Cefuroxime EP Impurity F | CAS 97170-19-9 - Request Quote
Cefuroxime EP Impurity F
| SZ CAT No: | SZ-C086007 |
| CAS No | 97170-19-9 |
| Mol.F. | C15H15N3O7S |
| Mol.Wt. | 381.4 |
| Inv. Status | In Stock |
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Usage Note:
Cefuroxime EP Impurity F is chemically (6R,7R)-7-[[(E)-(Furan-2-yl)(methoxyimino)acetyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP). It is also known as Descarbamoyl trans-Cefuroxime. Cefuroxime EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Cefuroxime EP Impurity F 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 Cefuroxime.
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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Cefuroxime EP Impurity F for Method Validation
Cefuroxime Reference Standard
Cefuroxime EP Impurity F for ANDA Filing
Cefuroxime EP Impurity F for Forced Degradation Studies
Cefuroxime EP Impurity F Identification Standards
Cefuroxime EP Impurity F for DMF Filing
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