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Product Information

Product Name
(Tetrahydrofuran-2-yl)methyl acrylate,98% (stabilized with MEHQ)
Brand Name
ChemScene
Product Number
CS-W018010
CAS
2399-48-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
94232
IUPAC Name
oxolan-2-ylmethyl prop-2-enoate
InChI Key
YNXCGLKMOXLBOD-UHFFFAOYSA-N
SMILES
C=CC(=O)OCC1CCCO1

Description

Product Introduction

Tetrahydrofurfuryl Acrylate (THFA, CAS No. 2399-48-6) is a functional monofunctional acrylate monomer containing a polymerizable acrylate group and a tetrahydrofuran ring.

The 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 reactive diluent and functional monomer for UV-curable and radiation-curable polymer systems.

Commercial THFA is commonly supplied as a stabilized liquid. TCI reports >98.0% GC purity, while other commercial grades are available at approximately 97–98% purity with polymerization inhibitors.

THFA is used in UV-curable resins, adhesives, coatings, inks, 3D-printing resins, and specialty polymer synthesis. Arkema describes its commercial THFA monomer as a low-viscosity, polar, monofunctional monomer that promotes adhesion to numerous substrates.

 

Polymerization / Reaction Principle

Tetrahydrofurfuryl Acrylate contains a polymerizable acrylate double bond:

CH₂=CHCOOCH₂C₄H₇O

Under suitable free-radical initiation conditions, THFA undergoes addition polymerization:

n CH₂=CHCOOCH₂C₄H₇O → –CH₂–CH(COOCH₂C₄H₇O)–

The tetrahydrofuran ring remains incorporated into the side chain of the resulting polymer.

THFA can also be copolymerized with other acrylate, methacrylate, or vinyl monomers to adjust:

  • Polymer polarity
  • Adhesion
  • Flexibility
  • Surface properties
  • Solvency
  • Crosslinking behavior
  • Film formation
  • Curing performance

The low viscosity and polar nature of THFA are particularly useful when formulating reactive resin systems.

 

Key Research Applications

1. UV-Curable Resin

THFA is widely used as a reactive monomer and reactive diluent in UV-curable resin systems.

Applications include:

  • UV-curable acrylic resins
  • Radiation-curable polymers
  • UV resin formulations
  • Photopolymer systems
  • Functional acrylic resins

Its 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.

 

2. 3D Printing Materials

THFA is used in the development of photopolymer resins for additive manufacturing.

Applications include:

  • SLA 3D printing
  • DLP 3D printing
  • UV-curable 3D-printing resins
  • Photopolymer formulation
  • Rapid prototyping materials

J&K Scientific specifically identifies Tetrahydrofurfuryl Acrylate for developing photopolymer resins used in 3D printing, while industry sources identify THFA among monomers used in UV-curable systems.

 

3. UV-Curable Adhesives

THFA can be incorporated into UV-curable adhesive formulations.

Applications include:

  • UV-curable adhesives
  • Pressure-sensitive adhesive research
  • Optical adhesives
  • Electronic-material adhesives
  • Specialty bonding materials

Its 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.

 

4. Coatings

THFA is an important functional monomer for acrylic and UV-curable coatings.

Applications include:

  • UV-curable coatings
  • Protective coatings
  • Industrial coatings
  • Metal coatings
  • Plastic coatings
  • Functional surface coatings
  • Outdoor coatings

Its 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.

 

5. UV-Curable Inks

THFA can be used in radiation-curable ink formulations.

Applications include:

  • UV printing inks
  • UV inkjet inks
  • Digital printing
  • Industrial printing
  • Functional inks

Its low viscosity and good dilution capability make it useful in reactive ink formulations. Kowa Chemicals identifies THFA for UV inkjet inks, while other commercial sources list UV inks among its applications.

 

6. Polymer and Copolymer Synthesis

THFA is a useful monomer for preparing specialty polymers and copolymers.

Applications include:

  • Acrylic copolymers
  • Functional polymers
  • Specialty resins
  • Hydrophobic/hydrophilic property modification
  • Polymer structure–property studies

Its cyclic ether group provides an additional structural feature compared with simple alkyl acrylates, allowing researchers to tune polymer polarity and substrate interactions.

 

7. Adhesives & Sealants

THFA can be used in adhesive and sealant formulations as a reactive monomer.

Applications include:

  • Industrial adhesives
  • UV adhesives
  • Sealants
  • Flexible adhesive systems
  • Specialty bonding formulations

Kowa Chemicals identifies THFA as a monomer used in adhesives and sealants, with functions including adhesion and low viscosity.

 

8. Bio-Based Polymer Materials

A bio-based version of THFA is commercially available, with TCI reporting approximately 62% bio-based carbon for its plant-derived-carbon product. This provides an option for research into more sustainable acrylate monomers and polymer formulations.

