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75160

Supelco

Methyl oleate

analytical standard

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Synonym(s):
Methyl cis-9-octadecenoate, Oleic acid methyl ester
Linear Formula:
CH3(CH2)7CH=CH(CH2)7CO2CH3
CAS Number:
Molecular Weight:
296.49
Beilstein/REAXYS Number:
1727037
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor pressure

10 mmHg ( 205 °C)

assay

≥98.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.452 (lit.)
n20/D 1.452

bp

218 °C/20 mmHg (lit.)

density

0.874 g/mL at 20 °C (lit.)

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

format

neat

functional group

ester

shipped in

ambient

storage temp.

2-8°C

SMILES string

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-

InChI key

QYDYPVFESGNLHU-KHPPLWFESA-N

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This Item
PHR1571311111268038
Methyl oleate analytical standard

75160

Methyl oleate

Methyl Oleate Pharmaceutical Secondary Standard; Certified Reference Material

PHR1571

Methyl Oleate

Methyl oleate 99%

311111

Methyl oleate

Methyl oleate technical grade, 70%

268038

Methyl oleate

grade

analytical standard

grade

certified reference material, pharmaceutical secondary standard

grade

-

grade

technical grade

application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

application(s)

pharmaceutical

application(s)

-

application(s)

-

format

neat

format

neat

format

-

format

-

vapor pressure

10 mmHg ( 205 °C)

vapor pressure

10 mmHg ( 205 °C)

vapor pressure

10 mmHg ( 205 °C)

vapor pressure

10 mmHg ( 205 °C)

assay

≥98.5% (GC)

assay

-

assay

99%

assay

70%

General description

Methyl oleate is a methyl ester of the monounsaturated fatty acid (MUFA), oleic acid, which is abundantly found in dietary fats and oils.

Application

This analytical standard can also be used as follows:

  • Determination of free fatty acids in plasma samples following their methylation by gas chromatography (GC)
  • Comparative analysis of gas chromatography-combustion-mass spectrometry and gas chromatography-flame ionization detector methods for the determination of fatty acid methyl esters (FAMEs) in biodiesel samples
  • Simultaneous determination of fatty acid methyl esters in commercial food oil samples by gas chromatography-vacuum ultraviolet (GC-VUV) spectroscopy
  • Measurement of fatty acid methyl ester composition of various edible oil samples by 1H nuclear magnetic resonance (1H NMR) spectroscopy combined with partial least squares (PLS) method
  • Simultaneous determination of fatty acids in bovine colostrum samples by GC-FID after their derivatization to ester forms using an acidic catalyst boron trifluoride

Other Notes

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113.0 °C - closed cup

ppe

Eyeshields, Gloves


Certificates of Analysis (COA)

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25G
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MMYOMAG-74K-13

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Selective transesterification of triolein with methanol to methyl oleate and glycerol using alumina loaded with alkali metal salt as a solid-base catalyst
Ebiura T, et al.
Applied Catalysis A: General, 283(1), 111-116 (2005)
Selective hydrogenation of methyl oleate into unsaturated alcohols: Relationships between catalytic properties and composition of cobalt?tin catalysts
Pouilloux.Y, et al.
Catalysis Today, 63(1), 87-100 (2000)
Annapurna Kumari et al.
Biotechnology for biofuels, 2(1), 1-1 (2009-01-16)
Transesterification of Jatropha oil was carried out in t-butanol solvent using immobilized lipase from Enterobacter aerogenes. The presence of t-butanol significantly reduced the negative effects caused by both methanol and glycerol. The effects of various reaction parameters on transesterification of
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
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

Articles

Separation of Methyl oleate; Caprylic acid; Heptanoic acid; Methyl decanoate; Methyl dodecanoate; Myristic acid; Methyl palmitate; Methyl palmitoleate; Methyl stearate; Methyl linoleate; Methyl linolenate; Acetic acid; Arachidic acid; Behenic acid; Propionic acid; Isobutyric acid; Valeric acid; Isovaleric acid; Isocaproic acid; Butyric acid

Protocols

Separation of Methyl decanoate; Methyl dodecanoate; Methyl myristate; Methyl palmitate; Methyl caprylate; Methyl oleate; Methyl linoleate; Methyl linolenate; Methyl stearate

-11-eicosenoate; Methyl elaidate; Methyl linoleate; Methyl myristate; Methyl myristoleate; Methyl palmitate; Methyl palmitoleate; Methyl oleate; Methyl pentadecanoate; Methyl tridecanoate; Methyl behenate; Methyl caprylate; Methyl erucate; Methyl heptadecanoate; Methyl arachidate

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