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Doxorubicin EP Impurity C - Request Quote

Picture of Doxorubicin EP Impurity C

Doxorubicin EP Impurity C

SZ CAT No:SZ-D051008
CAS No
NA
Mol.F.
C27H28BrNO10 : 2(H2O) : HBr
Mol.Wt.
606.4 : 2(18.0) : 80.9
Inv. Status
Synthesis on demand
Rel. CAS No65026-79-1 (free base) ; 60873-68-9 (HBr salt) ; 29742-67-4 (HCl salt)
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    Doxorubicin 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 dihydrate hydrobromide. It is also known as Doxorubicin BP Impurity C. Doxorubicin EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Doxorubicin 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.

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