Chemistry:Hydroxypyruvic acid
From HandWiki
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| Names | |
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| Preferred IUPAC name
3-Hydroxy-2-oxopropanoic acid | |
| Other names
Hydroxypyruvate
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| Identifiers | |
3D model (JSmol)
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| 1721079 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
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| KEGG | |
PubChem CID
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| UNII | |
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| Properties | |
| C3H4O4 | |
| Molar mass | 104.06 g/mol |
| Appearance | white solid |
| Melting point | 202 °C (396 °F; 475 K) |
| Hazards[1] | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H302, H314 | |
| P260, P264, P270, P280, P301+312, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P330, P363, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
Hydroxypyruvic acid is the organic compound with the formula HOCH2C(O)CO2H. It is a white solid. It is encountered in many biochemical contexts, being the oxidized derivative of lactic acid, a degradation product of RuBisCO, and the result of oxidative deamination of serine.[2]
See also
Notes
- ↑ "3-Hydroxypyruvic acid" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/964#section=Safety-and-Hazards.
- ↑ Timm, Stefan; Florian, Alexandra; Jahnke, Kathrin; Nunes-Nesi, Adriano; Fernie, Alisdair R.; Bauwe, Hermann (2011). "The Hydroxypyruvate-Reducing System in Arabidopsis: Multiple Enzymes for the Same End". Plant Physiology 155 (2): 694–705. doi:10.1104/pp.110.166538. PMID 21205613.
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