Article · Volume 13, Issue 2 · pp. 313–320
Synthesis, Characterization, RP-HPLC Method Development and Validation for Qualitative Estimation of (4Z) 3 Methyl 1 (4 Nitrobenzoyl) 1H Pyrazole 4,5 Dione 4[(4fluorophenyl) Hydrazone]
Harsha Ashtekar1, Natasha Aggarwal2, Chaitra Raviraj3, Gupta Dheeraj Rajesh4, Nimmy Varghese1
- 1Department of Pharmacology, NITTE (Deemed to be University), NGSM Institute of Pharmaceutical Sciences (NGSMIPS), Mangalore, Karnataka, INDIA.
- 2Department of Pharmaceutical Chemistry, Yenepoya University (Deemed to be University), Yenepoya Pharmacy College and Research Center, Mangalore, Karnataka, INDIA.
- 3Department of Advance Research Centre, (NGSMIPS), NITTE (Deemed to be University), NGSM Institute of Pharmaceutical Sciences Mangalore, Karnataka, INDIA.
- 4Department of Pharmaceutical Chemistry, NITTE (Deemed to be University), NGSM Institute of Pharmaceutical Sciences (NGSMIPS), Mangalore, Karnataka, INDIA.
Abstract
Aim: A new simple, accurate, precise, Reverse Phase High-performance Liquid Chromatography method was developed and validated for the estimation of newly synthesized (4Z) 3 methyl 1 (4 nitrobenzoyl) 1H pyrazole 4,5 dione 4[(4fluorophenyl)hydrazone] derivative of pyrazolone.Materials and Methods: The chromatogram was run through Luna 5µ C18 (2). 250 × 4.80 mm. 272817-7 HPLC column; mobile phase consisting of acetonitrile and water in the ratio 90:10 was pumped through the column at a flow rate of 0.8mL/min.Results: The optimized wavelength was 237 nm. The retention time of (4Z) 3 methyl 1 (4 nitrobenzoyl) 1H pyrazole 4,5 dione 4[(4fluorophenyl)hydrazone] was found to be 7.3 min. The percentage relative standard deviation was obtained as 0.3%.Conclusion: This method was accurate, precise, and sensitive; therefore, could be used for the quality control and bioanalytical evaluation of (4Z) 3 methyl 1 (4 nitrobenzoyl) 1H pyrazole 4,5 dione 4[(4fluorophenyl)hydrazone] in drug testing laboratory.
Keywords: Column Chromatography; HPLC; Pyrazolone derivative
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