Search Results for " Cefoxitin "
Cefoxitin EP Impurity A
| SZ CAT No: | SZ-C125002 |
| CAS No | 1158963-31-5 |
| Mol.F. | C15H15N2O6S2 : C6H14N |
| Mol.Wt. | 383.4 : 100.2 |
| Inv. Status | In Stock |
| Rel. CAS No | 54333-94-7 (free base) ; 37051-16-4 (K salt) ; 94089-00-6 (Na salt) |
Chemical Name: Cyclohexanaminium (6R,7S)-3-(hydroxymethyl)-7-methoxy-8-oxo-7-[[(thiophen-2-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (as per EP)
Synonym: Decarbamoylcefoxitin (EP)
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: O=C([C@@]1(OC)NC(CC2=CC=CS2)=O)N3[C@]1([H])SCC(CO)=C3C([O-])=O.[NH3+]C4CCCCC4
Cefoxitin EP Impurity A is chemically Cyclohexanaminium (6R,7S)-3-(hydroxymethyl)-7-methoxy-8-oxo-7-[[(thiophen-2-yl)acetyl]amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate (as per EP). It is also known as Decarbamoylcefoxitin (EP). Cefoxitin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Cefoxitin 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 Cefoxitin.
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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