Nystatin Butyrrate Impurity - 请求报价
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Nystatin Butyrrate Impurity is chemically (1R,3R,4R,7R,9R,11R,15S,16R,17R,18S,19E,21E,25E,27E,29E,31E,33R,35S,36S,37S)-33-(((2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-37-(butyryloxy)-1,3,4,7,9,11,17-heptahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,25,27,29,31-hexaene-36-carboxylic acid. Nystatin Butyrrate Impurity is supplied with detailed characterization data compliant with regulatory guideline. Nystatin Butyrrate 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 Nystatin.
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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Nystatin Butyrrate Impurity 成本
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Nystatin Butyrrate Impurity 用于方法验证
Nystatin 对照标准
Nystatin Butyrrate Impurity 用于ANDA申报
Nystatin Butyrrate Impurity 用于强制降解研究
Nystatin Butyrrate Impurity 鉴别标准
Nystatin Butyrrate Impurity 用于DMF申报
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