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46902-U

Supelco

cis-9-Octadecenoic methyl ester

certified reference material, 10 mg/mL in heptane

Sinónimos:

Oleic acid methyl ester

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About This Item

Número de CAS:
112-62-9
Número CE:
205-563-8
Código UNSPSC:
85151701
NACRES:
NA.24

grado

certified reference material
TraceCERT®

Línea del producto

TraceCERT®

formulario

liquid

CofA

current certificate can be downloaded

envase

ampule of 1 mL

concentración

10 mg/mL in heptane

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

food and beverages

formato

single component solution

grupo funcional

ester

temp. de almacenamiento

-10 to -25°C

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+

Clave InChI

QYDYPVFESGNLHU-ZHACJKMWSA-N

Aplicación

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

Otras notas

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Información legal

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Palabra de señalización

Danger

Frases de peligro

H225,H304,H315,H336,H410

Clasificaciones de peligro

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Órganos de actuación

Central nervous system

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 2

Punto de inflamabilidad (°F)

24.8 °F - closed cup

Punto de inflamabilidad (°C)

-4 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
LRAC9020
LRAB9327
XA14407V
XA14393V
LC13644

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cis-11-Hexadecenal 95%

Sigma-Aldrich

249084

cis-11-Hexadecenal

Linoleic Acid Methyl Ester Mix cis/trans, certified reference material, 10 mg/mL in dichloromethane

Supelco

CRM47791

Linoleic Acid Methyl Ester Mix

Methyl oleate technical grade, 70%

Sigma-Aldrich

268038

Methyl oleate

Methyl elaidate analytical standard

Supelco

45119

Methyl elaidate

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
L I Mazaletskaia et al.
Prikladnaia biokhimiia i mikrobiologiia, 46(2), 148-152 (2010-04-16)
Influence of the widely used food supplement lecithin on the effectiveness of the inhibiting effect of the natural antioxidants (quercitin, dihydroquercitin, and alpha-tocopherol) has been studied in dependence of the rate of free radicals generation in the model oxidation reactions.
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
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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