{"title":"Dental Resin Monomers","description":"\u003cp\u003eResin monomers are fundamental building blocks for many resin-based dental materials, including dental composites, adhesives, sealants, and restorative materials.\u003c\/p\u003e\n\u003cp\u003eThese materials can be selected according to requirements such as polymerization behavior, viscosity, adhesion, mechanical properties, water absorption, and biocompatibility.\u003c\/p\u003e\n\u003cdiv class=\"ace-line ace-line old-record-id-CVpOdM3hyoVqR4x4BFacI3L1nXg\"\u003e\n\u003cp\u003e\u003ca href=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/J_K_Scientific-Dental_Resin_Monomers.pdf?v=1788320159\" target=\"_blank\" title=\"J\u0026amp;K Dental Resin Monomers\" rel=\"noopener\"\u003e—\u0026gt;Download Product List\u003c\/a\u003e\u003c\/p\u003e\n\u003cp\u003e\u003ca href=\"https:\/\/www.jk-sci.com\/pages\/request-bulk-quote\" rel=\"noopener\" target=\"_blank\"\u003e—\u0026gt; Request a Bulk Quote\u003c\/a\u003e\u003c\/p\u003e\n\u003cp\u003e\u003ca href=\"https:\/\/www.jk-sci.com\/pages\/contact-form\" rel=\"noopener\" target=\"_blank\"\u003e—\u0026gt; Contact Our Technical Team\u003c\/a\u003e\u003c\/p\u003e\n\u003c\/div\u003e","products":[{"product_id":"a01999070","title":"Tetrahydrofurfuryl acrylate, 98%, stabilized with MEHQ | 2399-48-6","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display: none !important;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eTetrahydrofurfuryl acrylate, 98%, stabilized with MEHQ\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eJ\u0026amp;K\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e999070\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2399-48-6\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Formula\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eC8H12O3\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Weight\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e156.18\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eSDS Document\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003ca href=\"https:\/\/web.jkchemical.com\/partial\/productMsdsFileByProductId\/EN\/66360\/1\" target=\"_blank\" rel=\"noopener noreferrer\"\u003eView\/Download\u003c\/a\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSynonyms\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cul\u003e\n                            \n                                \u003cli\u003eAcrylic acid tetrahydrofurfuryl ester\u003c\/li\u003e\n                            \n                                \u003cli\u003eTHFA\u003c\/li\u003e\n                            \n                        \u003c\/ul\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eProperties\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eDensity\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e1.064\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eBoiling Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e87\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eFlash Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e113\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003en20D\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e1.4560 to 1.4600\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSignal Word\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Warning\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eHazard Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eH315\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eH319\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003ePrecautionary Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eP280\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP321\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP302+P352\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP332+P317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP362+P364\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP264+P265\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP305+P351+P338\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP337+P317\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003eProduct Introduction\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eTetrahydrofurfuryl Acrylate (THFA, CAS No. 2399-48-6)\u003c\/strong\u003e is a functional monofunctional acrylate monomer containing a polymerizable acrylate group and a tetrahydrofuran ring.\u003c\/p\u003e\n\u003cp\u003eThe molecule combines the high reactivity of an acrylate double bond with the polarity and cyclic ether functionality of the tetrahydrofuran group. This structure makes THFA useful as a \u003cstrong\u003ereactive diluent and functional monomer\u003c\/strong\u003e for UV-curable and radiation-curable polymer systems.\u003c\/p\u003e\n\u003cp\u003eCommercial THFA is commonly supplied as a stabilized liquid. TCI reports \u003cstrong\u003e\u0026gt;98.0% GC purity\u003c\/strong\u003e, while other commercial grades are available at approximately 97–98% purity with polymerization inhibitors.\u003c\/p\u003e\n\u003cp\u003eTHFA is used in \u003cstrong\u003eUV-curable resins, adhesives, coatings, inks, 3D-printing resins, and specialty polymer synthesis\u003c\/strong\u003e. Arkema describes its commercial THFA monomer as a low-viscosity, polar, monofunctional monomer that promotes adhesion to numerous substrates.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003ePolymerization \/ Reaction Principle\u003c\/h2\u003e\n\u003cp\u003eTetrahydrofurfuryl Acrylate contains a polymerizable acrylate double bond:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCH₂=CHCOOCH₂C₄H₇O\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eUnder suitable free-radical initiation conditions, THFA undergoes addition polymerization:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003en CH₂=CHCOOCH₂C₄H₇O → \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e–CH₂–CH(COOCH₂C₄H₇O)–\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eₙ\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe tetrahydrofuran ring remains incorporated into the side chain of the resulting polymer.\u003c\/p\u003e\n\u003cp\u003eTHFA can also be copolymerized with other acrylate, methacrylate, or vinyl monomers to adjust:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer polarity\u003c\/li\u003e\n\u003cli\u003eAdhesion\u003c\/li\u003e\n\u003cli\u003eFlexibility\u003c\/li\u003e\n\u003cli\u003eSurface properties\u003c\/li\u003e\n\u003cli\u003eSolvency\u003c\/li\u003e\n\u003cli\u003eCrosslinking behavior\u003c\/li\u003e\n\u003cli\u003eFilm formation\u003c\/li\u003e\n\u003cli\u003eCuring performance\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe low viscosity and polar nature of THFA are particularly useful when formulating reactive resin systems.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eKey Research Applications\u003c\/h2\u003e\n\u003ch3\u003e\u003cstrong\u003e1. UV-Curable Resin\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is widely used as a \u003cstrong\u003ereactive monomer and reactive diluent in UV-curable resin systems\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable acrylic resins\u003c\/li\u003e\n\u003cli\u003eRadiation-curable polymers\u003c\/li\u003e\n\u003cli\u003eUV resin formulations\u003c\/li\u003e\n\u003cli\u003ePhotopolymer systems\u003c\/li\u003e\n\u003cli\u003eFunctional acrylic resins\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts low viscosity can help reduce formulation viscosity while allowing the monomer to become part of the cured polymer network rather than acting solely as a conventional solvent.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e2. 3D Printing Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is used in the development of \u003cstrong\u003ephotopolymer resins for additive manufacturing\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSLA 3D printing\u003c\/li\u003e\n\u003cli\u003eDLP 3D printing\u003c\/li\u003e\n\u003cli\u003eUV-curable 3D-printing resins\u003c\/li\u003e\n\u003cli\u003ePhotopolymer formulation\u003c\/li\u003e\n\u003cli\u003eRapid prototyping materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eJ\u0026amp;K Scientific specifically identifies Tetrahydrofurfuryl Acrylate for developing photopolymer resins used in \u003cstrong\u003e3D printing\u003c\/strong\u003e, while industry sources identify THFA among monomers used in UV-curable systems.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e3. UV-Curable Adhesives\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA can be incorporated into UV-curable adhesive formulations.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable adhesives\u003c\/li\u003e\n\u003cli\u003ePressure-sensitive adhesive research\u003c\/li\u003e\n\u003cli\u003eOptical adhesives\u003c\/li\u003e\n\u003cli\u003eElectronic-material adhesives\u003c\/li\u003e\n\u003cli\u003eSpecialty bonding materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts low viscosity and ability to promote adhesion to various substrates make it useful in adhesive formulations. Arkema specifically describes THFA as promoting adhesion to numerous substrates.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e4. Coatings\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is an important functional monomer for \u003cstrong\u003eacrylic and UV-curable coatings\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable coatings\u003c\/li\u003e\n\u003cli\u003eProtective coatings\u003c\/li\u003e\n\u003cli\u003eIndustrial coatings\u003c\/li\u003e\n\u003cli\u003eMetal coatings\u003c\/li\u003e\n\u003cli\u003ePlastic coatings\u003c\/li\u003e\n\u003cli\u003eFunctional surface coatings\u003c\/li\u003e\n\u003cli\u003eOutdoor coatings\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts incorporation into polymer formulations can contribute to adhesion, water resistance, chemical resistance, and film-forming performance. Commercial application information identifies THFA for coatings requiring durability and environmental resistance.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e5. UV-Curable Inks\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA can be used in radiation-curable ink formulations.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV printing inks\u003c\/li\u003e\n\u003cli\u003eUV inkjet inks\u003c\/li\u003e\n\u003cli\u003eDigital printing\u003c\/li\u003e\n\u003cli\u003eIndustrial printing\u003c\/li\u003e\n\u003cli\u003eFunctional inks\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts low viscosity and good dilution capability make it useful in reactive ink formulations. Kowa Chemicals identifies THFA for \u003cstrong\u003eUV inkjet inks\u003c\/strong\u003e, while other commercial sources list UV inks among its applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e6. Polymer and Copolymer Synthesis\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is a useful monomer for preparing specialty polymers and copolymers.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eAcrylic copolymers\u003c\/li\u003e\n\u003cli\u003eFunctional polymers\u003c\/li\u003e\n\u003cli\u003eSpecialty resins\u003c\/li\u003e\n\u003cli\u003eHydrophobic\/hydrophilic property modification\u003c\/li\u003e\n\u003cli\u003ePolymer structure–property studies\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts cyclic ether group provides an additional structural feature compared with simple alkyl acrylates, allowing researchers to tune polymer polarity and substrate interactions.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e7. Adhesives \u0026amp; Sealants\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA can be used in adhesive and sealant formulations as a reactive monomer.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eIndustrial adhesives\u003c\/li\u003e\n\u003cli\u003eUV adhesives\u003c\/li\u003e\n\u003cli\u003eSealants\u003c\/li\u003e\n\u003cli\u003eFlexible adhesive systems\u003c\/li\u003e\n\u003cli\u003eSpecialty bonding formulations\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eKowa Chemicals identifies THFA as a monomer used in \u003cstrong\u003eadhesives and sealants\u003c\/strong\u003e, with functions including adhesion and low viscosity.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e8. Bio-Based Polymer Materials\u003c\/h3\u003e\n\u003cp\u003eA bio-based version of THFA is commercially available, with TCI reporting approximately \u003cstrong\u003e62% bio-based carbon\u003c\/strong\u003e for its plant-derived-carbon product. This provides an option for research into more sustainable acrylate monomers and polymer formulations.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eBio-based polymer research\u003c\/li\u003e\n\u003cli\u003eSustainable UV-curable materials\u003c\/li\u003e\n\u003cli\u003eRenewable-content acrylate formulations\u003c\/li\u003e\n\u003cli\u003eGreen polymer chemistry\u003c\/li\u003e\n\u003cli\u003eBio-based coatings and resins\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eAdvantages\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eHighly reactive acrylate functionality\u003c\/li\u003e\n\u003cli\u003eMonofunctional reactive monomer\u003c\/li\u003e\n\u003cli\u003eLow viscosity\u003c\/li\u003e\n\u003cli\u003ePolar molecular structure\u003c\/li\u003e\n\u003cli\u003eContains a cyclic ether group\u003c\/li\u003e\n\u003cli\u003eGood dilution capability\u003c\/li\u003e\n\u003cli\u003eCan improve adhesion to various substrates\u003c\/li\u003e\n\u003cli\u003eSuitable for UV and radiation curing\u003c\/li\u003e\n\u003cli\u003eUseful for polymer and copolymer synthesis\u003c\/li\u003e\n\u003cli\u003eApplicable to coatings and adhesives\u003c\/li\u003e\n\u003cli\u003eSuitable for UV inks\u003c\/li\u003e\n\u003cli\u003eUseful in 3D-printing resin development\u003c\/li\u003e\n\u003cli\u003eStabilized grades available\u003c\/li\u003e\n\u003cli\u003eBio-based versions available\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eArkema characterizes THFA as a \u003cstrong\u003elow-viscosity, polar, monofunctional monomer\u003c\/strong\u003e with adhesion-promoting properties, while commercial technical data also highlights its dilution capability and suitability for UV-curable applications.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eStorage \u0026amp; Handling\u003c\/h2\u003e\n\u003cp\u003eTetrahydrofurfuryl Acrylate is a reactive acrylate monomer and is commonly supplied with a polymerization inhibitor such as \u003cstrong\u003eMEHQ or hydroquinone\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eStore in a tightly closed container.\u003c\/li\u003e\n\u003cli\u003eKeep in a cool, dry and well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eProtect from heat and direct sunlight.\u003c\/li\u003e\n\u003cli\u003eAvoid contamination with polymerization initiators.\u003c\/li\u003e\n\u003cli\u003eKeep away from strong oxidizing agents and incompatible materials.\u003c\/li\u003e\n\u003cli\u003eMaintain the recommended inhibitor concentration during storage.\u003c\/li\u003e\n\u003cli\u003eAvoid unnecessary exposure to elevated temperatures.\u003c\/li\u003e\n\u003cli\u003eWear appropriate gloves, protective clothing, and eye protection.\u003c\/li\u003e\n\u003cli\u003eAvoid direct contact with skin and eyes.\u003c\/li\u003e\n\u003cli\u003eHandle in an appropriate fume hood or well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eConsult the current SDS before use.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTCI recommends storing its THFA product in a cool, dark location below \u003cstrong\u003e15°C\u003c\/strong\u003e. Its current safety information identifies hazards including skin irritation, serious eye damage, skin sensitization, and aquatic toxicity; other supplier SDS classifications can vary with formulation and grade.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eResearch Areas\u003c\/h2\u003e\n\u003cdiv\u003e\u003cdiv\u003e\u003ctable\u003e\n\u003cthead\u003e\u003ctr\u003e\n\u003cth\u003eResearch Area\u003c\/th\u003e\n\u003cth\u003eSpecific Industry \/ Application\u003c\/th\u003e\n\u003c\/tr\u003e\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eUV-Curable Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV-curable resins, radiation-curable polymers, photopolymer formulations\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003e3D Printing\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eSLA\/DLP photopolymer resins, UV-curable additive-manufacturing materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eCoatings Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV coatings, protective coatings, plastic coatings, metal coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eAdhesives \u0026amp; Sealants\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV adhesives, industrial adhesives, specialty sealants\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePrinting \u0026amp; Ink Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV inks, UV inkjet inks, digital printing materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePolymer Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic copolymers, specialty polymers, functional resins\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eElectronics Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV-curable functional coatings and adhesive materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSurface Engineering\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAdhesion promotion, surface modification, wettability control\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSustainable Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eBio-based acrylate monomers and renewable-content polymer research\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eMaterials Science\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eStructure–property studies of functional acrylate polymers\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\u003c\/div\u003e\u003c\/div\u003e\n\u003cp\u003e\u003cstrong\u003eNote:\u003c\/strong\u003e Compared with HEMA (868-77-9), whose application in dental materials is well established, the currently available evidence for \u003cstrong\u003e2399-48-6 in dental materials is not strong enough to make dentistry a primary commercial application\u003c\/strong\u003e. For an SEO product page, it is more accurate to prioritize \u003cstrong\u003eUV curing, coatings, adhesives, inks, 3D printing, and polymer materials\u003c\/strong\u003e.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch3\u003eQ1: What is Tetrahydrofurfuryl Acrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Tetrahydrofurfuryl Acrylate (THFA) is a functional monofunctional acrylate monomer with \u003cstrong\u003eCAS No. 2399-48-6\u003c\/strong\u003e, molecular formula \u003cstrong\u003eC₈H₁₂O₃\u003c\/strong\u003e, and molecular weight \u003cstrong\u003e156.18 g\/mol\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ2: What is Tetrahydrofurfuryl Acrylate used for?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e THFA is mainly used in \u003cstrong\u003eUV-curable resins, coatings, adhesives, UV inks, 3D-printing photopolymer resins, and specialty polymer synthesis\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ3: Is THFA a monomer?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is a \u003cstrong\u003emonofunctional acrylate monomer\u003c\/strong\u003e that can undergo free-radical polymerization and copolymerization.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ4: Is Tetrahydrofurfuryl Acrylate used in UV curing?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used as a reactive monomer\/reactive diluent in UV-curable and radiation-curable formulations.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ5: Is THFA used in 3D printing?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used in the development of \u003cstrong\u003ephotopolymer resins for 3D printing\u003c\/strong\u003e, including UV-curable additive-manufacturing materials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ6: Is THFA used in coatings?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used in UV-curable and functional coating formulations, where its properties can contribute to adhesion and other coating performance characteristics.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ7: Is THFA used in adhesives?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used in UV-curable adhesives and other adhesive formulations, particularly where low viscosity and adhesion to substrates are important.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ8: Is Tetrahydrofurfuryl Acrylate stabilized?