Haloperidol EP Impurity A | CAS 3109-12-4 - Request Quote
Haloperidol EP Impurity A
| SZ CAT No: | SZ-H010002 |
| CAS No | 3109-12-4 |
| Mol.F. | C21H24FNO2 |
| Mol.Wt. | 341.4 |
| Inv. Status | In Stock |
| Rel. CAS No | 4021-57-2 (HCl salt) |
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Usage Note:
Haloperidol EP Impurity A is chemically 1-(4-fluorophenyl)-4-(4-hydroxy-4-phenylpiperidin-1-yl)butan-1-one (as per EP). It is also known as Dechlorohaloperidol. Haloperidol EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Haloperidol 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 Haloperidol.
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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Haloperidol EP Impurity A for Method Validation
Haloperidol Reference Standard
Haloperidol EP Impurity A for ANDA Filing
Haloperidol EP Impurity A for Forced Degradation Studies
Haloperidol EP Impurity A Identification Standards
Haloperidol EP Impurity A for DMF Filing
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SynZeal will update these details as per new developments or findings in product specifications without further notice.


