N-Nitroso Nilotinib EP Impurity E - Request Quote
N-Nitroso Nilotinib EP Impurity E
| SZ CAT No: | SZ-N009058 |
| CAS No | NA |
| Mol.F. | C27H19F3N8O2 : HCl |
| Mol.Wt. | 544.5 : 36.5 |
| Inv. Status | Synthesis on demand |
| Shipping Condition | Room Temperature |
Chemical Name :
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Country of Origin :
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Usage Note:
N-Nitroso Nilotinib EP Impurity E is chemically N-(3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-(nitroso(4-(pyridin-3-yl)pyrimidin-2-yl)amino)benzamide hydrochloride. N-Nitroso Nilotinib EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Nilotinib 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 Nilotinib.
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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Nilotinib Reference Standard
N-Nitroso Nilotinib EP Impurity E for ANDA Filing
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N-Nitroso Nilotinib EP Impurity E Identification Standards
N-Nitroso Nilotinib EP Impurity E for DMF Filing
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