Veratraldehyde (3,4-dimethoxybenzaldehyde) is an organic compound that is widely used as a flavorant and odorant. The compound is structurally related to benzaldehyde.
Names | |
---|---|
Preferred IUPAC name
3,4-Dimethoxybenzaldehyde | |
Systematic IUPAC name
3,4-Dimethoxybenzenecarbaldehyde | |
Other names
Methylvanillin; Veratric aldehyde; Veratral; Veratryl aldehyde; Veratrum aldehyde; Vanillin methyl ether
| |
Identifiers | |
3D model (JSmol)
|
|
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.003.976 |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C9H10O3 | |
Molar mass | 166.176 g·mol−1 |
Appearance | Peach coloured crystals |
Density | 1.114 g/mL |
Melting point | 40 to 43 °C (104 to 109 °F; 313 to 316 K) |
Boiling point | 281 °C (538 °F; 554 K) |
organic solvents | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
|
Harmful |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
This compound is popular commercially because of its pleasant woody fragrance. It is derivative of vanillin, from which it is prepared by methylation.[1]
Uses
editVeratraldehyde can be used as an intermediate in the synthesis of some pharmaceutical drugs including amiquinsin, hoquizil, piquizil, prazosin, quinazoline, tiapamil, toborinone, verazide, and vetrabutine.[citation needed]
See also
editReferences
edit- ^ Karl-Georg Fahlbusch, Franz-Josef Hammerschmidt, Johannes Panten, Wilhelm Pickenhagen, Dietmar Schatkowski, , Kurt Bauer, Dorothea Garbe and Horst Surburg "Flavors and Fragrances" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2003. doi:10.1002/14356007.a11_141