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CAS RN: 7785-26-4 | Product Number: P0440

(1S)-(-)-α-Pinene


Purity: >97.0%(GC)
Synonyms:
Product Documents:
25ML
€16.00
4   30  
500ML
€51.00
1   ≥60 

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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, Ether, Chloroform
GHS
Pictogram Pictogram Pictogram 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 2902900000
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


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