باب
Levofloxacin
رقم CAS
100986-86-5
الصيغة الجزيئية
C18H20FN3O4
وزن جزيئي
361.37g/mol
مرادف

(2R)-7-fluoro-2-methyl-6-(4-methylpiperazin-1-yl)-10-oxo-4-oxa-1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8,11-tetraene-11-carboxylic acid;

الكلمات الرئيسية
Fine Chemicals
Pharmaceutical Standards
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Purity:

Above - 95.0%

Technical Data:

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Levofloxacin EP Impurity A is used as a reference standard in pharmaceutical quality control to identify and quantify related impurities during levofloxacin analysis. It supports method validation and ensures compliance with European Pharmacopoeia specifications for drug purity and safety.