Vamorolone 21 Propionate Impurity - 请求报价
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Vamorolone 21 Propionate Impurity is chemically 2-((8S,10S,13S,14S,16R,17R)-17-hydroxy-10,13,16-trimethyl-3-oxo-6,7,8,10,12,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl propionate. Vamorolone 21 Propionate Impurity is supplied with detailed characterization data compliant with regulatory guideline. Vamorolone 21 Propionate Impurity 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 Vamorolone.
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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Vamorolone 21 Propionate Impurity 成本
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Vamorolone 21 Propionate Impurity 分销商
Vamorolone 21 Propionate Impurity 用于方法验证
Vamorolone 对照标准
Vamorolone 21 Propionate Impurity 用于ANDA申报
Vamorolone 21 Propionate Impurity 用于强制降解研究
Vamorolone 21 Propionate Impurity 鉴别标准
Vamorolone 21 Propionate Impurity 用于DMF申报
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