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General Material Information

Preferred name bornyl salicylate
Trivial Name (1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl) 2-hydroxybenzoate
Short Description benzoic acid, 2-hydroxy-, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester, endo-
Formula C17 H22 O3
CAS Number 560-88-3
CAS Number 560-88-3 (SRR)
ECHA Number 209-213-5
FDA UNII 990G1O66KJ
Nikkaji Number J60.093H
MDL MFCD00213519
xLogP3-AA 4.90 (est)
NMR Predictor External link
Synonyms
  • benzoic acid, 2-hydroxy-, 1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester, endo-
  • endo-1,7,7-trimethyl bicyclo(2.2.1)hept-2-yl salicylate
  • (1,7,7-trimethyl norbornan-2-yl) 2-hydroxybenzoate
  • (1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl) 2-hydroxybenzoate
  • endo-1,7,7-trimethylbicyclo(2.2.1)hept-2-yl salicylate
  • (1,7,7-trimethylnorbornan-2-yl) 2-hydroxybenzoate

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Literature & References

(1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl) 2-hydroxybenzoate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:560-88-3
Pubchem (cid):98012
Pubchem (sid):135056854
[(1S,4R,6R)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] 2-hydroxybenzoate
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:560-88-3
Pubchem (cid):249579
Pubchem (sid):112451
Publications by PubMed
Synthesis, acute toxicity and anti-inflammatory effect of bornyl salicylate, a salicylic acid derivative.
The acid adducts hydrazinium 2-hydroxybenzoate-2-hydroxybenzoic acid (1/1) and hydrazinium 3-hydroxy-2-naphthoate-3-hydroxy-2-naphthoic acid (1/1).
Hydroquinone-salicylic acid conjugates as novel anti-melasma actives show superior skin targeting compared to the parent drugs.
Transporter-mediated uptake of 2-chloro- and 2-hydroxybenzoate by Pseudomonas huttiensis strain D1.
Purification and characterization of an oxygen-sensitive, reversible 3,4-dihydroxybenzoate decarboxylase from Clostridium hydroxybenzoicum.
Male sex pheromone of cockroachEurycotis floridana (walker) (Blattidae, Polyzosteriinae): Role and composition of tergites 2 and 8 secretions.
Salicylate activity. 2. Potentiation of atrazine.
Thermophilic, reversible gamma-resorcylate decarboxylase from Rhizobium sp. strain MTP-10005: purification, molecular characterization, and expression.
Smooth muscle relaxant action of benzyl benzoates and salicylic acid derivatives from Brickellia veronicaefolia on isolated guinea-pig ileum.
New chemical constituents from the endophyte Streptomyces species LR4612 cultivated on Maytenus hookeri.
Inhibition of phosphoglycerate kinase by salicylates.
Identification of a cocaine esterase in a strain of Pseudomonas maltophilia.

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
Export Tariff Code:2918.23.0000
ChemSpider:View

Suppliers

BOC Sciences

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 274.35995483398
Melting Point 22 to 24°C @ 760 mm Hg
Boiling Point 349 to 350°C @ 760 mm Hg
Flash Point TCC Value 93.33 °C TCC
logP (o/w) 5.763 est
Solubility
alcohol Yes
water, 0.4153 mg/L @ 25 °C (est) Yes
water No

Organoleptic Properties

Odor Type: Herbal
green, fresh, woody, orchid, fir needle, balsamic
Odor strength medium
Substantivity 400 hour(s) at 100.00 %
Luebke, William tgsc, (1987) At 100.00 %. green fresh woody salicylate pine needle bisabolene

Potential Uses

Applications
Odor purposes Fresh and clean, Herbal, Orchid, Woody
Other purposes Clean

Safety Information

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

Safety in use information

Category:
fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for bornyl salicylate usage levels up to:
8.0000 % in the fragrance concentrate.
Recommendation for bornyl salicylate flavor usage levels up to:
not for flavor use.

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 :98012
National Institute of Allergy and Infectious Diseases:Data
(1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl) 2-hydroxybenzoate
Chemidplus:0000560883
[(1S,4R,6R)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] 2-hydroxybenzoate