5427-02-1

Basic information

• Product Name: 2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one
• Synonyms: 2,6-Bis(1,1-dimethylethyl)-4-isopropylidenecyclohexa-2,5-dien-1-one; 2,6-Ditert-butyl-4-(1-methylethylidene)-2,5-cyclohexadien-1-one
• CAS NO: 5427-02-1
• Molecular Formula: C₁₇H₂₆O
• Molecular Weight: 246.3877
• Mol File: 5427-02-1.mol

Chemical Properties

• Boiling Point: 337.3°C at 760 mmHg
• Flash Point: 139.8°C
• Density: 0.948g/cm³
• Vapor Pressure: 0.000106mmHg at 25°C
• Refractive Index: 1.503
• CAS DataBase Reference: 2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one(5427-02-1)
• EPA Substance Registry System: 2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one(5427-02-1)

Safety Data

• Hazardous Substances Data: 5427-02-1(Hazardous Substances Data)

Usage

Uses

Used in Fragrance Industry:
2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one is used as a fragrance ingredient for its distinctive and long-lasting scent. It is commonly incorporated into perfumes and personal care products to enhance their aroma profiles.
Used in Plastics Production:
2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one is also utilized in the manufacturing process of plastics, contributing to the development of materials with specific properties and characteristics.
Used in Food Industry:
Furthermore, 2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one serves as a flavoring agent in the food industry, adding unique taste dimensions to various food products.
Despite its low acute toxicity, it is essential to handle and store 2,6-di-tert-butyl-4-(propan-2-ylidene)cyclohexa-2,5-dien-1-one with care to ensure safety in all its applications.

Upstream product

• 56-23-5 tetrachloromethane 
• 33768-37-5 2,6-Di-tert-butyl-4-isopropyl-phenoxyl 
• 108-86-1 bromobenzene 
• 110-82-7 cyclohexane 
• 5427-03-2 2,6-di-tert-butyl-4-isopropylphenol 
• 100-66-3 methoxybenzene 
• 100-47-0 benzonitrile 
• 108-90-7 chlorobenzene 
• 71-43-2 benzene 
• 58382-02-8 2,3-bis-(3,5-di-tert-butyl-4-hydroxy-phenyl)-2,3-dimethyl-butane 
• 99-89-8 4-Isopropylphenol 

Downstream Products

• 58382-02-8 2,3-bis-(3,5-di-tert-butyl-4-hydroxy-phenyl)-2,3-dimethyl-butane 
• 102175-20-2 2,6-Di-tert-butyl-4-(α-methoxy-isopropyl)-phenol 
• 87970-43-2 2,6-di-tert-butyl-4-<(2-cyano)isopropyl>phenol 
• 24416-95-3 5,7-di-tert-butyl-2,2-dimethyl-1-oxa-spiro[2.5]octa-4,7-dien-6-one 
• 19263-37-7 2,6-di-t-butyl-4-i-propenylphenol 
• 14035-33-7 1-(3,5-di-tert-butyl-4-hydroxyphenyl)ethanone 
• 87970-45-4 <2-methyl-2-<3,5-di-tert-butyl-4-hydroxyphenyl>-propyl>ammonium chloride 
• 103400-93-7 2,6,2',6'-tetra-tert-butyl-4,4'-bis-(α-methoxy-isopropyl)-4,4'-peroxy-bis-cyclohexa-2,5-dienone 

Relevant articles and documents

4,4′-(Trimethylene)bis(2,6-di-t-butylphenoxy) diradical: An application of the sequential redox-solid state photolysis (SRSSP) method

The oxidation of 4,4′-(trimethylene)bis(2,6-di-t-butylphenol) with lead dioxide underwent intramolecular cyclization at the 4,4′-positions to give a dispiro-compound. Irradiation of the dispiro-compound in a methylcyclohexane matrix at -150 °C produced 4,