Lactaldehyde
From Wikipedia, the free encyclopedia
| Lactaldehyde | |
|---|---|
| IUPAC name | 2-Hydroxypropanal |
| Other names | Hydroxypropionaldehyde |
| Identifiers | |
| CAS number | [3913-65-3], (R):3946-09-6 (S):3913-64-2 |
| PubChem | |
| SMILES | CC(C=O)O |
| Properties | |
| Molecular formula | C3H6O2 |
| Molar mass | 74.079 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Lactaldehyde is an intermediate in the methylglyoxal metabolic pathway. Methylglyoxal is converted to D-lactaldehyde by glycerol dehydrogenase (gldA). Lactaldehyde is then oxidized to lactic acid by aldehyde dehydrogenase.[1]
[edit] References
- ^ Huang PC, Miller ON (1958). "The metabolism of lactaldehyde". J. Biol. Chem. 231 (1): 201–5. PMID 13538961.

