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L2251

Sigma-Aldrich

Methyl linolelaidate

Sinonimo/i:

Linolelaidic acid methyl ester, Methyl trans,trans-9,12-octadecadienoate

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About This Item

Formula empirica (notazione di Hill):
C19H34O2
Numero CAS:
2566-97-4
Peso molecolare:
294.47
Beilstein:
1727615
Numero CE:
219-901-7
Numero MDL:
MFCD00069997
Codice UNSPSC:
12352211
ID PubChem:
24896306
NACRES:
NA.25

Tipo di lipide

unsaturated FAs

Stringa SMILE

CCCCC\C=C\C\C=C\CCCCCCCC(=O)OC

InChI

1S/C19H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h7-8,10-11H,3-6,9,12-18H2,1-2H3/b8-7+,11-10+
WTTJVINHCBCLGX-ZDVGBALWSA-N

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Confezionamento

Sealed ampule

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Elaidic acid ≥99.0% (GC)

Sigma-Aldrich

E4637

Elaidic acid

Methyl linoleate analytical standard

Supelco

62280

Methyl linoleate

Ethyl stearate ≥99% (capillary GC)

Sigma-Aldrich

S8269

Ethyl stearate

trans-9-Octadecenoic acid methyl ester certified reference material, 10 mg/mL in heptane, ampule of 1 mL

Supelco

CRM46903

trans-9-Octadecenoic acid methyl ester

Linolenic acid methyl ester isomer mix

Sigma-Aldrich

L6031

Linolenic acid methyl ester isomer mix

Methyl cis-11-octadecenoate analytical standard

Supelco

17264

Methyl cis-11-octadecenoate

B M Craven et al.
Journal of lipid research, 24(6), 784-789 (1983-06-01)
At 123 K, crystals of cholesteryl trans-9-trans-12-octadecadienoate (cholesteryl linolelaidate, C47H76O2) are monoclinic, space group P2(1) with cell dimensions a = 13.03(3), b = 8.76(2), c = 17.90(4) A, beta = 89.7(2) degrees, having two molecules per unit cell. The crystal
T H Fischer et al.
Biochimica et biophysica acta, 1022(2), 215-228 (1990-02-28)
Arachidonate, at concentrations up to 50 microM, induced dose-dependent calcium efflux from preloaded microsomes prepared from human platelets, but not from unilamellar egg phosphatidylcholine vesicles. Arachidonate-induced efflux from microsomes was not inhibited by indomethacin, 13-azaprostanoic acid, or catalase and superoxide
Effect of emeriamine, an inhibitor of fatty acid oxidation, on metabolic fate of a geometrical isomer of linoleic acid in perfused rat liver.
Fukuda N, Fukui M, Kai Y, Jayasooriya AP, et al.
J. Nutr. Sci. Vitaminol., 44, 525-535 (1998)
Mizuka Nagai et al.
Bioscience, biotechnology, and biochemistry, 73(11), 2501-2505 (2009-11-10)
Acyl arbutin was synthesized through the condensation of arbutin with a saturated fatty acid (C6-18) by the immobilized lipase in a batch reaction. The conversion at 10 and 20 g/l-solvent of immobilized lipase reached 45% over 2 d, but the
Philip T Lynett et al.
Organic & biomolecular chemistry, 9(9), 3320-3330 (2011-03-30)
It has long been recognized that garlic and petiveria, two plants of the Allium genus--which also includes onions, leeks and shallots--possess great medicinal value. In recent times, the biological activities of extracts of these plants have been ascribed to the
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