Thujone
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| Ball-and-stick model of (−)-α-thujone | |||
| Names | |||
|---|---|---|---|
| IUPAC names α: (1S,4R,5R)-4-Methyl-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-one β: (1S,4S,5R)-4-methyl-1-propan-2-ylbicyclo[3.1.0]hexan-3-one | |||
| Other names Bicyclo[3.1.0]hexan-3-one, 4-methyl-1-(1-methylethyl)-, [1S-(1α,4α,5α)]- α-Thujone β-Thujone Thujone, cis 3-Thujanone, (1S,4R,5R)-(−)- Thujon 3-Thujanone, (−)- l-Thujone; 4-Methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-one-, (1S,4R,5R)- 3-Thujone; cis-Thujone (Z)-Thujone (−)-Thujone; Bicyclo(3.1.0)hexan-3-one, 4-methyl-1-(1-methylethyl)-, (1S,4R,5R)- NSC 93742 1-isopropyl-4-methylbicyclo[3.1.0]hexan-3-one | |||
| Identifiers | |||
| 
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| 3D model (JSmol) | 
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| 4660369 | |||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.013.096 | ||
| EC Number | 
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| KEGG | |||
| PubChem CID | |||
| UNII | 
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| CompTox Dashboard (EPA) | |||
| 
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| 
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| Properties | |||
| C10H16O | |||
| Molar mass | 152.237 g·mol−1 | ||
| Density | 0.92 g/cm3 (β-thujone); 0.9116 g/cm3 (α-thujone) | ||
| Melting point | <25 °C | ||
| Boiling point | 203 °C (397 °F; 476 K) (alpha,beta-thujone) | ||
| 407 mg/L | |||
| Hazards | |||
| GHS labelling: | |||
| Warning | |||
| H302 | |||
| P264, P270, P301+P312, P330, P501 | |||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
Thujone (/ˈθuːdʒoʊn/ ⓘ) is a ketone and a monoterpene that occurs predominantly in two diastereomeric (epimeric) forms: (−)-α-thujone and (+)-β-thujone.
Though it is best known as a chemical compound in the spirit absinthe, it is only present in trace amounts and is unlikely to be responsible for the spirit's purported stimulant and psychoactive effects.
Thujone acts on the GABAA receptor as an antagonist. As a competitive antagonist of GABAA receptor, thujone alone is considered to be convulsant, though by interfering with the inhibitory transmitter GABA, it may convey stimulating, mood-elevating effects at low doses. It is also found in perfumery as a component of several essential oils.
In addition to the naturally occurring (−)-α-thujone and (+)-β-thujone, two other forms are possible: (+)-α-thujone and (−)-β-thujone. In 2016, they were found in nature as well, in Salvia officinalis.
- (−)-α-thujone
- (+)-α-thujone
- (+)-β-thujone
- (−)-β-thujone