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Moxifloxacin EP Impurity C

N° de SZ CAT:SZ-M033004
Número CAS1029364-75-7
Mol.F.C22H26FN3O4
Peso Molecular415.5
Status de FaturaIn Stock
Shipping Condition Ambient Temperature

Nome Químico: 1-Cyclopropyl-8-ethoxy-6-fluoro-7-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (as per EP) ; 1-Cyclopropyl-8-ethoxy-6-fluoro-1,4-dihydro-7-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-3-quinolinecarboxylic acid (as per USP)

Sinônimo: Moxifloxacin Ethyl Analog ; Moxifloxacin USP related compound C

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)=C3OCC)C1=O)O

Moxifloxacin EP Impurity C is chemically 1-Cyclopropyl-8-ethoxy-6-fluoro-7-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (as per EP) ; 1-Cyclopropyl-8-ethoxy-6-fluoro-1,4-dihydro-7-[(4aS,7aS)-octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl]-4-oxo-3-quinolinecarboxylic acid (as per USP). It is also known as Moxifloxacin Ethyl Analog ; Moxifloxacin USP related compound C. Moxifloxacin EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Moxifloxacin EP Impurity C 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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