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O3380

Sigma-Aldrich

Oleyl oleate

≥99%

Synonyme(s) :

Oleyl oleate, Oleic acid oleyl ester

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About This Item

Formule empirique (notation de Hill):
C36H68O2
Numéro CAS:
3687-45-4
Poids moléculaire :
532.92
Numéro CE :
222-980-0
Numéro MDL:
MFCD00072252
Code UNSPSC :
12352211
ID de substance PubChem :
24897979
Nomenclature NACRES :
NA.25

Pureté

≥99%

Forme

liquid

Groupe fonctionnel

ester
oleic acid

Type de lipide

unsaturated FAs

Conditions d'expédition

ambient

Température de stockage

−20°C

Chaîne SMILES 

CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC

InChI

1S/C36H68O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-38-36(37)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20H,3-16,21-35H2,1-2H3/b19-17-,20-18-

Clé InChI

BARWIPMJPCRCTP-CLFAGFIQSA-N

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Catégories apparentées

Application


  • Group 13 Lewis acid catalyzed synthesis of metal oxide nanocrystals via hydroxide transmetallation.: This research utilizes oleyl oleate as a solvent to facilitate the synthesis of metal oxide nanocrystals, showcasing its effectiveness in nanoparticle production and potential applications in various electronic and optical devices (Gibson et al., 2021).

  • High-level accumulation of oleyl oleate in plant seed oil by abundant supply of oleic acid substrates to efficient wax ester synthesis enzymes.: This article details the genetic engineering approaches to enhance oleyl oleate content in plant oils, aiming at industrial applications such as biofuels and biolubricants (Yu et al., 2018).

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

452.3 °F

Point d'éclair (°C)

233.5 °C

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José Aracil et al.
Journal of biotechnology, 124(1), 213-223 (2006-02-21)
A comparative study of the oleyl oleate production using conventional and enzymatic catalysts has been carried out. The present paper describes the flow diagrams for these processes and compares operation conditions for batch reaction and the downstream proceedings. In addition
J Zhang et al.
Chinese journal of biotechnology, 11(4), 243-251 (1995-01-01)
The effect of 14 different lipases on oleyl oleate synthesis were compared. The lipase from Candida sp.1619 had the highest esterification activity. The lipase was immobilized by adsorbing it on celite with 0.1 (w/w) coconut oil, Tween 80, and 1%
T Rostrup-Nielsen et al.
Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986), 48(4), 467-482 (1990-01-01)
The kinetics of enzymatic hydrolysis of oleyl oleate in the boundary layer between stagnant organic and aqueous phases was studied using a commercial lipase preparation which was dissolved in the aqueous phase. Three aspects of the reaction were investigated. (1)
K Ichihara et al.
Lipids, 31(5), 535-539 (1996-05-01)
An improved rapid procedure to determine the fatty acid composition of glycerolipids is described. The procedure includes KOH-catalyzed transesterification and high-speed gas chromatography. Glycerolipids (20-40 mg) were mixed with 2 mL of hexane and 0.2 mL of 2 M methanolic
Shi-You Jiang et al.
Nature communications, 9(1), 5138-5138 (2018-12-05)
Statins are inhibitors of HMG-CoA reductase, the rate-limiting enzyme of cholesterol biosynthesis, and have been clinically used to treat cardiovascular disease. However, a paradoxical increase of reductase protein following statin treatment may attenuate the effect and increase the side effects.
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