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. Commercial THFA is commonly supplied with polymerization inhibitors such as \u003cstrong\u003eMEHQ or hydroquinone\u003c\/strong\u003e to improve storage stability\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"J\u0026K Chemical","offers":[{"title":"1×50G","offer_id":45735529939134,"sku":"JK999070_50_G","price":48.0,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/374943.png?v=1791754126"},{"product_id":"a01283272","title":"Isobornyl methacrylate, 90%, stabilized with MEHQ | 7534-94-3","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display: none !important;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none 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5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eIsobornyl methacrylate, 90%, stabilized with MEHQ\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eJ\u0026amp;K\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e283272\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e7534-94-3\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Formula\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eC14H22O2\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Weight\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e222.32\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eSDS Document\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003ca href=\"https:\/\/web.jkchemical.com\/partial\/productMsdsFileByProductId\/EN\/27139\/1\" target=\"_blank\" rel=\"noopener noreferrer\"\u003eView\/Download\u003c\/a\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eProperties\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eDensity\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e0.983\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eBoiling Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e127-129\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eFlash Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e114\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003en20D\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e1.4770\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSignal Word\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Warning\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eHazard Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eH315\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eH319\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eH335\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003ePrecautionary Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eP280\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP321\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP261\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP271\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP319\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP405\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP501\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP302+P352\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP332+P317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP362+P364\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP264+P265\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP305+P351+P338\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP337+P317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP304+P340\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP403+P233\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003e\u003cspan\u003eProduct Introduction\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eIsobornyl Methacrylate is a sterically hindered methacrylate monomer derived from isoborneol and methacrylic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe molecule contains a bulky bicyclic isobornyl group attached to a methacrylate polymerizable unit. During polymerization, the methacrylate double bond participates in free-radical polymerization, while the rigid cyclic structure remains within the polymer backbone, contributing to increased hardness, dimensional stability, and hydrophobic properties.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eCompared with conventional low-molecular-weight methacrylate monomers, IBOMA provides enhanced rigidity and durability, making it an important monomer for high-performance polymer formulations.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eMechanism \/ Principle\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eIsobornyl Methacrylate polymerizes through the methacrylate vinyl group via free-radical polymerization.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eUnder UV irradiation, thermal initiation, or chemical initiation conditions, radicals attack the carbon–carbon double bond of the methacrylate group, forming polymer chains.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe bulky isobornyl group influences polymer chain mobility and molecular packing, which can improve:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eGlass transition temperature (Tg)\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eSurface hardness\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eChemical resistance\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eDimensional stability\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eMoisture resistance\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eThis makes IBOMA useful for designing high-performance acrylic polymers and resin systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eKey Research Applications\u003c\/span\u003e\u003c\/h2\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e1. UV-Curable Coatings\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIsobornyl Methacrylate is widely used in UV-curable resin research due to its rapid polymerization ability and contribution to coating hardness.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIt can be combined with photoinitiators and other acrylic monomers to develop protective coatings with improved durability, scratch resistance, and chemical resistance.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e2. Optical Materials and Optical Coatings\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA is investigated in optical polymer systems because its rigid bicyclic structure can contribute to dimensional stability, transparency, and controlled refractive properties.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eApplications include optical coatings, optical adhesives, and transparent polymer materials.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e3. Adhesives and Sealants\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe hydrophobic and rigid characteristics of IBOMA make it suitable for acrylic adhesive formulations.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eResearchers study its influence on adhesion strength, environmental resistance, flexibility, and long-term stability.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e4. Polymer Modification\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA is used as a functional monomer for modifying acrylic polymers and copolymers.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eBy incorporating IBOMA into polymer chains, researchers can adjust polymer hardness, Tg, water resistance, and mechanical properties.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e5. Advanced Acrylic Resins\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA is an important building block for high-performance acrylic resin systems used in coatings, inks, and specialty polymer formulations.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIts bulky structure helps improve polymer performance while maintaining methacrylate-based processing compatibility.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e6. Composite Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA can be incorporated into polymer composite systems to improve matrix properties, including rigidity, environmental stability, and resistance to moisture.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e7. Dental Materials Research\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eAlthough not as commonly used as Bis-GMA, HEMA, TEGDMA, or 10-MDP, IBOMA can be investigated as a hydrophobic methacrylate monomer in polymer-based dental material research.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIts rigid structure and hydrophobic characteristics may contribute to studies on resin formulation, water resistance, polymer network design, and dental composite matrix modification.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eAdvantages\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eRigid molecular structure:\u003c\/strong\u003e The bicyclic isobornyl group improves polymer rigidity and hardness.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eLow shrinkage characteristics:\u003c\/strong\u003e Suitable for applications requiring dimensional stability.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eHydrophobic performance:\u003c\/strong\u003e Helps improve moisture resistance of polymer materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eHigh compatibility:\u003c\/strong\u003e Can copolymerize with various acrylic and methacrylate monomers.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eImproved thermal properties:\u003c\/strong\u003e Contributes to higher Tg and enhanced polymer stability.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eBroad resin applications:\u003c\/strong\u003e Suitable for UV coatings, adhesives, optical polymers, and specialty acrylic materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCommercial stabilized grades:\u003c\/strong\u003e Usually supplied with MEHQ inhibitor for storage stability.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eStorage \u0026amp; Handling\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eStore in a \u003cstrong\u003ecool, dark, and well-ventilated area\u003c\/strong\u003e.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eRecommended storage temperature: \u003cstrong\u003ebelow 15 °C\u003c\/strong\u003e.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eProtect from heat, direct sunlight, and strong oxidizing conditions.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eKeep container tightly closed.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eCommercial products are generally stabilized with MEHQ to reduce premature polymerization.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eAvoid unnecessary exposure to polymerization initiators.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eWear appropriate protective gloves, clothing, and eye protection during handling.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eResearch Areas\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eThis product can support research, formulation development, and material innovation across the following specific industries:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eUV-Curable Materials\u003c\/strong\u003e – UV coatings, radiation-curable resins, protective coatings, and light-curing polymer systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003ePolymer Materials\u003c\/strong\u003e – Acrylic polymers, methacrylate copolymers, functional resin systems, and polymer modification.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCoatings Industry\u003c\/strong\u003e – High-hardness coatings, automotive coatings, industrial coatings, and protective surface coatings.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdhesives \u0026amp; Sealants\u003c\/strong\u003e – Acrylic adhesives, structural adhesives, and moisture-resistant bonding systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eOptical Materials\u003c\/strong\u003e – Optical polymers, transparent resins, optical adhesives, and functional coatings.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eComposite Materials\u003c\/strong\u003e – Polymer composites, reinforced resin systems, and hybrid materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e – Hydrophobic methacrylate resin systems, dental composite formulations, and polymer network research.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ1. What is Isobornyl Methacrylate?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIsobornyl Methacrylate (IBOMA) is a rigid cyclic methacrylate monomer used in UV-curable materials, coatings, adhesives, and polymer research.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ2. What are the main applications of IBOMA?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIBOMA is mainly used in UV-curable coatings, adhesives, optical materials, acrylic polymers, and specialty resin systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ3. Why is IBOMA used in polymer materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIts bulky rigid structure can improve polymer hardness, thermal properties, dimensional stability, and moisture resistance.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ4. Is IBOMA a monomer or polymer?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIBOMA is a \u003cstrong\u003emethacrylate monomer\u003c\/strong\u003e that can polymerize into acrylic and methacrylate-based polymers.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ5. Is IBOMA used in dental materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIBOMA can be investigated in dental polymer research as a hydrophobic methacrylate component, although common dental monomers include Bis-GMA, HEMA, TEGDMA, UDMA, and 10-MDP.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ6. Why is MEHQ added to IBOMA?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eMEHQ is added as a polymerization inhibitor to improve storage stability and prevent premature polymerization.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ7. How should IBOMA be stored?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eStore IBOMA in a cool, dark place below 15 °C and follow supplier SDS recommendations.\u003c\/span\u003e\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"J\u0026K Chemical","offers":[{"title":"1×250g","offer_id":45737926295742,"sku":"JK283272_250_G","price":53.0,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/223812_697d704b-39d4-4f94-9ef0-494db71969f5.png?v=1791770506"},{"product_id":"a01175528","title":"3-(Trimethoxysilyl)propyl methacrylate, 98% | 2530-85-0","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display: none !important;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e3-(Trimethoxysilyl)propyl methacrylate, 98%\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eJ\u0026amp;K\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e175528\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2530-85-0\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eSDS Document\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003ca href=\"https:\/\/web.jkchemical.com\/partial\/productMsdsFileByProductId\/EN\/14422\/1\" target=\"_blank\" rel=\"noopener noreferrer\"\u003eView\/Download\u003c\/a\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003e\u003cspan\u003eProduct Introduction\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is a functional silane coupling agent designed to improve adhesion between organic polymers and inorganic substrates.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe methacrylate functionality allows this molecule to participate in free-radical polymerization with acrylic and methacrylate-based resins, while the trimethoxysilane group undergoes hydrolysis and condensation reactions to form strong bonds with inorganic surfaces such as glass, silica, ceramics, and metal oxides.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eBecause of its dual reactivity, this compound is widely investigated in polymer–inorganic hybrid materials, composite reinforcement, dental resin systems, and surface-functionalized materials.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eMechanism \/ Principle\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eThe functionality of 3-(Trimethoxysilyl)propyl Methacrylate comes from its two reactive ends.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe \u003cstrong\u003etrimethoxysilane group\u003c\/strong\u003e can hydrolyze in the presence of moisture to generate silanol groups (Si–OH). These groups can subsequently condense with hydroxyl-containing surfaces such as silica, glass, ceramic, and metal oxides to form stable Si–O–Si or Si–O–M bonds.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe \u003cstrong\u003emethacrylate group\u003c\/strong\u003e can undergo free-radical polymerization with resin monomers, creating a covalent connection between inorganic fillers and organic polymer matrices.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThis mechanism allows improved interfacial adhesion, mechanical strength, durability, and compatibility in composite systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eKey Research Applications\u003c\/span\u003e\u003c\/h2\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e1. Dental Composite Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is widely studied as a silane coupling agent in dental composite materials. It can improve the bonding between inorganic fillers such as silica-based particles and methacrylate resin matrices.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIn dental restorative materials, silane coupling agents help enhance filler dispersion, interfacial bonding, mechanical properties, and long-term stability.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e2. Dental Adhesives and Restorative Systems\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThis compound is relevant to research on dental bonding systems, resin-based restorative materials, and filler-modified dental composites.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIts ability to connect inorganic dental fillers with polymer resin networks makes it valuable for improving adhesion and material performance.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e3. Polymer Composite Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe compound is commonly used in polymer composite research to improve compatibility between organic polymers and inorganic fillers.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eApplications include glass fiber reinforced polymers, silica-filled composites, ceramic-polymer composites, and hybrid material systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e4. Surface Modification\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is widely investigated for modifying glass, silica, ceramic, and metal oxide surfaces.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSurface treatment with this silane can introduce polymerizable methacrylate functionality onto inorganic surfaces for subsequent polymer coating or composite formation.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e5. Adhesives and Sealants\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eAs a coupling promoter, this compound can improve adhesion between polymer adhesives and inorganic substrates.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIt is relevant to acrylic adhesives, sealants, coating formulations, and bonding technologies.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e6. Coatings and Functional Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe molecule is used in research involving functional coatings, protective layers, hybrid organic-inorganic coatings, and surface-engineered materials.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e7. Organic-Inorganic Hybrid Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe dual functionality of 3-(Trimethoxysilyl)propyl Methacrylate makes it suitable for preparing hybrid materials that combine polymer properties with inorganic characteristics.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eAdvantages\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDual reactive functionality:\u003c\/strong\u003e Combines silane coupling capability and methacrylate polymerization ability.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eStrong interface bonding:\u003c\/strong\u003e Improves adhesion between organic polymers and inorganic surfaces.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental material compatibility:\u003c\/strong\u003e Suitable for silica-filled dental composites and resin systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eComposite reinforcement:\u003c\/strong\u003e Enhances filler–matrix interaction in polymer composites.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eSurface modification capability:\u003c\/strong\u003e Enables functionalization of glass, silica, ceramic, and metal oxide surfaces.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eBroad material applications:\u003c\/strong\u003e Applicable to adhesives, coatings, polymers, composites, and hybrid materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCommercial availability:\u003c\/strong\u003e Available in stabilized high-purity research grades.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eStorage \u0026amp; Handling\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eStore in a cool, dry, and well-ventilated area.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eProtect from moisture and direct light.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eStore under inert gas when possible.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eTCI recommends storage in a cool and dark place below 15 °C.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eAvoid prolonged exposure to humidity because silane groups are moisture sensitive.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eKeep away from heat sources and polymerization initiators.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eWear appropriate gloves, protective clothing, and eye protection during handling.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eAvoid skin and eye contact.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eResearch Areas\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eThis product can support research, formulation development, and material innovation across the following specific industries:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e – Dental composite resins, restorative materials, filler surface treatment, dental bonding systems, and resin-based dental materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental Restorative Materials\u003c\/strong\u003e – Silica-filled composites, ceramic-reinforced dental materials, and resin–filler interface optimization.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003ePolymer Composite Materials\u003c\/strong\u003e – Glass fiber composites, silica-filled polymers, ceramic-polymer composites, and hybrid composites.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdhesives \u0026amp; Sealants\u003c\/strong\u003e – Acrylic adhesives, bonding agents, and interface-enhanced adhesive formulations.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eSurface Modification\u003c\/strong\u003e – Functionalization of glass, silica, ceramics, and metal oxide surfaces.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCoatings \u0026amp; Surface Engineering\u003c\/strong\u003e – Protective coatings, functional coatings, and organic-inorganic hybrid coatings.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdvanced Materials\u003c\/strong\u003e – Hybrid materials, nanocomposites, and polymer-inorganic interface research.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ1. What is 3-(Trimethoxysilyl)propyl Methacrylate?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is a silane coupling agent containing both a methacrylate polymerizable group and a trimethoxysilane functional group.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ2. What is KH-570?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eKH-570 is a common commercial name for 3-(Trimethoxysilyl)propyl Methacrylate.