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Doxorubicin EP Impurity C

N° de SZ CAT:SZ-D051008
Número CASNA
Mol.F.C27H28BrNO10 : 2(H2O) : HBr
Peso Molecular606.4 : 2(18.0) : 80.9
Status de FaturaCustom Synthesis
Rel. CAS No65026-79-1 (free base) ; 60873-68-9 (HBr salt) ; 29742-67-4 (HCl salt)

Nome Químico: (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

Sinônimo: Doxorubicin BP Impurity C

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: OC1=C(C[C@](C(CBr)=O)(O)C[C@@H]2O[C@@](O[C@@H](C)[C@H]3O)([H])C[C@@H]3N)C2=C(O)C(C4=O)=C1C(C5=CC=CC(OC)=C45)=O.[2H2O].Br

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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