bornyl benzoate

borneol benzoate

CAS: 26927-90-2 C17 H22 O2 MW: 258.36074000 pine

Identification

Namebornyl benzoate
IUPAC[(1S,3R,4S)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] benzoate
CAS Number26927-90-2
FDA UNIISearch
Molecular FormulaC17 H22 O2
Molecular Weight258.36074000
Nikkaji NumberJ456.311E
XlogP35.00 (est)

Regulatory

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 mmHg @ 25.00 °C. (est)
Flash Point 300.00 °F. TCC ( 149.00 °C. ) (est)
logP (o/w) 5.365 (est)
Soluble in alcohol
Insoluble in water

Organoleptic Properties

Odor Strength low
Odor Description at 100.00 %.

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryinformation only not used for fragrances or flavors
Recommendation for bornyl benzoate usage levels up tonot for fragrance use.
Recommendation for bornyl benzoate flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

FR balsam FR herbal FR pine

Natural Occurrence

not found in nature

Synonyms

borneol benzoate [(1S,3R,4S)-4,7,7- trimethyl-3-bicyclo[2.2.1]heptanyl] benzoate 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.