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Chemical compound From Wikipedia, the free encyclopedia
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.[3] An less-common isomeric form, having one of the three alkene units in a different position, is α-myrcene.
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| Names | |
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| Preferred IUPAC name
7-Methyl-3-methylideneocta-1,6-diene | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.004.203 |
| KEGG | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C10H16 | |
| Molar mass | 136.238 g·mol−1 |
| Density | 0.794 g/cm3 |
| Melting point | < −10 °C (14 °F; 263 K) |
| Boiling point | 166 to 168 °C (331 to 334 °F; 439 to 441 K)[2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Myrcene is often produced commercially by the pyrolysis (400 °C) of β-pinene, which is obtained from turpentine.[3] It is rarely obtained directly from plants.[4]
Plants biosynthesize myrcene via geranyl pyrophosphate (GPP), which isomerizes into linalyl pyrophosphate. An elimination reaction, releasing the pyrophosphate (OPP) and a proton, completes the conversion.[5]
It could in principle be extracted from any number of plants, such as verbena or wild thyme,[4] the leaves of which contain up to 40% by weight of myrcene.[citation needed] Many other plants contain myrcene, sometimes in substantial amounts.[3] Some of these include cannabis,[6] hops, Houttuynia, lemon grass, mango, Myrcia, West Indian bay tree, and cardamom.[7]
Of the several terpenes extracted from Humulus lupulus (hops), the largest monoterpenes fraction is β-myrcene. One study of the chemical composition of the fragrance of Cannabis sativa found β-myrcene to compose between 29.4% and 65.8% of the steam-distilled essential oil for the set of fiber and drug strains tested.[8] Additionally, myrcene is thought to be the predominant terpene found in modern cannabis cultivars within North America. Interestingly, photo-oxidation of myrcene has been shown to rearrange the molecule into a novel terpene known as "hashishene" which is named for its abundance in hashish.[9]
It is found in the South African Adenandra villosa (50%).[10] & Brazilian Schinus molle (40%)[11] Myrcene is also found in Myrcia cuprea petitgrain (up to 48%),[12] bay leaf, juniper berry, cannabis, and hops.[3][13]
Myrcene is an intermediate used in the perfumery industry. It has a pleasant odor but is rarely used directly.[3] It is also unstable in air, tending to polymerize. Samples are stabilized by the addition of alkylphenols or tocopherol. It is thus more highly valued as an intermediate for the preparation of flavor and fragrance chemicals, such as menthol, citral, citronellol, citronellal, geraniol, nerol, and linalool.[4]
Both myrcene and myrcenol undergo Diels–Alder reactions with several dienophiles, such as acrolein, to give cyclohexene derivatives that are also useful fragrances, for instance Lyral.[2]
Myrcene also contributes a peppery and balsam aroma in beer.[14][15]
As of October 2018, the U.S. FDA withdrew authorization for the use of myrcene as a synthetic flavoring substance for use in food, without regard to its continuing stance that this substance does not pose a risk to public health under the conditions of its intended use.[16]
In 2015, beta-myrcene was added to California's Prop 65 list of chemicals known to the state of California to cause cancer or reproductive harm.[17]
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