Formula C10H12O Boiling point 216 °C | Molar mass 148.2 g/mol Density 946 kg/m³ | |
![]() | ||
Estragole (p-allylanisole, methyl chavicol) is a phenylpropene, a natural organic compound. Its chemical structure consists of a benzene ring substituted with a methoxy group and a propenyl group. It is an isomer of anethole, differing with respect to the location of the double bond. It is a colorless liquid, although impure samples can appear yellow. It is a component of various trees and plants, including turpentine (pine oil), anise, fennel, bay, tarragon, and basil. It is used in the preparation of fragrances.
Contents
![Estragole FileEstragolepng Wikimedia Commons](https://alchetron.com/cdn/estragole-24fd0d2e-fbe6-4c0c-9e6f-ce32f2454fc-resize-750.jpg)
Production
![Estragole FileEstragolesvg Wikimedia Commons](https://alchetron.com/cdn/estragole-6c316226-ebe8-4ba5-8d1d-772d4a4a91f-resize-750.jpg)
Hundreds of tonnes of basil oil are produced annually by steam distillation of Ocimum basilicum (common basil). This oil is mainly estragole but also contains substantial amounts of linalool. Estragole is the primary constituent of essential oil of tarragon (comprising 60–75%), pine oil, turpentine, fennel, anise (2%), Clausena anisata and Syzygium anisatum.
![Estragole httpsuploadwikimediaorgwikipediacommonsthu](https://alchetron.com/cdn/estragole-f383c0f4-196f-4338-9db0-ef84ba2d31e-resize-750.jpg)
Estragole is used in perfumes and as a food additive for flavor. Upon treatment with potassium hydroxide, estragole converts to anethole.
Safety
![Estragole Estragole analytical standard SigmaAldrich](https://alchetron.com/cdn/estragole-548573d7-dfd0-4daf-a862-1969e43d599-resize-750.jpg)
Estragole is suspected to be carcinogenic and genotoxic, as is indicated by a report of the European Union, Committee on Herbal Medicinal Products. Several studies have clearly established that the profiles of metabolism, metabolic activation, and covalent binding are dose dependent and that the relative importance diminishes markedly at low levels of exposure (i.e. these events are not linear with respect to dose). In particular, rodent studies show that these events are minimal probably in the dose range of 1–10 mg/kg body weight, which is approximately 100-1000 times the anticipated human exposure to this substance. For these reasons it is concluded that the present exposure to estragole resulting from consumption of herbal medicinal products (short time use in adults at recommended posology) does not pose a significant cancer risk. In the meantime exposure of estragole to sensitive groups such as young children, pregnant and breastfeeding women should be minimized.
![Estragole Estragole Wikipedia](https://alchetron.com/cdn/estragole-3235914a-08e3-4158-ae9c-29a776abdc8-resize-750.jpg)
The Scientific Committee on Food from the Health & Consumer Protection Directorate-General took a more concerned position and concluded that "Estragole has been demonstrated to be genotoxic and carcinogenic. Therefore the existence of a threshold cannot be assumed and the Committee could not establish a safe exposure limit. Consequently, reductions in exposure and restrictions in use levels are indicated."
![Estragole estragole Kovats Retention Index](https://alchetron.com/cdn/estragole-5764513b-41bf-4b13-b2ee-a4d7660c7af-resize-750.gif)
![Estragole Estragole CAS Number 140670](https://alchetron.com/cdn/estragole-0b3f77ff-e6f9-45ca-92c7-7fc74b8db27-resize-750.gif)
![Estragole FileEstragolesvg Wikimedia Commons](https://alchetron.com/cdn/estragole-b715e578-d716-497d-8067-d4b46cd051e-resize-750.jpg)