4-VINYLCYCLOHEXENE-1

PRODUCT IDENTIFICATION

CAS NO. 100-40-3

4-VINYLCYCLOHEXENE-1

EINECS NO. 202-848-9
FORMULA C6H9CH=CH2
MOL WT. 108.18
H.S. CODE 2902.19.0050
TOXICITY Oral rat LD50: 2,560 mg/kg
SYNONYMS 4-Ethenylcyclohexene; 4-Vinyl-1-cyclohexene; Butadiene dimer;
1,2,3,4-Tetrahydrostyrene; 4-Vinylcyclohexene; 1,2,3,4-Tetrahydrostyrene; 1-Vinylcyclohexene-3; 4-Ethenyl-1-cyclohexene; 4-Vinylcyclohexene; 4-Vinylcyclohexene-1;  Cyclohexenylethylene; Ethenyl-1-cyclohexene; Vinylcyclohexene; Other RN: 92619-43-7
SMILES C1[C@@H](CC=CC1)C=C

CLASSIFICATION

 

EXTRA NOTES

Overall Carcinogenic Evaluation: Group 2B

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE Slightly yellow liquid
MELTING POINT -108 C
BOILING POINT 129 C
SPECIFIC GRAVITY

0.8263

SOLUBILITY IN WATER Slightly
AUTOIGNITION  
pH  
VAPOR PRESSURE 15 mm Hg
HENRY LAW CONSTANT 0.045 (atm-m3/mole at 25 C)
OH RATE CONSTANT 8.93E-11 (cm3/molecule-sec at 25 C Atmospheric )

REFRACTIVE INDEX

 
NFPA RATINGS Health : 0 Flammability : 3 Reactivity : 2
FLASH POINT

16 C

STABILITY Stable under ordinary conditions

EXTERNAL LINKS & GENERAL DESCRIPTION

Wikipedia Linking

Material Safety Data Sheet

Google Scholar Search

http://monographs.iarc.fr/
Production: 4-Vinylcyclohexene is isolated as a by-product of other production processes involving 1,3-butadiene (see IARC, 1992), including the production of vinylnorbornene, dodecanedioic acid and 1,3-butadiene itself. The 4-vinylcyclohexene isolated in these processes may be sold or converted to the diepoxide, or may be recycled for further use within the production facility (Che mi cal Manufacturers Association, 1991). 4-VinylcycIohexene is prepared commercially by catalytic dimerization of 1,3-butadiene at LLO-425°C and 1.3-100 MPa. The catalysts used are tyically silicon carbide and copper or chromium salts (Kirshenbaum, 1978). No data were available to the Working Group on production volume. Use: 4-Vinylcyclohexene has been used as an intermediate for producing flame retardants, flavours and fragrances; in the manufacture of polyolefins; as a solvent; and in the manufacture of special chemicals such as the diepoxide (see monograph, p. 361) (DuPont Chemicals, undated).

Local:
Vinyl: the univalent chemical radical H2C=CHCl-, derived from ethylene. It is a highly reactive, easily polymerizing, and low cost monomer used as basic materials for one of largest-selling plastic. In addition to its application of polymerization to make plastics with huge amount, vinly- is an functional group involved in cycloaddition, addition reactions, and carbon skeleton expansion reactions including Suzuki reaction, Heck reaction. This radical is useful in biomolecules chemistry such as protein sequencing and enzyme inhibitors.

4-Vinyl-1-Cyclohexene is a polymerizable monomer and a co-monomer in polymerization of other monomers useful as a chemical intermediate applied for the wide range of products; e.g cyclohexene dioxide, flame retardants through halogenation, flavors, fragrances , insecticidal compounds with ethylene chlorohydrin, diepoxides, solvents, and in other organic synthesis.

SALES SPECIFICATION

APPEARANCE

Slightly yellow liquid
4-VINYLCYCLOHEXENE-1

97.0% min

1,5-CYCLOOCTADIENE 3.0% max
MOISTURE

0.2% max

TRANSPORTATION
PACKING 180kgs in Drum
HAZARD CLASS 3.1
UN NO. 1993
SAFETY INFORMATION
Hazard Symbols: XI F, Risk Phrases: 11-38, Safety Phrases: 9-16-29-33
PRICE INFORMATION