EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes

beta-sitosteryl acetate
stigmast-5-en-3-ol, acetate, (3b)- (9CI)

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CAS Number: 915-05-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg:213-019-6
Nikkaji Web:J149.402C
XlogP3-AA:9.90 (est)
Molecular Weight:456.75384000
Formula:C31 H52 O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:cosmetic ingredient for skin conditioning
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
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Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 514.52 °C. @ 760.00 mm Hg (est)
Flash Point: 504.00 °F. TCC ( 262.10 °C. ) (est)
logP (o/w): 11.583 (est)
Soluble in:
 water, 1.079e-006 mg/L @ 25 °C (est)
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: skin conditioning
stabilising agents
Santa Cruz Biotechnology
For experimental / research use only.
beta-Sitosteryl Acetate
Sigma-Aldrich: Sigma
For experimental / research use only.
beta-Sitosteryl acetate ∼97%
For experimental / research use only.
β-Sitosterol Acetate (contains Campesterol Acetate) >40.0%(GC)
Safety Information:
Preferred SDS: View
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Safety in Use Information:
cosmetic ingredient for skin conditioning
Recommendation for beta-sitosteryl acetate usage levels up to:
 not for fragrance use.
Recommendation for beta-sitosteryl acetate flavor usage levels up to:
 not for flavor use.
Safety References:
EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :5354503
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
 [(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5354503
Pubchem (sid):135051596
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
HMDB (The Human Metabolome Database):HMDB30151
Export Tariff Code:2915.39.3500
VCF-Online:VCF Volatile Compounds in Food
Potential Blenders and core components note
None Found
Potential Uses:
Occurrence (nature, food, other):note
 acacia leucophloea pods
Search Trop Picture
 mussaenda esquirolli leaf
Search Trop Picture
 acetic acid sitosteryl ester
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
beta-sitosterol 3-acetate
b-sitosterol acetate
beta-sitosterol acetate
 sitosteryl acetate
b-sitosteryl acetate
 stigmast-5-en-3-b-yl acetate
 stigmast-5-en-3-beta-yl acetate
 stigmast-5-en-3-ol, acetate (8CI)
 stigmast-5-en-3-ol, acetate, (3b,24R)-
 stigmast-5-en-3-ol, acetate, (3b)-
 stigmast-5-en-3-ol, acetate, (3b)- (9CI)
 stigmast-5-en-3-ol, acetate, (3beta)- (9CI)
(3b)-stigmast-5-en-3-yl acetate
 stigmast-5-en-3beta-ol, acetate
 stigmast-5-en-3beta-yl acetate


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PubMed:Chemical constituents from the seeds of Pongamia pinnata (L.) Pierre.
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PubMed:Characterization of effective chemopreventive agents in mammary gland in vitro using an initiation-promotion protocol.
Constit. of pods of kiker (Acacia leucophloea)
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