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| Names | |
|---|---|
| Preferred IUPAC name
 (1R,7aR)-7-(Hydroxymethyl)-2,3,5,7a-tetrahydro-1H-pyrrolizin-1-ol  | |
| Other names
 (+)-Retronecine; Retronecin; Senecifolinene  | |
| Identifiers | |
3D model (JSmol)  | 
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| Properties | |
| C8H13NO2 | |
| Molar mass | 155.197 g·mol−1 | 
| Melting point | 119 to 120 °C (246 to 248 °F; 392 to 393 K)[1] | 
| Hazards | |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)  | 
634 mg/kg (IV, mouse)[1] | 
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |
Retronecine is a pyrrolizidine alkaloid found in a variety of plants in the genera Senecio and Crotalaria, and the family Boraginaceae. It is the most common central core for other pyrrolizidine alkaloids.[1]
References
- 1 2 3 Retronecine, Merck Index, 12th Edition, 8334
 
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