Lubiprostone Impurity ll - 请求报价
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Lubiprostone Impurity ll is chemically 7-((1R,2R,3R)-2-(4,4-difluoro-3-oxo-1-octyl)-3-(phenylmethoxy)-5-oxo-cyclopentyl)heptanoic Acid. Lubiprostone Impurity ll is supplied with detailed characterization data compliant with regulatory guideline. Lubiprostone Impurity ll 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 Lubiprostone.
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.
应用与法规使用场景
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Lubiprostone Impurity ll 成本
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Lubiprostone Impurity ll 分销商
Lubiprostone Impurity ll 用于方法验证
Lubiprostone 对照标准
Lubiprostone Impurity ll 用于ANDA申报
Lubiprostone Impurity ll 用于强制降解研究
Lubiprostone Impurity ll 鉴别标准
Lubiprostone Impurity ll 用于DMF申报
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