Doxorubicin Hydrobromide EP Impurity C

Doxorubicin Hydrobromide EP Impurity C is chemically (8S,10S)-10[(3-Amino-2,3,6-trideoxy-α-l-lyxo-hexopyranosyl)oxy]-8-(bromoacetyl)-6,8,11-trihydroxy-1-methoxy-7,8,9,10-tetrahydrotetracene-5,12-dione hydrobromide (as per EP). It is also known as Doxorubicin BP Impurity C. Doxorubicin Hydrobromide EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Doxorubicin Hydrobromide EP Impurity C 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 Doxorubicin.

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.