CasNo: 123-35-3
Molecular Formula: C10H16
Appearance: clear to pale yellow liquid
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Myrcene is clear to pale yellow liquid, while it's Molecular Formula is C10H16. Myrcene is the suitable synthetic standard used in the identification of E-myrcenol (2-methyl-6-methylene-E-2,7-octadien-1-01) as a major hindgut constituent in Eurasian bark beetle Ips duplicatus by GC-MS.
The CAS number of Myrcene is 123-35-3.
More information of Myrcene 123-35-3 are:
Synonyms |
1,6-Octadiene,7-methyl-3-methylene-;2-Methyl-6-methylene-2,7-octadiene;3-Methylene-7-methyl-1,6-octadiene;7-Methyl-3-methylene-1,6-octadiene;NSC 406264;b-Geraniolene;b-Myrcene; |
CAS Number |
123-35-3 |
Molecular Formula |
C10H16 |
Molecular Weight |
136.237 |
Density |
0.769 g/cm3 |
Melting Point |
<-10 °C |
Boiling Point |
167 °C at 760 mmHg |
Flash Point |
44.4 °C |
HS CODE |
2901.29 Oral rat LD50: 5000 mg/kg |
PSA |
0.00000 |
LogP |
3.47500 |
β-Myrcene is a terpene that has been found in Cannabis and has antioxidative properties. It reduces thiobarbituric acid reactive substance (TBARS) and increases glutathione (GSH), catalase, GSH peroxidase, and CuZn superoxide dismutase levels in a rat model of persistent environmental pollutant-induced oxidative stress when administered at a dose of 200 mg/kg per day.
InChI:InChI=1/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H3
Articles related to Myrcene:
Article |
Source |
- |
Walker,Hawkins , p. 4209 (1952) |
Palladium-Catalyzed Reactions of Allylic Electrophiles with Organometallic Reagents. A Regioselective 1,4-Elimination and a Regio- and Stereoselective Reduction of Allylic Derivatives |
Matsushita, Hajime,Negishi, Ei-ichi , p. 4161 - 4165 (1982) |
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