Date published: 2025-10-2

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(+)-Borneol (CAS 464-43-7)

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Alternate Names:
(1R,3S,4R)-4,7,7-trimethylbicyclo[2.2.1]heptan-3-ol; endo-(1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
Application:
(+)-Borneol is originally isolated from various aromatic plants
CAS Number:
464-43-7
Purity:
≥95%
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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(+)-Borneol is an organic compound that has application in various fields of research due to its chiral properties and presence in essential oils. Within the area of organic synthesis, (+)-borneol serves as a chiral starting material or resolving agent, allowing chemists to study and produce enantiomerically pure substances, which are for understanding the role of chirality in chemical reactions and properties. It is also employed in studies examining the release of aromatic compounds in plant metabolism, contributing to a deeper comprehension of plant defense mechanisms and interactions with the environment. In materials science, researchers explore (+)-borneol′s potential as a green additive for the synthesis of polymers and other materials, investigating how its incorporation affects biodegradability and sustainability. Additionally, its role in the field of catalysis is of interest, with studies focusing on how it can influence reaction pathways and efficiencies, particularly in the development of environmentally friendly catalytic processes.


(+)-Borneol (CAS 464-43-7) References

  1. 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
  2. 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
  3. 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
  4. (+)-Borneol alleviates mechanical hyperalgesia in models of chronic inflammatory and neuropathic pain in mice.  |  Jiang, J., et al. 2015. Eur J Pharmacol. 757: 53-8. PMID: 25835611
  5. (+)-Borneol attenuates oxaliplatin-induced neuropathic hyperalgesia in mice.  |  Zhou, HH., et al. 2016. Neuroreport. 27: 160-5. PMID: 26730517
  6. (+)-Borneol is neuroprotective against permanent cerebral ischemia in rats by suppressing production of proinflammatory cytokines.  |  Chang, L., et al. 2017. J Biomed Res. 31: 306-314. PMID: 28808202
  7. (+)-Borneol suppresses conditioned fear recall and anxiety-like behaviors in mice.  |  Cao, B., et al. 2018. Biochem Biophys Res Commun. 495: 1588-1593. PMID: 29223397
  8. (+/-)-Borneol Reverses Mitoxantrone Resistance against P-Glycoprotein.  |  Yang, R., et al. 2021. J Chem Inf Model. 61: 252-262. PMID: 33378196
  9. Identification of (-)-bornyl diphosphate synthase from Blumea balsamifera and its application for (-)-borneol biosynthesis in Saccharomyces cerevisiae.  |  Ma, R., et al. 2022. Synth Syst Biotechnol. 7: 490-497. PMID: 34977393
  10. Aerial (+)-borneol modulates root morphology, auxin signalling and meristematic activity in Arabidopsis roots.  |  Fukuda, K., et al. 2022. Biol Lett. 18: 20210629. PMID: 35506238
  11. Muscone and (+)-Borneol Cooperatively Strengthen CREB Induction of Claudin 5 in IL-1β-Induced Endothelium Injury.  |  Li, YC., et al. 2022. Antioxidants (Basel). 11: PMID: 35892657
  12. Cardiotoxicity of (-)-borneol, (+)-borneol, and isoborneol in zebrafish embryos is associated with Na+ /K+ -ATPase and Ca2+ -ATPase inhibition.  |  Ni, X., et al. 2023. J Appl Toxicol. 43: 373-386. PMID: 36062847
  13. (+)-Borneol inhibits the generation of reactive oxygen species and neutrophil extracellular traps induced by phorbol-12-myristate-13-acetate.  |  Chen, H., et al. 2022. Front Pharmacol. 13: 1023450. PMID: 36419617
  14. (+)-Borneol enantiomer ameliorates epileptic seizure via decreasing the excitability of glutamatergic transmission.  |  Wang, Y., et al. 2023. Acta Pharmacol Sin.. PMID: 36973542

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(+)-Borneol, 1 g

sc-239408
1 g
$163.00