Iopamidol EP Impurity A | CAS 60166-98-5 - Request Quote
Iopamidol EP Impurity A
| SZ CAT No: | SZ-L060002 |
| CAS No | 60166-98-5 |
| Mol.F. | C14H18I3N3O6 |
| Mol.Wt. | 705.0 |
| Inv. Status | In Stock |
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Usage Note:
Iopamidol EP Impurity A is chemically 5-Amino-N,N’-bis[2-hydroxy-1-(hydroxymethyl)ethyl]-2,4,6-triiodobenzene-1,3-dicarboxamide (as per EP) ; N,N′-Bis-(1,3-dihydroxy-2-propyl)-5-amino-2,4,6-triiodoisophthalamide (as per USP). It is also known as Iopamidol BP Impurity A ; Iopamidol USP Related Compound A. Iopamidol EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Iopamidol EP Impurity A 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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Iopamidol EP Impurity A for Method Validation
Lopamidol Reference Standard
Iopamidol EP Impurity A for ANDA Filing
Iopamidol EP Impurity A for Forced Degradation Studies
Iopamidol EP Impurity A Identification Standards
Iopamidol EP Impurity A for DMF Filing
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