Paroxetine Impurity 5 - 请求报价
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Paroxetine Impurity 5 is chemically (2S,3R,4S,5R,6R)-2-(((2R,3S,4R,5R,6R)-6-((3S,4R)-3-((benzo[d][1,3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)piperidin-1-yl)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol. Paroxetine Impurity 5 is supplied with detailed characterization data compliant with regulatory guideline. Paroxetine Impurity 5 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 Paroxetine.
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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Paroxetine Impurity 5 用于方法验证
Paroxetine 对照标准
Paroxetine Impurity 5 用于ANDA申报
Paroxetine Impurity 5 用于强制降解研究
Paroxetine Impurity 5 鉴别标准
Paroxetine Impurity 5 用于DMF申报
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