Raltegravir EP Impurity G & F Mixture - 请求报价
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Raltegravir EP Impurity G & F Mixture is chemically Ethyl (E)-N-(2-((2-(4-((4-fluorobenzyl)carbamoyl)-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)propan-2-yl)amino)-2-oxoacetyl)acetohydrazonate compound with ethyl (Z)-N-(2-((2-(4-((4-fluorobenzyl)carbamoyl)-5-hydroxy-1-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)propan-2-yl)amino)-2-oxoacetyl)acetohydrazonate (1:1). Raltegravir EP Impurity G & F Mixture is supplied with detailed characterization data compliant with regulatory guideline. Raltegravir EP Impurity G & F Mixture 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 Raltegravir.
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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Raltegravir EP Impurity G & F Mixture 用于方法验证
Raltegravir 对照标准
Raltegravir EP Impurity G & F Mixture 用于ANDA申报
Raltegravir EP Impurity G & F Mixture 用于强制降解研究
Raltegravir EP Impurity G & F Mixture 鉴别标准
Raltegravir EP Impurity G & F Mixture 用于DMF申报
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