Deferoxamine EP Impurity H

N° de SZ CAT:	SZ-D131007
Número CAS	NA
Mol.F.	C41H78N10O12
Peso Molecular	903.1
Status de Fatura	Custom Synthesis

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Nome Químico: N1,N37-bis(5-aminopentyl)-N1,N37,11,27-tetrahydroxy-4,12,15,23,26,34-hexaoxo-5,11,16,22,27,33-hexaazaheptatriacontane-1,37-diamide (as per EP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: ON(C(CCC(NCCCCCNC(CCC(N(O)CCCCCNC(CCC(N(CCCCCN)O)=O)=O)=O)=O)=O)=O)CCCCCNC(CCC(N(O)CCCCCN)=O)=O

Deferoxamine EP Impurity H is chemically N1,N37-bis(5-aminopentyl)-N1,N37,11,27-tetrahydroxy-4,12,15,23,26,34-hexaoxo-5,11,16,22,27,33-hexaazaheptatriacontane-1,37-diamide (as per EP). Deferoxamine EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Deferoxamine EP Impurity H 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 Deferoxamine.

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.