|Product Name||Levofloxacin EP Impurity G|
|Synonyms||Levofloxacin USP Related Compound E; Levofloxacin Desethylene Impurity; N,N-Desethylene Levofloxacin; (-)-(S)-9-Fluoro-2,3-dihydro-3-methyl-10-[2-(methylamino)ethylamino]-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid HCl|
Levofloxacin EP Impurity G product with CAS: 1346603-62-0 is also known as Levofloxacin USP Related Compound E; Levofloxacin Desethylene Impurity. This product can be used as working standard or secondary reference standard (additional internal validation as per respective FDA regulations/guidelines may require). This product offered by SynThink is generally used for ANDA and DMF filing, toxicity study of respective drug formulation, Quality Control (QC) of Levofloxacin manufacturing. Please also find out other impurities of Levofloxacin developed by our R&D.
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All products / Impurities / standards are provided with certificate of analysis (CoA) along with the characterization data like 1H-NMR, MASS, HPLC Purity, MSDS (whatever relevant and possible). Moreover, additional data like 13C-NMR, 13C-DEPT NMR, GC, GC-MS, IC, Potency, TGA, Structure Elucidation etc. will be provided on request (extra charges may apply). Products provide by SynThink are for research and development (R&D) use only.
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