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ3. Is this product used in dental materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eYes. It is widely studied as a silane coupling agent for dental composite materials, especially for improving bonding between inorganic fillers and resin matrices.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ4. How does this compound improve composite materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIt forms chemical bridges between inorganic fillers and polymer matrices, improving interfacial adhesion and material performance.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ5. Is it a monomer or coupling agent?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIt can function as both a functional methacrylate monomer and a silane coupling agent.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ6. What materials can it modify?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIt is commonly used for glass, silica, ceramics, metal oxides, and other hydroxyl-containing inorganic surfaces.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ7. How should it be stored?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eStore tightly sealed in a cool, dry, dark environment and protect from moisture.\u003c\/span\u003e\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"J\u0026K Chemical","offers":[{"title":"1×100ML","offer_id":46416407855294,"sku":"JK175528_100_ML","price":35.2,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/282165.png?v=1791775608"},{"product_id":"a01969669","title":"2-Hydroxyethyl methacrylate, 98%, stabilized with 200 ppm MEHQ,  ＜20 APHA | 868-77-9","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display: none !important;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    border-bottom: none;\n  }\n\n  .section-row .row-key {\n    grid-column: 1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2-Hydroxyethyl methacrylate, 98%, stabilized with 200 ppm MEHQ,  ＜20 APHA\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eJ\u0026amp;K\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e969669\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e868-77-9\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Formula\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eC6H10O3\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Weight\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e130.14\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eSDS Document\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003ca href=\"https:\/\/web.jkchemical.com\/partial\/productMsdsFileByProductId\/EN\/61754\/1\" target=\"_blank\" rel=\"noopener noreferrer\"\u003eView\/Download\u003c\/a\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSynonyms\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eEthylene glycol monomethacrylate\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eProperties\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eDensity\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e1.073\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eMelting Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e-12\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eBoiling Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e205-208\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eFlash Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e101\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003en20D\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e1.4490-1.4540\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eGHS Symbols\u003c\/div\u003e\n                    \u003cdiv class=\"row-value ghs-symbols-row\"\u003e\n                        \n                            \u003cdiv class=\"hazard-symbol-container\"\u003e\u003cimg class=\"hazard-symbol\" src=\"https:\/\/supplier-images.jk-data.com\/jk-sci\/hazard\/GHS07.svg\" alt=\"Hazard Symbol\"\u003e\u003c\/div\u003e\n                        \n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSignal Word\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Warning\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eHazard Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eH315\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eH317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eH319\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003ePrecautionary Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eP280\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP321\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP261\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP272\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP501\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP302+P352\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP332+P317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP362+P364\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP333+P317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP264+P265\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP305+P351+P338\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP337+P317\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003eProduct Introduction\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003e2-Hydroxyethyl Methacrylate (HEMA, CAS No. 868-77-9)\u003c\/strong\u003e is a hydroxy-functional methacrylate monomer containing both a polymerizable methacrylate group and a terminal hydroxyl group. Its molecular formula is C₆H₁₀O₃ and molecular weight is 130.14 g\/mol.\u003c\/p\u003e\n\u003cp\u003eThe methacrylate double bond enables HEMA to participate in free-radical polymerization, while the hydroxyl group provides additional hydrophilicity and opportunities for hydrogen bonding, esterification, crosslinking, and surface modification.\u003c\/p\u003e\n\u003cp\u003eHEMA is an important building block for \u003cstrong\u003ehydrophilic polymers, hydrogels, biomaterials, dental materials, contact-lens materials, coatings, adhesives, and functional polymer systems\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003ch2\u003ePolymerization \/ Reaction Principle\u003c\/h2\u003e\n\u003cp\u003eHEMA contains a polymerizable carbon-carbon double bond:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCH₂=C(CH₃)COOCH₂CH₂OH\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eUnder suitable free-radical initiation conditions, HEMA undergoes addition polymerization to form \u003cstrong\u003epoly(2-hydroxyethyl methacrylate) (PHEMA)\u003c\/strong\u003e:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003en CH₂=C(CH₃)COOCH₂CH₂OH → \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e–CH₂–C(CH₃)(COOCH₂CH₂OH)–\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eₙ\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe resulting PHEMA contains hydrophilic hydroxyl groups and can absorb water, making it useful for hydrogel and biomaterial research.\u003c\/p\u003e\n\u003cp\u003eHEMA can also be copolymerized with other methacrylate or acrylic monomers to tune:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eHydrophilicity\u003c\/li\u003e\n\u003cli\u003eWater absorption\u003c\/li\u003e\n\u003cli\u003eMechanical properties\u003c\/li\u003e\n\u003cli\u003eCrosslinking density\u003c\/li\u003e\n\u003cli\u003eSurface wettability\u003c\/li\u003e\n\u003cli\u003eAdhesion\u003c\/li\u003e\n\u003cli\u003eOptical properties\u003c\/li\u003e\n\u003cli\u003eBiocompatibility-related material characteristics\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003ePHEMA and HEMA-based copolymers are widely investigated as hydrophilic polymer and hydrogel materials.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eKey Research Applications\u003c\/h2\u003e\n\u003ch3\u003e\u003cstrong\u003e1. Dental Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eHEMA is an important monomer in dental materials research\u003c\/strong\u003e, particularly in resin-based restorative and adhesive systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eDental adhesive systems\u003c\/li\u003e\n\u003cli\u003eDentin bonding research\u003c\/li\u003e\n\u003cli\u003eDental resin formulations\u003c\/li\u003e\n\u003cli\u003eDental composite materials\u003c\/li\u003e\n\u003cli\u003eResin-based restorative materials\u003c\/li\u003e\n\u003cli\u003eDental polymer materials\u003c\/li\u003e\n\u003cli\u003eDental bonding interfaces\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA can contribute hydrophilic characteristics and improve interaction between resin systems and moist dentin surfaces. HEMA and HEMA-based polymers have also been investigated in dental composite materials and dental-pulp-related research.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eResearch focus:\u003c\/strong\u003e dental resin formulation, polymerization behavior, dentin bonding, water uptake, interface stability, and dental biomaterials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e2. Contact Lens Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is historically important in the development of \u003cstrong\u003ehydrophilic contact-lens materials\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003ePolymerization of HEMA can produce hydrophilic PHEMA-based materials capable of absorbing and retaining water.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSoft contact lens materials\u003c\/li\u003e\n\u003cli\u003eHydrogel contact lenses\u003c\/li\u003e\n\u003cli\u003eHydrogel polymer research\u003c\/li\u003e\n\u003cli\u003eOphthalmic biomaterials\u003c\/li\u003e\n\u003cli\u003eContact-lens surface modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e3. Biomedical Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is widely used as a monomer for preparing hydrophilic polymers and hydrogel materials.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eBiomedical hydrogels\u003c\/li\u003e\n\u003cli\u003eBiomaterial development\u003c\/li\u003e\n\u003cli\u003eTissue-engineering materials\u003c\/li\u003e\n\u003cli\u003eDrug-delivery systems\u003c\/li\u003e\n\u003cli\u003eBiointerfaces\u003c\/li\u003e\n\u003cli\u003eFunctional polymeric biomaterials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTCI specifically classifies HEMA under \u003cstrong\u003eBiomaterials \/ Biocompatible Materials Research Reagents\u003c\/strong\u003e and \u003cstrong\u003eMonomers and Macromonomers\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e4. Drug Delivery\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA-based hydrogels can be designed to absorb water and provide controlled polymer networks.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eDrug-delivery hydrogels\u003c\/li\u003e\n\u003cli\u003eControlled-release materials\u003c\/li\u003e\n\u003cli\u003eStimuli-responsive polymer systems\u003c\/li\u003e\n\u003cli\u003eWater-soluble polymer systems\u003c\/li\u003e\n\u003cli\u003eBiomedical polymer research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA-based hydrogel systems have been investigated for drug-release and drug-delivery applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e5. Coatings\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can be incorporated into acrylic and methacrylate polymer systems to introduce hydroxyl functionality.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFunctional coatings\u003c\/li\u003e\n\u003cli\u003eAcrylic coatings\u003c\/li\u003e\n\u003cli\u003eUV-curable coatings\u003c\/li\u003e\n\u003cli\u003eProtective coatings\u003c\/li\u003e\n\u003cli\u003eSurface-modification coatings\u003c\/li\u003e\n\u003cli\u003ePolymer coating research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe hydroxyl group can provide additional sites for interactions and crosslinking with other components.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e6. Adhesives\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is used as a functional monomer in adhesive polymer systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eAcrylic adhesives\u003c\/li\u003e\n\u003cli\u003ePressure-sensitive adhesives\u003c\/li\u003e\n\u003cli\u003eStructural adhesive research\u003c\/li\u003e\n\u003cli\u003eWater-compatible adhesives\u003c\/li\u003e\n\u003cli\u003eDental adhesives\u003c\/li\u003e\n\u003cli\u003ePolymer adhesion research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe combination of a polymerizable methacrylate group and hydroxyl functionality makes HEMA useful for modifying adhesion and polymer–substrate interactions.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e7. Photosensitive Resins and UV-Curable Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can participate in polymerization and crosslinking reactions used to develop photosensitive polymer systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable resins\u003c\/li\u003e\n\u003cli\u003ePhotosensitive coatings\u003c\/li\u003e\n\u003cli\u003ePhotopolymer research\u003c\/li\u003e\n\u003cli\u003eResin modification\u003c\/li\u003e\n\u003cli\u003eFunctional acrylic polymers\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e8. Fiber and Textile Treatment\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can be incorporated into polymer systems designed to modify fiber surfaces.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFiber treatment agents\u003c\/li\u003e\n\u003cli\u003ePolymer surface modification\u003c\/li\u003e\n\u003cli\u003eTextile functionalization\u003c\/li\u003e\n\u003cli\u003eHydrophilic surface modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eCommercial application references also identify HEMA for fiber-treatment and acrylic resin modification.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eAdvantages\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eReactive methacrylate functional group\u003c\/li\u003e\n\u003cli\u003eHydroxyl-functional monomer\u003c\/li\u003e\n\u003cli\u003eSuitable for free-radical polymerization\u003c\/li\u003e\n\u003cli\u003eProduces hydrophilic polymers\u003c\/li\u003e\n\u003cli\u003eUseful for hydrogel preparation\u003c\/li\u003e\n\u003cli\u003eSuitable for copolymerization\u003c\/li\u003e\n\u003cli\u003eWidely used in dental materials research\u003c\/li\u003e\n\u003cli\u003eUseful for biomedical polymer research\u003c\/li\u003e\n\u003cli\u003eSuitable for contact-lens material development\u003c\/li\u003e\n\u003cli\u003eApplicable to coatings and adhesives\u003c\/li\u003e\n\u003cli\u003eUseful for surface functionalization\u003c\/li\u003e\n\u003cli\u003eAvailable in multiple purity grades\u003c\/li\u003e\n\u003cli\u003eCommercially available in stabilized formulations\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eStorage \u0026amp; Handling\u003c\/h2\u003e\n\u003cp\u003eHEMA is a reactive methacrylate monomer and is commonly supplied with a polymerization inhibitor such as \u003cstrong\u003eMEHQ\u003c\/strong\u003e to improve storage stability. Commercial specifications from Sigma-Aldrich include grades containing ≤50 ppm or ≤250 ppm MEHQ.\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eStore in a tightly closed container.\u003c\/li\u003e\n\u003cli\u003eStore in a cool, dry and well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eProtect from excessive heat and direct light.\u003c\/li\u003e\n\u003cli\u003eKeep away from strong oxidizing agents and incompatible chemicals.\u003c\/li\u003e\n\u003cli\u003eAvoid unnecessary exposure to heat because methacrylate monomers can polymerize.\u003c\/li\u003e\n\u003cli\u003eMaintain appropriate inhibitor concentration during storage.\u003c\/li\u003e\n\u003cli\u003eAvoid direct skin and eye contact.\u003c\/li\u003e\n\u003cli\u003eWear suitable gloves, protective clothing, and eye protection.\u003c\/li\u003e\n\u003cli\u003eHandle in a suitable fume hood or well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eConsult the current SDS before handling.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA can cause skin sensitization, so appropriate measures should be taken to minimize skin exposure. PubChem notes the sensitizing potential associated with methacrylates.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eResearch Areas\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003e2-Hydroxyethyl Methacrylate (CAS No. 868-77-9)\u003c\/strong\u003e can be positioned across several specific industries and research fields:\u003c\/p\u003e\n\u003cdiv\u003e\u003cdiv\u003e\u003ctable\u003e\n\u003cthead\u003e\u003ctr\u003e\n\u003cth\u003eResearch Area\u003c\/th\u003e\n\u003cth\u003eSpecific Industry \/ Application\u003c\/th\u003e\n\u003c\/tr\u003e\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eDental adhesives, dentin bonding, dental composites, resin-based restorative materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eContact Lens Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eSoft contact lenses, hydrogel lenses, ophthalmic biomaterials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eBiomedical Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrogels, biomaterials, biointerfaces, tissue-engineering materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDrug Delivery\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eControlled-release hydrogels, drug-delivery polymer systems\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eMedical Devices\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrophilic polymer coatings and functional polymer materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eCoatings\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic coatings, UV-curable coatings, functional surface coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eAdhesives\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic adhesives, pressure-sensitive adhesives, dental adhesives\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePolymer Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic\/methacrylate copolymers and functional polymer synthesis\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePhotosensitive Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003ePhotopolymerizable resins and photosensitive coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eFiber \u0026amp; Textile\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eFiber treatment and polymer-based surface modification\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSurface Engineering\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrophilic surface modification and polymer interface engineering\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\u003c\/div\u003e\u003c\/div\u003e\n\u003cp\u003eTCI's current application classification specifically includes \u003cstrong\u003eDental Materials Research Reagents\u003c\/strong\u003e, \u003cstrong\u003eBiomaterials\/ Biocompatible Materials\u003c\/strong\u003e, \u003cstrong\u003eMethacrylate Monomers\u003c\/strong\u003e, \u003cstrong\u003eDrug Delivery Systems\u003c\/strong\u003e, and \u003cstrong\u003eDouble Network Gel synthesis\u003c\/strong\u003e for HEMA.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch3\u003eQ1: What is 2-Hydroxyethyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e 2-Hydroxyethyl Methacrylate (HEMA) is a hydroxy-functional methacrylate monomer with \u003cstrong\u003eCAS No. 868-77-9\u003c\/strong\u003e, molecular formula \u003cstrong\u003eC₆H₁₀O₃\u003c\/strong\u003e, and molecular weight \u003cstrong\u003e130.14 g\/mol\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ2: What is HEMA used for?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e HEMA is used to prepare \u003cstrong\u003ehydrophilic polymers, hydrogels, dental materials, contact-lens materials, biomedical materials, coatings, adhesives, and functional acrylic polymers\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ3: Is HEMA used in dental materials?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is widely used in \u003cstrong\u003edental materials research\u003c\/strong\u003e, particularly in dental adhesive and resin systems. TCI explicitly lists HEMA under Dental Materials Research Reagents.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ4: Why is HEMA used in dental adhesives?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Its methacrylate group enables polymerization, while its hydroxyl group contributes hydrophilicity and interactions with substrates, making HEMA useful in dental adhesive formulations and dentin-bonding research.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ5: Is HEMA used for contact lenses?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is an important monomer for preparing \u003cstrong\u003ehydrophilic PHEMA-based hydrogel materials\u003c\/strong\u003e, historically associated with soft contact-lens materials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ6: What polymer is produced from HEMA?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Polymerization of HEMA produces \u003cstrong\u003epoly(2-hydroxyethyl methacrylate), or PHEMA\u003c\/strong\u003e, a hydrophilic polymer widely investigated in hydrogel and biomaterial research.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ7: Is HEMA used in biomedical research?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is used as a monomer for developing \u003cstrong\u003ehydrogels, biomaterials, drug-delivery systems, and other functional polymeric materials\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ8: Is HEMA supplied with an inhibitor?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. Commercial HEMA is commonly supplied in stabilized form, such as \u003cstrong\u003eMEHQ-stabilized HEMA\u003c\/strong\u003e, to reduce unwanted polymerization during storage.