باب
Zanamivir
رقم CAS
NA
الصيغة الجزيئية
C13H22N6O7
وزن جزيئي
374.4g/mol
مرادف

(2R,3R,4S)-3-Acetamido-4-(N′-carbamimidoylcarbamimidamido)-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid

الكلمات الرئيسية
Intermediates
Impurities
Pharmaceutical Standards
Fine Chemicals
Slide 1.GIF
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.

Zanamivir Impurity-E is a certified reference standard used in pharmaceutical analysis of zanamivir. It supports quality control, method validation, and stability testing, ensuring regulatory compliance and the safety of zanamivir drug products.