Cefixime EP Impurity D | CAS 97164-56-2 - Request Quote
Cefixime EP Impurity D
| SZ CAT No: | SZ-C081005 |
| CAS No | 97164-56-2 |
| Mol.F. | C16H15N5O7S2 |
| Mol.Wt. |
453.4 |
| Inv. Status |
In Stock |
| Rel. CAS No | 79369-28-1 (HCl salt) ; 1202055-17-1 (Na salt) ; 1202055-18-2 (K salt) ; 210702-16-2 (Sulfate) |
| Shipping Condition | Room Temperature |
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Usage Note:
Cefixime EP Impurity D is chemically (6R,7R)-7-[[(E)-2-(2-Aminothiazol-4-yl)-2-[(carboxymethoxy)imino]acetyl]amino]-3-ethenyl-8-oxo5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP). It is also known as Cefixime (E)-Isomer (EP). Cefixime EP Impurity D is supplied with detailed characterization data compliant with regulatory guideline. Cefixime EP Impurity D 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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Cefixime EP Impurity D for Method Validation
Cefixime Reference Standard
Cefixime EP Impurity D for ANDA Filing
Cefixime EP Impurity D for Forced Degradation Studies
Cefixime EP Impurity D Identification Standards
Cefixime EP Impurity D for DMF Filing
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