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46903

Supelco

Methyl elaidate

10 mg/mL in heptane, analytical standard

Synonyme(s) :

Ester méthylique d’acide élaïdique

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About This Item

Formule linéaire :
CH3(CH2)7CH=CH(CH2)7COOCH3
Numéro CAS:
1937-62-8
Poids moléculaire :
296.49
Numéro Beilstein :
1727038
Numéro CE :
205-563-8
Numéro MDL:
MFCD00066521
Code UNSPSC :
85151701

Qualité

analytical standard

CofA (certificat d'analyse)

certificate of analysis is enclosed in each package.

Conditionnement

ampule of 1 mL

Concentration

10 mg/mL in heptane

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Densité

0.871 g/mL at 20 °C (lit.)

Format

single component solution

Température de stockage

−20°C

Chaîne SMILES 

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+

Clé InChI

QYDYPVFESGNLHU-ZHACJKMWSA-N

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Application

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Réf. du produit
Description
Tarif

Mention d'avertissement

Danger

Mentions de danger

H225,H304,H315,H336,H410

Classification des risques

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

Organes cibles

Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

24.8 °F

Point d'éclair (°C)

-4 °C

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Certificats d'analyse (COA)

Lot/Batch Number
LC07864V
LC03765
LB86349
LB75258
LB62517

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

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
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
Farshad Darvishi et al.
New biotechnology, 28(6), 756-760 (2011-02-18)
The yeast Yarrowia lipolytica degrades efficiently low-cost hydrophobic substrates for the production of various added-value products such as lipases. To obtain yeast strains producing high levels of extracellular lipase, Y. lipolytica DSM3286 was subjected to mutation using ethyl methanesulfonate (EMS)
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
Cyril Thurier et al.
ChemSusChem, 1(1-2), 118-122 (2008-07-09)
Unsaturated vegetable oils are an attractive renewable feedstock, and the selective cleavage of unsaturated fatty esters is an important transformation in this respect. The efficient and selective cross-metathesis of methyl oleate with ethylene was achieved under mild conditions with ruthenium-alkylidene
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