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ChemicalBook > Product Catalogue >Biochemical Engineering >Amino Acids and proteins >Oxamic acid sodium salt

Oxamic acid sodium salt

Oxamic acid sodium salt Structure
  • ₹4829 - ₹13594
  • Product name: Oxamic acid sodium salt
  • CAS: 565-73-1
  • MF: C2H2NNaO3
  • MW: 111.03
  • EINECS:209-290-5
  • MDL Number:MFCD00044553
  • Synonyms:aminooxo-aceticacimonosodiumsalt ;AMINOOXOACETIC ACID SODIUM SALT;OXALIC ACID MONOAMIDE SODIUM SALT;OXAMIC ACID SODIUM SALT;oxamic acid sodium;OxamicacidsodiumsaltOxamicacidsodiumsalt;Aminooxoacetic acid sodium salt, Oxalic acid monoamide sodium salt, Oxamic acid sodium salt;2-Amino-2-oxoacetic acid sodium salt
2 prices
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Brand

  • ALFA India

Package

  • 5g
  • 25g
  • ManufacturerALFA India
  • Product numberALF-A16532-06
  • Product descriptionOxamic acid sodium salt, 98%
  • Packaging5g
  • Price₹4829
  • Updated2022-05-26
  • Buy
  • ManufacturerALFA India
  • Product numberALF-A16532-14
  • Product descriptionOxamic acid sodium salt, 98%
  • Packaging25g
  • Price₹13594
  • Updated2022-05-26
  • Buy
Manufacturer Product number Product description Packaging Price Updated Buy
ALFA India ALF-A16532-06 Oxamic acid sodium salt, 98% 5g ₹4829 2022-05-26 Buy
ALFA India ALF-A16532-14 Oxamic acid sodium salt, 98% 25g ₹13594 2022-05-26 Buy

Properties

Melting point :300 °C
storage temp. :Inert atmosphere,Room Temperature
solubility :PBS (pH 7.2): 10 mg/ml
form :solid
color :White to off-white
Water Solubility :Soluble in water (10 mg/ml).
BRN :6538153
InChI :InChI=1S/C2H3NO3.Na/c3-1(4)2(5)6;/h(H2,3,4)(H,5,6);/q;+1/p-1
InChIKey :RQVZIJIQDCGIKI-UHFFFAOYSA-M
SMILES :C(=O)(N)C([O-])=O.[Na+]
CAS DataBase Reference :565-73-1(CAS DataBase Reference)
EPA Substance Registry System :Sodium oxamate (565-73-1)

Safety Information

Symbol(GHS):
Signal word:
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
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Description

Sodium oxamate is a derivative of pyruvate that inhibits the conversion of pyruvate to lactate via lactate dehydrogenase, thus disrupting glycolysis. Because cancer cells produce a large amount of energy via aerobic glycolysis, sodium oxamate has been studied as an inhibitor of carbohydrate metabolism in various tumors.

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