Ethyl linoleate

• Catalog No.: L1751
• CAS Number: 544-35-4
• M. F.: C20H36O2
• M. W.: 308.49864
• Purity: ≥99%

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.)
• 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.