Chamazulene

Chamazulene
Names
Preferred IUPAC name
7-Ethyl-1,4-dimethylazulene
Other names
1,4-Dimethyl-7-ethylazulene; Ba 2784; Camazulene; Chamazulen; Dimethulen; Dimethulene
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.682
UNII
  • InChI=1S/C14H16/c1-4-12-7-5-10(2)13-8-6-11(3)14(13)9-12/h5-9H,4H2,1-3H3
    Key: GXGJIOMUZAGVEH-UHFFFAOYSA-N
  • InChI=1/C14H16/c1-4-12-7-5-10(2)13-8-6-11(3)14(13)9-12/h5-9H,4H2,1-3H3
    Key: GXGJIOMUZAGVEH-UHFFFAOYAM
  • c1(ccc(c2ccc(c2c1)C)C)CC
Properties
C14H16
Molar mass 184.282 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):
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 formed from sesquiterpene matricin after the loss of acetate, water and carbon dioxide during the steam distillation of chamomile blossoms. Oral ingestion of matricin results in chamazulene being found in blood plasma and artificial gastric fluid is able to convert matricin to chamazulene.

Chamazulene has anti-inflammatory properties in vivo and inhibits the CYP1A2 enzyme, but not CYP1A1.