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Merck

268038

Methyl oleate

technical grade, 70%

Synonym(s):

Methyl cis-9-octadecenoate, Oleic acid methyl ester

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About This Item

Linear Formula:
CH3(CH2)7CH=CH(CH2)7CO2CH3
CAS Number:
112-62-9
Molecular Weight:
296.49
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24856258
EC Number:
203-992-5
Beilstein/REAXYS Number:
1727037
MDL number:
MFCD00009578

Key Documents

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Product Name

Methyl oleate, technical grade, 70%

InChI key

QYDYPVFESGNLHU-KHPPLWFESA-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

grade

technical grade

vapor pressure

10 mmHg ( 205 °C)

assay

70%

form

liquid

refractive index

n20/D 1.452 (lit.)

bp

218 °C/20 mmHg (lit.)

density

0.874 g/mL at 20 °C (lit.)

functional group

ester

Quality Level

100

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Application

Methyl oleate was used to study the catalytic potential of molybdenum oxide/bipyridinedicarboxylate hybrid material.

General description

The methyl oleate monolayers at the air-water interface undergoes ozonolysis that results in rapid loss of material through cleavage of the C[double bond]C bond and evaporation/dissolution of reaction products.

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113.0 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5743
MKBF2291V
STBK9281
STBK1264
STBJ6278

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Hailey M Summers et al.
Bioresource technology, 196, 431-440 (2015-08-16)
The economic feasibility and environmental impact is investigated for the conversion of agricultural waste, delactosed whey permeate, through yeast fermentation to a renewable diesel via hydrothermal liquefaction. Process feasibility was demonstrated at laboratory-scale with data leveraged to validate systems models
Tatiana R Amarante et al.
Inorganic chemistry, 52(8), 4618-4628 (2013-03-28)
The reaction of MoO3, 2,2'-bipyridine-5,5-dicarboxylic acid (H2bpdc), water, and dimethylformamide in the mole ratio 1:1:1730:130 at 150 °C for 3 days in a rotating Teflon-lined digestion bomb leads to the isolation of the molybdenum oxide/bipyridinedicarboxylate hybrid material (DMA)[MoO3(Hbpdc)]·nH2O (1) (DMA
Christian Pfrang et al.
Physical chemistry chemical physics : PCCP, 16(26), 13220-13228 (2014-05-30)
Ozonolysis of methyl oleate monolayers at the air-water interface results in surprisingly rapid loss of material through cleavage of the C=C bond and evaporation/dissolution of reaction products. We determine using neutron reflectometry a rate coefficient of (5.7 ± 0.9) ×
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
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
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