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 |
Melting Point: | 38.00 to 39.00 °C. @ 760.00 mm Hg
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Boiling Point: | 244.00 to 245.00 °C. @ 760.00 mm Hg (est)
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Vapor Pressure: | 0.005000 mmHg @ 25.00 °C. (est) |
Flash Point: | 220.00 °F. TCC ( 104.50 °C. ) (est)
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logP (o/w): | 0.995 (est) |
Soluble in: |
| alcohol | | water, 1726 mg/L @ 25 °C (est) |
Insoluble in: |
| water |
Organoleptic Properties:
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Odor and/or flavor descriptions from others (if found). |
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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: |
intraperitoneal-rat LDLo 400 mg/kg BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD Annales Pharmaceutiques Francaises. Vol. 9, Pg. 338, 1951.
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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.
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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.
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Recommendation for oxypinocamphone flavor usage levels up to: |
| not for flavor use.
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Safety References:
References:
| 4-hydroxy-4,6,6-trimethylbicyclo[3.1.1]heptan-3-one |
NIST Chemistry WebBook: | Search Inchi |
Pubchem (cid): | 112005 |
Pubchem (sid): | 135068739 |
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
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- | oxy | pinone |
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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