Alfuzosin EP Impurity F is a meticulously characterized reference material that complies with rigorous regulatory requirements, including those defined by USP, EMA, JP, and BP. This product plays a crucial role in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial manufacturing of 2,4-Quinazolinediamine, 6,7-dimethoxy-N2,N2-dimethyl. It is further supported by a detailed Structure Elucidation Report (SER), ensuring high accuracy and reliability across a broad range of analytical applications. Alfuzosin EP Impurity F (cas no.-19216-53-6) IUPAC Name-6,7-dimethoxy-N2, N2-dimethylquinazoline-2,4-diamine; Molecular Formula- C12H16N4O2; Molecular weight-248.28; Alfuzosin EP Impurity F is an impurity of Alfuzosin. Alfuzosin is used in the treatment of benign prostatic hyperplasia. It’s a quinazoline derivative, it antagonizes a1-adrenoceptor selectively and competitively leading to contraction of the prostatic, prostatic capsule, bladder base, and proximal urethral smooth muscle, thereby re
References
Wilde, Michelle I., et al. “Alfuzosin.†Drugs, vol. 45, no. 3, Mar. 1993, pp. 410–29, https://doi.org/10.2165/00003495-199345030-00008.
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