oxypinocamphone
bicyclo(3.1.1)heptan-3-one, 2-hydroxy-2,6,6-trimethyl- (9CI)
 
Notes:
None found
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CAS Number: 10136-65-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 233-376-1
Nikkaji Web: J10.649F
XlogP3-AA: 1.20 (est)
Molecular Weight: 168.23592000
Formula: C10 H16 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Physical Properties:
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Melting Point: 38.00 to  39.00 °C. @ 760.00 mm Hg
Boiling Point: 244.00 to  245.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.005000 mmHg @ 25.00 °C. (est)
Flash Point: 220.00 °F. TCC ( 104.50 °C. ) (est)
logP (o/w): 0.995 (est)
Soluble in:
 alcohol
 water, 1726 mg/L @ 25 °C (est)
Insoluble in:
 water
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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:
intraperitoneal-rat LDLo  400 mg/kg
BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Annales Pharmaceutiques Francaises. Vol. 9, Pg. 338, 1951.

Dermal Toxicity:
subcutaneous-mouse LD50 500 mg/kg
BEHAVIORAL: COMA KIDNEY, URETER, AND BLADDER: URINE VOLUME INCREASED GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA"
Annales Pharmaceutiques Francaises. Vol. 9, Pg. 338, 1951.

Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for oxypinocamphone usage levels up to:
 not for fragrance use.
 
Recommendation for oxypinocamphone 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 : 112005
National Institute of Allergy and Infectious Diseases: Data
 4-hydroxy-4,6,6-trimethylbicyclo[3.1.1]heptan-3-one
Chemidplus: 0010136659
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References:
 4-hydroxy-4,6,6-trimethylbicyclo[3.1.1]heptan-3-one
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 112005
Pubchem (sid): 135068739
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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
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: 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
 cistus twig/leaf oil @ 0.4%
Data  GC  Search Trop  Picture
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Synonyms:
 bicyclo(3.1.1)heptan-3-one, 2-hydroxy-2,6,6-trimethyl- (9CI)
 bicyclo[3.1.1]heptan-3-one, 2-hydroxy-2,6,6-trimethyl-
 camphostene
2-hydroxy-2,6,6-trimethyl bicyclo(3.1.1)heptan-3-one
2-hydroxy-2,6,6-trimethylbicyclo(3.1.1)heptan-3-one
2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one
2-hydroxy-3-pinanone
4-hydroxy-4,6,6-trimethylbicyclo[3.1.1]heptan-3-one
2-hydroxypinan-3-one
2-hydroxypinocamphone
3-hydroxypinocamphone
 pinan-3-one, 2-hydroxy-
3-pinanone, 2-hydroxy-
oxypinone
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Articles:
PubMed: Synthesis of 2-(pyridin-3-yl)-1-azabicyclo[3.2.2]nonane, 2-(pyridin-3-yl)-1-azabicyclo[2.2.2]octane, and 2-(pyridin-3-yl)-1-azabicyclo[3.2.1]octane, a class of potent nicotinic acetylcholine receptor-ligands.
PubMed: A general, efficient and stereospecific route to sphingosine, sphinganines, phytosphingosines and their analogs.
PubMed: A general procedure for the enantioselective synthesis of the minor tobacco alkaloids nornicotine, anabasine, and anatabine.
PubMed: Synthesis, theoretical and structural analyses, and enantiopharmacology of 3-carboxy homologs of AMPA.
PubMed: Full stereochemical understanding in a new (2R,3R,4R)-4-hydroxyisoleucine synthesis.
PubMed: Two key chiral intermediates in a new 4-hydroxyisoleucine synthesis.
PubMed: Some of the amino acid chemistry going on in the Laboratory of Amino Acids, Peptides and Proteins.
PubMed: A novel enantioselective synthesis of (S)-(-)- and (R)-(+)-nornicotine via alkylation of a chiral 2-hydroxy-3-pinanone ketimine template.
PubMed: Syntheses ofγ-fluoro-α-amino acids.
PubMed: [Pharmacodynamics of oxypinocamphone].
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