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268038

Sigma-Aldrich

Methyl oleate

technical grade, 70%

Sinonimo/i:

Methyl cis-9-octadecenoate, Oleic acid methyl ester

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1 L
CHF 76.80

About This Item

Formula condensata:
CH3(CH2)7CH=CH(CH2)7CO2CH3
Numero CAS:
112-62-9
Peso molecolare:
296.49
Beilstein:
1727037
Numero CE:
203-992-5
Numero MDL:
MFCD00009578
Codice UNSPSC:
12352100
ID PubChem:
24856258
NACRES:
NA.22

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Grado

technical grade

Tensione di vapore

10 mmHg ( 205 °C)

Saggio

70%

Stato

liquid

Indice di rifrazione

n20/D 1.452 (lit.)

P. ebollizione

218 °C/20 mmHg (lit.)

Densità

0.874 g/mL at 20 °C (lit.)

Gruppo funzionale

ester

Stringa SMILE

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

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-
QYDYPVFESGNLHU-KHPPLWFESA-N

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Categorie correlate

Descrizione generale

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[1].

Applicazioni

Methyl oleate was used to study the catalytic potential of molybdenum oxide/bipyridinedicarboxylate hybrid material[2].

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113.0 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
MKBF2291V
STBK9281
STBK1264
STBJ6278
STBJ0658

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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
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
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