Applications include:

  • Bio-based polymer research
  • Sustainable UV-curable materials
  • Renewable-content acrylate formulations
  • Green polymer chemistry
  • Bio-based coatings and resins

 

Advantages

  • Highly reactive acrylate functionality
  • Monofunctional reactive monomer
  • Low viscosity
  • Polar molecular structure
  • Contains a cyclic ether group
  • Good dilution capability
  • Can improve adhesion to various substrates
  • Suitable for UV and radiation curing
  • Useful for polymer and copolymer synthesis
  • Applicable to coatings and adhesives
  • Suitable for UV inks
  • Useful in 3D-printing resin development
  • Stabilized grades available
  • Bio-based versions available

Arkema characterizes THFA as a low-viscosity, polar, monofunctional monomer with adhesion-promoting properties, while commercial technical data also highlights its dilution capability and suitability for UV-curable applications.

 

Storage & Handling

Tetrahydrofurfuryl Acrylate is a reactive acrylate monomer and is commonly supplied with a polymerization inhibitor such as MEHQ or hydroquinone.

  • Store in a tightly closed container.
  • Keep in a cool, dry and well-ventilated area.
  • Protect from heat and direct sunlight.
  • Avoid contamination with polymerization initiators.
  • Keep away from strong oxidizing agents and incompatible materials.
  • Maintain the recommended inhibitor concentration during storage.
  • Avoid unnecessary exposure to elevated temperatures.
  • Wear appropriate gloves, protective clothing, and eye protection.
  • Avoid direct contact with skin and eyes.
  • Handle in an appropriate fume hood or well-ventilated area.
  • Consult the current SDS before use.

TCI recommends storing its THFA product in a cool, dark location below 15°C. 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.

 

Research Areas

Research Area Specific Industry / Application
UV-Curable Materials UV-curable resins, radiation-curable polymers, photopolymer formulations
3D Printing SLA/DLP photopolymer resins, UV-curable additive-manufacturing materials
Coatings Industry UV coatings, protective coatings, plastic coatings, metal coatings
Adhesives & Sealants UV adhesives, industrial adhesives, specialty sealants
Printing & Ink Industry UV inks, UV inkjet inks, digital printing materials
Polymer Industry Acrylic copolymers, specialty polymers, functional resins
Electronics Materials UV-curable functional coatings and adhesive materials
Surface Engineering Adhesion promotion, surface modification, wettability control
Sustainable Materials Bio-based acrylate monomers and renewable-content polymer research
Materials Science Structure–property studies of functional acrylate polymers

Note: Compared with HEMA (868-77-9), whose application in dental materials is well established, the currently available evidence for 2399-48-6 in dental materials is not strong enough to make dentistry a primary commercial application. For an SEO product page, it is more accurate to prioritize UV curing, coatings, adhesives, inks, 3D printing, and polymer materials.

FAQ

Q1: What is Tetrahydrofurfuryl Acrylate?

A: Tetrahydrofurfuryl Acrylate (THFA) is a functional monofunctional acrylate monomer with CAS No. 2399-48-6, molecular formula C₈H₁₂O₃, and molecular weight 156.18 g/mol.

 

Q2: What is Tetrahydrofurfuryl Acrylate used for?

A: THFA is mainly used in UV-curable resins, coatings, adhesives, UV inks, 3D-printing photopolymer resins, and specialty polymer synthesis.

 

Q3: Is THFA a monomer?

A: Yes. THFA is a monofunctional acrylate monomer that can undergo free-radical polymerization and copolymerization.

 

Q4: Is Tetrahydrofurfuryl Acrylate used in UV curing?

A: Yes. THFA is used as a reactive monomer/reactive diluent in UV-curable and radiation-curable formulations.

 

Q5: Is THFA used in 3D printing?

A: Yes. THFA is used in the development of photopolymer resins for 3D printing, including UV-curable additive-manufacturing materials.

 

Q6: Is THFA used in coatings?

A: Yes. THFA is used in UV-curable and functional coating formulations, where its properties can contribute to adhesion and other coating performance characteristics.

 

Q7: Is THFA used in adhesives?

A: Yes. THFA is used in UV-curable adhesives and other adhesive formulations, particularly where low viscosity and adhesion to substrates are important.

 

Q8: Is Tetrahydrofurfuryl Acrylate stabilized?

A: Yes. Commercial THFA is commonly supplied with polymerization inhibitors such as MEHQ or hydroquinone to improve storage stability

References Data Source From Pubchem

Preparation of cellulose-based fluorescent elastomers via RAFT polymerization and lanthanide coordination

Publication Name: Cellulose
Publication Date: 2025-10-11
DOI: 10.1007/s10570-025-06809-z

A novel composite meniscus scaffold with shape memory and adhesive properties alleviates knee cartilage degeneration through minimally invasive and sutureless approach

Publication Name: Advanced Composites and Hybrid Materials
Publication Date: 2025-05-14
DOI: 10.1007/s42114-025-01325-x

Irradiation-cured graphene composite films: a comparison between UV and EB curing

Publication Name: Journal of Coatings Technology and Research
Publication Date: 2023-06-13
DOI: 10.1007/s11998-023-00776-5

Electron beam irradiation treatment of textiles materials: a review

Publication Name: Journal of Polymer Research
Publication Date: 2022-03-11
DOI: 10.1007/s10965-022-02952-4

UV-curable organic–inorganic hybrid hard coatings for metal sheets

Publication Name: Journal of Coatings Technology and Research
Publication Date: 2018-11-05
DOI: 10.1007/s11998-018-00154-6