Avapritinib Hydroxy Impurity - Request Quote
Avapritinib Hydroxy Impurity
| SZ CAT No: | SZ-A155019 |
| CAS No | NA |
| Mol.F. | C23H25FN8 |
| Mol.Wt. | 432.5 |
| Inv. Status | Under Synthesis |
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Avapritinib Hydroxy Impurity is chemically (S)-1-(4-fluorophenyl)-1-(2-(4-(6-methylpyrrolo[2,1-f][1,2,4]triazin-4-yl)piperazin-1-yl)pyrimidin-5-yl)ethan-1-amine. Avapritinib Hydroxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Avapritinib 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 Avapritinib.
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 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.


