Oxaloacetic acid

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Oxaloacetic acid
Chemical name	Oxobutanedioic acid
Other names	Oxaloacetic acid Oxalacetic acid Oxosuccinic acid
Chemical formula	C4H4O5
Molecular mass	132.07 g/mol
Melting point	161 °C
Density	? g/cm3
pKa value	2.22 3.89
CAS number	[328-42-7]
EINECS number	206-329-8
SMILES	OC(C(CC(O)=O)=O)=O
Thermodynamic data
Standard enthalpy of formation ΔfH°solid	-943.21 kJ/mol
Standard enthalpy of combustion ΔcH°solid	-1205.58 kJ/mol
Disclaimer and references

Oxaloacetic acid, also known as oxosuccinic acid or oxalacetic acid, is a four-carbon dicarboxylic acid appearing as an intermediate of the citric acid cycle and gluconeogenesis. In vivo, oxaloacetate (the ionised form of oxaloacetic acid) is formed by the oxidation of L-malate, catalysed by malate dehydrogenase, and reacts with Acetyl-CoA to form citrate, catalysed by citrate synthase. It is also formed in the mesophyll of plants by the condensation of CO₂ with phosphoenolpyruvate, catalysed by oxaloacetate decarboxylase. It can be formed from pyruvate as an anaplerotic reaction.

The enol forms of oxaloacetic acid are particularly stable, so much so that the two isomers have different melting points (152°C cis, 184°C trans). The enol proton has a pK_a value of 13.02. The enzyme fumarase A from E. coli catalyses the conversion between the keto and enol forms.

Oxaloacetic acid is unstable in solution, decomposing to pyruvic acid by decarboxylation over a period of hours (room temperature) or days (0°C). Refrigerator storage of the solid is recommended for long periods.

See also

Citric Acid Cycle Metabolic Pathway

Oxaloacetate Malate Fumarate Succinate Succinyl-CoA Acetyl-CoA NADH + H+ NAD+ H2O FADH2 FAD CoA + ATP(GTP) Pi + ADP(GDP) + H2O NADH + H+ + CO2 CoA NAD+ H2O H2O NAD(P)+ NAD(P)H + H+ CO2 Citrate cis-Aconitate Isocitrate Oxalosuccinate α-Ketoglutarate