| Estragole | |
|---|---|
| Chemical name | 1-methoxy-4-(2-propenyl)benzene |
| Chemical formula | C10H12O |
| Molecular mass | 148.20 g/mol |
| CAS number | * |
| Density | 0.946 g/cm3 |
| Melting point | ? °C |
| Boiling point | 216 °C 95-96 °C at 12 mmHg |
| SMILES | C=CCC1=CC=C(OC)C=C1 |
| Chemical infobox | |
Estragole, or p-allylanisole or methyl chavicol, is a natural organic compound. Its chemical structure consists of a benzene ring substituted with a methoxy group and a propenyl group. Estragole is a double-bond isomer of anethole. It is a colorless to pale yellow liquid. It is the primary constituent of tarragon oil making up 60-75% of the oil. It is also found in pine oil and turpentine.
Estragole is used in perfumes and as a food additive for flavor.
Estragole is known to be carcinogenic and genotoxic, as is indicated by a report of the European Union. A reduction in consumption is thus indicated. Special care is also to be taken with infant nourishment, since many teas or tea-like beverages contain estragole.
Aromatic compounds | Alkenes | Food additives | Perfumery | Phenylpropanoids
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"Estragole".
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