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45119

Supelco

Methyl elaidate

analytical standard

Sinônimo(s):

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:
217-712-4
Número MDL:
MFCD00066521
Código UNSPSC:
85151701
ID de substância PubChem:
329756582
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

Ensaio

≥99.0% (GC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.450

pf

9-10 °C

densidade

0.871 g/mL at 20 °C (lit.)

formato

neat

grupo funcional

ester

Condições de expedição

ambient

temperatura de armazenamento

2-8°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.

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BCCL1245
BCCH6578
BCCF2027
BCCD1930
BCBX4103

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Supelco

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Sigma-Aldrich

V1381

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trans-11-Vaccenic methyl ester certified reference material, 10 mg/mL in heptane, ampule of 1 mL

Supelco

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Methyl linoleate ≥98% (GC)

Sigma-Aldrich

L1876

Methyl linoleate

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
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
Chinmay A Deshmane et al.
Chemical communications (Cambridge, England), 46(34), 6347-6349 (2010-08-18)
Thermally stable mesoporous Ga-Nb mixed oxides, active in both acid-catalysed and redox reactions have been synthesized via self-assembly hydrothermal assisted approach. Methyl oleate, a major component of biodiesels, undergoes double bond and skeletal isomerisation as well as dehydrogenation over these
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