Succinylacetone
 | |
| Names | |
|---|---|
| IUPAC name
4,6-Dioxoheptanoic acid | |
| Other names
Succinyl acetone | |
| Identifiers | |
3D model (JSmol) |
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PubChem CID |
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| Properties | |
| C7H10O4 | |
| Molar mass | 158.15 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Succinylacetone is a chemical compound that is formed by the oxidation of glycine and is a precursor of methylglyoxal.[1]
References
- ↑ "Interplay Between Oxidative and Carbonyl Stresses: Molecular Mechanisms, Biological Effects and Therapeutic Strategies of Protection". Intechopen.com. Retrieved January 28, 2016.
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