Malondialdehyde
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| Names | |||
|---|---|---|---|
| IUPAC name propanedial | |||
| Other names Malonic aldehyde; Malonodialdehyde; Propanedial; 1,3-Propanedial ; Malonaldehyde ; Malonyldialdehyde | |||
| Identifiers | |||
| 3D model (JSmol) | 
 | ||
| Abbreviations | MDA | ||
| ChemSpider | |||
| KEGG | |||
| PubChem CID | |||
| UNII | |||
| CompTox Dashboard (EPA) | |||
| 
 | |||
| 
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| Properties | |||
| C3H4O2 | |||
| Molar mass | 72.063 g·mol−1 | ||
| Appearance | Needle-like solid | ||
| Density | 0.991 g/mL | ||
| Melting point | 72 °C (162 °F; 345 K) | ||
| Boiling point | 108 °C (226 °F; 381 K) | ||
| Hazards | |||
| NIOSH (US health exposure limits): | |||
| PEL (Permissible) | none | ||
| REL (Recommended) | Ca | ||
| IDLH (Immediate danger) | Ca [N.D.] | ||
| Related compounds | |||
| Related alkenals | Glucic acid | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |||
Malondialdehyde belong to the class of β-dicarbonyls. A colorless solid, malondialdehyde is a highly reactive compound that occurs as the enol. It is a physiological metabolite, and a marker for oxidative stress.