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Merck

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
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
24894579
EC Number:
217-712-4
Beilstein/REAXYS Number:
1727038
MDL number:
MFCD00066521

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
0000523443
0000523443
0000510269
0000510269
0000491600

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Byung-Jun Kollbe Ahn et al.
Journal of agricultural and food chemistry, 60(9), 2179-2189 (2012-02-07)
Toxic solvent and strong acid catalysts causing environmental issues have been mainly used for ring-opening of epoxidized oleochemicals. Here, we demonstrated that magnesium stearate (Mg-stearate) was a high efficient catalyst for solvent-free ring-opening of epoxidized methyl oleate, a model compound
Yoshiyuki Mochida et al.
Journal of oleo science, 58(9), 461-466 (2009-08-06)
The analysis or preparative isolation of a specimen by a packed column gas chromatograph is affected by the kind and amount (concentration) of the liquid phase coated on the stationary phase. In particular, compounds having the same or similar molecular
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
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
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)
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