Search Results for " Candesartan "
Candesartan Cilexetil EP Impurity E
| SZ目录编号: | SZ-C011006 |
| CAS 号 | 914613-35-7 |
| 分子式 | C35H38N6O6 |
| 分子量 | 638.7 |
| 投资状态 | In Stock |
化学名称: (1RS)-1-[[(cyclohexyloxy)carbonyl]oxy]ethyl 2-ethoxy-1-[[2′-(1-ethyl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-benzimidazole-7-carboxylate (as per EP)
异名: Candesartan Cilexetil N1-Ethyl Analog ;
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: CCOC1=NC2=C(C(C(O[C@@]([H])(C)OC(OC3CCCCC3)=O)=O)=CC=C2)N1CC(C=C4)=CC=C4C5=CC=CC=C5C6=NN=NN6CC
Candesartan Cilexetil EP Impurity E is chemically (1RS)-1-[[(cyclohexyloxy)carbonyl]oxy]ethyl 2-ethoxy-1-[[2′-(1-ethyl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-benzimidazole-7-carboxylate (as per EP). It is also known as Candesartan Cilexetil N1-Ethyl Analog ; . Candesartan Cilexetil EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Candesartan Cilexetil EP Impurity E 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 Candesartan.
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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