Bupropion Impurity 17 - 请求报价
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Bupropion Impurity 17 is chemically (3-Chlorophenyl)(2,4,4-trimethyloxazolidin-2-yl)methanone. Bupropion Impurity 17 is supplied with detailed characterization data compliant with regulatory guideline. Bupropion Impurity 17 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 Bupropion.
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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Bupropion Impurity 17 用于方法验证
Bupropion 对照标准
Bupropion Impurity 17 用于ANDA申报
Bupropion Impurity 17 用于强制降解研究
Bupropion Impurity 17 鉴别标准
Bupropion Impurity 17 用于DMF申报
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