Loperamide EP Impurity F | CAS 106900-12-3 - Request Quote

Loperamide EP Impurity F is chemically (1r,4r)-4-(4-Chlorophenyl)-1-[4-(N,N-dimethylamino)-3,3-diphenyl-4-oxobutyl]-4-hydroxypiperazine 1-oxide (as per EP) ; (1r,4s)-4-(4-Chlorophenyl)-1-[4-(dimethylamino)-4-oxo-3,3-diphenylbutyl]-4-hydroxypiperidine 1-oxide (as per USP). It is also known as Loperamide Trans-N-Oxide (USP) ; (loperamide oxide) (EP) ; Loperamide Related Compound F (USP). Loperamide EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Loperamide 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 Loperamide.

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.