497-39-2

Basic information

• Product Name: 4,6-DI-TERT-BUTYL-M-CRESOL
• Synonyms: 2,4-bis(1,1-dimethylethyl)-5-methylphenol;2,4-bis(1,1-dimethylethyl)-5-methyl-Phenol;2,4-di-t-butyl-5-methylphenol;3-methyl-4,6-di-tert-butylphenol;4,6-di-t-butyl-m-cresol;4,6-di-tert-butyl-m-creso;4,6-DI-TERT-BUTYL-M-CRESOL;4,6-DI-TERT-BUTYL-3-METHYLPHENOL
• CAS NO: 497-39-2
• Molecular Formula: C₁₅H₂₄O
• Molecular Weight: 220.35
• EINECS: 207-847-7
• Mol File: 497-39-2.mol
• Article Data: 1

Chemical Properties

• Melting Point: 62°C
• Boiling Point: 284℃
• Flash Point: 128℃
• Appearance: /
• Density: 0.927
• Vapor Pressure: 0.0018mmHg at 25°C
• Refractive Index: 1.5021 (estimate)
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
• PKA: 11.68±0.23(Predicted)
• Merck: 14,2837
• CAS DataBase Reference: 4,6-DI-TERT-BUTYL-M-CRESOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-DI-TERT-BUTYL-M-CRESOL(497-39-2)
• EPA Substance Registry System: 4,6-DI-TERT-BUTYL-M-CRESOL(497-39-2)

Safety Data

• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• RTECS: GO7800000
• Hazardous Substances Data: 497-39-2(Hazardous Substances Data)

Usage

Description

4,6-Di-tert-butyl-m-cresol is an organic compound characterized by its molecular structure that features two tert-butyl groups and a methyl group attached to a cresol backbone. It is known for its chemical stability and is commonly used as an intermediate in the synthesis of various compounds.

Uses

Used in Chemical Industry:
4,6-Di-tert-butyl-m-cresol is used as an intermediate for the production of rubber chemicals and modified phenolic resins. Its chemical structure provides enhanced stability and performance characteristics to the final products, making it a valuable component in the development of these materials.
Used in Fragrance Industry:
In the fragrance industry, 4,6-Di-tert-butyl-m-cresol is used as a precursor for the synthesis of synthetic musks of the ambrette type. These synthetic musks are valued for their unique scent profiles and are used in the creation of various perfumes and fragrances.
Used in Food Industry:
The condensation of 4,6-Di-tert-butyl-m-cresol can produce di-tert-butyl-m-cresyl phosphonite, which is a regulated food additive. This additive is utilized in the food industry to enhance the flavor and aroma of certain products, contributing to a more enjoyable consumer experience.

Upstream product

• 108-39-4 3-methyl-phenol 
• 75-65-0 tert-butyl alcohol 
• 7664-93-9 sulfuric acid 
• 115-11-7 isobutene 

Downstream Products

• 24456-96-0 2-tert-butyl-5-methyl-1,4-benzoquinone 
• 3114-65-6 4,6-Di-tert-butyl-3-methyl-2-nitro-phenol 
• 3996-59-6 2.6-dinitro-3-hydroxy-1-methyl-4-tert-butyl-benzene 
• 52751-71-0 2,4-dibromo-6-tert-butyl-3-methyl-phenol 
• 15460-09-0 2-bromo-3-methyl-4,6-di-tert-butylphenol 
• 6319-31-9 4,6-di-tert-butyl-2-chloro-3-methyl-phenol 
• 855411-56-2 6-tert-butyl-2,4,4-trichloro-3-methyl-cyclohexa-2,5-dienone 
• 101354-87-4 4,6-di-tert-butyl-3-methyl-2,4-dinitro-cyclohexa-2,5-dienone 
• 26411-30-3 4,6,4',6'-tetra-tert-butyl-3,3'-dimethyl-2,2'-sulfanediyl-di-phenol 
• 108-39-4 3-methyl-phenol 
• 115-11-7 isobutene 
• 29666-43-1 2-tert-Butyl-6-chloro-5-methyl-1,4-benzoquinone 
• 6390-68-7 3,5,3',5'-Tetra-tert-butyl-6,6'-dimethyl-biphenyl-2,2'-diol 
• 97434-41-8 (1,3,5-Tri-tert-butyl-4-oxo-cyclohexa-2,5-dienyl)-(3-methyl-4,6-di-tert-butyl-phenyl)-ether 

Relevant articles and documents

Alkylation of Phenols with tert-Butanol Catalyzed by H-Form of Y Zeolites with a Hierarchical Porous Structure

tert-Butyl-substituted phenols have been synthesized via the reaction of phenol, o-, m-, and p-cresols with tert-butanol under the action of CBr4-promoted Y-zeolites in the H-form with a hierarchical porous structure.