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Levofloxacin EP Impurity E  | CAS 178964-53-9 - Request Quote

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Levofloxacin EP Impurity E 

SZ CAT No:SZ-L020006
CAS No
178964-53-9
Mol.F.
C17H20FN3O2
Mol.Wt.
317.4
Inv. Status
In Stock

Chemical Name :

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Usage Note:

Levofloxacin EP Impurity E  is chemically (3S)-9-Fluoro-3-methyl-10-(4-methylpiperazin-1-yl)-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazin-7-one (as per EP) ; (S)-9-Fluoro-2,3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1,2,3-de][1,4]benzoxazine (as per USP). It is also known as Levofloxacin Decarboxy Impurity ; Decarboxylate Impurity. Levofloxacin EP Impurity E  is supplied with detailed characterization data compliant with regulatory guideline. Levofloxacin EP Impurity E  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 Levofloxacin.

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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Levofloxacin EP Impurity E  for Method Validation

Levofloxacin Reference Standard

Levofloxacin EP Impurity E  for ANDA Filing

Levofloxacin EP Impurity E  for Forced Degradation Studies

Levofloxacin EP Impurity E  Identification Standards

Levofloxacin EP Impurity E  for DMF Filing

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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

SynZeal will update these details as per new developments or findings in product specifications without further notice.

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