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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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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
Philipp Roesle et al.
Journal of the American Chemical Society, 134(42), 17696-17703 (2012-10-18)
The weakly coordinated triflate complex [(P^P)Pd(OTf)](+)(OTf)(-) (1) (P^P = 1,3-bis(di-tert-butylphosphino)propane) is a suitable reactive precursor for mechanistic studies of the isomerizing alkoxcarbonylation of methyl oleate. Addition of CH(3)OH or CD(3)OD to 1 forms the hydride species [(P^P)PdH(CH(3)OH)](+)(OTf)(-) (2-CH(3)OH) or the
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
B Kollbe Ahn et al.
Advanced materials (Deerfield Beach, Fla.), 24(16), 2123-2129 (2012-03-21)
Amphiphilic reduced graphene oxide is obtained by oleo-functionalization with epoxidized methyl oleate (renewable feedstock) using a green process. The excellent diverse solvent-dispersivity of the oleo-reduced amphiphilic graphene and its reduction chemistry are confirmed in this study. Oleo-reduction of amphiphilic graphene
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
View All Related Papers

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