Piperonal
| Names | |
|---|---|
| Preferred IUPAC name
2H-1,3-Benzodioxole-5-carbaldehyde | |
| Other names
Heliotropin; Heliotropine; Piperonyl aldehyde; Protocatechuic aldehyde methylene ether; 3,4-methylenedioxybenzaldehyde; | |
| Identifiers | |
3D model (JSmol) |
|
| 131691 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.004.009 |
| EC Number |
|
| 4186 | |
| KEGG | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C8H6O3 | |
| Molar mass | 150.133 g·mol−1 |
| Appearance | Colorless crystals |
| Density | 1.337 g/cm3 |
| Melting point | 37 °C (99 °F; 310 K) |
| Boiling point | 263 °C (505 °F; 536 K) |
| Soluble in 500 parts | |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H317 | |
| P261, P272, P280, P302+P352, P321, P333+P313, P363, P501 | |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose) |
2700 mg/kg (orally in rats) |
| Legal status |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Piperonal, also known as heliotropin, is an organic compound which is commonly found in fragrances and flavors. The molecule is structurally related to other aromatic aldehydes such as benzaldehyde and vanillin.