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

sitostenone
stigmast-4-en-3-one (8CI)(9CI)

Supplier Sponsors

Name:(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
CAS Number: 1058-61-3Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J83.547A
XlogP3-AA:9.30 (est)
Molecular Weight:412.70076000
Formula:C29 H48 O
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 503.80 °C. @ 760.00 mm Hg (est)
Flash Point: 507.00 °F. TCC ( 263.70 °C. ) (est)
logP (o/w): 10.240 (est)
Soluble in:
 water, 2.284e-005 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Sitostenone
Coompo
For experimental / research use only.
Sitostenone from Plants ≥96%
 
Safety Information:
 
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
 
Pictogram
 
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:
Category:
natural substances and extractives
Recommendation for sitostenone usage levels up to:
 not for fragrance use.
 
Recommendation for sitostenone 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 :5484202
National Institute of Allergy and Infectious Diseases:Data
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
Chemidplus:0001058613
 
References:
 (8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5484202
Pubchem (sid):135051184
 
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
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB33934
FooDB:FDB012138
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 cardamom seed
Search Trop Picture
 corn
Search Trop Picture
 date palm stem
Search Trop Picture
 quassia amara wood
Search Trop Picture
 soybean tissue culture
Search Trop Picture
 
Synonyms:
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one
 stigmast-4-en-3-one
 stigmast-4-en-3-one (8CI)(9CI)
4-stigmasten-3-one
 

Articles:

PubMed:[Chemical constituents of chloroform fraction from leaves of Chimonanthus salicifolius].
PubMed:Oleodaphnoic acid and coriaceol, two new natural products from the stem bark of Wikstroemia coriacea.
PubMed:Bioactive constituents in Prunus africana: geographical variation throughout Africa and associations with environmental and genetic parameters.
PubMed:Chemical constituents from the roots of Xanthium sibiricum.
PubMed:Antituberculosis cycloartane triterpenoids from Radermachera boniana.
PubMed:Amides from the stem of Capsicum annuum.
PubMed:A new pyrrole derivative from the extracts of the fungus monascus pilosus-fermented rice.
PubMed:Isolation of new esters from the stems of Cinnamomum reticulatum Hay.
PubMed:A new sesquiterpene isolated from the extracts of the fungus Monascus pilosus-fermented rice.
PubMed:[Studies on the chemical constituents from Euphorbia chrysocoma].
PubMed:Secondary metabolites and cytotoxic activities from the stem bark of Zanthoxylum nitidum.
PubMed:Bioactive metabolites from Spilanthes acmella Murr.
PubMed:Isolation of antibacterial diterpenoids from Cryptomeria japonica bark.
PubMed:[Triterpenoids and steroids from Excoecaria agallocha].
PubMed:A new cytotoxic amide from the stem wood of Hibiscus tiliaceus.
PubMed:Cytotoxic chromenes from Myriactis humilis.
PubMed:A cytotoxic butenolide, two new dolabellane diterpenoids, a chroman and a benzoquinol derivative formosan Casearia membranacea.
PubMed:Proposed active constituents of Dipladenia martiana.
PubMed:A new phorbol diester from Aleurites moluccana.
PubMed:Steroids from Harrisonia abyssinica.
PubMed:[Cleavage of the side chain of sitosterol by R, S and M mycobacteria variants].
 
Notes:
Constit. of the wood of Quassia amara (Surinam quassia)
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