Oxamic acid (High Purity)

<strong>Oxamic acid (High Purity)</strong>_x000D_ <strong>Catalog number:</strong> B2010690_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 5 g_x000D_ <strong>Molecular Weight or Concentration:</strong> 89.05 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various chemical and biochemical applications_x000D_ <strong>Storage:</strong> RT_x000D_ <strong>Keywords:</strong> Oxalic acid monoamide, Aminooxoacetic acid_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Espinoza LC, Sepúlveda P, García A, Martins de Godoi D, Salazar R. Degradation of oxamic_acid using dimensionally stable anodes (DSA) based on a mixture of RuO(2) and IrO(2) nanoparticles Chemosphere. 2020 Jul;251:126674._x000D_ 2: Lan Y, Wang C, Yuan F, Fereja TH, Lou B, Han S, Li J, Xu G. Electrochemiluminescence of 3,4,9,10-perylenetetracarboxylic acid/oxamic hydrazide and its application in the detection of tannic acid Analyst. 2019 Aug 7;144(15):4493-4498._x000D_ 3: Rodríguez-Páez L, Chena-Taboada MA, Cabrera-Hernández A, Cordero-Martínez J, Wong C. Oxamic_acid analogues as LDH-C4-specific competitive inhibitors J Enzyme Inhib Med Chem. 2011 Aug;26(4):579-86._x000D_ 4: Ruddraraju KV, Aggarwal D, Niu C, Baker EA, Zhang RY, Wu L, Zhang ZY. Highly Potent and Selective N-Aryl Oxamic_Acid-Based Inhibitors for Mycobacterium tuberculosis Protein Tyrosine Phosphatase B J Med Chem. 2020 Sep 10;63(17):9212-9227._x000D_ 5: Choi SR, Beeler AB, Pradhan A, Watkins EB, Rimoldi JM, Tekwani B, Avery MA. Generation of oxamic acid libraries: antimalarials and inhibitors of Plasmodium falciparum lactate dehydrogenase J Comb Chem. 2007 Mar-Apr;9(2):292-300._x000D_ 6: Orge CA, Faria JL, Pereira MF. Removal of oxalic acid, oxamic acid and aniline by a combined photolysis and ozonation process Environ Technol. 2015 May-Jun;36(9-12):1075-83._x000D_ 7: Koch RL, Goldman P. The anaerobic metabolism of metronidazole forms N-(2-hydroxyethyl)-oxamic acid J Pharmacol Exp Ther. 1979 Mar;208(3):406-10._x000D_ 8: Yang L, Liu L, Olsen BA, Nussbaum MA. The determination of oxalic acid, oxamic_acid, and oxamide in a drug substance by ion-exclusion chromatography J Pharm Biomed Anal. 2000 Apr;22(3):487-93._x000D_ 9: Aksenov AN, Krayushkin MM, Yarovenko VN. Synthesis of (2-chloroquinolin-3-yl)-1,3,4-thiadiazole-2-carboxamides Russ Chem Bull. 2021;70(6):1131-1134._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/1899891">10: Chiarino D, Grancini G, Frigeni V, Biasini I, Carenzi A. N-(4-Isoxazolylthiazol-2-yl)oxamic acid derivatives as potent orally active antianaphylactic agents J Med Chem. 1991 Feb;34(2):600-5. </a>_x000D_ _x000D_ <strong>Products Related to Oxamic acid (High Purity)</strong><a href="https://moleculardepot.com/product-category/Chemicals/">: Chemicals</a>