(Z)-2-heptene

cis-2-heptene

CAS: 6443-92-1 C7 H14 MW: 98.18858000

Identification

Name(Z)-2-heptene
IUPAC(Z)-hept-2-ene
CAS Number6443-92-1
EINECS229-242-7
FDA UNII250X978P9Q
Molecular FormulaC7 H14
Molecular Weight98.18858000
MDL NumberMFCD00063976
Nikkaji NumberJ147.997K

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 0.70800 to 0.71100 @ 20.00 °C.
Pounds per Gallon - (est). 5.898 to 5.923
Refractive Index 1.40600 to 1.40900 @ 20.00 °C.
Boiling Point 98.40 °C. @ 760.00 mm Hg
Vapor Pressure 45.800000 mmHg @ 25.00 °C. (est)
Flash Point 21.00 °F. TCC ( -6.11 °C. )
logP (o/w) 3.960 (est)
Soluble in water, 31.08 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryinformation only not used for fragrances or flavors
Recommendation for (Z)-2-heptene usage levels up tonot for fragrance use.
Recommendation for (Z)-2-heptene flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

(Z)- hept-2-ene cis-2- heptene PubMed: Inverse solvent effects in the heterogeneous and homogeneous epoxidation of cis-2-heptene with [2-percarboxyethyl]-functionalized silica and meta-chloroperbenzoic acid. PubMed: Addition of the phenoxathiin cation radical to alkenes and nonconjugated dienes. Formation of (E)- and (Z)-(10-phenoxathiiniumyl)alkenes and (E)- and (Z)-(10-phenoxathiiniumyl)dienes on basic alumina. PubMed: Improved operational stability of peroxidases by coimmobilization with glucose oxidase. PubMed: Oxidation of aliphatic olefins by toluene dioxygenase: enzyme rates and product identification.