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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

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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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Michael A Rogers et al.
Langmuir : the ACS journal of surfaces and colloids, 25(15), 8556-8566 (2009-03-31)
The solvent type strongly affects the nucleation behavior of 12HSA and therefore strongly influences the peak nucleation rate, fiber length, spatial distribution of mass, and degree of branching. Using nonisothermal kinetic models, a correlation was established among the activation energy
Catherine M Klapperich et al.
Journal of biomedical materials research. Part A, 91(2), 378-384 (2008-11-05)
We describe a new class of biomaterials with potential for a variety of applications in tissue engineering, wound healing, and transdermal drug delivery. These materials are based on oleic methyl ester (OME), which is derived from various plant oils including
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
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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