Risperidone EP Impurity A | CAS 691007-09-7 - Request Quote
Risperidone EP Impurity A
| SZ CAT No: | SZ-R016002 |
| CAS No | 691007-09-7 |
| Mol.F. | C23H28F2N4O2 |
| Mol.Wt. | 430.5 |
| Inv. Status | In Stock |
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Risperidone EP Impurity A is chemically 3-[2-[4-[(E)-(2,4-difluorophenyl)(hydroxyimino)methyl]piperidin-1-yl]ethyl]-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one, (as per EP & USP). It is also known as Risperidone E-Oxime (USP). Risperidone EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Risperidone EP Impurity A 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 Risperidone.
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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Risperidone EP Impurity A for Method Validation
Risperidone Reference Standard
Risperidone EP Impurity A for ANDA Filing
Risperidone EP Impurity A for Forced Degradation Studies
Risperidone EP Impurity A Identification Standards
Risperidone EP Impurity A for DMF Filing
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