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n               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#e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2-Hydroxyethyl methacrylate, 98%, stabilized with 200 ppm MEHQ\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eJ\u0026amp;K\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e225147\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e868-77-9\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Formula\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eC6H10O3\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eMolecular Weight\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e130.14\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eSDS Document\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003ca href=\"https:\/\/web.jkchemical.com\/partial\/productMsdsFileByProductId\/EN\/20449\/1\" target=\"_blank\" rel=\"noopener noreferrer\"\u003eView\/Download\u003c\/a\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSynonyms\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eEthylene glycol monomethacrylate\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eProperties\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eDensity\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e1.073\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eMelting Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e-12\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eBoiling Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e205-208\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eFlash Point\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e101\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003en20D\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e1.4490-1.4540\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eSafety Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSignal Word\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Warning\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eHazard Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eH315\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eH317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eH319\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003ePrecautionary Statement\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        \u003cdiv class=\"hazard-grid\"\u003e\n                            \n                                \u003cdiv\u003eP280\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP321\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP261\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP272\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP501\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP302+P352\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP332+P317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP362+P364\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP333+P317\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP264+P265\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP305+P351+P338\u003c\/div\u003e\n                            \n                                \u003cdiv\u003eP337+P317\u003c\/div\u003e\n                            \n                        \u003c\/div\u003e\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n\n            \n\n            \n\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eStorage Condition\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003e\n                        Store at 2-8℃\n                    \u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003eProduct Introduction\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003e2-Hydroxyethyl Methacrylate (HEMA, CAS No. 868-77-9)\u003c\/strong\u003e is a hydroxy-functional methacrylate monomer containing both a polymerizable methacrylate group and a terminal hydroxyl group. Its molecular formula is C₆H₁₀O₃ and molecular weight is 130.14 g\/mol.\u003c\/p\u003e\n\u003cp\u003eThe methacrylate double bond enables HEMA to participate in free-radical polymerization, while the hydroxyl group provides additional hydrophilicity and opportunities for hydrogen bonding, esterification, crosslinking, and surface modification.\u003c\/p\u003e\n\u003cp\u003eHEMA is an important building block for \u003cstrong\u003ehydrophilic polymers, hydrogels, biomaterials, dental materials, contact-lens materials, coatings, adhesives, and functional polymer systems\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003ch2\u003ePolymerization \/ Reaction Principle\u003c\/h2\u003e\n\u003cp\u003eHEMA contains a polymerizable carbon-carbon double bond:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCH₂=C(CH₃)COOCH₂CH₂OH\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eUnder suitable free-radical initiation conditions, HEMA undergoes addition polymerization to form \u003cstrong\u003epoly(2-hydroxyethyl methacrylate) (PHEMA)\u003c\/strong\u003e:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003en CH₂=C(CH₃)COOCH₂CH₂OH → \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e–CH₂–C(CH₃)(COOCH₂CH₂OH)–\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eₙ\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe resulting PHEMA contains hydrophilic hydroxyl groups and can absorb water, making it useful for hydrogel and biomaterial research.\u003c\/p\u003e\n\u003cp\u003eHEMA can also be copolymerized with other methacrylate or acrylic monomers to tune:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eHydrophilicity\u003c\/li\u003e\n\u003cli\u003eWater absorption\u003c\/li\u003e\n\u003cli\u003eMechanical properties\u003c\/li\u003e\n\u003cli\u003eCrosslinking density\u003c\/li\u003e\n\u003cli\u003eSurface wettability\u003c\/li\u003e\n\u003cli\u003eAdhesion\u003c\/li\u003e\n\u003cli\u003eOptical properties\u003c\/li\u003e\n\u003cli\u003eBiocompatibility-related material characteristics\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003ePHEMA and HEMA-based copolymers are widely investigated as hydrophilic polymer and hydrogel materials.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eKey Research Applications\u003c\/h2\u003e\n\u003ch3\u003e\u003cstrong\u003e1. Dental Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eHEMA is an important monomer in dental materials research\u003c\/strong\u003e, particularly in resin-based restorative and adhesive systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eDental adhesive systems\u003c\/li\u003e\n\u003cli\u003eDentin bonding research\u003c\/li\u003e\n\u003cli\u003eDental resin formulations\u003c\/li\u003e\n\u003cli\u003eDental composite materials\u003c\/li\u003e\n\u003cli\u003eResin-based restorative materials\u003c\/li\u003e\n\u003cli\u003eDental polymer materials\u003c\/li\u003e\n\u003cli\u003eDental bonding interfaces\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA can contribute hydrophilic characteristics and improve interaction between resin systems and moist dentin surfaces. HEMA and HEMA-based polymers have also been investigated in dental composite materials and dental-pulp-related research.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eResearch focus:\u003c\/strong\u003e dental resin formulation, polymerization behavior, dentin bonding, water uptake, interface stability, and dental biomaterials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e2. Contact Lens Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is historically important in the development of \u003cstrong\u003ehydrophilic contact-lens materials\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003ePolymerization of HEMA can produce hydrophilic PHEMA-based materials capable of absorbing and retaining water.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSoft contact lens materials\u003c\/li\u003e\n\u003cli\u003eHydrogel contact lenses\u003c\/li\u003e\n\u003cli\u003eHydrogel polymer research\u003c\/li\u003e\n\u003cli\u003eOphthalmic biomaterials\u003c\/li\u003e\n\u003cli\u003eContact-lens surface modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e3. Biomedical Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is widely used as a monomer for preparing hydrophilic polymers and hydrogel materials.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eBiomedical hydrogels\u003c\/li\u003e\n\u003cli\u003eBiomaterial development\u003c\/li\u003e\n\u003cli\u003eTissue-engineering materials\u003c\/li\u003e\n\u003cli\u003eDrug-delivery systems\u003c\/li\u003e\n\u003cli\u003eBiointerfaces\u003c\/li\u003e\n\u003cli\u003eFunctional polymeric biomaterials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTCI specifically classifies HEMA under \u003cstrong\u003eBiomaterials \/ Biocompatible Materials Research Reagents\u003c\/strong\u003e and \u003cstrong\u003eMonomers and Macromonomers\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e4. Drug Delivery\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA-based hydrogels can be designed to absorb water and provide controlled polymer networks.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eDrug-delivery hydrogels\u003c\/li\u003e\n\u003cli\u003eControlled-release materials\u003c\/li\u003e\n\u003cli\u003eStimuli-responsive polymer systems\u003c\/li\u003e\n\u003cli\u003eWater-soluble polymer systems\u003c\/li\u003e\n\u003cli\u003eBiomedical polymer research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA-based hydrogel systems have been investigated for drug-release and drug-delivery applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e5. Coatings\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can be incorporated into acrylic and methacrylate polymer systems to introduce hydroxyl functionality.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFunctional coatings\u003c\/li\u003e\n\u003cli\u003eAcrylic coatings\u003c\/li\u003e\n\u003cli\u003eUV-curable coatings\u003c\/li\u003e\n\u003cli\u003eProtective coatings\u003c\/li\u003e\n\u003cli\u003eSurface-modification coatings\u003c\/li\u003e\n\u003cli\u003ePolymer coating research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe hydroxyl group can provide additional sites for interactions and crosslinking with other components.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e6. Adhesives\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is used as a functional monomer in adhesive polymer systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eAcrylic adhesives\u003c\/li\u003e\n\u003cli\u003ePressure-sensitive adhesives\u003c\/li\u003e\n\u003cli\u003eStructural adhesive research\u003c\/li\u003e\n\u003cli\u003eWater-compatible adhesives\u003c\/li\u003e\n\u003cli\u003eDental adhesives\u003c\/li\u003e\n\u003cli\u003ePolymer adhesion research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe combination of a polymerizable methacrylate group and hydroxyl functionality makes HEMA useful for modifying adhesion and polymer–substrate interactions.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e7. Photosensitive Resins and UV-Curable Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can participate in polymerization and crosslinking reactions used to develop photosensitive polymer systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable resins\u003c\/li\u003e\n\u003cli\u003ePhotosensitive coatings\u003c\/li\u003e\n\u003cli\u003ePhotopolymer research\u003c\/li\u003e\n\u003cli\u003eResin modification\u003c\/li\u003e\n\u003cli\u003eFunctional acrylic polymers\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e8. Fiber and Textile Treatment\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can be incorporated into polymer systems designed to modify fiber surfaces.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFiber treatment agents\u003c\/li\u003e\n\u003cli\u003ePolymer surface modification\u003c\/li\u003e\n\u003cli\u003eTextile functionalization\u003c\/li\u003e\n\u003cli\u003eHydrophilic surface modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eCommercial application references also identify HEMA for fiber-treatment and acrylic resin modification.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eAdvantages\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eReactive methacrylate functional group\u003c\/li\u003e\n\u003cli\u003eHydroxyl-functional monomer\u003c\/li\u003e\n\u003cli\u003eSuitable for free-radical polymerization\u003c\/li\u003e\n\u003cli\u003eProduces hydrophilic polymers\u003c\/li\u003e\n\u003cli\u003eUseful for hydrogel preparation\u003c\/li\u003e\n\u003cli\u003eSuitable for copolymerization\u003c\/li\u003e\n\u003cli\u003eWidely used in dental materials research\u003c\/li\u003e\n\u003cli\u003eUseful for biomedical polymer research\u003c\/li\u003e\n\u003cli\u003eSuitable for contact-lens material development\u003c\/li\u003e\n\u003cli\u003eApplicable to coatings and adhesives\u003c\/li\u003e\n\u003cli\u003eUseful for surface functionalization\u003c\/li\u003e\n\u003cli\u003eAvailable in multiple purity grades\u003c\/li\u003e\n\u003cli\u003eCommercially available in stabilized formulations\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eStorage \u0026amp; Handling\u003c\/h2\u003e\n\u003cp\u003eHEMA is a reactive methacrylate monomer and is commonly supplied with a polymerization inhibitor such as \u003cstrong\u003eMEHQ\u003c\/strong\u003e to improve storage stability. Commercial specifications from Sigma-Aldrich include grades containing ≤50 ppm or ≤250 ppm MEHQ.\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eStore in a tightly closed container.\u003c\/li\u003e\n\u003cli\u003eStore in a cool, dry and well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eProtect from excessive heat and direct light.\u003c\/li\u003e\n\u003cli\u003eKeep away from strong oxidizing agents and incompatible chemicals.\u003c\/li\u003e\n\u003cli\u003eAvoid unnecessary exposure to heat because methacrylate monomers can polymerize.\u003c\/li\u003e\n\u003cli\u003eMaintain appropriate inhibitor concentration during storage.\u003c\/li\u003e\n\u003cli\u003eAvoid direct skin and eye contact.\u003c\/li\u003e\n\u003cli\u003eWear suitable gloves, protective clothing, and eye protection.\u003c\/li\u003e\n\u003cli\u003eHandle in a suitable fume hood or well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eConsult the current SDS before handling.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA can cause skin sensitization, so appropriate measures should be taken to minimize skin exposure. PubChem notes the sensitizing potential associated with methacrylates.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eResearch Areas\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003e2-Hydroxyethyl Methacrylate (CAS No. 868-77-9)\u003c\/strong\u003e can be positioned across several specific industries and research fields:\u003c\/p\u003e\n\u003cdiv\u003e\u003cdiv\u003e\u003ctable\u003e\n\u003cthead\u003e\u003ctr\u003e\n\u003cth\u003eResearch Area\u003c\/th\u003e\n\u003cth\u003eSpecific Industry \/ Application\u003c\/th\u003e\n\u003c\/tr\u003e\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eDental adhesives, dentin bonding, dental composites, resin-based restorative materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eContact Lens Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eSoft contact lenses, hydrogel lenses, ophthalmic biomaterials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eBiomedical Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrogels, biomaterials, biointerfaces, tissue-engineering materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDrug Delivery\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eControlled-release hydrogels, drug-delivery polymer systems\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eMedical Devices\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrophilic polymer coatings and functional polymer materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eCoatings\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic coatings, UV-curable coatings, functional surface coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eAdhesives\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic adhesives, pressure-sensitive adhesives, dental adhesives\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePolymer Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic\/methacrylate copolymers and functional polymer synthesis\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePhotosensitive Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003ePhotopolymerizable resins and photosensitive coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eFiber \u0026amp; Textile\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eFiber treatment and polymer-based surface modification\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSurface Engineering\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrophilic surface modification and polymer interface engineering\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\u003c\/div\u003e\u003c\/div\u003e\n\u003cp\u003eTCI's current application classification specifically includes \u003cstrong\u003eDental Materials Research Reagents\u003c\/strong\u003e, \u003cstrong\u003eBiomaterials\/ Biocompatible Materials\u003c\/strong\u003e, \u003cstrong\u003eMethacrylate Monomers\u003c\/strong\u003e, \u003cstrong\u003eDrug Delivery Systems\u003c\/strong\u003e, and \u003cstrong\u003eDouble Network Gel synthesis\u003c\/strong\u003e for HEMA.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch3\u003eQ1: What is 2-Hydroxyethyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e 2-Hydroxyethyl Methacrylate (HEMA) is a hydroxy-functional methacrylate monomer with \u003cstrong\u003eCAS No. 868-77-9\u003c\/strong\u003e, molecular formula \u003cstrong\u003eC₆H₁₀O₃\u003c\/strong\u003e, and molecular weight \u003cstrong\u003e130.14 g\/mol\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ2: What is HEMA used for?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e HEMA is used to prepare \u003cstrong\u003ehydrophilic polymers, hydrogels, dental materials, contact-lens materials, biomedical materials, coatings, adhesives, and functional acrylic polymers\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ3: Is HEMA used in dental materials?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is widely used in \u003cstrong\u003edental materials research\u003c\/strong\u003e, particularly in dental adhesive and resin systems. TCI explicitly lists HEMA under Dental Materials Research Reagents.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ4: Why is HEMA used in dental adhesives?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Its methacrylate group enables polymerization, while its hydroxyl group contributes hydrophilicity and interactions with substrates, making HEMA useful in dental adhesive formulations and dentin-bonding research.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ5: Is HEMA used for contact lenses?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is an important monomer for preparing \u003cstrong\u003ehydrophilic PHEMA-based hydrogel materials\u003c\/strong\u003e, historically associated with soft contact-lens materials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ6: What polymer is produced from HEMA?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Polymerization of HEMA produces \u003cstrong\u003epoly(2-hydroxyethyl methacrylate), or PHEMA\u003c\/strong\u003e, a hydrophilic polymer widely investigated in hydrogel and biomaterial research.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ7: Is HEMA used in biomedical research?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is used as a monomer for developing \u003cstrong\u003ehydrogels, biomaterials, drug-delivery systems, and other functional polymeric materials\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ8: Is HEMA supplied with an inhibitor?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. Commercial HEMA is commonly supplied in stabilized form, such as \u003cstrong\u003eMEHQ-stabilized HEMA\u003c\/strong\u003e, to reduce unwanted polymerization during storage.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n               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1 \/ 3;\n    font-weight: bold;\n    align-self: center;\n  }\n\n  .section-row .row-value {\n    grid-column: 3 \/ 9;\n  }\n\n  .section-row ul li {\n    line-height: 2rem !important;\n    font-size: 1.3rem;\n  }\n\n  .html-area {\n    padding: 10px;\n    width: 100%;\n    overflow-x: auto;\n  }\n\n  .html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(1R,2R,4R)-1,7,7-Trimethylbicyclo\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2.2.1\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eheptan-2-yl methacrylate\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eChemScene\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eCS-W014235\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e7534-94-3\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003e\u003cspan\u003eProduct Introduction\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003e1,7,7-Trimethylbicyclo\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2.2.1\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eheptan-2-yl methacrylate is a sterically hindered methacrylate monomer derived from isoborneol and methacrylic acid.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe molecule contains a bulky bicyclic isobornyl group attached to a methacrylate polymerizable unit. During polymerization, the methacrylate double bond participates in free-radical polymerization, while the rigid cyclic structure remains within the polymer backbone, contributing to increased hardness, dimensional stability, and hydrophobic properties.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eCompared with conventional low-molecular-weight methacrylate monomers, IBOMA provides enhanced rigidity and durability, making it an important monomer for high-performance polymer formulations.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eMechanism \/ Principle\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003e1,7,7-Trimethylbicyclo\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2.2.1\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eheptan-2-yl methacrylate polymerizes through the methacrylate vinyl group via free-radical polymerization.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eUnder UV irradiation, thermal initiation, or chemical initiation conditions, radicals attack the carbon–carbon double bond of the methacrylate group, forming polymer chains.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe bulky isobornyl group influences polymer chain mobility and molecular packing, which can improve:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eGlass transition temperature (Tg)\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eSurface hardness\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eChemical resistance\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eDimensional stability\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eMoisture resistance\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan\u003eThis makes IBOMA useful for designing high-performance acrylic polymers and resin systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eKey Research Applications\u003c\/span\u003e\u003c\/h2\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e1. UV-Curable Coatings\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003e1,7,7-Trimethylbicyclo\u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e2.2.1\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eheptan-2-yl methacrylate is widely used in UV-curable resin research due to its rapid polymerization ability and contribution to coating hardness.