Molecular structure of (−)-Borneol, CAS Number: 464-45-9
(-)-Borneol (CAS 464-45-9)
Alternate Names:
endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
Application:
(−)-Borneol is originally isolated from various aromatic plants
CAS Number:
464-45-9
Molecular Weight:
154.25
Molecular Formula:
C10H18O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
(−)-Borneol is an optical isomer of Borneol. Borneol is a bicyclic organic component of some aromatic plant essential oils. In a study on Tanacetum parthenium, Borneol was isolated from the extratred essential oil. Additionally this compound has been isolated from the essential oils of Zingiber officinale Roscoe as determined via gas chromatography and GC-MS.
(-)-Borneol (CAS 464-45-9) References
- (+)- And (-)-borneol: efficacious positive modulators of GABA action at human recombinant alpha1beta2gamma2L GABA(A) receptors. | Granger, RE., et al. 2005. Biochem Pharmacol. 69: 1101-11. PMID: 15763546
- Composition of a monoterpenoid-rich essential oil from the rhizome of Zingiber officinale from north western Himalayas. | Gupta, S., et al. 2011. Nat Prod Commun. 6: 93-6. PMID: 21366054
- Chemical composition, antibacterial activity and cytotoxicity of essential oils of Tanacetum parthenium in different developmental stages. | Mohsenzadeh, F., et al. 2011. Pharm Biol. 49: 920-6. PMID: 21592001
- Investigation of mechanisms involved in (-)-borneol-induced vasorelaxant response on rat thoracic aorta. | Silva-Filho, JC., et al. 2012. Basic Clin Pharmacol Toxicol. 110: 171-7. PMID: 21883938
- Borneol alleviates oxidative stress via upregulation of Nrf2 and Bcl-2 in SH-SY5Y cells. | Hur, J., et al. 2013. Pharm Biol. 51: 30-5. PMID: 23134284
- Borneol Dehydrogenase from Pseudomonas sp. Strain TCU-HL1 Catalyzes the Oxidation of (+)-Borneol and Its Isomers to Camphor. | Tsang, HL., et al. 2016. Appl Environ Microbiol. 82: 6378-6385. PMID: 27542933
- Different effects of (+)‑borneol and (‑)‑borneol on the pharmacokinetics of osthole in rats following oral administration. | Luo, DD., et al. 2017. Mol Med Rep. 15: 4239-4246. PMID: 28440419
- New insights on relaxant effects of (-)-borneol monoterpene in rat aortic rings. | Santos, SE., et al. 2019. Fundam Clin Pharmacol. 33: 148-158. PMID: 30240490
- Analytical techniques to recognize inclusion complexes formation involving monoterpenes and cyclodextrins: A study case with (-) borneol, a food ingredient. | Santana, DVS., et al. 2021. Food Chem. 339: 127791. PMID: 32860997
- Borneol in cardio-cerebrovascular diseases: Pharmacological actions, mechanisms, and therapeutics. | Liu, S., et al. 2021. Pharmacol Res. 169: 105627. PMID: 33892091
- A comparative analysis of morphology, microstructure, and volatile metabolomics of leaves at varied developmental stages in Ainaxiang (Blumea balsamifera (Linn.) DC.). | Chen, X., et al. 2023. Front Plant Sci. 14: 1285616. PMID: 38034556
- Functional Characterization and Catalytic Activity Improvement of Borneol Acetyltransferase from Wurfbainia longiligularis. | Chen, Y., et al. 2024. J Agric Food Chem. 72: 13250-13261. PMID: 38813660
- Effects of (−)-borneol on the growth and morphology of Aspergillus fumigatus and Epidermophyton floccosom | Lee, S. Y., Kim, S. H., Hong, C. Y., Park, M. J., & Choi, I. G. 2013. Flavour and Fragrance Journal. 28(2): 129-134.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(-)-Borneol, 100 g | sc-239409 | 100 g | $111.00 |