Candesartan Impurity 2, also known as Candesartan Ethyl Ester Desethyl Analog; Candesartan Ethyl Ester Impurity is a highly characterized reference material. It fully complies with stringent regulatory standards, including those set by USP, EMA, JP, and BP. This product is essential for use in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Candesartan. Moreover, it comes with a detailed Structure Elucidation Report (SER), ensuring its accuracy and reliability for a wide range of analytical applications. Candesartan Impurity 2 (CAS No: 1225044-20-1) Or 2,3-Dihydro-2-oxo-3-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-1H-Benzimidazole-4-carboxylic Acid Ethyl Ester, it is an one of the impurity of Candestran,Candesartant angiotensin II receptor type 1 in vascular smooth muscle,which is used to heart attacks and kidney problems.
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