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L2501

Sigma-Aldrich

Ethyl linolenate

≥98%

Sinonimo/i:

9,12,15-Octadecatrienoic acid ethyl ester, Linolenic acid ethyl ester

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About This Item

Formula condensata:
CH3(CH2CH=CH)3(CH2)7COOC2H5
Numero CAS:
1191-41-9
Peso molecolare:
306.48
Beilstein:
1728340
Numero CE:
214-734-6
Numero MDL:
MFCD07371452
Codice UNSPSC:
12352211
ID PubChem:
24896316
NACRES:
NA.25

Origine biologica

Linum usitatissimum

Saggio

≥98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.468 (lit.)

P. eboll.

166-168 °C/1 mmHg (lit.)

Densità

0.892 g/mL at 25 °C (lit.)

Gruppo funzionale

ester

Tipo di lipide

omega FAs

Condizioni di spedizione

ambient

Temperatura di conservazione

−20°C

Stringa SMILE

CCOC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC

InChI

1S/C20H34O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20(21)22-4-2/h5-6,8-9,11-12H,3-4,7,10,13-19H2,1-2H3/b6-5-,9-8-,12-11-
JYYFMIOPGOFNPK-AGRJPVHOSA-N

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Categorie correlate

Azioni biochim/fisiol

Ethyl linolenate may be used as a reference molecule in systems developed to measure fatty acid esters derived from tissues, membranes and lipids, especially associated with alcohol abuse. Ethyl linolenate is being studied as a possible skin whitening agent with anti-melanogenesis activity.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves

Certificati d'analisi (COA)

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K S Bjerve et al.
The American journal of clinical nutrition, 46(4), 570-576 (1987-10-01)
Treatment of human alpha-linolenic acid deficiency (ALAD) with ethyl linolenate is reported. The patient's scaly dermatitis nearly disappeared after 5-d supplementation with 0.1 mL ethyl linolenate. Pretreatment content of various n-3 fatty acids in RBC was 0-15% of healthy controls.
Yukiko Mizutani et al.
Journal of agricultural and food chemistry, 52(11), 3570-3576 (2004-05-27)
The effects of heat treatment on the interaction of lipid and zein in a dry powder system were investigated. Linolenic acid ethyl ester (LAE) was mixed with the zein powder. The glass transition temperature (T(g)) for the dry powder zein
Yukiko Mizutani et al.
Journal of agricultural and food chemistry, 51(1), 229-235 (2002-12-28)
The effects of water activity (A(w)) and lipid addition on the secondary structure of powdery zein were investigated using Fourier transform infrared spectroscopy. Two fatty acid esters, i.e., the linolenic and eicosapentaenoic acid ethyl esters (LAE and EPE), were mixed
Kristýna Floková et al.
Phytochemistry, 122, 230-237 (2015-12-18)
Jasmonates (JAs) are plant hormones that integrate external stress stimuli with physiological responses. (+)-7-iso-JA-L-Ile is the natural JA ligand of COI1, a component of a known JA receptor. The upstream JA biosynthetic precursor cis-(+)-12-oxo-phytodienoic acid (cis-(+)-OPDA) has been reported to
Simona Pichini et al.
Journal of pharmaceutical and biomedical analysis, 48(3), 927-933 (2008-09-13)
Fatty acid ethyl esters (FAEEs) in meconium emerged as a reliable, direct biological marker for establishing fetal exposure to ethanol. We developed an LC-MS/MS method for ethyl laurate, ethyl myristate, ethyl palmitate, ethyl palmitoleate, ethyl stearate, ethyl oleate, ethyl linoleate
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