Sodium oxamate

Base Information

• Chemical Name: Sodium oxamate
• CAS No.: 565-73-1
• Molecular Formula: C2H2NNaO3
• Molecular Weight: 111.03
• Hs Code.: 29241990
• European Community (EC) Number: 209-290-5
• DSSTox Substance ID: DTXSID1060342
• Nikkaji Number: J188.429H
• ChEMBL ID: CHEMBL1256289
• Mol file: 565-73-1.mol

Synonyms:sodium oxamate;565-73-1;Oxamic acid sodium salt;Sodium 2-amino-2-oxoacetate;Aminooxoacetic acid sodium salt;Oxamic acid, sodium salt;Acetic acid, aminooxo-, monosodium salt;Oxamate (sodium);Oxamic acid (sodium);EINECS 209-290-5;Acetic acid, 2-amino-2-oxo-, sodium salt (1:1);sodium;oxamate;Oxalic acid monoamide sodium salt;Oxamic acid sodium;MFCD00044553;Lopac-O-2751;C2H3NO3.Na;C2-H3-N-O3.Na;SCHEMBL2370295;CHEMBL1256289;DTXSID1060342;3-n-phthaloylglyaminomethylaniline;HMS3262H08;HY-W013032A;Tox21_500913;BDBM50144744;AKOS024462579;CCG-222217;LP00913;NCGC00016183-01;NCGC00016183-02;NCGC00094224-01;NCGC00261598-01;CS-0109107;EU-0100913;FT-0632400;O 2751;A853818

Chemical Property of Sodium oxamate

Chemical Property:

• Appearance/Colour: white crystalline powder
• Vapor Pressure: 0.000177mmHg at 25°C
• Melting Point: 300 °C
• Boiling Point: 306.3 °C at 760 mmHg
• Flash Point: 139 °C
• PSA: 83.22000
• LogP: -2.07810
• Storage Temp.: Store at RT.
• Water Solubility.: Soluble in water (10 mg/ml).
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 110.99323721
• Heavy Atom Count: 7
• Complexity: 90.9

Purity/Quality:

99% ^*data from raw suppliers

Sodium oxamate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F
• Hazard Codes: F
• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(=O)(C(=O)[O-])N.[Na+]
• Uses: Oxamic acid sodium salt is a lactate dehydrogenase (LDH) inhibitor. It is a suitable compound to investigate cancer cells that utilize the glycolytic pathway.This compound is suitable for lactate dehydrogenase (LDH) related research. It can be used as an inhibitor of gluconeogenesis useful for anticancer research.