(+)-Borneol TCI B6417

Chemical Identity

Other names: (1R,2S,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol · endo-(1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol
CAS No.: 464-43-7
PubChem: CID 6552009
Formula: C10H18O
Molecular weight: 154.25 g/mol
Purity: >95.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (1R,2S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol
SMILES: CC1(C2CCC1(C(C2)O)C)C
InChIKey: DTGKSKDOIYIVQL-WEDXCCLWSA-N
MDL: MDL00066427

Rp 1.167.600,00

~~Rp 831.600,00~~ Rp 1.167.600,00

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TCI B6417 (+)-Borneol (CAS 464-43-7) is a bicyclic monoterpene alcohol supplied as a crude medicine ingredient intended for research and experimental use. It is commonly employed as a reference compound in phytochemical studies and in the characterisation of plant-derived extracts. The single-enantiomer form also makes it useful for stereochemistry-oriented investigations and for the synthesis of bornyl derivatives. Store the material in a tightly closed container in a cool, dry place away from light, and always consult the manufacturer's safety data sheet before handling.

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Terpenes 2025-09-22 · p. 5

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Ma et al. (2023). Comparison of pharmacological activity and safety of different stereochemical configurations of borneol: L-borneol, D-borneol, and synthetic borneol. Biomedicine & Pharmacotherapy doi:10.1016/j.biopha.2023.114668
(2016). Preparation of borneol loaded hollow mesoporous silica nanoparticles and effect on borneol volatility. China Journal of Chinese Materia Medica doi:10.4268/cjcmm20161510
Ma et al. (2017). Microcalorimetric study of the effect of l-borneol, d-borneol and synthetic borneol on the growth of P. aeruginosa. Journal of Thermal Analysis and Calorimetry doi:10.1007/s10973-017-6627-3

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.