Cabergoline EP Impurity B | CAS 166533-36-4 - Solicitar cotización

Cabergoline EP Impurity B is chemically (6aR,9R,10aR)-N9-[3-(dimethylamino)propyl]-N4-ethyl-7-(prop-2-enyl)-6a,7,8,9,10,10a-hexahydroindolo[4,3-fg]quinoline-4,9(6H)-dicarboxamide (as per EP & USP). It is also known as Cabergoline USP Related Compound B ; N8-Desethylcarbamoyl-N1-ethylcarbamoyl Cabergoline. Cabergoline EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Cabergoline EP Impurity B 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 Cabergoline.

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.