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Ethyl trans-3-hexenoate

ethyl cis-3-hexenoate

CAS: 2396-83-0

Molecular Formula: C8H14O2

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Ethyl trans-3-hexenoate - Names and Identifiers

Name ethyl cis-3-hexenoate
Synonyms FEMA 3342
ETHYL 3-HEXENOATE
Ethyl 3-hexenoate
ethyl hex-3-enoate
ETHYL T3 HEXENOATE
ETHYL CIS-3-HEXENOATE
ethyl cis-3-hexenoate
Ethyl (3E)-3-hexenoate
ETHYL TRANS-3-HEXENOATE
ethyl (3E)-hex-3-enoate
3-Hexenoicacid,ethylester
CAS 2396-83-0
EINECS 219-257-7
InChI InChI=1/C8H14O2/c1-3-5-6-7-8(9)10-4-2/h5-6H,3-4,7H2,1-2H3/b6-5+

Ethyl trans-3-hexenoate - Physico-chemical Properties

Molecular FormulaC8H14O2
Molar Mass142.2
Density0.896g/mLat 25°C(lit.)
Melting Point-65.52°C (estimate)
Boling Point63-64°C12mm Hg(lit.)
Flash Point139°F
JECFA Number335
Vapor Presure1.55mmHg at 25°C
Storage ConditionSealed in dry,Room Temperature
Refractive Indexn20/D 1.426(lit.)
Physical and Chemical PropertiesColorless liquid, the aroma of fruit. Boiling point of 63~64 degrees C (1600pa). Slightly soluble in water, soluble in most organic solvents. Natural products are present in pineapple and the like.

Ethyl trans-3-hexenoate - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
R10 - Flammable
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
S24/25 - Avoid contact with skin and eyes.
UN IDsUN 3272 3/PG 3
WGK Germany3
TSCAYes
HS Code29161900
Hazard NoteIrritant
Hazard Class3
Packing GroupIII

Ethyl trans-3-hexenoate - Reference Information

FEMA3342 | ETHYL 3-HEXENOATE
NIST chemical information Information provided by: webbook.nist.gov (external link)
EPA chemical information Information provided by: ofmpub.epa.gov (external link)
toxicity GRAS(FEMA).
usage limit FEMA(mg/kg): soft drinks, cold drinks, jelly, pudding, jam, candied fruit, 2.0; Candy, baked goods, 4.0.
use GB 2760-1996 specified as allowed food spices.
Production method is composed of 3-hexenoic acid and biscyclohexylcarbodiimide. It is obtained by fermentation of 3-hexenoic acid with brewer's yeast at 20°C.
Last Update:2024-04-10 22:29:15
Ethyl trans-3-hexenoate
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