Lazertinib Hydroxy Impurity - Request Quote
Lazertinib Hydroxy Impurity
| SZ CAT No: | SZ-L127008 |
| CAS No | NA |
| Mol.F. | C29H32N8O3 |
| Mol.Wt. | 540.6 |
| Inv. Status | Synthesis on demand |
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Usage Note:
Lazertinib Hydroxy Impurity is chemically N-(5-((4-(4-((Dimethylamino)methyl)-3-phenyl-1H-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-hydroxy-2-morpholinophenyl)acrylamide. Lazertinib Hydroxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Lazertinib Hydroxy Impurity 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 Lazertinib.
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.


