| Identification | More | [Name]
Chelidamic acid | [CAS]
138-60-3 | [Synonyms]
1,4-DIHYDRO-4-OXO-2,6-PYRIDINEDICARBOXYLIC ACID
4-HYDROXY-2,6-PYRIDINEDICARBOXYLIC ACID
4-HYDROXYPYRIDINE-2,6-DICARBOXYLIC ACID
4-PYRIDONE-2,6-DICARBOXYLIC ACID
AKOS 90653
CHELIDAMIC ACID
CHELIDAMIC ACID HYDRATE
1,4-Dihydro-4-oxo-2,6-pyridinedicarboxylic acid hydrate
4-Hydroxypyridine-2,6-dicarboxylic acid hydrate
chelidamic acid approx. 95%
Chelidamic aicd
1,4-dihydro-4-oxopyridine-2,6-dicarboxylic acid
.HELIDAMIC AICD
4-Hydroxy-2,6-pyridenedicarboxylic acid
Ammox-chelidonic acid
4-Oxo-1,4-dihydro-2,6-pyridinedicarboxylic acid
Chelidamic acid (4-Hydroxypyridine-2,6-dicarboxylic acid)
1,4-Dihydro-4-oxo-2,6-pyridinedicarboxylic acid hydrate, 4-Hydroxypyridine-2,6-dicarboxylic acid
2,6-Pyridinedicarboxylic acid, 1,4-dihydro-4-oxo-
4-Oxo-1H-pyridine-2,6-dicarboxylic acid | [EINECS(EC#)]
205-335-8 | [Molecular Formula]
C7H5NO5 | [MDL Number]
MFCD00066478 | [Molecular Weight]
183.12 | [MOL File]
138-60-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
265-270 °C | [Boiling point ]
428.3±45.0 °C(Predicted) | [density ]
1.726±0.06 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
powder | [pka]
0.12±0.40(Predicted) | [color ]
brown | [Detection Methods]
HPLC,NMR | [BRN ]
476229 | [InChIKey]
XTLJJHGQACAZMS-UHFFFAOYSA-N | [CAS DataBase Reference]
138-60-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [HS Code ]
29333990 |
| Hazard Information | Back Directory | [Chemical Properties]
Light yellow powder | [Uses]
Chelidamic acid hydrate has been used in eluent solution as a complexing additive in high-performance chelation ion chromatography (HPCIC) for speciation of iron. It has also been used as an organic ligand for the polyoxometalate (POM)-based lanthanoid hybrid compounds. | [Biochem/physiol Actions]
Among the most potent of the tested "conformationally restricted glutamate analogs" as an inhibitor of glutamate decarboxylase. |
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