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Merck

46903

Supelco

trans-9-Octadecensäure-methylester

10 mg/mL in heptane, analytical standard

Synonym(e):

Methylelaidat, trans-9-Octadecensäure-methylester, Methyl-elaidat

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About This Item

Lineare Formel:
CH3(CH2)7CH=CH(CH2)7COOCH3
CAS-Nummer:
Molekulargewicht:
296.49
Beilstein:
1727038
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
85151701

Qualität

analytical standard

Analysenzertifikat (CofA)

certificate of analysis is enclosed in each package.

Verpackung

ampule of 1 mL

Konzentration

10 mg/mL in heptane

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Dichte

0.871 g/mL at 20 °C (lit.)

Format

single component solution

Lagertemp.

−20°C

SMILES String

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+

InChIKey

QYDYPVFESGNLHU-ZHACJKMWSA-N

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Anwendung

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

Ersetzt durch

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Central nervous system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

24.8 °F

Flammpunkt (°C)

-4 °C


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Analysenzertifikate (COA)

Lot/Batch Number

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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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