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75160

Supelco

Methyl oleate

analytical standard

Sinonimo/i:

Methyl cis-9-octadecenoate, Oleic acid methyl ester

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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:
85151701
ID PubChem:
329766226
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Tensione di vapore

10 mmHg ( 205 °C)

Saggio

≥98.5% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

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

P. ebollizione

218 °C/20 mmHg (lit.)

Densità

0.874 g/mL at 20 °C (lit.)

applicazioni

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Formato

neat

Gruppo funzionale

ester

Condizioni di spedizione

ambient

Temperatura di conservazione

2-8°C

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

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

Applicazioni

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

Altre note

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

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCG3546
BCCD8407
BCCC4265
BCBZ8853
BCBW2906

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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
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
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