albicanol
[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl]methanol
 
Notes:
None found
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CAS Number: 54632-04-1Picture of molecule3D/inchi
Nikkaji Web: J13.110E
XlogP3-AA: 4.10 (est)
Molecular Weight: 222.37142000
Formula: C15 H26 O
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 299.34 °C. @ 760.00 mm Hg (est)
Flash Point: 225.00 °F. TCC ( 107.30 °C. ) (est)
logP (o/w): 4.661 (est)
Soluble in:
 water, 7.289 mg/L @ 25 °C (est)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
 None found
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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
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for albicanol usage levels up to:
 not for fragrance use.
 
Recommendation for albicanol flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 171360
National Institute of Allergy and Infectious Diseases: Data
 [(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methanol
Chemidplus: 0054632041
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References:
 [(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methanol
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 171360
Pubchem (sid): 135127295
Pherobase: View
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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): Search
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 found in nature
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Synonyms:
1-naphthalenemethanol, decahydro-5,5,8a-trimethyl-2-methylene-, (1S,4aS,8aS)-
[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylenedecahydronaphthalen-1-yl]methanol
[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methanol
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Articles:
PubMed: Bioassay-Guided Isolation of Cytotoxic Isocryptoporic Acids from Cryptoporus volvatus.
PubMed: Further drimane sesquiterpenes from Drimys brasiliensis stem barks with cytotoxic potential.
PubMed: Compounds from Dryopteris fragrans (L.) Schott with cytotoxic activity.
PubMed: Cytotoxic metabolites from Perenniporia tephropora, an endophytic fungus from Taxus chinensis var. mairei.
PubMed: First syntheses of (-)-tauranin and antibiotic (-)-BE-40644 based on lipase-catalyzed optical resolution of albicanol.
PubMed: A concise Diels-Alder strategy for the asymmetric synthesis of (+)-albicanol, (+)-albicanyl acetate, (+)-dihydrodrimenin, and (-)-dihydroisodrimeninol.
PubMed: Concise syntheses of coronarin A, coronarin E, austrochaparol and pacovatinin A.
PubMed: [Study on terpene of Dryopteris fragrans L].
PubMed: Total syntheses of (+)-chloropuupehenone and (+)-chloropuupehenol and their analogues and evaluation of their bioactivities.
PubMed: African elephant sesquiterpenes. II. Identification and synthesis of new derivatives of 2,3-dihydrofarnesol.
PubMed: Cryptoporic and isocryptoporic acids from the fungal cultures of Polyporus arcularius and P. ciliatus.
PubMed: First synthesis of (+)-alpha- and (+)-gamma-polypodatetraenes.
PubMed: Total synthesis of (+)-albicanol and (+)-albicanyl acetate.
PubMed: Ichthyotoxic phloroglucinol derivatives from Dryopteris fragrans and their anti-tumor promoting activity.
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