Baclofen EP Impurity H - Request Quote
Baclofen EP Impurity H
| SZ CAT No: | SZ-B050009 |
| CAS No | NA |
| Mol.F. | C21H20Cl2N2O4 |
| Mol.Wt. | 435.3 |
| Inv. Status | In Stock |
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Usage Note:
Baclofen EP Impurity H is chemically Mixture of the 4 stereoisomers of (3Ξ)-3-(4-chlorophenyl)-4-[(4Ξ)-4-(4-chlorophenyl)-2-oxopyrrolidine-1-carboxamido]butanoic acid (as per EP). Baclofen EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Baclofen EP Impurity H 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 Baclofen.
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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Baclofen Reference Standard
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Baclofen EP Impurity H Identification Standards
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SynZeal will update these details as per new developments or findings in product specifications without further notice.


