Category:natural substances and extractives
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Assay: | 95.00 to 100.00
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Food Chemicals Codex Listed: | No |
Soluble in: |
| water, 3.642 mg/L @ 25 °C (est) |
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found). |
Cosmetic Information:
Suppliers:
Safety Information:
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Hazards identification |
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Classification of the substance or mixture |
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
None found. |
GHS Label elements, including precautionary statements |
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Pictogram | |
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Hazard statement(s) |
None found. |
Precautionary statement(s) |
None found. |
Oral/Parenteral Toxicity: |
Not determined
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Dermal Toxicity: |
Not determined
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Inhalation Toxicity: |
Not determined
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Safety in Use Information:
Category: | natural substances and extractives |
Recommendation for 5alpha-androst-16-en-3beta-ol usage levels up to: | | not for fragrance use.
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Recommendation for 5alpha-androst-16-en-3beta-ol flavor usage levels up to: |
| not for flavor use.
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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 :151449 |
National Institute of Allergy and Infectious Diseases:Data |
(3S,5S,8R,9S,10S,13R,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol |
Chemidplus:0007148518 |
References:
| (3S,5S,8R,9S,10S,13R,14S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol |
NIST Chemistry WebBook: | Search Inchi |
Pubchem (cid): | 151449 |
Pubchem (sid): | 135108710 |
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
(3beta,5alpha)- | androst-16-en-3-ol | | androst-16-en-3-ol, (3beta,5alpha)- (9CI) | 5alpha- | androst-16-en-3beta-ol (8CI) | (3S,5S,8R,9S,10S,13R,14S)-10,13- | dimethyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol | | JNF 55 |
Articles:
PubMed:Capillary gas chromatography with chemical ionization negative ion mass spectrometry in the identification of odorous steroids formed in metabolic studies of the sulphates of androsterone, DHA and 5alpha-androst-16-en-3beta-ol with human axillary bacterial isolates. |
PubMed:Metabolism of androstenone, 17β-estradiol and dihydrotestosterone in primary cultured pig hepatocytes and the role of 3β-hydroxysteroid dehydrogenase in this process. |
PubMed:A simplified and accurate method for the analysis of urinary metabolites of testosterone-related steroids using gas chromatography/combustion/isotope ratio mass spectrometry. |
PubMed:Development of a candidate reference method for the simultaneous quantitation of the boar taint compounds androstenone, 3α-androstenol, 3β-androstenol, skatole, and indole in pig fat by means of stable isotope dilution analysis-headspace solid-phase microextraction-gas chromatography/mass spectrometry. |
PubMed:The biosynthesis of androst-16-enes in boar testis tissue. |
PubMed:Determination of 13C/12C ratios of endogenous urinary steroids: method validation, reference population and application to doping control purposes. |
PubMed:Odor thresholds of the C(19)-Δ(16)-steroids responsible for boar odor in pork. |
PubMed:Evaluation of the contribution of skatole, indole, androstenone and androstenols to boar-taint in back fat of pigs by HPLC and capillary gas chromatography (CGC). |
PubMed:Androgen metabolism by rat epididymis. Metabolic conversion of 3H 5alpha-androstane-3alpha,17beta-diol, in vitro. |
PubMed:Changes with age in the occurrence of C19 steroids in the testis and submaxillary gland of the boar. |
PubMed:Studies on the metabolism of 5alpha-androst-16-en-3-one in boar tests in vivo. |
PubMed:Studies on the biosynthesis in vivo and excretion of 16-unsaturated C 19 steroids in the boar. |
PubMed:16-unsaturated C 19 3-oxo steroids as metabolic intermediates in boar testis. |
PubMed:Studies on the biosynthesis of 16-dehydro steroids. The metabolism of [4-14C]pregnenolone by boar adrenal and testis tissue in vitro. |
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