Name | L(-)-Borneol |
Synonyms | Linderol (-)-Borneol L(-)-Borneol l-2-Bornanol Bornencamphor l-2-Camphanol [(1S)-endo]-(?-Borneol endo-2-Hy-droxycamphane Borneol, (1S,2R,4S)-(-)- (1S,2S)-1,7,7-trimethylnorbornan-2-ol endo-(1S)-1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol (1S,2R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol |
CAS | 464-45-9 |
EINECS | 207-353-1 |
InChI | InChI=1/C10H18O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7?,8-,10+/m0/s1 |
Molecular Formula | C10H18O |
Molar Mass | 154.25 |
Density | 0.8389 (rough estimate) |
Melting Point | 206-209°C |
Boling Point | 210°C(lit.) |
Specific Rotation(α) | -36.2 º (c=5, C2H5OH) |
Flash Point | 150°F |
Water Solubility | INSOLUBLE |
Solubility | almost transparency in EtOH |
Vapor Presure | 33.5 mm Hg ( 25 °C) |
Vapor Density | 5.31 (vs air) |
Appearance | Crystalline Powder or Crystals |
Color | White to light yellow |
Merck | 14,1338 |
BRN | 3587558 |
pKa | 15.36±0.60(Predicted) |
Storage Condition | Store below +30°C. |
Refractive Index | -36 ° (C=5, EtOH) |
MDL | MFCD00066426 |
Use | This product is for scientific research only and shall not be used for other purposes. |
Risk Codes | R11 - Highly Flammable R43 - May cause sensitization by skin contact |
Safety Description | S16 - Keep away from sources of ignition. S36/37 - Wear suitable protective clothing and gloves. |
UN IDs | UN 1312 4.1/PG 3 |
WGK Germany | 2 |
RTECS | DT5095000 |
TSCA | Yes |
HS Code | 29061900 |
Hazard Class | 4.1 |
Packing Group | III |
Toxicity | LD50 orally in Rabbit: 5800 mg/kg |
Raw Materials | Oil of turpentine |
Reference Show more | 1. [IF=3.772] Z.-Y. Zeng et al."Inhibitory effects of essential oils from Asteraceae plant against pathogenic fungi of Panax notoginseng."J Appl Microbiol. 2021 Feb;130(2):592-603 |
FEMA | 2157 | BORNEOL |
LogP | 2.75 at 20℃ |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
use | a bicyclic monoterpene found in essential oils has been used to study its anti-apoptosis, antioxidant and neuroprotective effects in human neuroblastoma cells (SH-SY5Y). |
production method | 1. produced from camphor through reduction reaction. 2. produced from turpentine as raw material. |