Search Results for " Olmesartan "
Olmesartan Medoxomil EP Impurity C
| SZ目录编号: | SZ-O006004 |
| CAS 号 | 879562-26-2 |
| 分子式 | C29H28N6O5 |
| 分子量 | 540.6 |
| 投资状态 | In Stock |
化学名称: (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-(1-methylethenyl)-2-propyl-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-imidazole-5-carboxylate (as per EP)
异名: Dehydro Olmesartan Medoxomil ; Anhydro Olmesartan Medoxomil ; Olmesartan Medoxomil Olefinic Impurity (USP) ; Olmesartan Medoxomil Methylvinyl Impurity
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: O=C(C1=C(C(C)=C)N=C(CCC)N1CC2=CC=C(C3=CC=CC=C3C4=NNN=N4)C=C2)OCC5=C(C)OC(O5)=O
Olmesartan Medoxomil EP Impurity C is chemically (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl 4-(1-methylethenyl)-2-propyl-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-imidazole-5-carboxylate (as per EP). It is also known as Dehydro Olmesartan Medoxomil ; Anhydro Olmesartan Medoxomil ; Olmesartan Medoxomil Olefinic Impurity (USP) ; Olmesartan Medoxomil Methylvinyl Impurity. Olmesartan Medoxomil EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Olmesartan Medoxomil EP Impurity C 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 Olmesartan.
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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