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46903

Supelco

trans-9-Octadecenoic methyl ester

10 mg/mL in heptane, analytical standard

Sinônimo(s):

Methyl elaidate, Elaidic acid methyl ester, Methyl trans-9-octadecenoate

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About This Item

Fórmula linear:
CH3(CH2)7CH=CH(CH2)7COOCH3
Número CAS:
1937-62-8
Peso molecular:
296.49
Beilstein:
1727038
Número CE:
205-563-8
Número MDL:
MFCD00066521
Código UNSPSC:
85151701

grau

analytical standard

Certificado de análise (CofA)

certificate of analysis is enclosed in each package.

embalagem

ampule of 1 mL

concentração

10 mg/mL in heptane

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

densidade

0.871 g/mL at 20 °C (lit.)

formato

single component solution

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

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

InChI

1S/C19H36O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-2/h10-11H,3-9,12-18H2,1-2H3/b11-10+

chave InChI

QYDYPVFESGNLHU-ZHACJKMWSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

substituído por

Nº do produto
Descrição
Preços

Palavra indicadora

Danger

Frases de perigo

H225,H304,H315,H336,H410

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Órgãos-alvo

Central nervous system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

24.8 °F

Ponto de fulgor (°C)

-4 °C

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Certificados de análise (COA)

Lot/Batch Number
LC07864V
LC03765
LB86349
LB75258
LB62517

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Atanu Biswas et al.
Journal of agricultural and food chemistry, 56(14), 5611-5616 (2008-06-19)
An environmentally friendly water-based pathway to form the azide derivatives of soybean oil and fatty esters is reported. This entails first the formation of epoxides and then the azidization of the epoxides. The azidization reaction is carried out at high
Renee M Thomas et al.
Journal of the American Chemical Society, 133(19), 7490-7496 (2011-04-23)
N-Aryl,N-alkyl N-heterocyclic carbene (NHC) ruthenium metathesis catalysts are highly selective toward the ethenolysis of methyl oleate, giving selectivity as high as 95% for the kinetic ethenolysis products over the thermodynamic self-metathesis products. The examples described herein represent some of the
Farshad Darvishi et al.
New biotechnology, 28(6), 756-760 (2011-02-18)
The yeast Yarrowia lipolytica degrades efficiently low-cost hydrophobic substrates for the production of various added-value products such as lipases. To obtain yeast strains producing high levels of extracellular lipase, Y. lipolytica DSM3286 was subjected to mutation using ethyl methanesulfonate (EMS)
Ursula Biermann et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(26), 8201-8207 (2012-05-18)
A kinetic study of the dodecanethiol-catalyzed cis/trans isomerization of methyl oleate (cis-2) without added initiator was performed by focusing on the initiation of the radical chain reaction. The reaction orders of the rate of isomerization were 2 and 0.5 for
Cyril Thurier et al.
ChemSusChem, 1(1-2), 118-122 (2008-07-09)
Unsaturated vegetable oils are an attractive renewable feedstock, and the selective cleavage of unsaturated fatty esters is an important transformation in this respect. The efficient and selective cross-metathesis of methyl oleate with ethylene was achieved under mild conditions with ruthenium-alkylidene
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