Azithromycin EP Impurity H

Azithromycin EP Impurity H

VS CAT No VS-A040009
CAS No 612069-30-4
Mol.F. C45H77N3O15S
Mol.Wt. 932.2
Inv. Status Custom Synthesis

Chemical Name: 3′-N-[[4-(acetylamino)phenyl]sulfonyl]-3′-N-demethylazithromycin (as per EP) ; 3'-N-{[4-(Acetylamino)phenyl]sulfonyl}-3'-N-demethylazithromycin (as per USP)

Synonym: Azithromycin USP Related Compound H

Shipping Temperature: Ambient

Country of Origin: India

Smiles: C[C@@H]([C@@H]([C@H](C(O[C@@H]([C@@](C)(O)[C@@H]1O)CC)=O)C)O[C@@](O[C@@H](C)[C@@H]2O)([H])C[C@@]2(C)OC)[C@H]([C@](O)(C[C@H](CN([C@@H]1C)C)C)C)O[C@@](O[C@H](C)C[C@@H]3N(C)[S](=O)(C4=CC=C(NC(C)=O)C=C4)=O)([H])[C@@H]3O

Azithromycin EP Impurity H is chemically 3′-N-[[4-(acetylamino)phenyl]sulfonyl]-3′-N-demethylazithromycin (as per EP) ; 3'-N-{[4-(Acetylamino)phenyl]sulfonyl}-3'-N-demethylazithromycin (as per USP). It is also known as Azithromycin USP Related Compound H. Azithromycin EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Azithromycin EP Impurity H 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 Azithromycin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. Vsquare products are for analytical purpose only and not for human use.