Search Results for " Lopamidol "
Iopamidol EP Impurity E
| SZ目录编号: | SZ-L060006 |
| CAS 号 | 60166-92-9 |
| 分子式 | C19H24I3N3O9 |
| 分子量 | 819.1 |
| 投资状态 | In Stock |
化学名称: (1S)-2-[[3,5-bis[[2-hydroxy-1-(hydroxymethyl)ethyl]carbamoyl]-2,4,6-triiodophenyl]amino]-1-methyl-2-oxoethyl acetate (as per EP) ; (S)-5-[[2-(acetyloxy)-1-oxopropyl]amino]-N,N'-bis[2-hydroxy-1-(hydroxymethyl)ethyl]-2,4,6-triiodo-1,3-Benzenedicarboxamide (as per USP)
异名: O-Acetyl Iopamidol (USP) ; Iopamidol BP Impurity E
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: CC(O[C@@H](C)C(NC1=C(I)C(C(NC(CO)CO)=O)=C(I)C(C(NC(CO)CO)=O)=C1I)=O)=O
Iopamidol EP Impurity E is chemically (1S)-2-[[3,5-bis[[2-hydroxy-1-(hydroxymethyl)ethyl]carbamoyl]-2,4,6-triiodophenyl]amino]-1-methyl-2-oxoethyl acetate (as per EP) ; (S)-5-[[2-(acetyloxy)-1-oxopropyl]amino]-N,N'-bis[2-hydroxy-1-(hydroxymethyl)ethyl]-2,4,6-triiodo-1,3-Benzenedicarboxamide (as per USP). It is also known as O-Acetyl Iopamidol (USP) ; Iopamidol BP Impurity E. Iopamidol EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Iopamidol 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 Lopamidol.
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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