4,5-Imidazoledicarboxylic acid

4,5-Imidazoledicarboxylic acid
  • CAS No.:570-22-9
Other grades of this product :
4,5-Imidazoledicarboxylic acid Basic information
Product Name:4,5-Imidazoledicarboxylic acid
Synonyms:4,5-IMIDAZOLEDICARBOXYLIC ACID;IMIDAZOLE-4,5-DICARBOXYLIC ACID;IFLAB-BB F1918-0019;AKOS BBS-00002898;AKOS AUF2071;alpha,beta-Imidazoledicarboxylic acid;alpha-beta-imidazolecarboxylicacid;Glycoxalinedicarboxylic acid
CAS:570-22-9
MF:C5H4N2O4
MW:156.1
EINECS:209-327-5
Product Categories:Alcohols;Monomers;Polymer Science;Building Blocks;Heterocyclic Building Blocks;Imidazoles;Imidazoles, Pyrroles, Pyrazoles, Pyrrolidines;Imidazol&Benzimidazole;Heterocyclic Compounds;Imidaxoles;1
Mol File:570-22-9.mol
4,5-Imidazoledicarboxylic acid Chemical Properties
Melting point 280-285 °C (dec.) (lit.)
Boiling point 280.29°C (rough estimate)
density 1,749 g/cm3
refractive index 1.4800 (estimate)
storage temp. Store below +30°C.
solubility 0.5g/l
pka3.59±0.10(Predicted)
form Fine Crystalline Powder
color Light yellow to yellow-brown
PH3.7 (0.5g/l, H2O, 20℃)
Water Solubility 0.5g/L(20 ºC)
BRN 147774
InChIKeyZEVWQFWTGHFIDH-UHFFFAOYSA-N
CAS DataBase Reference570-22-9(CAS DataBase Reference)
NIST Chemistry Reference4,5-Imidazole dicarboxylic acid(570-22-9)
EPA Substance Registry System1H-Imidazole-4,5-dicarboxylic acid (570-22-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39
WGK Germany 3
RTECS NI4760000
TSCA Yes
HS Code 29332990
MSDS Information
ProviderLanguage
4,5-Imidazoledicarboxylic acid English
SigmaAldrich English
ACROS English
ALFA English
4,5-Imidazoledicarboxylic acid Usage And Synthesis
Chemical Propertieslight yellow to yellow-brown fine cryst. powder
Uses4,5-Imidazoledicarboxylic acid is an imidazole used for research purposes.
Uses4,5-Imidazoledicarboxylic Acid is an intermediate used in the synthesis of N-substituted cyclic imides with anticancer and anti-inflammatory activities. it is also used to prepare imidazolecarboxamide derivatives with cannabinoid CB2 receptor antagonistic activities.

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