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Merck
CN

E4762

Methyl elaidate

≥99% (capillary GC)

Synonym(s):

Elaidic acid methyl ester, Methyl trans-9-octadecenoate

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About This Item

Linear Formula:
CH3(CH2)7CH=CH(CH2)7COOCH3
CAS Number:
1937-62-8
Molecular Weight:
296.49
MDL number:
MFCD00066521
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
24894579
EC Number:
217-712-4
Beilstein/REAXYS Number:
1727038

Key Documents

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Product Name

Methyl elaidate, ≥99% (capillary GC)

InChI key

QYDYPVFESGNLHU-ZHACJKMWSA-N

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+

SMILES string

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

assay

≥99% (capillary GC)

form

liquid

density

0.871 g/mL at 20 °C (lit.)

functional group

ester

lipid type

unsaturated FAs

shipped in

ambient

storage temp.

−20°C

Quality Level

200

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Packaging

Sealed ampule.

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000510269
0000510269
0000491600
0000491600
0000383137

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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
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)
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
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
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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