Acetazolamide EP Impurity F

Spectrophotometric determination of acetazolamide in bulk and tablet dosage form by area under curve and first order derivative methods
By Dudhe, P. B.; Lahane, A. V.; Borhade, K. D.; Shelke, P. S.; Chavare, P. D.
From International Journal of ChemTech Research (2017), 10(6), 261-268

Acetazolamide EP Impurity F is chemically N-[5-[(5-Acetamido-1,3,4-thiadiazol-2-yl)sulfonyl]sulfamoyl-1,3,4-thiadiazol-2-yl]acetamide (as per EP) N,N′-{5,5′-[(Hydrosulfonylamino)sulfonyl]bis(1,3,4-thiadiazole-5,2-diyl)}diacetamide (as per USP). It is also known as Acetazolamide Dimer (USP). Acetazolamide EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Acetazolamide EP Impurity F 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 Acetazolamide.

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.