4-Imidazolecarboxylic acid, 98%

Code: 425842-5G D2-231

Application

4-Imidazolecarboxylic acid (ICA) was used in the synthesis of triphenymethyl-protected 4-imidazole carboxylic acid (trityl-ImCOOH) which is employed to functional...


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€189.00 5G
€232.47 inc. VAT

Application

4-Imidazolecarboxylic acid (ICA) was used in the synthesis of triphenymethyl-protected 4-imidazole carboxylic acid (trityl-ImCOOH) which is employed to functionalize poly(propylene imine) dendrimers.It may be used in the following studies:In the synthesis of lanthanide sulfate–carboxylates, [Ln(HIMC)(SO4)(H2O)] (Ln = Dy and Eu, HIMC = 4-imidazolecarboxylic acid) by in situ decarboxylation in the presence of Cu(II) ions.As an internal standard to obtain calibration curve by plotting the peak area ratios of histamine (HA) and several metabolites isolated from C3H/HeNCrj mice hair relative to ICA.In the synthesis of tetranuclear manganese carboxylate complexes possessing imidazole-based N/O chelating ligands.

General description

4-Imidazolecarboxylic acid (1H-imidazole-4-carboxylic acid, H2imc) is an imidazole derivative that contains an imidazole group and a carboxylate group. It has been widely utilized to generate different types of coordination polymers. The anion of 4-imidazolecarboxylic acid has been reported to stabilize binuclear hydroxo complexes of trivalent lanthanides in the pH range 7-10.

Other Notes

For a review of imidazoles, see Science of Synthesis.

Packaging

1, 5 g in poly bottle

assay98%
InChI keyNKWCGTOZTHZDHB-UHFFFAOYSA-N
InChI1S/C4H4N2O2/c7-4(8)3-1-5-2-6-3/h1-2H,(H,5,6)(H,7,8)
mp294-295 °C (lit.)
Quality Level100
SMILES stringOC(=O)c1c[nH]cn1
Cas Number1072-84-0
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