Fluorocitric acid
Names | |
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IUPAC name
3-C-Carboxy-2,4-dideoxy-2-fluoropentaric acid | |
Other names
2-Fluorocitric acid; 2-Fluorocitrate; 1-Fluoro-2-hydroxypropane-1,2,3-tricarboxylic acid | |
Identifiers | |
357-89-1 | |
3D model (Jmol) | Interactive image |
ChemSpider | 96829 |
PubChem | 107647 |
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Properties | |
C6H7FO7 | |
Molar mass | 210.11 g·mol−1 |
Appearance | Odorless, white crystals |
Density | 1.37 |
Melting point | 35.2°C |
Boiling point | 165°C |
Soluble | |
Hazards | |
Main hazards | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Fluorocitric acid is a fluorinated carboxylic acid derived from citric acid by substitution of one hydrogen by a fluorine atom. The appropriate anion is called fluorocitrate. It is a metabolite of fluoroacetic acid and is very toxic because it is not processable using aconitase in the citrate cycle (where fluorocitrate takes place of citrate as the substrate). The enzyme is inhibited and the cycle stops working.[1]
See also
References
External links
- PubChem: Fluorocitrate
- Human Metabolome Database (HMDB): Fluorocitric acid
- The Chemical and Biochemical Properties of Fluorocitric Acid Pdf
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