cholesteryl succinate

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cholesterol hydrogen succinate

CAS: 1510-21-0 C31 H50 O4 MW: 486.73630000
All Ingredients Aromatic Ingredients CAS Numbers EINECS Numbers

Identification

Namecholesteryl succinate
IUPAC4-[[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4-oxobutanoic acid
CAS Number1510-21-0
EINECS216-148-6
FDA UNIIT3J4KS4201
Molecular FormulaC31 H50 O4
Molecular Weight486.73630000
MDL NumberMFCD00037705
Nikkaji NumberJ206.716A

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 585.97 °C. @ 760.00 mm Hg (est)
Flash Point 355.00 °F. TCC ( 179.60 °C. ) (est)
logP (o/w) 10.708 (est)
Soluble in water, 1.702e-005 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesskin conditioning

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryemollients, skin conditioning
Recommendation for cholesteryl succinate usage levels up tonot for fragrance use.
Recommendation for cholesteryl succinate flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

butanedioic acid, mono[(3b)-cholest-5-en-3-yl] ester 4-[(3b)- cholest-5-en-3-yloxy]-4-oxobutanoic acid cholest-5-en-3beta-yl hydrogen succinate cholesterol hydrogen succinate cholesteryl hemisuccinate cholesteryl hydrogen succinate cholesterylhemisuccinate 4-[[(3S,8S,9S,10R,13R,14S,17R)-10,13- dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4-oxobutanoic acid 3b- hydroxy-5-cholestene3-hemisuccinate PubMed: Combinatorial approach for the rapid determination of thermochromic behavior of binary and ternary cholesteric liquid crystalline mixtures. PubMed: Cholesterol quantitation by GLC: artifactual formation of short-chain steryl esters. PubMed: [Physiochemical studies on the phase transition of the mixture of cholesteryl-propionate and cholesterol].