Esketamine EP Impurity A | CAS 6740-87-0 - Request Quote
Esketamine EP Impurity A
| SZ CAT No: | SZ-E061002 |
| CAS No | 6740-87-0 |
| Mol.F. | C13H16ClNO |
| Mol.Wt. | 237.7 |
| Inv. Status | In Stock |
| Rel. CAS No | 90717-16-1 (HCl salt) |
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Usage Note:
Esketamine EP Impurity A is chemically 1-[(2-Chlorophenyl)(methylimino)methyl]cyclopentanol (as per EP). Esketamine EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Esketamine 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 Esketamine Hydrochloride.
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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Esketamine EP Impurity A for Method Validation
Esketamine Hydrochloride Reference Standard
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Esketamine EP Impurity A for Forced Degradation Studies
Esketamine EP Impurity A Identification Standards
Esketamine 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.


