bornyl benzoate
borneol benzoate
 
Notes:
Flavouring compound [Flavornet]
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[(1S,3R,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] benzoate (Click)
CAS Number: 26927-90-2Picture of molecule
Nikkaji Web: J456.311E
XlogP3: 5.00 (est)
Molecular Weight: 258.36074000
Formula: C17 H22 O2
NMR Predictor: Predict (works with chrome or firefox)
Category: information only not used for fragrances or flavors
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
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Physical Properties:
Appearance: colorless solid (est)
Assay: 95.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 328.00 to  329.00 °C. @ 760.00 mm Hg (est)
Vapor Pressure: 0.000184 mm/Hg @ 25.00 °C. (est)
Flash Point: 300.00 °F. TCC ( 149.00 °C. ) (est)
logP (o/w): 5.365 (est)
Soluble in:
 alcohol
 water, 0.6179 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
Odor Type: pine
Odor Strength: low
 pine  balsamic  herbal  
Odor Description:
at 100.00 %. 
pine balsam herbal
  
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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: information only not used for fragrances or flavors
Recommendation for bornyl benzoate usage levels up to:
 not for fragrance use.
 
Recommendation for bornyl benzoate flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 6428443
National Institute of Allergy and Infectious Diseases: Data
 [(1S,3R,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] benzoate
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References:
 [(1S,3R,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] benzoate
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 6428443
Pubchem (sid): 10544224
Flavornet: 26927-90-2
Pherobase: View
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (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
FooDB: FDB029760
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
 balsam 
 herbal 
 pine 
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Occurrence (nature, food, other): note
 not found in nature
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Synonyms:
 borneol benzoate
[(1S,3R,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] benzoate
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Articles:
PubMed: Contact and fumigant toxicity of Pinus densiflora needle hydrodistillate constituents and related compounds and efficacy of spray formulations containing the oil to Dermatophagoides farinae.
PubMed: Antimicrobial activity of synthetic bornyl benzoates against Trypanosoma cruzi.
PubMed: Synthesis, acute toxicity and anti-inflammatory effect of bornyl salicylate, a salicylic acid derivative.
PubMed: Acaricidal activities of major constituents of essential oil of Juniperus chinensis leaves against house dust and stored food mites.
PubMed: Fabrication and characterization of a novel inclusion complex of chiral monomer derived from (+)-camphor with beta-cyclodextrins.
PubMed: Xanthine oxidase inhibitory activity of alkyl gallates.
PubMed: Asymmetric methoxyselenenylations and cyclizations with 3-camphorseleno electrophiles containing oxime substituents at C-2. Formation of an unusual oxaselenazole from an oxime-substituted selenenyl bromide.
PubMed: [Chemical constituents of fructus Amomi].
PubMed: Mechanism of the pyrophosphate migration in the enzymatic cyclization of geranyl and linalyl pyrophosphates to (+)- and (-)-bornyl pyrophosphates.
PubMed: Biosynthesis of monoterpenes: preliminary characterization of bornyl pyrophosphate synthetase from sage (Salvia officinalis) and demonstration that Geranyl pyrophosphate is the preferred substrate for cyclization.
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