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Merck

68878

(+)-Borneol

analytical standard

Sinónimos:

endo-(1R)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol

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About This Item

Fórmula empírica (notación de Hill):
C10H18O
Número CAS:
464-43-7
Peso molecular:
154.25
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329761192
EC Number:
208-080-0
Beilstein/REAXYS Number:
2038056
MDL number:
MFCD00066427

Nombre del producto

(+)-Borneol, analytical standard

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

DTGKSKDOIYIVQL-WEDXCCLWSA-N

SMILES string

[H][C@@]12CC[C@@](C)([C@@H](O)C1)C2(C)C

grade

analytical standard

assay

≥97.5% (GC)

optical activity

[α]20/D 37.0±2.0°, c = 5 in ethanol

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

206-209 °C (lit.)

application(s)

food and beverages

format

neat

storage temp.

2-8°C

Quality Level

100

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Application

(+)-Borneol has been reported exert highly efficient positive modulating gamma-aminobutyric action (GABA) action at human recombinant α1β2γ2L GABAA receptors.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

Borneol, a bicyclic monoterpenoid alcohol which is a major constituent of medicinal plants is grouped under the volatile organic compounds (VOCs) family of chemicals. It is employed as analgesic and anesthetic in traditional Chinese and Japanese medicines.

Other Notes

This compound is commonly found in plants of the genus: angelica cinnamomum curcuma echinacea salvia thymus valeriana zingiber

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

pictograms

Flame
GHS02

signalword

Warning

hcodes

H228

pcodes

P210

Hazard Classifications

Flam. Sol. 2

Clase de almacenamiento

4.1B - Flammable solid hazardous materials

wgk

WGK 3

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

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Certificados de análisis (COA)

Lot/Batch Number
0000232161
0000232161
0000191236
0000188086
0000186727

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Visite la Librería de documentos

The enhancing effect of synthetical borneol on the absorption of tetramethylpyrazine phosphate in mouse.
Yan-Yu X, et al.
International Journal of Pharmaceutics, 337(1-2), 74-79 (2007)
Supercritical carbon dioxide extraction of volatiles from spices: comparison with simultaneous distillation-extraction.
Diaz-Maroto MC, et al.
Journal of Chromatography A, 947(1), 23-29 (2002)
(+)-And (-)-borneol: efficacious positive modulators of GABA action at human recombinant a 1 ? 2 ? 2L GABA A receptors.
Granger RE, et al.
Biochemical Pharmacology, 69(7), 1101-1111 (2005)
Eva Horváthová et al.
Mutagenesis, 27(5), 581-588 (2012-05-01)
Experimental evidences suggest that most essential oils possess a wide range of biological and pharmacological activities that may protect tissues against oxidative damage. In this study, we investigated DNA-protective effect of borneol, a component of many essential oils, against oxidative
Zhen-Yu Xiong et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 38(6), 786-790 (2013-05-31)
Borneol is a major component of many medicinal plant essential oils, as well as a popular traditional Chinese medicine. This essay collects the results of the latest domestic and foreign studies, and summarizes and analyzes its activity and reaction mechanism
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