Nilotinib EP Impurity D, also known as Nilotinib Carboxylic Acid 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 Nilotinib. Moreover, it comes with a detailed Structure Elucidation Report (SER), ensuring its accuracy and reliability for a wide range of analytical applications. Also known as Nilotinib Carboxylic Acid Impurity, it is an impurity present in Nilotinib is a synthetic amino pyrimidine, a second-generation tyrosine kinase inhibitor used for the treatment of imatinib-resistant chronic myelogenous leukemia in the form of nilotinib hydrochloride monohydrate salt.
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