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46903

Supelco

trans-9-Octadecenoic methyl ester

10 mg/mL in heptane, analytical standard

Sinonimo/i:

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

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About This Item

Formula condensata:
CH3(CH2)7CH=CH(CH2)7COOCH3
Numero CAS:
1937-62-8
Peso molecolare:
296.49
Beilstein:
1727038
Numero CE:
205-563-8
Numero MDL:
MFCD00066521
Codice UNSPSC:
85151701

Grado

analytical standard

CdA

certificate of analysis is enclosed in each package.

Confezionamento

ampule of 1 mL

Concentrazione

10 mg/mL in heptane

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Densità

0.871 g/mL at 20 °C (lit.)

Formato

single component solution

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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Applicazioni

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

Sostituito da

N° Catalogo
Descrizione
Determinazione del prezzo

Avvertenze

Danger

Indicazioni di pericolo

H225,H304,H315,H336,H410

Classi di pericolo

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

Organi bersaglio

Central nervous system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

24.8 °F

Punto d’infiammabilità (°C)

-4 °C

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Certificati d'analisi (COA)

Lot/Batch Number
LC07864V
LC03765
LB86349
LB75258
LB62517

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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)
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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
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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
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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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