Moxifloxacin EP Impurity A is a structurally related fluoroquinolone derivative characterized by a quinolone core substituted with a fluorinated piperazine ring and a methyl group at the C-8 position. It retains the parent drug's 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid scaffold but features an additional methoxy group at the C-5 position, distinguishing it from the parent compound. This impurity arises during synthetic processes due to premature termination of side-chain alkylation. It serves as a critical HPLC reference standard for quantifying process-related impurities in moxifloxacin bulk drug substance.
On Request| Std | Catalog # | Quantity | Price |
|---|---|---|---|
| USP | 1448617 โ | 25 mg | USD 903.00 |
C1C[C@H]2CN(C[C@H]2NC1)C3=C(C=C4C(=C3F)N(C=C(C4=O)C(=O)O)C5CC5)F
InChI=1S/C20H21F2N3O3/c21-14-6-12-17(25(11-3-4-11)8-13(19(12)26)20(27)28)16(22)18(14)24-7-10-2-1-5-23-15(10)9-24/h6,8,10-11,15,23H,1-5,7,9H2,(H,27,28)/t10-,15+/m0/s1
WEXQOLCYKFJAJZ-ZUZCIYMTSA-N