Structure via PubChem · Public domain (PubChem)
myrcene
Sign in to saveAlso known as 7-methyl-3-methyleneocta-1,6-diene, 7-methyl-3-methylene-1,6-octadiene, 7-Methyl-3-methylene-1,6-octadiene (myrcene), FEMA 2762, 7-Methyl-3-methyleneoctadiene-(1,6), 3-Methylene-7-methyl-1,6-octadiene, 7-Methyl-3-methylideneocta-1,6-diene, 7-Methyl-3-methylene-1,6-octadiene (beta -myrcene)
Myrcene, or β-myrcene, is a monoterpene. A colorless oil, it occurs widely in essential oils. It is produced mainly semi-synthetically from Myrcia, from which it gets its name. It is an intermediate in the production of several fragrances. A less-common isomeric form, having one of the three alkene units in a different position, is α-myrcene.
Chemical data
- Formula
- C10H16
- Molecular weight
- 136.23 g/mol
- IUPAC name
- 7-methyl-3-methylideneocta-1,6-diene
- SMILES
- CC(=CCCC(=C)C=C)C
- InChIKey
- UAHWPYUMFXYFJY-UHFFFAOYSA-N
- XLogP
- 4.3
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Wikidata facts
- Mass
- 136.125201
Show 3 more facts
- chemical formula
- C₁₀H₁₆
- Commons category
- Myrcene
- canonical SMILES
- CC(=CCCC(=C)C=C)C
Sources (3)
via Wikidata · CC0
~3 min read
Article
6 sectionsContents
- Production
- Occurrence
- Use in fragrance and flavor industries
- Health and safety
- See also
- References
Myrcene, or β-myrcene, is a monoterpene. A colorless oil, it occurs widely in essential oils. It is produced mainly semi-synthetically from Myrcia, from which it gets its name. It is an intermediate in the production of several fragrances. A less-common isomeric form, having one of the three alkene units in a different position, is α-myrcene.
==Production== thumb|244 px|left|Biosynthesis of myrcene from geranyl pyrophosphate. Myrcene is often produced commercially by the pyrolysis (400 °C) of β-pinene, which is obtained from turpentine. It is rarely obtained directly from plants.