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68878

Supelco

(+)-Borneol

analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C10H18O
CAS Number:
Molecular Weight:
154.25
Beilstein:
2038056
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

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

SMILES string

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

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

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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.

Application

(+)-Borneol has been reported exert highly efficient positive modulating gamma-aminobutyric action (GABA) action at human recombinant α1β2γ2L GABAA receptors.
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Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

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

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Flam. Sol. 2

Storage Class Code

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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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)
Jianyu Su et al.
Journal of food science, 77(6), C658-C664 (2012-05-16)
The aims of this study were to optimize the preparation conditions of natural borneol/β-cyclodextrin (NB/β-CD) inclusion complex by ultrasound method, and to investigate its improvement of stability and solubility. The complex was characterized by different various spectroscopic techniques including Fourier
Xiao Song et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 36(18), 2489-2492 (2012-01-20)
To investigate the absorption characteristic of borneol. Using single pass perfusion model, the active ingredient of borneol were detected by GC. The drug concentration, perfusion rate and pH value on the absorption of borneol were studied. Perfusion rate on the

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