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIt can be combined with photoinitiators and other acrylic monomers to develop protective coatings with improved durability, scratch resistance, and chemical resistance.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e2. Optical Materials and Optical Coatings\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA is investigated in optical polymer systems because its rigid bicyclic structure can contribute to dimensional stability, transparency, and controlled refractive properties.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eApplications include optical coatings, optical adhesives, and transparent polymer materials.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e3. Adhesives and Sealants\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe hydrophobic and rigid characteristics of IBOMA make it suitable for acrylic adhesive formulations.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eResearchers study its influence on adhesion strength, environmental resistance, flexibility, and long-term stability.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e4. Polymer Modification\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA is used as a functional monomer for modifying acrylic polymers and copolymers.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eBy incorporating IBOMA into polymer chains, researchers can adjust polymer hardness, Tg, water resistance, and mechanical properties.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e5. Advanced Acrylic Resins\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA is an important building block for high-performance acrylic resin systems used in coatings, inks, and specialty polymer formulations.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIts bulky structure helps improve polymer performance while maintaining methacrylate-based processing compatibility.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e6. Composite Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eIBOMA can be incorporated into polymer composite systems to improve matrix properties, including rigidity, environmental stability, and resistance to moisture.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e7. Dental Materials Research\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eAlthough not as commonly used as Bis-GMA, HEMA, TEGDMA, or 10-MDP, IBOMA can be investigated as a hydrophobic methacrylate monomer in polymer-based dental material research.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIts rigid structure and hydrophobic characteristics may contribute to studies on resin formulation, water resistance, polymer network design, and dental composite matrix modification.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eAdvantages\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eRigid molecular structure:\u003c\/strong\u003e The bicyclic isobornyl group improves polymer rigidity and hardness.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eLow shrinkage characteristics:\u003c\/strong\u003e Suitable for applications requiring dimensional stability.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eHydrophobic performance:\u003c\/strong\u003e Helps improve moisture resistance of polymer materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eHigh compatibility:\u003c\/strong\u003e Can copolymerize with various acrylic and methacrylate monomers.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eImproved thermal properties:\u003c\/strong\u003e Contributes to higher Tg and enhanced polymer stability.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eBroad resin applications:\u003c\/strong\u003e Suitable for UV coatings, adhesives, optical polymers, and specialty acrylic materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCommercial stabilized grades:\u003c\/strong\u003e Usually supplied with MEHQ inhibitor for storage stability.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eStorage \u0026amp; Handling\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eStore in a \u003cstrong\u003ecool, dark, and well-ventilated area\u003c\/strong\u003e.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eRecommended storage temperature: \u003cstrong\u003ebelow 15 °C\u003c\/strong\u003e.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eProtect from heat, direct sunlight, and strong oxidizing conditions.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eKeep container tightly closed.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eCommercial products are generally stabilized with MEHQ to reduce premature polymerization.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eAvoid unnecessary exposure to polymerization initiators.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eWear appropriate protective gloves, clothing, and eye protection during handling.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eResearch Areas\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eThis product can support research, formulation development, and material innovation across the following specific industries:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eUV-Curable Materials\u003c\/strong\u003e – UV coatings, radiation-curable resins, protective coatings, and light-curing polymer systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003ePolymer Materials\u003c\/strong\u003e – Acrylic polymers, methacrylate copolymers, functional resin systems, and polymer modification.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCoatings Industry\u003c\/strong\u003e – High-hardness coatings, automotive coatings, industrial coatings, and protective surface coatings.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdhesives \u0026amp; Sealants\u003c\/strong\u003e – Acrylic adhesives, structural adhesives, and moisture-resistant bonding systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eOptical Materials\u003c\/strong\u003e – Optical polymers, transparent resins, optical adhesives, and functional coatings.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eComposite Materials\u003c\/strong\u003e – Polymer composites, reinforced resin systems, and hybrid materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e – Hydrophobic methacrylate resin systems, dental composite formulations, and polymer network research.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ1. What is 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl methacrylate?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003e1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl methacrylate (IBOMA) is a rigid cyclic methacrylate monomer used in UV-curable materials, coatings, adhesives, and polymer research.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ2. What are the main applications of IBOMA?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIBOMA is mainly used in UV-curable coatings, adhesives, optical materials, acrylic polymers, and specialty resin systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ3. Why is IBOMA used in polymer materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIts bulky rigid structure can improve polymer hardness, thermal properties, dimensional stability, and moisture resistance.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ4. Is IBOMA a monomer or polymer?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIBOMA is a \u003cstrong\u003emethacrylate monomer\u003c\/strong\u003e that can polymerize into acrylic and methacrylate-based polymers.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ5. Is IBOMA used in dental materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIBOMA can be investigated in dental polymer research as a hydrophobic methacrylate component, although common dental monomers include Bis-GMA, HEMA, TEGDMA, UDMA, and 10-MDP.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ6. Why is MEHQ added to IBOMA?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eMEHQ is added as a polymerization inhibitor to improve storage stability and prevent premature polymerization.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ7. How should IBOMA be stored?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eStore IBOMA in a cool, dark place below 15 °C and follow supplier SDS recommendations.\u003c\/span\u003e\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = 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.html-area {\n    padding: 10px;\n  }\n\n  .html-area p {\n    margin: 0 !important;\n  }\n\n  .hazard-grid {\n    display: grid;\n    grid-template-columns: repeat(6, 1fr);\n    gap: 0 10px;\n    font-size: 1.3rem;\n  }\n\n  .reference-item {\n    padding: 10px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content .reference-item:last-child {\n    border-bottom: none;\n  }\n\n  .reference-item h3 {\n    font-size: 1.5rem !important;\n  }\n\n  .reference-item .publication-item {\n    font-size: 1.3rem !important;\n    line-height: 1.5rem !important;\n  }\n\n  \/* SDS Search *\/\n  .section-row .coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    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2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e3-(Trimethoxysilyl)propyl methacrylate\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eChemScene\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eCS-0158068\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2530-85-0\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003e\u003cspan\u003eProduct Introduction\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is a functional silane coupling agent designed to improve adhesion between organic polymers and inorganic substrates.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe methacrylate functionality allows this molecule to participate in free-radical polymerization with acrylic and methacrylate-based resins, while the trimethoxysilane group undergoes hydrolysis and condensation reactions to form strong bonds with inorganic surfaces such as glass, silica, ceramics, and metal oxides.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eBecause of its dual reactivity, this compound is widely investigated in polymer–inorganic hybrid materials, composite reinforcement, dental resin systems, and surface-functionalized materials.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eMechanism \/ Principle\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eThe functionality of 3-(Trimethoxysilyl)propyl Methacrylate comes from its two reactive ends.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe \u003cstrong\u003etrimethoxysilane group\u003c\/strong\u003e can hydrolyze in the presence of moisture to generate silanol groups (Si–OH). These groups can subsequently condense with hydroxyl-containing surfaces such as silica, glass, ceramic, and metal oxides to form stable Si–O–Si or Si–O–M bonds.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThe \u003cstrong\u003emethacrylate group\u003c\/strong\u003e can undergo free-radical polymerization with resin monomers, creating a covalent connection between inorganic fillers and organic polymer matrices.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eThis mechanism allows improved interfacial adhesion, mechanical strength, durability, and compatibility in composite systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eKey Research Applications\u003c\/span\u003e\u003c\/h2\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e1. Dental Composite Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is widely studied as a silane coupling agent in dental composite materials. It can improve the bonding between inorganic fillers such as silica-based particles and methacrylate resin matrices.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIn dental restorative materials, silane coupling agents help enhance filler dispersion, interfacial bonding, mechanical properties, and long-term stability.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e2. Dental Adhesives and Restorative Systems\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThis compound is relevant to research on dental bonding systems, resin-based restorative materials, and filler-modified dental composites.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIts ability to connect inorganic dental fillers with polymer resin networks makes it valuable for improving adhesion and material performance.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e3. Polymer Composite Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe compound is commonly used in polymer composite research to improve compatibility between organic polymers and inorganic fillers.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eApplications include glass fiber reinforced polymers, silica-filled composites, ceramic-polymer composites, and hybrid material systems.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e4. Surface Modification\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is widely investigated for modifying glass, silica, ceramic, and metal oxide surfaces.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eSurface treatment with this silane can introduce polymerizable methacrylate functionality onto inorganic surfaces for subsequent polymer coating or composite formation.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e5. Adhesives and Sealants\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eAs a coupling promoter, this compound can improve adhesion between polymer adhesives and inorganic substrates.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003eIt is relevant to acrylic adhesives, sealants, coating formulations, and bonding technologies.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e6. Coatings and Functional Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe molecule is used in research involving functional coatings, protective layers, hybrid organic-inorganic coatings, and surface-engineered materials.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cspan\u003e\u003cstrong\u003e7. Organic-Inorganic Hybrid Materials\u003c\/strong\u003e\u003c\/span\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cspan\u003eThe dual functionality of 3-(Trimethoxysilyl)propyl Methacrylate makes it suitable for preparing hybrid materials that combine polymer properties with inorganic characteristics.\u003c\/span\u003e\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eAdvantages\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDual reactive functionality:\u003c\/strong\u003e Combines silane coupling capability and methacrylate polymerization ability.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eStrong interface bonding:\u003c\/strong\u003e Improves adhesion between organic polymers and inorganic surfaces.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental material compatibility:\u003c\/strong\u003e Suitable for silica-filled dental composites and resin systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eComposite reinforcement:\u003c\/strong\u003e Enhances filler–matrix interaction in polymer composites.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eSurface modification capability:\u003c\/strong\u003e Enables functionalization of glass, silica, ceramic, and metal oxide surfaces.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eBroad material applications:\u003c\/strong\u003e Applicable to adhesives, coatings, polymers, composites, and hybrid materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCommercial availability:\u003c\/strong\u003e Available in stabilized high-purity research grades.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eStorage \u0026amp; Handling\u003c\/span\u003e\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003eStore in a cool, dry, and well-ventilated area.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eProtect from moisture and direct light.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eStore under inert gas when possible.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eTCI recommends storage in a cool and dark place below 15 °C.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eAvoid prolonged exposure to humidity because silane groups are moisture sensitive.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eKeep away from heat sources and polymerization initiators.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eWear appropriate gloves, protective clothing, and eye protection during handling.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003eAvoid skin and eye contact.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eResearch Areas\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eThis product can support research, formulation development, and material innovation across the following specific industries:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e – Dental composite resins, restorative materials, filler surface treatment, dental bonding systems, and resin-based dental materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental Restorative Materials\u003c\/strong\u003e – Silica-filled composites, ceramic-reinforced dental materials, and resin–filler interface optimization.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003ePolymer Composite Materials\u003c\/strong\u003e – Glass fiber composites, silica-filled polymers, ceramic-polymer composites, and hybrid composites.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdhesives \u0026amp; Sealants\u003c\/strong\u003e – Acrylic adhesives, bonding agents, and interface-enhanced adhesive formulations.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eSurface Modification\u003c\/strong\u003e – Functionalization of glass, silica, ceramics, and metal oxide surfaces.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCoatings \u0026amp; Surface Engineering\u003c\/strong\u003e – Protective coatings, functional coatings, and organic-inorganic hybrid coatings.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdvanced Materials\u003c\/strong\u003e – Hybrid materials, nanocomposites, and polymer-inorganic interface research.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ1. What is 3-(Trimethoxysilyl)propyl Methacrylate?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003e3-(Trimethoxysilyl)propyl Methacrylate is a silane coupling agent containing both a methacrylate polymerizable group and a trimethoxysilane functional group.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ2. What is KH-570?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eKH-570 is a common commercial name for 3-(Trimethoxysilyl)propyl Methacrylate.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ3. Is this product used in dental materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eYes. It is widely studied as a silane coupling agent for dental composite materials, especially for improving bonding between inorganic fillers and resin matrices.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ4. How does this compound improve composite materials?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIt forms chemical bridges between inorganic fillers and polymer matrices, improving interfacial adhesion and material performance.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ5. Is it a monomer or coupling agent?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIt can function as both a functional methacrylate monomer and a silane coupling agent.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ6. What materials can it modify?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eIt is commonly used for glass, silica, ceramics, metal oxides, and other hydroxyl-containing inorganic surfaces.\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003cp\u003e\u003cspan\u003e\u003cstrong\u003eQ7. How should it be stored?\u003c\/strong\u003e\u003c\/span\u003e\u003cbr\u003e\u003cspan\u003eStore tightly sealed in a cool, dry, dark environment and protect from moisture.\u003c\/span\u003e\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"ChemScene","offers":[{"title":"1×100g","offer_id":46683753971902,"sku":"TS246CS-0158068_100_G","price":19.6,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/282165_d30e6d3f-09ed-4128-8344-5e4f995a461c.png?v=1791645649"},{"product_id":"ts246cs-0158066","title":"2-(Trimethylsilyloxy)ethyl methacrylate, 96% | 17407-09-9","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    display:  unset ;\n  }\n\n  \/* Hide sku *\/\n  .product-sku, \n  #leadtimetext {\n    display: none !important;\n  }\n\n  \/* Square brackets *\/\n  span.l_bracket:before {\n    content: \"[\";\n  }\n  span.r_bracket:after {\n    content: \"]\";\n  }\n\n  \/* Hazard Symbols *\/\n  .ghs-symbols-row {\n    display: flex;\n    flex-wrap: wrap;\n    gap: 10px;\n  }\n\n  .hazard-symbol-container {\n    width: 50px;\n  }\n\n  .hazard-symbol {\n    object-fit: contain;\n    aspect-ratio: 1 \/ 1;\n    width: 100%;\n  }\n\n  \/* Section *\/\n  .section-header {\n    font-size: 2rem;\n    font-weight: bold;\n    color: #239ab7;\n    background-color: #f2f2f2;\n    padding: 10px;\n    border-radius: 4px;\n  }\n\n  .section-row {\n    display: grid;\n    grid-template-columns: repeat(8, 1fr);\n    padding: 6px 10px;\n    border-bottom: 1px solid #e0e0e0;\n  }\n\n  .section-content {\n    padding-bottom: 6px;\n  }\n\n  .section-content .section-row:last-child {\n    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.coa-search-container {\n    display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2-(Trimethylsilyloxy)ethyl methacrylate\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eChemScene\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eCS-0158066\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e17407-09-9\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003eProduct Introduction\u003c\/h2\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate (CAS 17407-09-9) is a silicon-containing functional methacrylate monomer featuring a polymerizable methacrylate group and a trimethylsilyloxy-functional side chain. The methacrylate group enables free-radical polymerization and copolymerization, while the trimethylsilyl group provides protected hydroxyl functionality.