P2144
Peanut oil
delivery vehicle for lipophilic compounds
Synonym(s):
Arachis Oil
Product Name
Peanut oil, delivery vehicle for lipophilic compounds
biological source
peanut oil
form
liquid
composition
Unsaturated fatty acids, ~80%
density
0.91 g/mL at 25 °C (lit.)
functional group
oleic acid
lipid type
oils
shipped in
ambient
storage temp.
room temp
Quality Level
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Related Categories
Application
Non-polar solvent, largely consisiting of long-chain glycerides of fatty acids, used for the delivery of lipophilic compounds.
Peanut oil has been used in the preparation of tamoxifen stock solution. It has also been used for dissolving the pesticide and fungicide compounds for in vivo study.
General description
Peanut oil is extracted from Arachis hypogaea L, is a source of edible oil in the tropical region. Peanut oil has high concentration of oleic and linoleic acid. It has many industrial applications like soap, cosmetics etc.
Storage Class
10 - Combustible liquids
wgk
awg
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves
Regulatory Information
监管及禁止进口产品
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The combined antiandrogenic effects of five commonly used pesticides
Birkhoj M, et al.
Toxicology and Applied Pharmacology, 201(1), 10-20 (2004)
Sergio Parra et al.
BMC pharmacology & toxicology, 15, 29-29 (2014-06-06)
Regulator of G protein signaling (RGS) proteins suppress G protein coupled receptor signaling by catalyzing the hydrolysis of Gα-bound guanine nucleotide triphosphate. Transgenic mice in which RGS-mediated regulation of Gαi2 is lost (RGS insensitive Gαi2G184S) exhibit beneficial (protection against ischemic
Inducible gene targeting in the neonatal vasculature and analysis of retinal angiogenesis in mice
Pitulescu ME, et al.
Nature Protocols, 5(9), 1518-1518 (2010)
Chemical analyses of groundnut (Arachis hypogaea) oil
Anyasor GN, et al.
Pakistan journal of nutrition, 8(3), 269-272 (2009)
Mechanisms of action underlying the antiandrogenic effects of the fungicide prochloraz
Laier P, et al.
Toxicology and Applied Pharmacology, 213(2), 160-171 (2006)
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