| Names | |
|---|---|
|
IUPAC name
7-Ethyl-1,4-dimethylazulene
|
|
| Other names
1,4-Dimethyl-7-ethylazulene; Ba 2784; Camazulene; Chamazulen; Dimethulen; Dimethulene
|
|
| Identifiers | |
|
3D model (Jmol)
|
|
| ChemSpider | |
| ECHA InfoCard | 100.007.682 |
|
PubChem CID
|
|
|
|
|
|
| Properties | |
| C14H16 | |
| Molar mass | 184.28 g·mol−1 |
| Appearance | Blue oil |
| Density | 0.9883 (at 20 °C) |
| Boiling point | 161 °C (322 °F; 434 K) (at 12 mmHg) |
| Hazards | |
| Lethal dose or concentration (LD, LC): | |
|
LD50 (median dose)
|
3 g/kg (i.m., mouse) |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
| Infobox references | |
Chamazulene is an aromatic chemical compound with the molecular formula C14H16 found in a variety of plants including in chamomile (Matricaria chamomilla), wormwood (Artemisia absinthium), and yarrow (Achillea millefolium). It is a blue-violet derivative of azulene which is biosynthesized from the sesquiterpene matricin.
Chamazulene has anti-inflammatory properties in vivo and inhibits the CYP1A2 Enzyme.