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Published TCIMAIL newest issue No.201
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CAS RN: 7785-26-4 | Product Number: P0440
(1S)-(-)-α-Pinene
Purity: >97.0%(GC)
Synonyms:
Product Documents:
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| Product Number | P0440 |
Purity / Analysis Method
|
>97.0%(GC) |
| Molecular Formula / Molecular Weight | C__1__0H__1__6 = 136.24 |
| Physical State (20 deg.C) | Liquid |
Storage Temperature
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| CAS RN | 7785-26-4 |
| Reaxys Registry Number | 1903790 |
| PubChem Substance ID | 87574637 |
| SDBS (AIST Spectral DB) | 2898 |
| Merck Index (14) | 7445 |
| MDL Number | MFCD00064145 |
Specifications
| Appearance | Colorless to Almost colorless clear liquid |
| Purity(GC) | min. 97.0 % |
| Optical purity(GC) | min. 85.0 ee% |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | -64 °C |
| Boiling Point | 155 °C |
| Flash point | 32 °C |
| Specific Gravity (20/20) | 0.86 |
| Specific Rotation | -45.5° (neat) |
| Refractive Index | 1.46 |
| Solubility in water | Insoluble |
| Solubility (soluble in) | Ethanol, Chloroform, Ether |
GHS
| Pictogram |
|
| Signal Word | Warning |
| Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. H317 : May cause an allergic skin reaction. H400 : Very toxic to aquatic life. H226 : Flammable liquid and vapour. |
| Precautionary Statements | P273 : Avoid release to the environment. P261 : Avoid breathing mist or vapours. P210 : Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. P280 : Wear protective gloves/ protective clothing/ eye protection/ face protection/ hearing protection. P370 + P378 : In case of fire: Use dry sand, dry chemical or alcohol-resistant foam to extinguish. P391 : Collect spillage. |
Related Laws:
| EC Number | 232-077-3 |
Transport Information:
| UN Number | UN2368 |
| Class | 3 |
| Packing Group | III |
| HS Number | 2902190000 |
Application
(-)-α-Pinene: A Bicyclic Monoterpene with Diverse Biological Activities
α-Pinenes ((+)-α-pinene [P1099] and (-)-α-pinene) are bicyclic monoterpenes found in pine trees and many other conifers, with diverse biological activities.1,2) In addition, α-pinenes are used for the synthesis of chiral cyclic compounds.3) (The product is for research purpose only.)
References
- 1) Taming THC: potential cannabis synergy and phytocannabinoid-terpenoid entourage effects (a review)
- 2) Differences in bioactivity between the enantiomers of α-pinene
- 3) Chiral cyclic synthetic intermediates from readily available monoterpenoids (a review)
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