Ball and stick model of oxamic acid
| |
Names | |
---|---|
Preferred IUPAC name
Oxamic acid
[1] | |
Other names
Amino(oxo)acetic acid
[1]
2-Amino-2-oxoacetic acid 2-oxoglycine Aminooxoacetic acid Oxalamic acid Oxamidic acid 2-Amino-2-oxoethanoic acid | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.006.768 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
Properties | |
NH2C(O)COOH | |
Molar mass | 89.050 g·mol−1 |
Appearance | White solid |
Melting point | 209 °C [2] |
Soluble | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Oxamic acid is an organic compound with the formula NH2C(O)COOH. It is a white, water-soluble solid. It is the mono amide of oxalic acid. [3] Oxamic acid inhibits lactate dehydrogenase A. [4] The active site of lactate dehydrogenase (LDH) is closed off once oxamic acid attaches to the LDH- NADH complex, effectively inhibiting it. [5]
Oxamic acid also has applications in polymer chemistry. It increases the water solubility of certain polymers, including polyester, epoxide, and acrylic upon binding with them. [6]
Ball and stick model of oxamic acid
| |
Names | |
---|---|
Preferred IUPAC name
Oxamic acid
[1] | |
Other names
Amino(oxo)acetic acid
[1]
2-Amino-2-oxoacetic acid 2-oxoglycine Aminooxoacetic acid Oxalamic acid Oxamidic acid 2-Amino-2-oxoethanoic acid | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.006.768 |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
Properties | |
NH2C(O)COOH | |
Molar mass | 89.050 g·mol−1 |
Appearance | White solid |
Melting point | 209 °C [2] |
Soluble | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Oxamic acid is an organic compound with the formula NH2C(O)COOH. It is a white, water-soluble solid. It is the mono amide of oxalic acid. [3] Oxamic acid inhibits lactate dehydrogenase A. [4] The active site of lactate dehydrogenase (LDH) is closed off once oxamic acid attaches to the LDH- NADH complex, effectively inhibiting it. [5]
Oxamic acid also has applications in polymer chemistry. It increases the water solubility of certain polymers, including polyester, epoxide, and acrylic upon binding with them. [6]