Enquire about " Ceftaroline Impurity 12 - 1277090-04-6"
Ceftaroline Impurity 12
| SZ CAT No: | SZ-C142015 |
| CAS No | 1277090-04-6 |
| Mol.F. | C28H35N12O10PS4 |
| Mol.Wt. |
858.9 |
| Inv. Status |
Synthesis on demand |
Chemical Name: (R)-2-((6S,9R,Z)-1-amino-6-carboxy-1-imino-8,11-dioxo-12-(5-(phosphonoamino)-1,2,4-thiadiazol-3-yl)-14-oxa-2,7,10,13-tetraazahexadec-12-en-9-yl)-5-((4-(1-methylpyridin-1-ium-4-yl)thiazol-2-yl)thio)-3,6-dihydro-2H-1,3-thiazine-4-carboxylate
Shipping Temperature:
HSN Code: 38229010
Country of Origin: India
Smiles: O=C(N[C@H](C(O)=O)CCCNC(N)=N)[C@H]([C@]1([H])NC(C([O-])=O)=C(SC2=NC(C3=CC=[N+](C)C=C3)=CS2)CS1)NC(/C(C4=NSC(N[P](O)(O)=O)=N4)=N\OCC)=O
Ceftaroline Impurity 12 is chemically (R)-2-((6S,9R,Z)-1-amino-6-carboxy-1-imino-8,11-dioxo-12-(5-(phosphonoamino)-1,2,4-thiadiazol-3-yl)-14-oxa-2,7,10,13-tetraazahexadec-12-en-9-yl)-5-((4-(1-methylpyridin-1-ium-4-yl)thiazol-2-yl)thio)-3,6-dihydro-2H-1,3-thiazine-4-carboxylate. Ceftaroline Impurity 12 is supplied with detailed characterization data compliant with regulatory guideline. Ceftaroline Impurity 12 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 Ceftaroline Fosamil.
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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