Levofloxacin EP Impurity G (HCl salt) | CAS 1346603-62-0 - Request Quote
Levofloxacin EP Impurity G (HCl salt)
| SZ CAT No: | SZ-L020010 |
| CAS No | 1346603-62-0 |
| Mol.F. | C16H18FN3O4 : HCl |
| Mol.Wt. | 335.3 : 36.5 |
| Inv. Status | In Stock |
| Rel. CAT No | SZ-L020025 |
| Rel. CAS No | 151250-76-9 (free base) |
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Usage Note:
Levofloxacin EP Impurity G (HCl salt) is chemically (S)-9-fluoro-3-methyl-10-((2-(methylamino)ethyl)amino)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid hydrochloride ; N,N’-Desethylene Levofloxacin Hydrochloride; . It is also known as Levofloxacin USP Related Compound E ; Levofloxacin Desethylene Impurity ; Diamine derivative. Levofloxacin EP Impurity G (HCl salt) is supplied with detailed characterization data compliant with regulatory guideline. Levofloxacin EP Impurity G (HCl salt) 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 Levofloxacin.
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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Levofloxacin EP Impurity G (HCl salt) for Method Validation
Levofloxacin Reference Standard
Levofloxacin EP Impurity G (HCl salt) for ANDA Filing
Levofloxacin EP Impurity G (HCl salt) for Forced Degradation Studies
Levofloxacin EP Impurity G (HCl salt) Identification Standards
Levofloxacin EP Impurity G (HCl salt) for DMF Filing
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