Deferoxamine EP Impurity I - 请求报价
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Deferoxamine EP Impurity I is chemically N1-(5-aminopentyl)-N4-[5-(4-[(5-aminopentyl)(hydroxy)amino]-4-oxobutanamido)pentyl]- N1-hydroxybutanediamide (as per EP). Deferoxamine EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Deferoxamine 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 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.
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Deferoxamine EP Impurity I 成本
Deferoxamine EP Impurity I 供应商
Deferoxamine EP Impurity I 分销商
Deferoxamine EP Impurity I 用于方法验证
Deferoxamine 对照标准
Deferoxamine EP Impurity I 用于ANDA申报
Deferoxamine EP Impurity I 用于强制降解研究
Deferoxamine EP Impurity I 鉴别标准
Deferoxamine EP Impurity I 用于DMF申报
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