Spectrophotometric Determination of Paracetamol using a Newly Synthesized Chromogenic Reagent 4-[(2-amino-1, 3thiazol-4-yl)amino]nitro benzene | ||
Egyptian Journal of Chemistry | ||
Article 2, Volume 63, Issue 12, December 2020, Pages 4681-4693 PDF (1.86 M) | ||
Document Type: Original Article | ||
DOI: 10.21608/ejchem.2020.17136.2053 | ||
Authors | ||
Ruba F. Abbas* 1; Amjad G Allawi2; Nagham M Abdulhassan2; Nawal H Mahmoud3 | ||
1Department of Chemistry, College of Science-University of AL-Mustansiriyah- Baghdad-Iraq | ||
2chemistry department, collage of science, al mustansiriyah university | ||
3chemistry department, collage of science, al mustansiriyah unversity | ||
Abstract | ||
This study describes the new simple and accurate spectrophotometric method for the determination of paracetamol after the formation of azo dye with a new chromogenic reagent 4 [(2-amino-1,3thiazol-4-yl)amino] nitrobenzene to form an orange-coloured product measured at 425 nm. The molecular structure of the newly synthesized compound was confirmed by several spectroscopic techniques such as UV-visible, FTIR, 1HNMR, and mass spectroscopy. Newly synthesized compound was in vitro screened against several bacterial species. The experimental conditions that affect the reaction were carefully optimized and under the optimized conditions, a linear relationship was obtained in the concentration range of 5–25mg.L−1 of paracetamol. A reaction with a new chromogenic reagent has been occurred at a stoichiometric ratio of 1:1. This method has a limit of detection of 1.334 mg.L-1 and Sandell's sensitivity of 0.0235 mg.cm-1 for new azo dye product. | ||
Keywords | ||
Paracetamol; Azo dye; Antibacterial activity; Thiazol; IHNMR; Spectrophotometric | ||
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