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Ethyl linoleate_Molecular_structure_CAS_544-35-4)
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Ethyl linoleate

Catalog No. L1751 Name Sigma Aldrich
CAS Number 544-35-4 Website http://www.sigmaaldrich.com
M. F. C20H36O2 Telephone 1-800-521-8956
M. W. 308.49864 Fax
Purity ≥99% Email
Storage Chembase ID: 102246

SYNONYMS

Title
亚油酸乙酯
IUPAC name
ethyl octadeca-9,12-dienoate
IUPAC Traditional name
ethyl octadeca-9,12-dienoate
Synonyms
亚麻油酸乙酯
Linoleic acid ethyl ester

DATABASE IDS

EC Number 208-868-4
PubChem SID 24896290
CAS Number 544-35-4
MDL Number MFCD00009535
Beilstein Number 1727827

PROPERTIES

Linear Formula CH3(CH2)3(CH2CH=CH)2(CH2)7COOC2H5
Purity ≥99%
Boiling Point 224 °C/17 mmHg(lit.)
Density 0.876 g/mL at 25 °C(lit.)
Flash Point 113 °C
Flash Point 235.4 °F
Refractive Index n20/D 1.455(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
Storage Temperature -20°C
German water hazard class 1

DETAILS

Description (English)
Packaging
1, 5, 25 g in glass bottle
Biochem/physiol Actions
Ethyl linoleate may be used as a reference material in assays that quantify fatty acid ethyl esters (FAEEs) for detection of alcohol abuse. Linoleic acid ethyl ester (Ethyl linoleate) may be used and studied as an acetylcholinesterase (AChE) inhibitor.
Ethyl linoleate solated from Oxalis triangularis inhibits forskolin-induced melanogenesis and tyrosinase activity in mouse B16 melanoma cells . This anti-melanogenic effect is mediated by inhibiting cAMP production.
Description (简体中文)
包装
1, 5, 25 g in glass bottle
Biochem/physiol Actions
Ethyl linoleate solated from Oxalis triangularis inhibits forskolin-induced melanogenesis and tyrosinase activity in mouse B16 melanoma cells 1. This anti-melanogenic effect is mediated by inhibiting cAMP production.

REFERENCES