\u003c\/p\u003e\n\u003cp\u003eThis monomer is particularly useful in research involving functional polymer materials, hydrogel systems, biomedical polymers, dental materials, and post-polymerization functionalization. It is also specifically identified as a monomer and adhesive promoter in dental application materials.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003ePolymerization \/ Reaction Principle\u003c\/h2\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate contains a reactive methacrylate double bond that can undergo free-radical polymerization and copolymerization with other vinyl monomers.\u003c\/p\u003e\n\u003cp\u003eThe trimethylsilyloxy group serves as a protected hydroxyl functionality. After polymerization, appropriate deprotection can expose hydroxyl groups, allowing the resulting polymer to undergo further chemical modification. Research applications describe the use of this protecting-group strategy to prepare controlled polymer architectures and subsequently obtain PHEMA-type materials.\u003c\/p\u003e\n\u003cp\u003eThis protected-functional-group strategy enables researchers to introduce hydroxyl functionality into polymer systems while controlling the timing of subsequent functionalization.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eSimplified reaction pathway:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate\u003cbr\u003e→ Polymerization \/ Copolymerization\u003cbr\u003e→ TMS-Protected Functional Polymer\u003cbr\u003e→ Deprotection\u003cbr\u003e→ Hydroxyl-Functional Polymer\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eKey Research Applications\u003c\/h2\u003e\n\u003ch3\u003e\u003cstrong\u003e1. Dental Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate is used as a functional monomer and adhesive promoter in dental materials research.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eDental adhesive systems\u003c\/li\u003e\n\u003cli\u003eMethacrylate-based dental resins\u003c\/li\u003e\n\u003cli\u003eResin–substrate adhesion studies\u003c\/li\u003e\n\u003cli\u003eDental polymer formulation research\u003c\/li\u003e\n\u003cli\u003eFunctional monomer evaluation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts polymerizable methacrylate group enables incorporation into resin systems, while its silicon-containing structure provides an additional chemical feature for studying adhesion and interfacial interactions in dental materials. Commercial dental-material literature specifically identifies this compound as a monomer and adhesive promoter.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e2. Hydrogel Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate is a useful protected-functional monomer for developing functional polymer networks and hydrogel materials.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFunctional hydrogel synthesis\u003c\/li\u003e\n\u003cli\u003eHydrophilic polymer networks\u003c\/li\u003e\n\u003cli\u003eHydrogel composition control\u003c\/li\u003e\n\u003cli\u003eWater-uptake studies\u003c\/li\u003e\n\u003cli\u003ePolymer network modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe trimethylsilyl group protects the hydroxyl functionality during polymer synthesis and can subsequently be removed to generate hydroxyl-containing polymers. This provides a route for controlling polymer architecture and modifying hydrogel functionality and hydration behavior.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e3. Biomedical Polymer Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate can be used as a functional building block for biomedical polymer and hydrogel research.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFunctional biomedical polymers\u003c\/li\u003e\n\u003cli\u003ePHEMA-related materials\u003c\/li\u003e\n\u003cli\u003eBiomedical hydrogel research\u003c\/li\u003e\n\u003cli\u003ePolymer surface engineering\u003c\/li\u003e\n\u003cli\u003eBiocompatible material development\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts protected hydroxyl functionality provides a synthetic route toward hydroxyl-containing polymer materials that can be further modified for biomedical research. Research literature and application protocols describe its use as a precursor to PHEMA-type materials and polymeric systems investigated for drug-delivery applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e4. Functional Polymer Modification\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate provides a protected hydroxyl functionality for post-polymerization modification of functional polymers.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eHydroxyl-functional polymer preparation\u003c\/li\u003e\n\u003cli\u003ePost-polymerization modification\u003c\/li\u003e\n\u003cli\u003ePolymer grafting\u003c\/li\u003e\n\u003cli\u003eCrosslinking studies\u003c\/li\u003e\n\u003cli\u003eFunctional polymer platform development\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe trimethylsilyl protecting group can be removed after polymerization to expose hydroxyl groups, providing reactive sites for subsequent chemical modification. This approach allows researchers to develop functional polymers with controlled structures and tailored chemical properties.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eAdvantages\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eFunctional methacrylate monomer:\u003c\/strong\u003e Provides a reactive methacrylate group for polymerization and copolymerization.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eProtected hydroxyl functionality:\u003c\/strong\u003e The trimethylsilyloxy group provides a protected hydroxyl precursor.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePost-polymerization modification:\u003c\/strong\u003e Deprotection enables further chemical functionalization of polymer structures.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSilicon-containing structure:\u003c\/strong\u003e Provides an additional structural feature for advanced polymer-material research.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eHydrogel research compatibility:\u003c\/strong\u003e Useful for developing functional hydrogel and polymer-network systems.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eBiomedical polymer potential:\u003c\/strong\u003e Suitable for research involving functional biomedical polymers and hydrogel materials.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eDental materials relevance:\u003c\/strong\u003e Identified as a monomer and adhesive promoter in dental application materials. \u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCommercial stabilized grades:\u003c\/strong\u003e Available in stabilized research-grade formulations, including BHT-stabilized grades. \u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eStorage \u0026amp; Handling\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eStore according to the current product-specific SDS and specification.\u003c\/li\u003e\n\u003cli\u003eKeep the container tightly closed when not in use.\u003c\/li\u003e\n\u003cli\u003eProtect from moisture, excessive heat, and direct light.\u003c\/li\u003e\n\u003cli\u003eAvoid contamination with polymerization initiators or other reactive materials.\u003c\/li\u003e\n\u003cli\u003eBecause it is a polymerizable methacrylate monomer, avoid conditions that may promote unintended polymerization.\u003c\/li\u003e\n\u003cli\u003eCommercial grades may contain BHT or other polymerization inhibitors.\u003c\/li\u003e\n\u003cli\u003eTCI recommends storage in a cool and dark place below 15°C, under inert gas, with protection from moisture. \u003c\/li\u003e\n\u003cli\u003eHandle in a well-ventilated laboratory environment.\u003c\/li\u003e\n\u003cli\u003eWear appropriate gloves, eye protection, and protective laboratory clothing.\u003c\/li\u003e\n\u003cli\u003eAlways consult the current SDS before handling, transportation, or disposal.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eResearch Areas\u003c\/h2\u003e\n\u003cdiv\u003e\u003cdiv\u003e\u003ctable\u003e\n\u003cthead\u003e\u003ctr\u003e\n\u003cth\u003eResearch Area\u003c\/th\u003e\n\u003cth\u003eSpecific Industry \/ Application\u003c\/th\u003e\n\u003c\/tr\u003e\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eDental adhesives, methacrylate-based dental resins, resin–substrate adhesion\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eHydrogel Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eFunctional hydrogels, polymer networks, hydration and swelling studies\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eBiomedical Polymer Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eBiomedical hydrogels, functional polymers, polymeric biomaterials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePolymer Chemistry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eFunctional methacrylate polymers, controlled polymerization and copolymer research\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSurface Engineering\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003ePolymer surface functionalization, grafting and interface modification\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDrug Delivery Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eFunctional hydrogel carriers, polymeric drug-delivery systems\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eAdvanced Polymer Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eFunctional polymer platforms and structure–property studies\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\u003c\/div\u003e\u003c\/div\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch3\u003eWhat is 2-(Trimethylsilyloxy)ethyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e2-(Trimethylsilyloxy)ethyl Methacrylate is a silicon-containing functional methacrylate monomer with CAS No. 17407-09-9. It contains a polymerizable methacrylate group and a trimethylsilyloxy-functional side chain.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eWhat is the molecular formula of 2-(Trimethylsilyloxy)ethyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003eThe molecular formula is C₉H₁₈O₃Si.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eWhat is the molecular weight of 2-(Trimethylsilyloxy)ethyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003eThe molecular weight is 202.32 g\/mol.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eIs 2-(Trimethylsilyloxy)ethyl Methacrylate a monomer?\u003c\/h3\u003e\n\u003cp\u003eYes. It is a functional methacrylate monomer that can undergo polymerization and copolymerization through its methacrylate double bond. TCI classifies it among monomers and silicon compounds.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eWhat is 2-(Trimethylsilyloxy)ethyl Methacrylate used for?\u003c\/h3\u003e\n\u003cp\u003eIt is used in research involving dental materials, hydrogels, biomedical polymer materials, functional polymer modification, surface engineering, specialty resin systems, and advanced polymer research.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eIs 2-(Trimethylsilyloxy)ethyl Methacrylate used in dental materials?\u003c\/h3\u003e\n\u003cp\u003eYes. Sigma-Aldrich's dental materials documentation specifically identifies CAS 17407-09-9 as a \u003cstrong\u003emonomer and adhesive promoter\u003c\/strong\u003e for dental applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eWhy is the trimethylsilyl group important?\u003c\/h3\u003e\n\u003cp\u003eThe trimethylsilyl group functions as a protected hydroxyl functionality. It can remain protected during polymer synthesis and subsequently be removed to generate hydroxyl-containing polymer structures, providing a route for further functionalization.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eHow should 2-(Trimethylsilyloxy)ethyl Methacrylate be stored?\u003c\/h3\u003e\n\u003cp\u003eStorage conditions depend on the specific grade. TCI recommends a cool, dark environment below 15°C, under inert gas and protected from moisture.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"ChemScene","offers":[{"title":"1×25g","offer_id":46683754791102,"sku":"TS246CS-0158066_25_G","price":43.7,"currency_code":"USD","in_stock":true},{"title":"1×100g","offer_id":46683754823870,"sku":"TS246CS-0158066_100_G","price":169.1,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/423895.png?v=1791645655"},{"product_id":"ts246cs-w018010","title":"(Tetrahydrofuran-2-yl)methyl acrylate,98% (stabilized with MEHQ), 98% (stabilized with MEHQ) | 2399-48-6","description":"\u003cstyle\u003e\n  \/* isQuote *\/\n  div.swatch.clearfix {\n    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display: flex;\n    align-items: center;\n    margin-top: 6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e(Tetrahydrofuran-2-yl)methyl acrylate,98% (stabilized with MEHQ)\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eChemScene\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eCS-W018010\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2399-48-6\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n        \u003ch2 class=\"section-header\"\u003eGeneral Information\u003c\/h2\u003e\n        \u003cdiv class=\"section-content\"\u003e\n            \n\n            \n            \u003cdiv class=\"section-row\"\u003e\n                \u003cdiv class=\"row-key\"\u003ePubChem CID\u003c\/div\u003e\n                \u003cdiv class=\"row-value\"\u003e94232\u003c\/div\u003e\n            \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eIUPAC Name\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eoxolan-2-ylmethyl prop-2-enoate\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eInChI Key\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eYNXCGLKMOXLBOD-UHFFFAOYSA-N\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n\n            \n                \u003cdiv class=\"section-row\"\u003e\n                    \u003cdiv class=\"row-key\"\u003eSMILES\u003c\/div\u003e\n                    \u003cdiv class=\"row-value\"\u003eC=CC(=O)OCC1CCCO1\u003c\/div\u003e\n                \u003c\/div\u003e\n            \n        \u003c\/div\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003eProduct Introduction\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eTetrahydrofurfuryl Acrylate (THFA, CAS No. 2399-48-6)\u003c\/strong\u003e is a functional monofunctional acrylate monomer containing a polymerizable acrylate group and a tetrahydrofuran ring.\u003c\/p\u003e\n\u003cp\u003eThe molecule combines the high reactivity of an acrylate double bond with the polarity and cyclic ether functionality of the tetrahydrofuran group. This structure makes THFA useful as a \u003cstrong\u003ereactive diluent and functional monomer\u003c\/strong\u003e for UV-curable and radiation-curable polymer systems.\u003c\/p\u003e\n\u003cp\u003eCommercial THFA is commonly supplied as a stabilized liquid. TCI reports \u003cstrong\u003e\u0026gt;98.0% GC purity\u003c\/strong\u003e, while other commercial grades are available at approximately 97–98% purity with polymerization inhibitors.\u003c\/p\u003e\n\u003cp\u003eTHFA is used in \u003cstrong\u003eUV-curable resins, adhesives, coatings, inks, 3D-printing resins, and specialty polymer synthesis\u003c\/strong\u003e. Arkema describes its commercial THFA monomer as a low-viscosity, polar, monofunctional monomer that promotes adhesion to numerous substrates.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003ePolymerization \/ Reaction Principle\u003c\/h2\u003e\n\u003cp\u003eTetrahydrofurfuryl Acrylate contains a polymerizable acrylate double bond:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCH₂=CHCOOCH₂C₄H₇O\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eUnder suitable free-radical initiation conditions, THFA undergoes addition polymerization:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003en CH₂=CHCOOCH₂C₄H₇O → \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e–CH₂–CH(COOCH₂C₄H₇O)–\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eₙ\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe tetrahydrofuran ring remains incorporated into the side chain of the resulting polymer.\u003c\/p\u003e\n\u003cp\u003eTHFA can also be copolymerized with other acrylate, methacrylate, or vinyl monomers to adjust:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer polarity\u003c\/li\u003e\n\u003cli\u003eAdhesion\u003c\/li\u003e\n\u003cli\u003eFlexibility\u003c\/li\u003e\n\u003cli\u003eSurface properties\u003c\/li\u003e\n\u003cli\u003eSolvency\u003c\/li\u003e\n\u003cli\u003eCrosslinking behavior\u003c\/li\u003e\n\u003cli\u003eFilm formation\u003c\/li\u003e\n\u003cli\u003eCuring performance\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe low viscosity and polar nature of THFA are particularly useful when formulating reactive resin systems.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eKey Research Applications\u003c\/h2\u003e\n\u003ch3\u003e\u003cstrong\u003e1. UV-Curable Resin\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is widely used as a \u003cstrong\u003ereactive monomer and reactive diluent in UV-curable resin systems\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable acrylic resins\u003c\/li\u003e\n\u003cli\u003eRadiation-curable polymers\u003c\/li\u003e\n\u003cli\u003eUV resin formulations\u003c\/li\u003e\n\u003cli\u003ePhotopolymer systems\u003c\/li\u003e\n\u003cli\u003eFunctional acrylic resins\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts low viscosity can help reduce formulation viscosity while allowing the monomer to become part of the cured polymer network rather than acting solely as a conventional solvent.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e2. 3D Printing Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is used in the development of \u003cstrong\u003ephotopolymer resins for additive manufacturing\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSLA 3D printing\u003c\/li\u003e\n\u003cli\u003eDLP 3D printing\u003c\/li\u003e\n\u003cli\u003eUV-curable 3D-printing resins\u003c\/li\u003e\n\u003cli\u003ePhotopolymer formulation\u003c\/li\u003e\n\u003cli\u003eRapid prototyping materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eJ\u0026amp;K Scientific specifically identifies Tetrahydrofurfuryl Acrylate for developing photopolymer resins used in \u003cstrong\u003e3D printing\u003c\/strong\u003e, while industry sources identify THFA among monomers used in UV-curable systems.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e3. UV-Curable Adhesives\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA can be incorporated into UV-curable adhesive formulations.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable adhesives\u003c\/li\u003e\n\u003cli\u003ePressure-sensitive adhesive research\u003c\/li\u003e\n\u003cli\u003eOptical adhesives\u003c\/li\u003e\n\u003cli\u003eElectronic-material adhesives\u003c\/li\u003e\n\u003cli\u003eSpecialty bonding materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts low viscosity and ability to promote adhesion to various substrates make it useful in adhesive formulations. Arkema specifically describes THFA as promoting adhesion to numerous substrates.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e4. Coatings\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is an important functional monomer for \u003cstrong\u003eacrylic and UV-curable coatings\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable coatings\u003c\/li\u003e\n\u003cli\u003eProtective coatings\u003c\/li\u003e\n\u003cli\u003eIndustrial coatings\u003c\/li\u003e\n\u003cli\u003eMetal coatings\u003c\/li\u003e\n\u003cli\u003ePlastic coatings\u003c\/li\u003e\n\u003cli\u003eFunctional surface coatings\u003c\/li\u003e\n\u003cli\u003eOutdoor coatings\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts incorporation into polymer formulations can contribute to adhesion, water resistance, chemical resistance, and film-forming performance. Commercial application information identifies THFA for coatings requiring durability and environmental resistance.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e5. UV-Curable Inks\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA can be used in radiation-curable ink formulations.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV printing inks\u003c\/li\u003e\n\u003cli\u003eUV inkjet inks\u003c\/li\u003e\n\u003cli\u003eDigital printing\u003c\/li\u003e\n\u003cli\u003eIndustrial printing\u003c\/li\u003e\n\u003cli\u003eFunctional inks\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts low viscosity and good dilution capability make it useful in reactive ink formulations. Kowa Chemicals identifies THFA for \u003cstrong\u003eUV inkjet inks\u003c\/strong\u003e, while other commercial sources list UV inks among its applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e6. Polymer and Copolymer Synthesis\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA is a useful monomer for preparing specialty polymers and copolymers.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eAcrylic copolymers\u003c\/li\u003e\n\u003cli\u003eFunctional polymers\u003c\/li\u003e\n\u003cli\u003eSpecialty resins\u003c\/li\u003e\n\u003cli\u003eHydrophobic\/hydrophilic property modification\u003c\/li\u003e\n\u003cli\u003ePolymer structure–property studies\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIts cyclic ether group provides an additional structural feature compared with simple alkyl acrylates, allowing researchers to tune polymer polarity and substrate interactions.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e7. Adhesives \u0026amp; Sealants\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eTHFA can be used in adhesive and sealant formulations as a reactive monomer.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eIndustrial adhesives\u003c\/li\u003e\n\u003cli\u003eUV adhesives\u003c\/li\u003e\n\u003cli\u003eSealants\u003c\/li\u003e\n\u003cli\u003eFlexible adhesive systems\u003c\/li\u003e\n\u003cli\u003eSpecialty bonding formulations\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eKowa Chemicals identifies THFA as a monomer used in \u003cstrong\u003eadhesives and sealants\u003c\/strong\u003e, with functions including adhesion and low viscosity.