79-96-9

Basic information

• Product Name: 4,4'-ISOPROPYLIDENEBIS(2-T-BUTYLPHENOL)
• Synonyms: 4,4'-ISOPROPYLIDENEBIS(2-T-BUTYLPHENOL);(2,2’-di-tert-butyl-4,4’-isopropylene)di-pheno;4,4’-(1-methylethylidene)bis(2-(1,1-dimethylethyl)-pheno;4,4’-(1-methylethylidene)bis[2-(1,1-dimethylethyl)-pheno;4,4’-isopropylidenebis(2-tert-butyl-pheno;4,4'-isopropylidenebis(o-tert-butylphenol);4,4'-Isopropylidenebis(2-tert-butylphenol);tert-Butylbisphenol A
• CAS NO: 79-96-9
• Molecular Formula: C₂₃H₃₂O₂
• Molecular Weight: 340.5
• EINECS: 201-239-5
• Mol File: 79-96-9.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 436.28°C (rough estimate)
• Appearance: /
• Density: 0.9832 (rough estimate)
• Refractive Index: 1.5100 (estimate)
• CAS DataBase Reference: 4,4'-ISOPROPYLIDENEBIS(2-T-BUTYLPHENOL)(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4'-ISOPROPYLIDENEBIS(2-T-BUTYLPHENOL)(79-96-9)
• EPA Substance Registry System: 4,4'-ISOPROPYLIDENEBIS(2-T-BUTYLPHENOL)(79-96-9)

Safety Data

• Hazardous Substances Data: 79-96-9(Hazardous Substances Data)

Usage

General Description

4,4'-Isopropylidenebis(2-t-butylphenol) is a chemical compound commonly used as an antioxidant in rubber and plastics. It is a white or pale yellow solid that is insoluble in water but soluble in organic solvents. 4,4'-ISOPROPYLIDENEBIS(2-T-BUTYLPHENOL) is known for its ability to protect against the degradation of materials caused by exposure to heat, oxygen, or light. It functions by preventing the oxidation of the material it is added to, thereby extending its lifespan and maintaining its physical properties. Additionally, it is often used as a stabilizer in various industrial processes and products, making it a valuable additive in the manufacturing of polymers and other materials.

Upstream product

• 88-18-6 2-tert-Butylphenol 
• 67-64-1 acetone 
• 74-99-7 prop-1-yne 
• 32565-67-6 2-tert.-Butyl-4-isopropenyl-phenol 
• 108-95-2 phenol 

Downstream Products

• 457658-13-8 5,5'-di-tert-butyl-6,6'-dihydroxy-3,3'-(propane-2,2-diyl)dibenzaldehyde 
• 333334-76-2 2-(tert-butyl)-4-(1-(5-(tert-butyl)-3-(chloromethyl)-4-hydroxyphenyl)isopropyl)-6-(chloromethyl)phenol 
• 333334-74-0 1-(tert-butyl)-5-(1-(3-(tert-butyl)-4-methoxyphenyl)isopropyl)-2-methoxybenzene 
• 122041-35-4 6-(tert-butyl)-4-(1-(5-(tert-butyl)-4-hydroxy-3-(hydroxymethyl)phenyl)isopropyl)-2-(hydroxymethyl)phenol 
• 32565-67-6 2-tert.-Butyl-4-isopropenyl-phenol 

Relevant articles and documents

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Highly enantioselective epoxidation of unfunctionalized olefins catalyzed by a novel recyclable chiral poly-salen-Mn(III) complex

A new soluble recyclable poly-salen-Mn(III) complex has been synthesized and found to give high enantioselectivities (up to 97% ee) for the asymmetric epoxidation of unfunctionalized olefins.

Phenolic compounds

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