| Identifiers | |
|---|---|
3D model (JSmol) | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.012.152 |
| EC Number |
|
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C11H14O | |
| Molar mass | 162.232 g·mol−1 |
| Appearance | colourless liquid |
| Density | 0.97 |
| Boiling point | 248.7 °C (479.7 °F; 521.8 K) |
| 120 mg/L | |
| Hazards | |
| GHS labelling: [1] | |
| | |
| Danger | |
| H301, H302, H317, H334, H361, H410 | |
| P203, P233, P260, P261, P264, P270, P271, P272, P273, P280, P284, P301+P316, P301+P317, P302+P352, P304+P340, P318, P321, P330, P333+P317, P342+P316, P362+P364, P391, P403, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
4-tert-Butylbenzaldehyde is an aromatic aldehyde and an important intermediate for the synthesis of synthetic aroma compounds.
4-tert-Butylbenzaldehyde is notable as a rare example of industrial-scale electrochemistry. It is produced by BASF and Givaudan (typically as its methanol acetal) through a double anodic oxidation of 4-tert-butyltoluene on greater than 10,000 ton per year scale. [2] [3]
Aldol condensation with either propionaldehyde or acetaldehyde, followed by hydrogenation, gives the fragrance compounds lilial and bourgeonal, respectively.