
CAS 464-43-7: d-Borneol
Formula:C10H18O
InChI:InChI=1S/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7-,8+,10+/m1/s1
InChI key:InChIKey=DTGKSKDOIYIVQL-WEDXCCLWSA-N
SMILES:C[C@@]12C(C)(C)[C@@](C[C@@H]1O)(CC2)[H]
Synonyms:- (+)-(2S)-Borneol
- (+)-2-Borneol
- (+)-endo-Borneol
- (1R)-(+)-Borneol
- (1R)-endo-Borneol
- (1R,2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
- (1R,2S,4R)-borneol
- (2S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
- Asparagus Root
- Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R,2S,4R)-
- Bicyclo[2.2.1]heptan-2-ol, 1,7,7-trimethyl-, (1R-endo)-
- See more synonyms
Sort by
Found 18 products.
Smart Solutions™ TerpiMix Kit 2500 μg/mL in Isopropanol
CAS:Controlled Product- 10458-14-7
- 105-87-3
- 106-22-9
- 106-24-1
- 106-25-2
- 111-02-4
- 112-14-1
- 1139-30-6
- 116-26-7
- 1196-01-6
- 123-35-3
- 124-76-5
- 125-12-2
- 127-91-3
- 13466-78-9
- 13877-91-3
- 138-86-3
- 2217-02-9
- 2244-16-8
- 22567-21-1
- 3387-41-5
- 4602-84-0
- 4630-07-3
- 464-43-7
- 464-45-9
- 4674-50-4
- 4695-62-9
- 469-61-4
- 470-82-6
- 489-86-1
- 498-15-7
- 499-75-2
- 502-61-4
- 515-69-5
- 527-84-4
- 535-77-3
- 5392-40-5
- 546-79-2
- 546-80-5
- 562-74-3
- 586-62-9
- 638-36-8
- 675-20-7
- 6753-98-6
- 7212-44-4
- 7541-49-3
- 76-22-2
- 77-53-2
- 7787-20-4
- 78-70-6
- 79-92-5
- 80-56-8
- 87-44-5
- 89-78-1
- 89-79-2
- 89-81-6
- 89-82-7
- 89-83-8
- 98-55-5
- 99-83-2
- 99-85-4
- 99-86-5
- 99-87-6
Color and Shape:Kit(+)-Borneol
CAS:Controlled Product(+)-Borneol is a bicyclic organic compound, which is a naturally occurring terpene obtained from various essential oils, particularly those derived from the camphor tree and certain herbaceous plants. As a monoterpenoid, it exhibits a unique bicyclic structure contributing to its characteristic camphoraceous odor and physical properties. The mode of action of (+)-Borneol is multifaceted, including its ability to interact with various biological pathways. It is known to modulate ion channels and neurotransmitter systems, providing it with potential anti-inflammatory and analgesic effects. Furthermore, it exhibits antioxidant properties by scavenging free radicals and protecting cellular components from oxidative damage. Due to these properties, (+)-Borneol is widely used in the pharmaceutical and cosmeceutical industries. It serves as a precursor in the synthesis of camphor and is also incorporated into traditional medicine formulations for its therapeutic benefits, including pain relief and improved circulation. Additionally, its pleasant aroma makes it a valuable component in perfumes and flavoring agents. Researchers explore its potential applications in neurology and cardiology, aiming to harness its bioactive properties for clinical advancements.Formula:C10H18OPurity:Min. 95%Color and Shape:PowderMolecular weight:154.25 g/mol(+)-BORNEOL
CAS:(+)-BORNEOL: natural bicyclic monoterpene, used in traditional Chinese medicine for pain relief and anesthesia; boosts GABA activity, EC50 248 μM.Formula:C10H18OPurity:99.6% - ≥95%Color and Shape:White To Off-White Crystals Than Water And Insoluble In Water Used To Make PerfumesMolecular weight:154.25(+)-Borneol
CAS:Formula:C10H18OPurity:>95.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:154.25(+)-Borneol-D3 (Contains up to 1% D0)
CAS:Controlled ProductFormula:C10H15D3OColor and Shape:NeatMolecular weight:157.27(+)-Borneol
CAS:Controlled ProductApplications (+)-Borneol is used for analgesia and anesthesia in traditional Chinese and Japanese medicine. (+)-Borneol has hightly efficacious positive modulating action at human recombinant α1β2γ2L GABAA receptors. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Granger, R.E., et. al.: Biochem. Pharmacol., 69, 1101 (2005)Formula:C10H18OColor and Shape:White To Off-WhiteMolecular weight:154.25(+)-Borneol
CAS:(+)-Borneol analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C10H18OPurity:(GC) ≥96% (sum of enantiomers)Color and Shape:SolidMolecular weight:154.25