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Lazertinib Hydroxy Impurity

SZ CAT No:SZ-L127008
CAS No
NA
Mol.F.
C29H32N8O3
Mol.Wt.
540.6
Inv. Status
Synthesis on demand

Chemical Name :

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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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Lazertinib Hydroxy Impurity for Method Validation

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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

SynZeal will update these details as per new developments or findings in product specifications without further notice.

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