N-Nitroso Cefixime EP Impurity A - Request Quote
N-Nitroso Cefixime EP Impurity A
| SZ CAT No: | SZ-C081034 |
| CAS No | NA |
| Mol.F. | C16H16N6O9S2 |
| Mol.Wt. |
500.5 |
| Inv. Status |
Synthesis on demand |
| Shipping Condition | Room Temperature |
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Usage Note:
N-Nitroso Cefixime EP Impurity A is chemically 2-((Z)-2-(2-Aminothiazol-4-yl)-2-((carboxymethoxy)imino)acetamido)-2-((2R)-5-methyl-1-nitroso-7-oxo-1,2,5,7-tetrahydro-4H-furo[3,4-d][1,3]thiazin-2-yl)acetic acid. N-Nitroso Cefixime EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Cefixime 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 Cefixime.
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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N-Nitroso Cefixime EP Impurity A for Method Validation
Cefixime Reference Standard
N-Nitroso Cefixime EP Impurity A for ANDA Filing
N-Nitroso Cefixime EP Impurity A for Forced Degradation Studies
N-Nitroso Cefixime EP Impurity A Identification Standards
N-Nitroso Cefixime EP Impurity A for DMF Filing
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