Home Categories Biochemical Engineering Oxamic acid
A6554912

Oxamic acid , >97.0%(T) , 471-47-6

Synonym(s):
Aminooxoacetic acid;Oxalic acid monoamide

CAS NO.:471-47-6

Empirical Formula: C2H3NO3

Molecular Weight: 89.05

MDL number: MFCD00008006

EINECS: 207-443-0

Pack Size Price Stock Quantity
1g RMB79.20 In Stock
5G RMB187.20 In Stock
25G RMB749.60 In Stock
100g RMB2399.20 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 207-210 °C (dec.) (lit.)
Boiling point: 165.08°C (rough estimate)
Density  1.6193 (rough estimate)
refractive index  1.4264 (estimate)
storage temp.  2-8°C(protect from light)
solubility  DMSO (Slightly), Methanol (Slightly), Water (Slightly)
form  Crystalline Powder
pka 1.60±0.20(Predicted)
color  White
Water Solubility  Soluble in water 108 mg/mL.
Merck  14,6917
BRN  1743294
InChI InChI=1S/C2H3NO3/c3-1(4)2(5)6/h(H2,3,4)(H,5,6)
InChIKey SOWBFZRMHSNYGE-UHFFFAOYSA-N
SMILES C(O)(=O)C(N)=O
CAS DataBase Reference 471-47-6(CAS DataBase Reference)
EPA Substance Registry System Oxamic acid (471-47-6)

Description and Uses

Oxamic acids also known to as oxalic acid monoamides have emerged as potent precursors for the generation of the carbamoyl radical. Oxamic acids can easily undergo decarboxylation through a single electron oxidation resulting in the generation of the reactive carbamoyl radical, which can then engage in diverse radical reactions or undergo a second single electron oxidation as originally unveiled by Minisci. Oxamic acids are thus versatile intermediates for the synthesis of nitrogen-containing organic molecules[1]. The oxidative decarboxylation of oxamic acids can be mediated through thermal, photochemical, electrochemical or photoelectrochemical means, generating carbamoyl radicals, which may further add to unsaturated systems to provide a broad range of important amides. Oxidative decarboxylation of oxamic acids also offers a straightforward entry for the preparation of urethanes, ureas, and thioureas.

Oxamic acid is an ozone oxidation product and is used in the synthesis of hydroxybenzimidazoles preparation as potential anti tumor agents targeting human lactate dehydrogenase A.This compound is suitable for lactate dehydrogenase (LDH) related research.

Safety

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3
TSCA  Yes
HS Code  29241990

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