| Name | (-)-borneol |
|---|---|
| Synonyms |
L-BORNYL ALCOHOL
1-Bornyl alcohol Camphane-6-ol L-BORNEOL CRYSTALS REGULADE 2-Camphanol L-BORNEO CAMPHOR L(-)-Borneol (1S,2R,4S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol (1S,2R,4S)-(-)-Borneol=(1S)-endo-(-)Borneol BORNEOL CRYSTALS L(-)-BORNEOL (1S-endo)-1,7,7-Trimethylbicyclo(2.2.1)heptan-2-ol (−)-Borneol Bornencamphor (-)-(1S,4S)-Borneol (-) - camphor alcohol [(1S)-ENDO]-(-)-BORNEOL MFCD00003759 (1S)-(-)-BORNEOL (-)-BORNEOL BORNEOL LAEVO CRIST (?)-Borneol (1S-endo)-1,7,7-trimethylbicyclo[2.2.1]htan-2-ol l-2-Camphanol L-BORNEOL NATURAL endo-2-Bornanol L-BORNEOL CRYSTALS ENDO-(1S)-1,7,7-TRIMETHYLBICYCLO[2.2.1]HTAN-2-OL [1S,2R,4S,(-)]-1,7,7-Trimethylbicyclo[2.2.1]htan-2-ol (1s,2r,4s)-(-)-borneo endo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol endo-2-Hy-droxycamphane 7,7-trimethyl-(1s-endo)-bicyclo(2.2.1)htan-2-o 1,7,7-trimethyl-,(1S-endo)-Bicyclo[2.2.1]htan-2-ol (-)-Borneol predominantly endo ngaicamphor Ngai camphor bornel L-BORNEOL BORNYL ALCOHOL 1-bornylalcohol Malayancam-phor l-2-Bornanol Borneol endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol Celosia seed extract (1S)-(-)-BORNEOL endo-2-hydroxycamphane L(-)-Borneol, R (-)-BORNEOL, TERPENE STANDD syntheticd-borneol BORNEO CAMPHOR (-)-Borneol solution [(1s)-endo]-(-)-borneol CAMPHOL-(+)-BORNOL BORNEOL FLAKES ((1S)-END))-(-)BORNEOL [1S,2R,4S,(-)]-Bornan-2-ol EINECS 207-353-1 L-2-HYDROXYBORNANE 2-HYDROXYBORNANE FEMA 2157 Borneol, (1S,2R,4S)-(-) (1S)-endo-(-)-Borneol 2-bornanol Bornan-2-ol 2-camphanol 1,7,7-trimethyl-endo-Bicyclo[2.2.1]htan-2-ol Bicyclo2.2.1htan-2-ol, 1,7,7-trimethyl-, (1S,2R,4S) Linderol (-)-BORNEOL WITH 7,7-trimethyl-(1s-endo)-bicyclo[2.2.1]htan-2-o endo-2-camphanol |
| Description | (-)-Borneol has a highly efficacious positive modulating action at GABA receptor with an EC50 of 237 μM. |
|---|---|
| Related Catalog | |
| Target |
EC50: 237 μM (GABA receptor)[1] |
| In Vitro | (-)-Borneol is an enantiomer of (+)-Borneol. (+)-Borneol is a natural bicyclic monoterpene used for analgesia and anesthesia in traditional Chinese medicine; enhances GABA receptor activity with an EC50 of 248 μM. At high concentrations (>1.5 mM), (-)-Borneol directly activates GABAA receptors producing 84% of the maximal GABA response indicative of a weak partial agonist action. (-)-Borneol produces dose-dependent positive modulation of the Cl- conductance generated by extremely low dose GABA at α1β2γ2L GABAA receptors[1]. |
| References |
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 212.0±0.0 °C at 760 mmHg |
| Melting Point | 206-209 °C |
| Molecular Formula | C10H18O |
| Molecular Weight | 154.249 |
| Flash Point | 65.6±0.0 °C |
| Exact Mass | 154.135757 |
| PSA | 20.23000 |
| LogP | 2.71 |
| Vapour density | 5.31 (vs air) |
| Vapour Pressure | 0.0±0.9 mmHg at 25°C |
| Index of Refraction | 1.502 |
| Water Solubility | INSOLUBLE |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
|
| Symbol |
GHS02, GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H228-H317 |
| Precautionary Statements | P210-P280 |
| Personal Protective Equipment | Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
| Hazard Codes | F:Flammable; |
| Risk Phrases | R11 |
| Safety Phrases | S16-S36/37 |
| RIDADR | UN 1312 4.1/PG 3 |
| WGK Germany | 2 |
| RTECS | DT5095000 |
| Packaging Group | III |
| Hazard Class | 4.1 |
| HS Code | 29061900 |
| Precursor 5 | |
|---|---|
| DownStream 10 | |
| HS Code | 2906199090 |
|---|---|
| Summary | 2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |