cholesteryl butyrate

cholest-5-en-3b-ol butyrate

CAS: 521-13-1 C31 H52 O2 MW: 456.75384000

Identification

Namecholesteryl butyrate
IUPAC[(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] butanoate
CAS Number521-13-1
EINECS208-304-7
FDA UNII50QA4YCP7F
Molecular FormulaC31 H52 O2
Molecular Weight456.75384000
MDL NumberMFCD00021144
Nikkaji NumberJ60.879C

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 518.00 °C. @ 760.00 mm Hg (est)
Flash Point 508.00 °F. TCC ( 264.30 °C. ) (est)
logP (o/w) 11.770 (est)
Soluble in water, 9.339e-007 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

Categorycosmetic ingredient for skin conditioning
Recommendation for cholesteryl butyrate usage levels up tonot for fragrance use.
Recommendation for cholesteryl butyrate flavor usage levels up tonot for flavor use.

TCI AMERICA

Moving Your Chemistry Forward

We continuously strive to advance our technology.

View All Website 1-800-423-8616 Sales-US@TCIchemicals.com;

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

butanoic acid, (3b)-cholest-5-en-3-yl ester butyric acid cholesteryl ester cholest-5-en-3b-ol butyrate cholest-5-en-3beta-ol butyrate 5- cholesten-3b-ol 3-butyrate cholesterol butyrate cholesteryl butanoate cholesteryl N-butyrate [(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] butanoate 3b- hydroxy-5-cholestene 3-butyrate PubMed: Solid lipid nanoparticles of cholesteryl butyrate inhibit the proliferation of cancer cells in vitro and in vivo models. PubMed: Cholesteryl butyrate solid lipid nanoparticles inhibit the adhesion and migration of colon cancer cells. PubMed: Influence of supercritical CO(2) pressurization on the phase behavior of mixed cholesteryl esters. PubMed: Solid lipid nanoparticles as anti-inflammatory drug delivery system in a human inflammatory bowel disease whole-blood model. PubMed: Application of comprehensive two-dimensional gas chromatography to sterols analysis. PubMed: Cholesterylbutyrate solid lipid nanoparticles as a butyric acid prodrug. PubMed: Solid lipid nanoparticles: could they help to improve the efficacy of pharmacologic treatments for brain tumors? PubMed: Cholesteryl butyrate solid lipid nanoparticles inhibit adhesion of human neutrophils to endothelial cells. PubMed: Cytotoxicity of anticancer drugs incorporated in solid lipid nanoparticles on HT-29 colorectal cancer cell line. PubMed: Cholesteryl butyrate solid lipid nanoparticles as a butyric acid pro-drug: effects on cell proliferation, cell-cycle distribution and c-myc expression in human leukemic cells. PubMed: In vitro effects of cholesteryl butyrate solid lipid nanospheres as a butyric acid pro-drug on melanoma cells: evaluation of antiproliferative activity and apoptosis induction. PubMed: The effect of formulation and concentration of cholesteryl butyrate solid lipid nanospheres (SLN) on NIH-H460 cell proliferation. PubMed: Fatty acid steryl, stanyl, and steroid esters by esterification and transesterification in vacuo using Candida rugosa lipase as catalyst. PubMed: Cholesteryl butyrate in solid lipid nanospheres as an alternative approach for butyric acid delivery. PubMed: Cholesterol quantitation by GLC: artifactual formation of short-chain steryl esters. PubMed: Use of the minimal function for partial structure development in direct methods. PubMed: Crystal structure of cholesteryl butanoate at 123 K. PubMed: Simultaneous estimation of urinary steroids by semi-automated gas chromatography. Investigation of neo-natal infants and children with abnormal steroid synthesis.