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e8. Bio-Based Polymer Materials\u003c\/h3\u003e\n\u003cp\u003eA bio-based version of THFA is commercially available, with TCI reporting approximately \u003cstrong\u003e62% bio-based carbon\u003c\/strong\u003e for its plant-derived-carbon product. This provides an option for research into more sustainable acrylate monomers and polymer formulations.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eBio-based polymer research\u003c\/li\u003e\n\u003cli\u003eSustainable UV-curable materials\u003c\/li\u003e\n\u003cli\u003eRenewable-content acrylate formulations\u003c\/li\u003e\n\u003cli\u003eGreen polymer chemistry\u003c\/li\u003e\n\u003cli\u003eBio-based coatings and resins\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eAdvantages\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eHighly reactive acrylate functionality\u003c\/li\u003e\n\u003cli\u003eMonofunctional reactive monomer\u003c\/li\u003e\n\u003cli\u003eLow viscosity\u003c\/li\u003e\n\u003cli\u003ePolar molecular structure\u003c\/li\u003e\n\u003cli\u003eContains a cyclic ether group\u003c\/li\u003e\n\u003cli\u003eGood dilution capability\u003c\/li\u003e\n\u003cli\u003eCan improve adhesion to various substrates\u003c\/li\u003e\n\u003cli\u003eSuitable for UV and radiation curing\u003c\/li\u003e\n\u003cli\u003eUseful for polymer and copolymer synthesis\u003c\/li\u003e\n\u003cli\u003eApplicable to coatings and adhesives\u003c\/li\u003e\n\u003cli\u003eSuitable for UV inks\u003c\/li\u003e\n\u003cli\u003eUseful in 3D-printing resin development\u003c\/li\u003e\n\u003cli\u003eStabilized grades available\u003c\/li\u003e\n\u003cli\u003eBio-based versions available\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eArkema characterizes THFA as a \u003cstrong\u003elow-viscosity, polar, monofunctional monomer\u003c\/strong\u003e with adhesion-promoting properties, while commercial technical data also highlights its dilution capability and suitability for UV-curable applications.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eStorage \u0026amp; Handling\u003c\/h2\u003e\n\u003cp\u003eTetrahydrofurfuryl Acrylate is a reactive acrylate monomer and is commonly supplied with a polymerization inhibitor such as \u003cstrong\u003eMEHQ or hydroquinone\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eStore in a tightly closed container.\u003c\/li\u003e\n\u003cli\u003eKeep in a cool, dry and well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eProtect from heat and direct sunlight.\u003c\/li\u003e\n\u003cli\u003eAvoid contamination with polymerization initiators.\u003c\/li\u003e\n\u003cli\u003eKeep away from strong oxidizing agents and incompatible materials.\u003c\/li\u003e\n\u003cli\u003eMaintain the recommended inhibitor concentration during storage.\u003c\/li\u003e\n\u003cli\u003eAvoid unnecessary exposure to elevated temperatures.\u003c\/li\u003e\n\u003cli\u003eWear appropriate gloves, protective clothing, and eye protection.\u003c\/li\u003e\n\u003cli\u003eAvoid direct contact with skin and eyes.\u003c\/li\u003e\n\u003cli\u003eHandle in an appropriate fume hood or well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eConsult the current SDS before use.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTCI recommends storing its THFA product in a cool, dark location below \u003cstrong\u003e15°C\u003c\/strong\u003e. Its current safety information identifies hazards including skin irritation, serious eye damage, skin sensitization, and aquatic toxicity; other supplier SDS classifications can vary with formulation and grade.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eResearch Areas\u003c\/h2\u003e\n\u003cdiv\u003e\u003cdiv\u003e\u003ctable\u003e\n\u003cthead\u003e\u003ctr\u003e\n\u003cth\u003eResearch Area\u003c\/th\u003e\n\u003cth\u003eSpecific Industry \/ Application\u003c\/th\u003e\n\u003c\/tr\u003e\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eUV-Curable Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV-curable resins, radiation-curable polymers, photopolymer formulations\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003e3D Printing\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eSLA\/DLP photopolymer resins, UV-curable additive-manufacturing materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eCoatings Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV coatings, protective coatings, plastic coatings, metal coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eAdhesives \u0026amp; Sealants\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV adhesives, industrial adhesives, specialty sealants\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePrinting \u0026amp; Ink Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV inks, UV inkjet inks, digital printing materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePolymer Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic copolymers, specialty polymers, functional resins\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eElectronics Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eUV-curable functional coatings and adhesive materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSurface Engineering\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAdhesion promotion, surface modification, wettability control\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSustainable Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eBio-based acrylate monomers and renewable-content polymer research\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eMaterials Science\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eStructure–property studies of functional acrylate polymers\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\u003c\/div\u003e\u003c\/div\u003e\n\u003cp\u003e\u003cstrong\u003eNote:\u003c\/strong\u003e Compared with HEMA (868-77-9), whose application in dental materials is well established, the currently available evidence for \u003cstrong\u003e2399-48-6 in dental materials is not strong enough to make dentistry a primary commercial application\u003c\/strong\u003e. For an SEO product page, it is more accurate to prioritize \u003cstrong\u003eUV curing, coatings, adhesives, inks, 3D printing, and polymer materials\u003c\/strong\u003e.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch3\u003eQ1: What is Tetrahydrofurfuryl Acrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Tetrahydrofurfuryl Acrylate (THFA) is a functional monofunctional acrylate monomer with \u003cstrong\u003eCAS No. 2399-48-6\u003c\/strong\u003e, molecular formula \u003cstrong\u003eC₈H₁₂O₃\u003c\/strong\u003e, and molecular weight \u003cstrong\u003e156.18 g\/mol\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ2: What is Tetrahydrofurfuryl Acrylate used for?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e THFA is mainly used in \u003cstrong\u003eUV-curable resins, coatings, adhesives, UV inks, 3D-printing photopolymer resins, and specialty polymer synthesis\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ3: Is THFA a monomer?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is a \u003cstrong\u003emonofunctional acrylate monomer\u003c\/strong\u003e that can undergo free-radical polymerization and copolymerization.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ4: Is Tetrahydrofurfuryl Acrylate used in UV curing?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used as a reactive monomer\/reactive diluent in UV-curable and radiation-curable formulations.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ5: Is THFA used in 3D printing?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used in the development of \u003cstrong\u003ephotopolymer resins for 3D printing\u003c\/strong\u003e, including UV-curable additive-manufacturing materials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ6: Is THFA used in coatings?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used in UV-curable and functional coating formulations, where its properties can contribute to adhesion and other coating performance characteristics.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ7: Is THFA used in adhesives?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. THFA is used in UV-curable adhesives and other adhesive formulations, particularly where low viscosity and adhesion to substrates are important.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ8: Is Tetrahydrofurfuryl Acrylate stabilized?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. Commercial THFA is commonly supplied with polymerization inhibitors such as \u003cstrong\u003eMEHQ or hydroquinone\u003c\/strong\u003e to improve storage stability\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await 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6px;\n  }\n\n  .section-row .coa-search-container input {\n    border: 1px solid #e0e0e0;\n    height: 2.5rem;\n    border-top-left-radius: 0.5rem !important;\n    border-bottom-left-radius: 0.5rem !important;\n    padding: 3px 5px;\n  }\n\n  .section-row .coa-search-container button {\n    height: 2.5rem;\n    line-height: 2.5rem;\n    border-radius: 0 0.5rem 0.5rem 0;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content {\n    display: flex;\n    align-items: center;\n    justify-content: center;\n    gap: 3px;\n  }\n\n  .section-row .coa-search-container button .coa-search-button-content .search-spin {\n    display: none;\n    width: 2rem;\n  }\n\n  .section-row .coa-search-container .coa-not-found {\n    display: none;\n    margin: 0 0 0 2rem;\n    color: #ad2031;\n    font-size: 1.3rem;\n  }\n\n  \/* Table *\/\n  .html-area table {\n    width: 100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2-Hydroxyethyl methacrylate\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eChemScene\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eCS-W013439\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e868-77-9\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003eProduct Introduction\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003e2-Hydroxyethyl Methacrylate (HEMA, CAS No. 868-77-9)\u003c\/strong\u003e is a hydroxy-functional methacrylate monomer containing both a polymerizable methacrylate group and a terminal hydroxyl group. Its molecular formula is C₆H₁₀O₃ and molecular weight is 130.14 g\/mol.\u003c\/p\u003e\n\u003cp\u003eThe methacrylate double bond enables HEMA to participate in free-radical polymerization, while the hydroxyl group provides additional hydrophilicity and opportunities for hydrogen bonding, esterification, crosslinking, and surface modification.\u003c\/p\u003e\n\u003cp\u003eHEMA is an important building block for \u003cstrong\u003ehydrophilic polymers, hydrogels, biomaterials, dental materials, contact-lens materials, coatings, adhesives, and functional polymer systems\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003e \u003c\/p\u003e\n\u003ch2\u003ePolymerization \/ Reaction Principle\u003c\/h2\u003e\n\u003cp\u003eHEMA contains a polymerizable carbon-carbon double bond:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eCH₂=C(CH₃)COOCH₂CH₂OH\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eUnder suitable free-radical initiation conditions, HEMA undergoes addition polymerization to form \u003cstrong\u003epoly(2-hydroxyethyl methacrylate) (PHEMA)\u003c\/strong\u003e:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003en CH₂=C(CH₃)COOCH₂CH₂OH → \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e–CH₂–C(CH₃)(COOCH₂CH₂OH)–\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eₙ\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe resulting PHEMA contains hydrophilic hydroxyl groups and can absorb water, making it useful for hydrogel and biomaterial research.\u003c\/p\u003e\n\u003cp\u003eHEMA can also be copolymerized with other methacrylate or acrylic monomers to tune:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eHydrophilicity\u003c\/li\u003e\n\u003cli\u003eWater absorption\u003c\/li\u003e\n\u003cli\u003eMechanical properties\u003c\/li\u003e\n\u003cli\u003eCrosslinking density\u003c\/li\u003e\n\u003cli\u003eSurface wettability\u003c\/li\u003e\n\u003cli\u003eAdhesion\u003c\/li\u003e\n\u003cli\u003eOptical properties\u003c\/li\u003e\n\u003cli\u003eBiocompatibility-related material characteristics\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003ePHEMA and HEMA-based copolymers are widely investigated as hydrophilic polymer and hydrogel materials.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eKey Research Applications\u003c\/h2\u003e\n\u003ch3\u003e\u003cstrong\u003e1. Dental Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eHEMA is an important monomer in dental materials research\u003c\/strong\u003e, particularly in resin-based restorative and adhesive systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eDental adhesive systems\u003c\/li\u003e\n\u003cli\u003eDentin bonding research\u003c\/li\u003e\n\u003cli\u003eDental resin formulations\u003c\/li\u003e\n\u003cli\u003eDental composite materials\u003c\/li\u003e\n\u003cli\u003eResin-based restorative materials\u003c\/li\u003e\n\u003cli\u003eDental polymer materials\u003c\/li\u003e\n\u003cli\u003eDental bonding interfaces\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA can contribute hydrophilic characteristics and improve interaction between resin systems and moist dentin surfaces. HEMA and HEMA-based polymers have also been investigated in dental composite materials and dental-pulp-related research.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eResearch focus:\u003c\/strong\u003e dental resin formulation, polymerization behavior, dentin bonding, water uptake, interface stability, and dental biomaterials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e2. Contact Lens Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is historically important in the development of \u003cstrong\u003ehydrophilic contact-lens materials\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003ePolymerization of HEMA can produce hydrophilic PHEMA-based materials capable of absorbing and retaining water.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSoft contact lens materials\u003c\/li\u003e\n\u003cli\u003eHydrogel contact lenses\u003c\/li\u003e\n\u003cli\u003eHydrogel polymer research\u003c\/li\u003e\n\u003cli\u003eOphthalmic biomaterials\u003c\/li\u003e\n\u003cli\u003eContact-lens surface modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e3. Biomedical Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is widely used as a monomer for preparing hydrophilic polymers and hydrogel materials.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eBiomedical hydrogels\u003c\/li\u003e\n\u003cli\u003eBiomaterial development\u003c\/li\u003e\n\u003cli\u003eTissue-engineering materials\u003c\/li\u003e\n\u003cli\u003eDrug-delivery systems\u003c\/li\u003e\n\u003cli\u003eBiointerfaces\u003c\/li\u003e\n\u003cli\u003eFunctional polymeric biomaterials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eTCI specifically classifies HEMA under \u003cstrong\u003eBiomaterials \/ Biocompatible Materials Research Reagents\u003c\/strong\u003e and \u003cstrong\u003eMonomers and Macromonomers\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e4. Drug Delivery\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA-based hydrogels can be designed to absorb water and provide controlled polymer networks.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eDrug-delivery hydrogels\u003c\/li\u003e\n\u003cli\u003eControlled-release materials\u003c\/li\u003e\n\u003cli\u003eStimuli-responsive polymer systems\u003c\/li\u003e\n\u003cli\u003eWater-soluble polymer systems\u003c\/li\u003e\n\u003cli\u003eBiomedical polymer research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA-based hydrogel systems have been investigated for drug-release and drug-delivery applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e5. Coatings\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can be incorporated into acrylic and methacrylate polymer systems to introduce hydroxyl functionality.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFunctional coatings\u003c\/li\u003e\n\u003cli\u003eAcrylic coatings\u003c\/li\u003e\n\u003cli\u003eUV-curable coatings\u003c\/li\u003e\n\u003cli\u003eProtective coatings\u003c\/li\u003e\n\u003cli\u003eSurface-modification coatings\u003c\/li\u003e\n\u003cli\u003ePolymer coating research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe hydroxyl group can provide additional sites for interactions and crosslinking with other components.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e6. Adhesives\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA is used as a functional monomer in adhesive polymer systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eAcrylic adhesives\u003c\/li\u003e\n\u003cli\u003ePressure-sensitive adhesives\u003c\/li\u003e\n\u003cli\u003eStructural adhesive research\u003c\/li\u003e\n\u003cli\u003eWater-compatible adhesives\u003c\/li\u003e\n\u003cli\u003eDental adhesives\u003c\/li\u003e\n\u003cli\u003ePolymer adhesion research\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eThe combination of a polymerizable methacrylate group and hydroxyl functionality makes HEMA useful for modifying adhesion and polymer–substrate interactions.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e7. Photosensitive Resins and UV-Curable Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can participate in polymerization and crosslinking reactions used to develop photosensitive polymer systems.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eUV-curable resins\u003c\/li\u003e\n\u003cli\u003ePhotosensitive coatings\u003c\/li\u003e\n\u003cli\u003ePhotopolymer research\u003c\/li\u003e\n\u003cli\u003eResin modification\u003c\/li\u003e\n\u003cli\u003eFunctional acrylic polymers\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e8. Fiber and Textile Treatment\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHEMA can be incorporated into polymer systems designed to modify fiber surfaces.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eFiber treatment agents\u003c\/li\u003e\n\u003cli\u003ePolymer surface modification\u003c\/li\u003e\n\u003cli\u003eTextile functionalization\u003c\/li\u003e\n\u003cli\u003eHydrophilic surface modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eCommercial application references also identify HEMA for fiber-treatment and acrylic resin modification.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eAdvantages\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eReactive methacrylate functional group\u003c\/li\u003e\n\u003cli\u003eHydroxyl-functional monomer\u003c\/li\u003e\n\u003cli\u003eSuitable for free-radical polymerization\u003c\/li\u003e\n\u003cli\u003eProduces hydrophilic polymers\u003c\/li\u003e\n\u003cli\u003eUseful for hydrogel preparation\u003c\/li\u003e\n\u003cli\u003eSuitable for copolymerization\u003c\/li\u003e\n\u003cli\u003eWidely used in dental materials research\u003c\/li\u003e\n\u003cli\u003eUseful for biomedical polymer research\u003c\/li\u003e\n\u003cli\u003eSuitable for contact-lens material development\u003c\/li\u003e\n\u003cli\u003eApplicable to coatings and adhesives\u003c\/li\u003e\n\u003cli\u003eUseful for surface functionalization\u003c\/li\u003e\n\u003cli\u003eAvailable in multiple purity grades\u003c\/li\u003e\n\u003cli\u003eCommercially available in stabilized formulations\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eStorage \u0026amp; Handling\u003c\/h2\u003e\n\u003cp\u003eHEMA is a reactive methacrylate monomer and is commonly supplied with a polymerization inhibitor such as \u003cstrong\u003eMEHQ\u003c\/strong\u003e to improve storage stability. Commercial specifications from Sigma-Aldrich include grades containing ≤50 ppm or ≤250 ppm MEHQ.\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eStore in a tightly closed container.\u003c\/li\u003e\n\u003cli\u003eStore in a cool, dry and well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eProtect from excessive heat and direct light.\u003c\/li\u003e\n\u003cli\u003eKeep away from strong oxidizing agents and incompatible chemicals.\u003c\/li\u003e\n\u003cli\u003eAvoid unnecessary exposure to heat because methacrylate monomers can polymerize.\u003c\/li\u003e\n\u003cli\u003eMaintain appropriate inhibitor concentration during storage.\u003c\/li\u003e\n\u003cli\u003eAvoid direct skin and eye contact.\u003c\/li\u003e\n\u003cli\u003eWear suitable gloves, protective clothing, and eye protection.\u003c\/li\u003e\n\u003cli\u003eHandle in a suitable fume hood or well-ventilated area.\u003c\/li\u003e\n\u003cli\u003eConsult the current SDS before handling.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eHEMA can cause skin sensitization, so appropriate measures should be taken to minimize skin exposure. PubChem notes the sensitizing potential associated with methacrylates.