Safrole
| Names | |
|---|---|
| Preferred IUPAC name 5-(Prop-2-en-1-yl)-2H-1,3-benzodioxole | |
| Other names 5-(2-Propenyl)-1,3-benzodioxole 5-Allylbenzo[d][1,3]dioxole 3,4-Methylenedioxyphenyl-2-propene | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.133 | 
| EC Number | 
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| KEGG | |
| PubChem CID | |
| RTECS number | 
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| UNII | |
| UN number | 3082 | 
| CompTox Dashboard (EPA) | |
| 
 | |
| 
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| Properties | |
| C10H10O2 | |
| Molar mass | 162.188 g·mol−1 | 
| Density | 1.096 g/cm3 | 
| Melting point | 11 °C (52 °F; 284 K) | 
| Boiling point | 232 to 234 °C (450 to 453 °F; 505 to 507 K) | 
| −97.5×10−6 cm3/mol | |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H302, H341, H350 | |
| P201, P281, P308+P313 | |
| Legal status | 
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| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Safrole is an organic compound with the formula CH2O2C6H3CH2CH=CH2. It is a colorless oily liquid, although impure samples can appear yellow. A member of the phenylpropanoid family of natural products, it is found in sassafras plants, among others. Small amounts are found in a wide variety of plants, where it functions as a natural antifeedant. Ocotea pretiosa, which grows in Brazil, and Sassafras albidum, which grows in eastern North America, are the main natural sources of safrole. It has a characteristic "sweet-shop" aroma.
It is a precursor in the synthesis of the insecticide synergist piperonyl butoxide, the fragrance piperonal via isosafrole, and the empathogenic/entactogenic substance MDMA.