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Fórmula empírica (notación de Hill):
C10H18O
Número CAS:
Peso molecular:
154.25
UNSPSC Code:
12352212
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-352-6
Beilstein/REAXYS Number:
2038056
MDL number:
Assay:
97%
Form:
solid
Servicio técnico
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Permítanos ayudarleQuality Level
assay
97%
form
solid
optical activity
[α]20/D +36°, c = 5 in ethanol
mp
206-209 °C (lit.)
functional group
hydroxyl
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
Gene Information
human ... UGT1A4(54657)
General description
(+)-Borneol, a bicyclic monoterpene, is found in the essential oils of medicinal plants and is commonly used in traditional Chinese medicine for analgesia and anaesthesia.
Application
(+)-Borneol has been used to study its antiapoptotic, antioxidative and neuroprotective effect in human neuroblastoma cells (SH-SY5Y).
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
signalword
Warning
hcodes
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
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Borneol alleviates oxidative stress via upregulation of Nrf2 and Bcl-2 in SH-SY5Y cells.
Hur J, et al.
Pharmaceutical Analysis, 51(1), 30-35 (2013)
(+)-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
