Tartronic acid
 ![]()  | |
| Names | |
|---|---|
|  IUPAC name
 2-hydroxypropanedioic acid  | |
|  Other names
 tartronic acid, 2-tartronic acid, hydroxymalonic acid, 2-hydroxymalonic acid, hydroxypropanedioic acid  | |
| Identifiers | |
|  80-69-3  | |
| ChEBI |  CHEBI:16513  | 
| ChemSpider |  44  | 
| EC Number | 201-301-1 | 
| Jmol interactive 3D | Image | 
| KEGG |  C02287  | 
| PubChem | 45 | 
 
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  | |
| Properties | |
| C3H4O5 | |
| Molar mass | 120.06 g/mol | 
| Appearance | beige powder | 
| Melting point | 159 °C (318 °F; 432 K) (decomposes) | 
| Hazards | |
| NFPA 704 | |
| Related compounds | |
|   Related carboxylic acids  | 
 Tartaric acid Malic acid mesoxalic acid Lactic acid 3-Hydroxypropionic acid Malonic acid Propionic acid Oxalic acid  | 
|   Related compounds  | 
 Glyceric acid Glyceraldehyde Tartonaldehyde Glycerol  | 
|   Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  | |
|   | |
| Infobox references | |
Tartronic acid or 2-hydroxymalonic acid is a dicarboxylic acid with the structural formula of HOOCCH(OH)COOH.
Its derivative, 2-methyltartronic acid, is isomalic acid.
Uses
Tartronic acids are best known as a reactant in the catalytic oxidation with air to form mesoxalic acid, another type of hydroxydicarboxylic acid.[1]
References
- ↑ Fordham P., Besson M., Gallezot P. (1997). "Catalytic oxidation with air of tartronic acid to mesoxalic acid on bismuth-promoted platinum". Catal. Lett. 46 (3–4): 195–199(5). doi:10.1023/A:1019082905366. Retrieved 2007-07-06.
 
- Hall A. N., Kulka D., Walker T. K. (1955). "Formation of arabinose, ribulose and tartronic acid from 2-keto-d-gluconic acid". Biochem J. 60 (2): 271–274(4). PMC 1215693. PMID 14389236. Retrieved 2007-07-06.
 
External links
- US-Patent 4319045: "Process for production of a tartronic acid solution", max 20% Tartronic acid besides other dicarbonic acids
 - US-Patent 5750037: Use of tartronic acid as an oxygen scavenger
 - Literature overview about synthesis
 
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