Verapamil EP Impurity I (HCl salt) | CAS 1794-55-4 - Solicitar cotización

Verapamil EP Impurity I (HCl salt) is chemically (2RS)-2-(3,4-dimethoxyphenyl)-4-[[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino]-2-(propan-2-yl)butanenitrile hydrochloride (as per EP) ; (4-[(3,4-Dimethoxyphenethyl)(methyl)amino]-2-(3,4-dimethoxyphenyl)-2-isopropylbutanenitrile hydrochloride) (as per USP). It is also known as Verapamil USP Related Compound B (HCl salt). Verapamil EP Impurity I (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Verapamil EP Impurity I (HCl salt) 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 Verapamil.

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.