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Vinorelbine EP Impurity I - Request Quote

Picture of Vinorelbine EP Impurity I

Vinorelbine EP Impurity I

SZ CAT No:SZ-V020011
CAS No
NA
Mol.F.
C45H53BrN4O8
Mol.Wt.
857.9
Inv. Status
Synthesis on demand
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    Vinorelbine EP Impurity I is chemically 17-Bromo-4′-deoxy-3′,4′-didehydro-8′-norvincaleukoblastine (as per EP). Vinorelbine EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Vinorelbine 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 Pharmaceutical Reference Standards.

    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.

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