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Nicergoline EP Impurity I
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- Product Overview
- Description
Description
Chemical Name: [(6aR,6a′R,9R,9′R,10aS,10a′S)-9′-[[[(5-bromopyridin-3-yl)carbonyl]oxy]methyl]-10a,10a′-dimethoxy-7,7′-dimethyl-4′,6′,6a,6a′,7,7′,8,8′,9,9′,10,10′,10a,10a′-tetradecahydro-6H-4,5′-biindolo[4,3-fg]quinoline-9-yl]methyl 5-bromopyridine-3-carboxylate Shipping Temperature: Ambient HSN Code: 38229010Country of Origin: IndiaSmiles: BrC1=CN=CC(C(OC[C@@]2([H])CN(C)[C@@](CC3=CN(C4=C(C5=C6C=CC=C5N4)C[C@@]([C@]6(OC)C7)([H])N(C)C[C@]7([H])COC(C8=CC(Br)=CN=C8)=O)C9=CC=CC%10=C39)([H])[C@]%10(OC)C2)=O)=C1
Additional Information
Nicergoline EP Impurity I is chemically [(6aR,6a′R,9R,9′R,10aS,10a′S)-9′-[[[(5-bromopyridin-3-yl)carbonyl]oxy]methyl]-10a,10a′-dimethoxy-7,7′-dimethyl-4′,6′,6a,6a′,7,7′,8,8′,9,9′,10,10′,10a,10a′-tetradecahydro-6H-4,5′-biindolo[4,3-fg]quinoline-9-yl]methyl 5-bromopyridine-3-carboxylate. Nicergoline EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Nicergoline EP Impurity I 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 Nicergoline.The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. ISP Standards products are for analytical purpose only and not for human use.
