Fenofibrate EP Impurity F, also referred to in pharmacopoeias as Fenofibrate Ether, is a meticulously characterized reference standard. It adheres to stringent regulatory guidelines, including those established by USP, EMA, JP, and BP. This product plays a vital role in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial manufacturing of Fenofibrate. Furthermore, it is accompanied by a comprehensive Structure Elucidation Report (SER), ensuring its accuracy and reliability across various analytical applications. Fenofibrate EP Impurity F (CAS No.: 154356-96-4) ((4-Chlorophenyl)[4-(1-methylethoxy)phenyl]methanone) is a photoproduct of the antihyperlipoproteinemic drug Fenofibrate. Fenofibrate is widely used for the treatment of dyslipidemia and activates the nuclear receptor and peroxisome proliferator-activated receptor.
References
Miranda, Miguel A., et al. “PHOTOSENSITIZATION by FENOFIBRATE. II. In Vitro PHOTOTOXICITY of the MAJOR METABOLITES.â€Â Photochemistry and Photobiology, vol. 59, no. 2, Feb. 1994, pp. 171–74, https://doi.org/10.1111/j.1751-1097.1994.tb05018.x.
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