Diclofenac Desacetate Impurity is a well-characterized reference material that meets stringent regulatory standards set by USP, EMA, JP, and BP. It plays a key role in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Diclofenac. Diclofenac Desacetate Impurity (CAS No: 15307-93-4)Â is a potent non-steroidal anti-inflammatory drug that is used for treating various inflammatory and painful diseases of rheumatic and nonrheumatic origin that include musculoskeletal, joint, peri-articular, and soft-tissue disorders, renal colic, acute gout, dysmenorrhoea, and migraine.
References
Banaschik, Robert, et al. “Degradation and Intermediates of Diclofenac as Instructive Example for Decomposition of Recalcitrant Pharmaceuticals by Hydroxyl Radicals Generated with Pulsed Corona Plasma in Water.†Journal of Hazardous Materials, vol. 342, Jan. 2018, pp. 651–60, https://doi.org/10.1016/j.jhazmat.2017.08.058. Orlandini, S., et al. “A Comprehensive Strategy in the Development of a Cyclodextrin-Modified Microemulsion Electrokinetic Chromatographic Method for the Assay of Diclofenac an
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