Doxapram EP Impurity B | CAS 1688-76-2 - Request Quote
Doxapram EP Impurity B
| SZ CAT No: | SZ-D201003 |
| CAS No | 1688-76-2 |
| Mol.F. | C22H29N3O |
| Mol.Wt. | 351.5 |
| Inv. Status | Synthesis on demand |
| Rel. CAS No | 100106-91-0 (HCl salt) |
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Usage Note:
Doxapram EP Impurity B is chemically (4RS)-1-ethyl-4-[2-[(2-hydroxyethyl)amino]ethyl]-3,3-diphenylpyrrolidin-2-one (as per EP) ; 1-Ethyl-4-{2-[(2-hydroxyethyl)amino]ethyl}-3,3-diphenylpyrrolidin-2-one (as per USP). It is also known as Doxapram USP Related Compound B. Doxapram EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Doxapram EP Impurity B 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 Doxapram.
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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Doxapram EP Impurity B for Method Validation
Doxapram Reference Standard
Doxapram EP Impurity B for ANDA Filing
Doxapram EP Impurity B for Forced Degradation Studies
Doxapram EP Impurity B Identification Standards
Doxapram EP Impurity B for DMF Filing
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