Alfuzosin EP Impurity A Hydrochloride

Stability-indicating HPTLC method for the simultaneous detection and quantification of alfuzosin hydrochloride, solifenacin succinate along with four of their official impurities
Mahmoud A. Tantawy, Soheir A. Weshahy, Mina Wadie , Mamdouh R. Rezk
Microchemical Journal Volume 157, September 2020, 104905
 
An improved and commercially viable process for the preparation of Alfuzosin hydrochloride
Manne Satyanarayana Reddy*a , Bairy Kondal Reddya , Chepyala Kista Reddyb , Muppa Kishore Kumara , Srinivasan Thirumalai Rajana and Venkatesh Mummadi
ARKIVOC 2007 (xiii) 41-46
 
Thermoanalytical study of alfuzosin hcl
Ali k. attia1,*, nagiba y. hassan2, a. el-bayoumi2, samar. g. abdel-hamid1
Int J Curr Pharm Res, Vol 4, Issue 3, 101-105

Alfuzosin EP Impurity A Hydrochloride is chemically N-[3-[(4-Amino-6,7-dimethoxyquinazolin-2-yl)methylamino]propyl]furan-2-carboxamide Hydrochloride (as per EP & USP). It is also known as Alfuzosin Tetradehydro Impurity ; Furamide Alfuzosin (USP). Alfuzosin EP Impurity A Hydrochloride is supplied with detailed characterization data compliant with regulatory guideline. Alfuzosin EP Impurity A Hydrochloride can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Alfuzosin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.