3,5-Dimethoxy-4-hydroxybenzene carbonal, Gallaldehyde 3,5-dimethyl ether, 4-Hydroxy-3,5-dimethoxybenzaldehyde, Syringic aldehyde
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||182.17 g/mol|
|Melting point||110 to 113 °C (230 to 235 °F; 383 to 386 K)|
|Boiling point||192 to 193 °C (378 to 379 °F; 465 to 466 K) at 19 kPa|
|Main hazards||Irritant (Xi)|
|Safety data sheet||External MSDS|
|S-phrases (outdated)||S24/25, S28A, S37, S45|
|NFPA 704 (fire diamond)|
|Flash point||> 110 °C (230 °F; 383 K) c.c.|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Syringaldehyde is an organic compound that occurs in trace amounts widely in nature. Some species of insects use syringaldehyde in their chemical communication systems. Scolytus multistriatus uses it as a signal to find a host tree during oviposition.
Because it contains many functional groups, it can be classified in many ways - aromatic, aldehyde, phenol. It is a colorless solid (impure samples appear yellowish) that is soluble in alcohol and polar organic solvents. Its refractive index is 1.53.
- Vanillin and Syringaldehyde as Attractants for Scolytus multistriatus (Coleoptera: Scolytidae). Meyer H.J. and Norris D.M., Annals of the Entomological Society of America, 17 July 1967, Volume 60, Number 4, pages 858-859, (abstract)
- R.H.J. Creighton; J.L. McCarthy; H. Hibbert (1941). "Aromatic Aldehyde from Spruce and Maple Woods". J. Am. Chem. Soc. 63: 312. doi:10.1021/ja01846a501.
- C. F. H. Allen and Gerhard W. Leubner (1963). "Syringic aldehyde". Organic Syntheses.; Collective Volume, 4, p. 866