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E4762

Sigma-Aldrich

Methyl elaidate

≥99% (capillary GC)

Sinonimo/i:

Elaidic acid methyl ester, Methyl trans-9-octadecenoate

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500 MG
CHF 111.00
1 G
CHF 371.00

CHF 111.00


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Cambia visualizzazione
500 MG
CHF 111.00
1 G
CHF 371.00

About This Item

Formula condensata:
CH3(CH2)7CH=CH(CH2)7COOCH3
Numero CAS:
Peso molecolare:
296.49
Beilstein:
1727038
Numero CE:
Numero MDL:
Codice UNSPSC:
12352211
ID PubChem:
NACRES:
NA.25

CHF 111.00


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Saggio

≥99% (capillary GC)

Stato

liquid

Densità

0.871 g/mL at 20 °C (lit.)

Gruppo funzionale

ester

Tipo di lipide

unsaturated FAs

Condizioni di spedizione

ambient

Temperatura di conservazione

−20°C

Stringa SMILE

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+
QYDYPVFESGNLHU-ZHACJKMWSA-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, multi-purpose combination respirator cartridge (US)


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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)
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
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
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

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