4-Aminoantipyrine (AAP) is scarcely administered as an analgesic drug because of the potential side effects. The residue of AAP in the environment possesses a potential threat to human health. In this article, the binding mode of AAP with the important
4-Aminoantipyrine (4-amino-1,5-dimethyl-2-phenylpyrazole-3-one) and its analogues have been found to be compounds of interest for their anti-inflammatory, analgesic, antiviral, antipyretic, antirheumatic and antimicrobial activities. In the present study, Schiff base analogues of 4-aminoantipyrine were synthesized by the condensation reaction with substituted
Journal of hazardous materials, 186(2-3), 1076-1081 (2010-12-21)
In this work, the immobilization of 4-aminoantipyrine onto bentonite was carried out and it was then used to investigate the adsorption behavior of Cr(III), Hg(II) and Pb(II) ions from aqueous solutions. The separation and preconcentration conditions of analytes were investigated
Journal of hazardous materials, 190(1-3), 574-581 (2011-04-19)
4-Aminoantipyrine (AAP) is widely used in the pharmaceutical industry, in biochemical experiments and in environmental monitoring. AAP as an aromatic pollutant in the environment poses a great threat to human health. To evaluate the toxicity of AAP at the protein
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 104, 213-221 (2012-12-27)
A novel series of copper(II) and palladium(II) with 4-derivatives benzaldehyde pyrazolone (L(n)) were synthesized. The mixed ligand complexes were prepared by using 1,10-phenanthroline (Phen) as second ligand. The structure of these complexes was identified and confirm by elemental analysis, molar
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