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Moxifloxacin EP Impurity G

N° de SZ CAT:SZ-M033007
Número CAS268545-13-7
Mol.F.C21H24FN3O4
Peso Molecular401.4
Status de FaturaLimited Stock
Rel. CAS No1394029-14-1 (HCl salt)

Nome Químico: 1-Cyclopropyl-6-fluoro-8-methoxy-7-[(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Sinônimo: Moxifloxacin USP Related Compound G ; d-Moxifloxacin

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C(C1=CN(C2CC2)C3=C(C=C(F)C(N(C4)C[C@@]5([H])[C@]4([H])CCCN5)=C3OC)C1=O)O

Moxifloxacin EP Impurity G is chemically 1-Cyclopropyl-6-fluoro-8-methoxy-7-[(4aR,7aR)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid. It is also known as Moxifloxacin USP Related Compound G ; d-Moxifloxacin. Moxifloxacin EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. Moxifloxacin EP Impurity G 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 Moxifloxacin.

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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