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Sku CI33860_1_KG
Chem Impex
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Product Information

Product Name
2,6-Di-tert-butyl-4-methylphenol
Brand Name
Chem Impex
Product Number
33860
CAS
128-37-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
31404
IUPAC Name
2,6-ditert-butyl-4-methylphenol
InChI Key
NLZUEZXRPGMBCV-UHFFFAOYSA-N
SMILES
CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C

Application

2,6-Di-tert-butyl-4-methylphenol is widely utilized in research focused on:

Antioxidant Applications: This compound is primarily used as a powerful antioxidant in various industrial products, helping to prevent oxidation and extend the shelf life of materials like plastics, rubber, and fuels.

Food Preservation: In the food industry, it acts as a food preservative, protecting oils and fats from rancidity, thereby maintaining flavor and quality in packaged foods.

Cosmetics and Personal Care: It is incorporated into cosmetics and personal care products to enhance stability and prevent degradation of sensitive ingredients, ensuring product efficacy over time.

Pharmaceuticals: The compound is used in the formulation of pharmaceuticals, where it helps to stabilize active ingredients, improving the overall effectiveness and safety of medications.

Polymer Manufacturing: In the polymer industry, it serves as a stabilizer, protecting polymers from thermal degradation during processing and extending the lifespan of finished products.

References

Publisher Correction: Selective and Efficient Oxidation of Aldehydes To Corresponding Carboxylic Acids Using Titanium(IV) Oxyacetylacetonate and Dioxygen

Publication Name: Chemistry Africa
Publication Date: 2025-11-14
DOI: 10.1007/s42250-025-01346-5|10.1007/s42250-025-01481-z

Mapping of chemical distribution and semi-quantitative evaluation of compatibility in polypropylene based on confocal Raman

Publication Name: Journal of Polymer Research
Publication Date: 2025-07-28
DOI: 10.1007/s10965-025-04493-y

The phytopathogenic fungus Macrophomina phaseolina: a potential resource for biosynthesis and biotransformation of bioactive compounds

Publication Name: Phytochemistry Reviews
Publication Date: 2025-07-24
DOI: 10.1007/s11101-025-10168-9

Ovarian toxicity of 2,6-di-tert-butyl-hydroxytoluene on female Ruditapes philippinarum: Reproductive endocrine disruption and oxidative stress

Publication Name: Journal of Hazardous Materials
Publication Date: 2025-07-15
DOI: 10.1016/j.jhazmat.2025.138289