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68878

Supelco

(+)-Borneol

analytical standard

Sinonimo/i:

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

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About This Item

Formula empirica (notazione di Hill):
C10H18O
Numero CAS:
464-43-7
Peso molecolare:
154.25
Beilstein:
2038056
Numero CE:
208-080-0
Numero MDL:
MFCD00066427
Codice UNSPSC:
85151701
ID PubChem:
329761192
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥97.5% (GC)

Attività ottica

[α]20/D 37.0±2.0°, c = 5 in ethanol

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

206-209 °C (lit.)

applicazioni

food and beverages

Formato

neat

Temperatura di conservazione

2-8°C

Stringa SMILE

[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
DTGKSKDOIYIVQL-WEDXCCLWSA-N

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Categorie correlate

Descrizione generale

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.

Applicazioni

(+)-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.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Altre note

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

Pittogrammi

Flame
GHS02

Avvertenze

Warning

Indicazioni di pericolo

H228

Consigli di prudenza

P210

Classi di pericolo

Flam. Sol. 2

Codice della classe di stoccaggio

4.1B - Flammable solid hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

149.0 °F - closed cup

Punto d’infiammabilità (°C)

65 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
0000232161
0000186727
0000191236
0000188086
BCBM3284V

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Sigma-Aldrich

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D-Camphor

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
Jinyoung Hur et al.
Pharmaceutical biology, 51(1), 30-35 (2012-11-09)
The β-amyloid (Aβ) peptide aggregation with accompanying oxidative stress plays the major role in the pathogenesis of Alzheimer's disease (AD). Some natural compounds, including borneol, shed promising light on AD treatment. The present study was designed to investigate the antioxidative
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