| Names | |
|---|---|
| Other names
Aldehyde 13-13 | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.030.900 |
| EC Number |
|
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C13H26O | |
| Molar mass | 198.350 g·mol−1 |
| Appearance | colorless liquid |
| Density | 0.825±0.06 g/cm3 |
| Melting point | 14 °C (57 °F; 287 K) |
| Boiling point | 126–138 °C (259–280 °F; 399–411 K) 15 Torr |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H314, H315, H319, H335, H411 | |
| P260, P264, P264+P265, P271, P273, P280, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P317, P319, P321, P332+P317, P337+P317, P362+P364, P363, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Tridecanal is an organic compound with the formula C13H26O CH3(CH2)11CHO. A colorless oily liquid, it is the aldehyde derivative of tridecane. It is produced by hydroformylation of 1-dodecene. Hydrogenation of tridecanal gives 1-tridecanol.
It is used as a fragrance and is well-tolerated. It is a trace component emitted from the combustion of diesel fuel and exposure of synthetic carpets to ozone.