Oxobutanedioic acid

Oxobutanedioic acid
  • CAS No.:328-42-7
Other grades of this product :
Oxobutanedioic acid Basic information
Product Name:Oxobutanedioic acid
Synonyms:OXOBUTANEDIOIC ACID;OXOBUTANEDIOTIC ACID;OXOSUCCINIC ACID;OXLACETIC ACID;OXALACETIC ACID;OXALEACETIC ACID;OXALOACETIC ACID;OAA
CAS:328-42-7
MF:C4H4O5
MW:132.07
EINECS:206-329-8
Product Categories:Aliphatics;Intermediates & Fine Chemicals;Fatty & Aliphatic Acids, Esters, Alcohols & Derivatives;Pharmaceuticals
Mol File:328-42-7.mol
Oxobutanedioic acid Chemical Properties
Melting point 161 °C (dec.)(lit.)
Boiling point 163.94°C (rough estimate)
density 1.3067 (rough estimate)
vapor pressure 0.003Pa at 20℃
refractive index 1.4000 (estimate)
Fp 88°C
storage temp. -20°C
solubility H2O: 100 mg/mL
form powder
pka2.22(at 25℃)
color White to off-white
PH3.05(1 mM solution);2.29(10 mM solution);1.68(100 mM solution)
Water Solubility soluble
Merck 14,6909
BRN 1705475
Stability:Stable. Incompatible with strong oxidizing agents. Keep refrigerated.
LogP-1.04 at 20℃
CAS DataBase Reference328-42-7(CAS DataBase Reference)
NIST Chemistry ReferenceOxalacetic acid(328-42-7)
EPA Substance Registry SystemOxalacetic acetic (328-42-7)
Safety Information
Hazard Codes C
Risk Statements 34
Safety Statements 26-36/37/39-45
RIDADR UN 3261 8/PG 2
WGK Germany 3
TSCA Yes
HazardClass 8
PackingGroup II
HS Code 29183000
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
Oxobutanedioic acid Usage And Synthesis
DescriptionOxaloacetic acid is an α-keto acid and a key component of cellular metabolism in its conjugate base form, oxaloacetate. Oxaloacetate reacts with acetyl-coenzyme A (acetyl-CoA; ) and water to form citrate in the first step of the citric acid cycle and is regenerated by oxidation of L-malate in the final step. It is an intermediate in gluconeogenesis that is formed in mitochondria via carboxylation of pyruvate and subsequently decarboxylated and phosphorylated to form phosphoenolpyruvate. It can be converted to aspartate via addition of an amino group from glutamate. Oxaloacetate (30 μmol/min per 100 g for 30 minutes, i.v.) reduces blood glutamate levels, severity of neurological dysfunction, and brain edema in a rat model of closed head injury.
Chemical Propertiesoff-white crystals
UsesA four carbon dicarboxylic acid that is an intermediate in the citric acid cycle and glucogenesis. It has been shown to inhibit succinate dehydrogenase.
UsesUse as a TCA (Krebs cycle) intermediate supplement in hybridoma cell culture applications. Enhances hybridoma growth and productivity.
UsesOxaloacetic acid is a substrate for malate dehydrogenase and oxaloacetate decarboxylase. It is an inhibitor of succinic dehydrogenase. It is an intermediate in the citric acid cycle and glucogenesis.
DefinitionChEBI: An oxodicarboxylic acid that is succinic acid bearing a single oxo group.
General DescriptionOxaloacetic acid is a dicarboxylic acid. It is an intermediate in the citric acid cycle. It is highly soluble in water and is present ubiquitously. It is produced in the mitochondria by the action of pyruvate carboxylase on pyruvate. Breakdown products of oxaloacetate includes malate, pyruvate and aspartic acid.
Flammability and ExplosibilityNotclassified
Biological ActivityOxalacetic acid (Oxaloacetic acid, 2-Oxosuccinic acid, Ketosuccinic acid) is an intermediate of the citric acid cycle, where it reacts with acetyl-CoA to form citrate, catalysed by citrate synthase. It is also involved in gluconeogenesis, urea cycle, glyoxylate cycle, amino acid synthesis, and fatty acid synthesis. Oxaloacetate is also a potent inhibitor of Complex II.
Biochem/physiol ActionsOxaloacetic acid being an intermediate in the tri carboxylic cycle is central to metabolism. It is part of gluconeogenesis pathway. Mutation in pyruvate carboxylase leads to decreased production of oxaloacetate. It inhibits succinate dehydrogenase and is a key regulator of mitochondrial metabolism.
Purification MethodsCrystallise it from boiling EtOAc, or from hot Me2CO/hot *C6H6. [Beilstein 3 IV 1808.]

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