Cefalotin EP Impurity A | CAS 34691-02-6 - Request Quote
Cefalotin EP Impurity A
| SZ CAT No: | SZ-C087002 |
| CAS No | 34691-02-6 |
| Mol.F. | C14H14N2O4S2 |
| Mol.Wt. | 338.4 |
| Inv. Status | Synthesis on demand |
| Rel. CAS No | 37049-55-1 (Na salt) ; 94735-30-5 (K salt) |
| Shipping Condition | Room Temperature |
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Usage Note:
Cefalotin EP Impurity A is chemically (6R,7R)-3-Methyl-8-oxo-7-[(thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP). It is also known as Deacetoxy Cefalotin (EP). Cefalotin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Cefalotin 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 Cefalotin.
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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Cefalotin EP Impurity A for Method Validation
Cefalotin Reference Standard
Cefalotin EP Impurity A for ANDA Filing
Cefalotin EP Impurity A for Forced Degradation Studies
Cefalotin EP Impurity A Identification Standards
Cefalotin EP Impurity A for DMF Filing
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