Tacrolimus Dehydro Impurity | CAS 129212-37-9 - 请求报价
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Tacrolimus Dehydro Impurity is chemically 15,19-Epoxy-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,20,21(4H,23H)-tetrone, 8,11,12,13,14,15,16,17,18,19,24,25,26,26a-tetradecahydro-19-hydroxy-3-[2-(4-hydroxy-3-methoxycyclohexyl)-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(2-propenyl)-, [3S-[3R*[E(1S*,3S*,4S*)],4S*,5E,8R*,9E,12R*,14R*,15S*,16R*,18S*,26aR*]]- (9CI). Tacrolimus Dehydro Impurity is supplied with detailed characterization data compliant with regulatory guideline. Tacrolimus Dehydro 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 Tacrolimus.
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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Tacrolimus Dehydro Impurity 成本
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Tacrolimus Dehydro Impurity 用于方法验证
Tacrolimus 对照标准
Tacrolimus Dehydro Impurity 用于ANDA申报
Tacrolimus Dehydro Impurity 用于强制降解研究
Tacrolimus Dehydro Impurity 鉴别标准
Tacrolimus Dehydro Impurity 用于DMF申报
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