Chemistry:Homocitric acid
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Names | |
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Preferred IUPAC name
2-Hydroxybutane-1,2,4-tricarboxylic acid | |
Other names
Homocitric acid
Homocitrate | |
Identifiers | |
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Properties | |
C7H10O7 | |
Molar mass | 206.150 g·mol−1 |
Appearance | Colorless solid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
Homocitric acid is an organic compound with the formula HOC(CO2H)(CH2CO2H)(C2H4CO2H). This tricarboxylic acid occurs naturally as a component of the iron-molybdenum cofactor of certain nitrogenase proteins.[1] Biochemists often refer to this cofactor as homocitrate, which is the conjugate bases that predominate in neutral aqueous solutions of this species.
The molecule is related to citric acid by the addition of one methylene unit, hence the prefix "homo." Unlike citric acid, homocitric acid is chiral. The acid exists in equilibrium with the lactone.
See also
References
- ↑ Rees, Douglas C. (2002). "Great Metalloclusters in Enzymology". Annual Review of Biochemistry 71: 221–46. doi:10.1146/annurev.biochem.71.110601.135406. PMID 12045096. https://authors.library.caltech.edu/7659/1/REEarb02.pdf.
![]() | Original source: https://en.wikipedia.org/wiki/Homocitric acid.
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