Tadalafil EP Impurity D - Request Quote
Tadalafil EP Impurity D
| SZ CAT No: | SZ-T007005 |
| CAS No | NA |
| Mol.F. | C22H19N3O6 |
| Mol.Wt. | 421.4 |
| Inv. Status | Under Synthesis |
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Usage Note:
Tadalafil EP Impurity D is chemically (6bR)-12-(1,3-Benzodioxol-5-yl)-12a-hydroxy-8-methyl- 6a,6b,8,9,12,12a-hexahydropyrazino[1′,2′:1,2]pyrrolo[3,4-c]quinoline-6,7,10(5H)-trione (as per EP). Tadalafil EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Tadalafil EP Impurity D 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 Tadalafil.
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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SynZeal will update these details as per new developments or findings in product specifications without further notice.