((6aR,6'aR,9R,9'R,10aS,10'aS)-10a,10'a-dimethoxy-7,7'-dimethyl-4',6a,6',6'a,7,7',8,8',9,9',10,10a,10',10'a-tetradecahydro-6H-[4,5'-biindolo[4,3-fg]quinoline]-9,9'-diyl)bis(methylene) bis(5-bromonicotinate)
Nicergoline EP Impurity I is a fully characterized chemical compound used as a reference standard of API Nicergoline. The standard offered is compliant with regulatory guidelines. Nicergoline EP Impurity I 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 - NA
