Tioconazole EP Impurity C is chemically 1-[(2RS)-2-[(5-bromo-2-chlorothiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole (as per EP) ; 1-{2-[(5-Bromo-2-chlorothiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole hydrochloride (as per USP). It is also known as Tioconazole USP Related Compound C. Tioconazole EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Tioconazole EP Impurity C 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 Tioconazole.

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.