Dehydro Loperamide; 4-(4-(4-chlorophenyl)-5,6-dihydropyridin-1(2H)-yl)-N,N-dimethyl-2,2-diphenylbutanamide; 4-(4-(4-chlorophenyl)-5,6-dihydropyridin-1(2H)-yl)-N,N-dimethyl-2,2-diphenylbutanamide;1(2H)-Pyridinebutanamide, 4-(4-chlorophenyl)-3,6-dihydro-N,N-dimethyl-alpha,alpha-diphenyl-;4-[4-(4-chlorophenyl)-3,6-dihydro-2H-pyridin-1-yl]-N,N-dimethyl-2,2-diphenylbutanamide
Loperamide EP Impurity H is a fully characterized chemical compound used as a reference standard of API Loperamide. The standard offered is compliant with regulatory guidelines. Loperamide EP Impurity H is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - 61299-42-1
