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O3380

Sigma-Aldrich

Oleyl oleate

≥99%

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Synonym(s):
Oleyl oleate, Oleic acid oleyl ester
Empirical Formula (Hill Notation):
C36H68O2
CAS Number:
Molecular Weight:
532.92
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.25

assay

≥99%

form

liquid

functional group

ester
oleic acid

lipid type

unsaturated FAs

shipped in

ambient

storage temp.

−20°C

SMILES string

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-

InChI key

BARWIPMJPCRCTP-CLFAGFIQSA-N

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This Item
O7501E4637C9253
vibrant-m

O3380

Oleyl oleate

vibrant-m

O7501

Sodium oleate

vibrant-m

E4637

Elaidic acid

vibrant-m

C9253

Cholesteryl oleate

assay

≥99%

assay

≥99%

assay

≥99.0% (GC)

assay

≥98% (HPLC; detection at 205 nm)

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

shipped in

ambient

shipped in

ambient

shipped in

ambient

shipped in

ambient

form

liquid

form

powder

form

powder

form

powder

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

452.3 °F

flash_point_c

233.5 °C


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Cetyl palmitate United States Pharmacopeia (USP) Reference Standard

USP

1103105

Cetyl palmitate

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)
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
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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