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eResearch Areas\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003e2-Hydroxyethyl Methacrylate (CAS No. 868-77-9)\u003c\/strong\u003e can be positioned across several specific industries and research fields:\u003c\/p\u003e\n\u003cdiv\u003e\u003cdiv\u003e\u003ctable\u003e\n\u003cthead\u003e\u003ctr\u003e\n\u003cth\u003eResearch Area\u003c\/th\u003e\n\u003cth\u003eSpecific Industry \/ Application\u003c\/th\u003e\n\u003c\/tr\u003e\u003c\/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eDental adhesives, dentin bonding, dental composites, resin-based restorative materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eContact Lens Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eSoft contact lenses, hydrogel lenses, ophthalmic biomaterials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eBiomedical Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrogels, biomaterials, biointerfaces, tissue-engineering materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eDrug Delivery\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eControlled-release hydrogels, drug-delivery polymer systems\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eMedical Devices\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrophilic polymer coatings and functional polymer materials\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eCoatings\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic coatings, UV-curable coatings, functional surface coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eAdhesives\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic adhesives, pressure-sensitive adhesives, dental adhesives\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePolymer Industry\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eAcrylic\/methacrylate copolymers and functional polymer synthesis\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003ePhotosensitive Materials\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003ePhotopolymerizable resins and photosensitive coatings\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eFiber \u0026amp; Textile\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eFiber treatment and polymer-based surface modification\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd\u003e\u003cstrong\u003eSurface Engineering\u003c\/strong\u003e\u003c\/td\u003e\n\u003ctd\u003eHydrophilic surface modification and polymer interface engineering\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\u003c\/div\u003e\u003c\/div\u003e\n\u003cp\u003eTCI's current application classification specifically includes \u003cstrong\u003eDental Materials Research Reagents\u003c\/strong\u003e, \u003cstrong\u003eBiomaterials\/ Biocompatible Materials\u003c\/strong\u003e, \u003cstrong\u003eMethacrylate Monomers\u003c\/strong\u003e, \u003cstrong\u003eDrug Delivery Systems\u003c\/strong\u003e, and \u003cstrong\u003eDouble Network Gel synthesis\u003c\/strong\u003e for HEMA.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch3\u003eQ1: What is 2-Hydroxyethyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e 2-Hydroxyethyl Methacrylate (HEMA) is a hydroxy-functional methacrylate monomer with \u003cstrong\u003eCAS No. 868-77-9\u003c\/strong\u003e, molecular formula \u003cstrong\u003eC₆H₁₀O₃\u003c\/strong\u003e, and molecular weight \u003cstrong\u003e130.14 g\/mol\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ2: What is HEMA used for?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e HEMA is used to prepare \u003cstrong\u003ehydrophilic polymers, hydrogels, dental materials, contact-lens materials, biomedical materials, coatings, adhesives, and functional acrylic polymers\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ3: Is HEMA used in dental materials?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is widely used in \u003cstrong\u003edental materials research\u003c\/strong\u003e, particularly in dental adhesive and resin systems. TCI explicitly lists HEMA under Dental Materials Research Reagents.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ4: Why is HEMA used in dental adhesives?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Its methacrylate group enables polymerization, while its hydroxyl group contributes hydrophilicity and interactions with substrates, making HEMA useful in dental adhesive formulations and dentin-bonding research.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ5: Is HEMA used for contact lenses?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is an important monomer for preparing \u003cstrong\u003ehydrophilic PHEMA-based hydrogel materials\u003c\/strong\u003e, historically associated with soft contact-lens materials.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ6: What polymer is produced from HEMA?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Polymerization of HEMA produces \u003cstrong\u003epoly(2-hydroxyethyl methacrylate), or PHEMA\u003c\/strong\u003e, a hydrophilic polymer widely investigated in hydrogel and biomaterial research.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ7: Is HEMA used in biomedical research?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. HEMA is used as a monomer for developing \u003cstrong\u003ehydrogels, biomaterials, drug-delivery systems, and other functional polymeric materials\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ8: Is HEMA supplied with an inhibitor?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. Commercial HEMA is commonly supplied in stabilized form, such as \u003cstrong\u003eMEHQ-stabilized HEMA\u003c\/strong\u003e, to reduce unwanted polymerization during storage.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n               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100%;\n    border-collapse: collapse;\n    margin: 15px 0;\n  }\n\n  .html-area table th,\n  .html-area table td {\n    border: 1px solid #e0e0e0;\n    padding: 5px 8px;\n  }\n\n  @media (max-width: 600px) {\n    .section-row {\n      grid-template-columns: repeat(1, 1fr);\n    }\n\n    .section-row .row-key {\n      grid-column: 1 \/ 2;\n    }\n\n    .section-row .row-value {\n      grid-column: 1 \/ 2;\n    }\n\n    .hazard-grid {\n      grid-template-columns: repeat(2, 1fr);\n      gap: 0 20px;\n    }\n  }\n  \n\u003c\/style\u003e\n\n\u003cdiv class=\"section\"\u003e\n  \n\n    \u003c!-- Order Info --\u003e\n    \u003ch2 class=\"section-header\"\u003eProduct Information\u003c\/h2\u003e\n    \u003cdiv class=\"section-content\"\u003e\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eHexadecyl methacrylate\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n        \n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eBrand Name\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eChemScene\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eProduct Number\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003eCS-0698155\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCAS\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e2495-27-4\u003c\/div\u003e\n        \u003c\/div\u003e\n        \n\n        \n\n        \n\n        \n\n        \u003cdiv class=\"section-row\"\u003e\n            \u003cdiv class=\"row-key\"\u003eCertificate of Analysis (COA)​\u003c\/div\u003e\n            \u003cdiv class=\"row-value\"\u003e\n                \u003cdiv class=\"coa-search-container\"\u003e\n                    \u003cinput id=\"coa-link-input\" type=\"text\" placeholder=\"Enter Lot No.\"\u003e\n                    \u003cbutton id=\"coa-search-button\"\u003e\n                        \u003cdiv class=\"coa-search-button-content\"\u003e\n                            \u003csvg class=\"search-spin\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" viewbox=\"0 0 200 200\"\u003e\u003cradialgradient id=\"a7\" cx=\".66\" fx=\".66\" cy=\".3125\" fy=\".3125\" gradienttransform=\"scale(1.5)\"\u003e\u003cstop offset=\"0\" stop-color=\"#FFFFFF\"\u003e\u003c\/stop\u003e\u003cstop offset=\".3\" stop-color=\"#FFFFFF\" stop-opacity=\".9\"\u003e\u003c\/stop\u003e\u003cstop offset=\".6\" stop-color=\"#FFFFFF\" stop-opacity=\".6\"\u003e\u003c\/stop\u003e\u003cstop offset=\".8\" stop-color=\"#FFFFFF\" stop-opacity=\".3\"\u003e\u003c\/stop\u003e\u003cstop offset=\"1\" stop-color=\"#FFFFFF\" stop-opacity=\"0\"\u003e\u003c\/stop\u003e\u003c\/radialgradient\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" stroke=\"url(#a7)\" stroke-width=\"15\" stroke-linecap=\"round\" stroke-dasharray=\"200 1000\" stroke-dashoffset=\"0\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003canimatetransform type=\"rotate\" attributename=\"transform\" calcmode=\"spline\" dur=\"2\" values=\"360;0\" keytimes=\"0;1\" keysplines=\"0 0 1 1\" repeatcount=\"indefinite\"\u003e\u003c\/animatetransform\u003e\u003c\/circle\u003e\u003ccircle transform-origin=\"center\" fill=\"none\" opacity=\".2\" stroke=\"#FFFFFF\" stroke-width=\"15\" stroke-linecap=\"round\" cx=\"100\" cy=\"100\" r=\"70\"\u003e\u003c\/circle\u003e\u003c\/svg\u003e\n                            \u003cspan\u003eSearch\u003c\/span\u003e\n                        \u003c\/div\u003e\n                    \u003c\/button\u003e\n                    \u003cspan class=\"coa-not-found\"\u003eCOA not found\u003c\/span\u003e\n                \u003c\/div\u003e\n            \u003c\/div\u003e\n        \u003c\/div\u003e\n\n    \u003c\/div\u003e\n\n    \u003c!-- General Info --\u003e\n    \n\n    \u003c!-- Properties --\u003e\n    \n\n    \u003c!-- Safety Info --\u003e\n    \n\n    \u003c!-- Description --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eDescription\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch2\u003eProduct Introduction\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eHexadecyl Methacrylate (CAS 2495-27-4)\u003c\/strong\u003e is a long-chain methacrylate monomer consisting of a polymerizable methacrylate group and a hydrophobic C16 alkyl chain.\u003c\/p\u003e\n\u003cp\u003eIts combination of a reactive methacrylate double bond and long hydrophobic alkyl segment makes it useful for preparing polymers with controlled \u003cstrong\u003esurface energy, water resistance, flexibility, hydrophobicity, and compatibility with nonpolar materials\u003c\/strong\u003e.\u003c\/p\u003e\n\u003cp\u003eHexadecyl Methacrylate is also known as \u003cstrong\u003eCetyl Methacrylate\u003c\/strong\u003e. Commercial suppliers offer stabilized grades, commonly using inhibitors such as hydroquinone or MEHQ to minimize unwanted polymerization during storage.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003ePolymerization Principle\u003c\/h2\u003e\n\u003cp\u003eHexadecyl Methacrylate contains a carbon-carbon double bond capable of undergoing free-radical polymerization.\u003c\/p\u003e\n\u003ch3\u003eFree-Radical Polymerization\u003c\/h3\u003e\n\u003cp\u003eUnder suitable initiation conditions:\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003en CH₂=C(CH₃)COO(CH₂)₁₅CH₃ → \u003cspan class=\"l_bracket\"\u003e\u003c\/span\u003e–CH₂–C(CH₃)(COO(CH₂)₁₅CH₃)–\u003cspan class=\"r_bracket\"\u003e\u003c\/span\u003eₙ\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eThe methacrylate double bond participates in polymerization, while the long C16 alkyl chain remains attached to the polymer backbone.\u003c\/p\u003e\n\u003cp\u003eThis structure can impart:\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eHydrophobicity\u003c\/li\u003e\n\u003cli\u003eFlexible side chains\u003c\/li\u003e\n\u003cli\u003eLow surface energy\u003c\/li\u003e\n\u003cli\u003eWater resistance\u003c\/li\u003e\n\u003cli\u003eTunable glass-transition behavior\u003c\/li\u003e\n\u003cli\u003eCompatibility with other alkyl methacrylates\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eKey Research Applications\u003c\/h2\u003e\n\u003ch3\u003e\u003cstrong\u003e1. Polymer and Copolymer Synthesis\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHexadecyl Methacrylate is primarily used as a monomer for polymer synthesis.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eHomopolymer synthesis\u003c\/li\u003e\n\u003cli\u003eCopolymer synthesis\u003c\/li\u003e\n\u003cli\u003eFunctional polymer development\u003c\/li\u003e\n\u003cli\u003eHydrophobic polymer materials\u003c\/li\u003e\n\u003cli\u003eSpecialty methacrylate polymers\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eIt can be copolymerized with other acrylic or methacrylic monomers to tune polymer properties.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e2. Hydrophobic Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eThe long C16 alkyl chain provides strong hydrophobic character.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eWater-repellent polymers\u003c\/li\u003e\n\u003cli\u003eHydrophobic coatings\u003c\/li\u003e\n\u003cli\u003eSurface modification\u003c\/li\u003e\n\u003cli\u003eLow-surface-energy materials\u003c\/li\u003e\n\u003cli\u003eWater-resistant polymer systems\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e3. Coatings\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHexadecyl Methacrylate can be incorporated into coating formulations to modify surface and environmental resistance.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eProtective coatings\u003c\/li\u003e\n\u003cli\u003eFunctional coatings\u003c\/li\u003e\n\u003cli\u003eHydrophobic coatings\u003c\/li\u003e\n\u003cli\u003eIndustrial coatings\u003c\/li\u003e\n\u003cli\u003eSurface-engineered polymer films\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eBASF lists C16\/C18 long-chain methacrylate products among applications including coatings, adhesives, plastics\/rubber, construction, lubricants, and related polymer applications.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e4. Adhesives and Sealants\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eLong-chain methacrylate monomers can be incorporated into adhesive and sealant formulations to adjust flexibility, hydrophobicity, and compatibility.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003ePressure-sensitive adhesives\u003c\/li\u003e\n\u003cli\u003eSpecialty adhesives\u003c\/li\u003e\n\u003cli\u003eSealants\u003c\/li\u003e\n\u003cli\u003ePolymer modifiers\u003c\/li\u003e\n\u003cli\u003eFlexible polymer systems\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e5. Lubricant and Oilfield Materials\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eLong-chain alkyl methacrylates are used in polymeric materials for lubricant and oilfield applications.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eLubricant additives\u003c\/li\u003e\n\u003cli\u003eViscosity-modifying polymers\u003c\/li\u003e\n\u003cli\u003eOil-soluble polymers\u003c\/li\u003e\n\u003cli\u003eOilfield polymer systems\u003c\/li\u003e\n\u003cli\u003eFunctional polymer additives\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003e\u003cstrong\u003e6. Surface Engineering\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003eHexadecyl Methacrylate can be used to introduce long hydrophobic side chains into polymer surfaces.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eApplications include:\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003eSurface functionalization\u003c\/li\u003e\n\u003cli\u003eWettability control\u003c\/li\u003e\n\u003cli\u003eHydrophobic surface preparation\u003c\/li\u003e\n\u003cli\u003ePolymer interface engineering\u003c\/li\u003e\n\u003cli\u003eSurface-energy modification\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eAdvantages\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eLong-chain hydrophobic methacrylate monomer\u003c\/li\u003e\n\u003cli\u003eContains a readily polymerizable methacrylate group\u003c\/li\u003e\n\u003cli\u003eUseful for homopolymer and copolymer synthesis\u003c\/li\u003e\n\u003cli\u003eProvides C16 hydrophobic side chains\u003c\/li\u003e\n\u003cli\u003eCan improve water resistance\u003c\/li\u003e\n\u003cli\u003eUseful for surface-energy modification\u003c\/li\u003e\n\u003cli\u003eSuitable for specialty polymer research\u003c\/li\u003e\n\u003cli\u003eCompatible with other acrylic and methacrylic monomers\u003c\/li\u003e\n\u003cli\u003eStabilized commercial grades available\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003eStorage \u0026amp; Handling\u003c\/h2\u003e\n\u003cul\u003e\n\u003cli\u003eStore in a \u003cstrong\u003etightly closed container\u003c\/strong\u003e.\u003c\/li\u003e\n\u003cli\u003eKeep away from heat, sparks, flames, and direct sunlight.\u003c\/li\u003e\n\u003cli\u003eStore under supplier-recommended temperature conditions.\u003c\/li\u003e\n\u003cli\u003eProtect from excessive heat because methacrylate monomers can polymerize when exposed to unsuitable conditions.\u003c\/li\u003e\n\u003cli\u003eMaintain the recommended inhibitor level during storage.\u003c\/li\u003e\n\u003cli\u003eAvoid contamination with strong oxidizers or polymerization initiators.\u003c\/li\u003e\n\u003cli\u003eHandle in a well-ventilated area or suitable fume hood.\u003c\/li\u003e\n\u003cli\u003eWear appropriate gloves, protective clothing, and eye protection.\u003c\/li\u003e\n\u003cli\u003eFollow the current product SDS for specific storage and handling requirements.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eCommercial Hexadecyl Methacrylate is available in stabilized form; one supplier specifies \u003cstrong\u003e100 ppm hydroquinone\u003c\/strong\u003e and long-term storage at \u003cstrong\u003e2–8°C\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch2\u003e \u003c\/h2\u003e\n\u003ch2\u003e\u003cspan\u003eResearch Areas\u003c\/span\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cspan\u003eThis product can support research, formulation development, and material innovation across multiple scientific and industrial fields, including:\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eDental Materials\u003c\/strong\u003e – Research and development of dental resin composites, dental adhesives, restorative materials, orthodontic bonding materials, and other resin-based dental systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003ePolymer Materials\u003c\/strong\u003e – Polymer synthesis, modification, crosslinking, and structure–property studies.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eCoatings \u0026amp; Surface Materials\u003c\/strong\u003e – Development of functional coatings, surface treatments, and polymer-based protective materials.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdhesives \u0026amp; Sealants\u003c\/strong\u003e – Formulation and performance optimization of adhesive and sealant systems.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eBiomedical Materials\u003c\/strong\u003e – Research on functional polymeric materials and other material systems for biomedical applications.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eChemical Synthesis\u003c\/strong\u003e – Use as a reagent, monomer, additive, crosslinker, or initiator in laboratory and industrial chemical synthesis, depending on its chemical functionality.\u003c\/span\u003e\u003c\/li\u003e\n\u003cli\u003e\u003cspan\u003e\u003cstrong\u003eAdvanced Materials Research\u003c\/strong\u003e – Development and optimization of high-performance functional materials for emerging technologies.\u003c\/span\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- Faq --\u003e\n    \n    \u003ch2 class=\"section-header\"\u003eFAQ\u003c\/h2\u003e\n    \u003cdiv class=\"html-area\"\u003e\n        \u003ch3\u003eQ1: What is Hexadecyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Hexadecyl Methacrylate is a long-chain alkyl methacrylate monomer with \u003cstrong\u003eCAS No. 2495-27-4\u003c\/strong\u003e, molecular formula \u003cstrong\u003eC₂₀H₃₈O₂\u003c\/strong\u003e, and molecular weight approximately \u003cstrong\u003e310.51 g\/mol\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ2: Is Hexadecyl Methacrylate the same as Cetyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. \u003cstrong\u003eCetyl Methacrylate\u003c\/strong\u003e is a commonly used synonym for Hexadecyl Methacrylate.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ3: What is Hexadecyl Methacrylate used for?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e It is primarily used as a \u003cstrong\u003emethacrylate monomer for polymer and copolymer synthesis\u003c\/strong\u003e, especially when hydrophobicity, flexibility, water resistance, or surface-property modification is desired.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ4: What is the molecular formula of Hexadecyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e The molecular formula is \u003cstrong\u003eC₂₀H₃₈O₂\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ5: What is the molecular weight of Hexadecyl Methacrylate?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e The molecular weight is approximately \u003cstrong\u003e310.51 g\/mol\u003c\/strong\u003e.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ6: Can Hexadecyl Methacrylate be used in copolymer synthesis?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Yes. Its methacrylate group allows it to participate in free-radical polymerization and copolymerization with compatible acrylic and methacrylic monomers.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ7: Why is Hexadecyl Methacrylate useful for hydrophobic polymers?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Its \u003cstrong\u003elong C16 alkyl chain\u003c\/strong\u003e provides a hydrophobic side group that can increase the hydrophobic character and reduce surface energy of the resulting polymer.\u003c\/p\u003e\n\u003ch3\u003e \u003c\/h3\u003e\n\u003ch3\u003eQ8: Is Hexadecyl Methacrylate stabilized?\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003eA:\u003c\/strong\u003e Commercial products are commonly supplied with polymerization inhibitors such as hydroquinone or MEHQ. The specific inhibitor and concentration should be confirmed in the product specification or SDS.\u003c\/p\u003e\n    \u003c\/div\u003e\n    \n\n    \u003c!-- References --\u003e\n    \n\n\n    \u003cscript\u003e\n        const coaSearchButton = document.getElementById('coa-search-button');\n        coaSearchButton.addEventListener('click', async function() {\n            const coaLinkInput = document.getElementById('coa-link-input');\n            const spinElement = document.querySelector('.search-spin');\n            const notFoundElement = document.querySelector('.coa-not-found');\n\n            const lot = coaLinkInput.value.trim().toUpperCase();\n            if (lot.length \u003e 0) {\n                spinElement.style.display = 'block';\n                notFoundElement.style.display = 'none';\n\n                const url = `https:\/\/web.jkchemical.com\/partial\/coaFileLotNumber\/${lot}`;\n                await fetch(url).then((res) =\u003e {\n                    if (res.status === 200) {\n                        window.open(url, '_blank');\n                    } else {\n                        notFoundElement.style.display = 'block';\n                    }\n                }).finally(() =\u003e {\n                    spinElement.style.display = 'none';\n                });\n            }\n        });\n    \u003c\/script\u003e\n\n\n\u003c\/div\u003e","brand":"ChemScene","offers":[{"title":"1×5g","offer_id":48237178126526,"sku":"TS246CS-0698155_5_G","price":40.3,"currency_code":"USD","in_stock":true},{"title":"1×1g","offer_id":48237178159294,"sku":"TS246CS-0698155_1_G","price":13.8,"currency_code":"USD","in_stock":true},{"title":"1×100g","offer_id":48237178192062,"sku":"TS246CS-0698155_100_G","price":426.7,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0506\/0005\/0878\/files\/d887a3425965e1c2643fdfb89f03555f.jpg?v=1791615188"}],"url":"https:\/\/www.jk-sci.com\/collections\/dental-resin-monomers.oembed","provider":"J\u0026K Scientific LLC","version":"1.0","type":"link"}