13131-76-5

Basic information

• Product Name: 1-Isobutyl-3,5-dimethylcyclohexane
• Synonyms: 1-Isobutyl-3,5-dimethylcyclohexane
• CAS NO: 13131-76-5
• Molecular Formula: C₂₇H₃₀O
• Molecular Weight: 370.53
• Mol File: 13131-76-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 510.9°Cat760mmHg
• Flash Point: 218.7°C
• Appearance: /
• Density: 1.051g/cm³
• Vapor Pressure: 1.49E-10mmHg at 25°C
• Refractive Index: 1.579
• CAS DataBase Reference: 1-Isobutyl-3,5-dimethylcyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Isobutyl-3,5-dimethylcyclohexane(13131-76-5)
• EPA Substance Registry System: 1-Isobutyl-3,5-dimethylcyclohexane(13131-76-5)

Safety Data

• Hazardous Substances Data: 13131-76-5(Hazardous Substances Data)

Usage

Type of compound

Cycloalkane

Structure

Cyclohexane ring with two methyl groups and an isobutyl group attached

Industrial applications

Solvent in the production of paints, coatings, and adhesives

Toxicity

Relatively low, not considered a significant health hazard

Safety precautions

Handle with care and follow proper safety measures when working with it

Versatility

Several practical uses in manufacturing and chemical industries

InChI:InChI=1/C27H30O/c1-26(2,3)22-17-21(18-23(25(22)28)27(4,5)6)24(19-13-9-7-10-14-19)20-15-11-8-12-16-20/h7-18H,1-6H3

Upstream product

• 13145-54-5 3,5-di-tert-butyl-4-hydroxyphenyldiphenylmethane 
• 91-01-0 1,1-Diphenylmethanol 
• 128-39-2 2,6-di-tert-butylphenol 

Downstream Products

• 13145-54-5 3,5-di-tert-butyl-4-hydroxyphenyldiphenylmethane 
• 13343-57-2 2,6-Di-t-butyl-4-(α,α-diphenyl)-pentylphenol 
• 13343-53-8 2,6-Di-tert-butyl-4-[(9H-fluoren-9-yl)-diphenyl-methyl]-phenol 
• 13319-99-8 2,6-Di-tert-butyl-4-(2-methanesulfonyl-1,1-diphenyl-ethyl)-phenol 
• 13343-52-7 4-[2-(4-Benzenesulfonyl-phenyl)-1,1-diphenyl-ethyl]-2,6-di-tert-butyl-phenol 
• 13343-55-0 2-{3,5-di-tert-butyl-4-hydroxyphenyl}-2,2-diphenylacetonitrile 
• 57196-37-9 α,α-Diphenyl-α-methoxy-2,6-di-tert.-butyl-p-cresol 
• 13145-53-4 3,5-Di-tert.-butyl-4-hydroxy-triphenylcarbinol 
• 13343-59-4 2,6-Di-tert-butyl-4-(methoxy-diphenyl-methyl)-biphenyl 
• 13343-60-7 2,6-Di-tert-butyl-4-(ethoxy-diphenyl-methyl)-biphenyl 
• 13343-51-6 4-[2-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-2,2-diphenyl-ethyl]-benzonitrile 
• 13343-49-2 3-(3,5-Di-tert-butyl-4-hydroxy-phenyl)-3,3-diphenyl-propionitrile 
• 119-61-9 benzophenone 
• 113894-06-7 (3,5-di-tert-4-methoxyphenyl)diphenylmethane 

Relevant articles and documents

ELECTRO-ORGANIC REACTIONS. PART 32. ELECTROGENERATED BASES FROM QUINONEMETHIDES

The radical-anion of fuchsone (1), and the dianions of related quinonemethides, are generated at low cathodic potentials and act as bases in high yielding Wittig reactions; the phenolic product may be oxidatively reconverted into quinonemethide.