باب
Abacavir
رقم CAS
208762-35-0
الصيغة الجزيئية
C₁₄H₂₀N₆O
وزن جزيئي
288.35 g/mol
مرادف

[(1R,4S)-3-[2-Amino-6-(cyclopropylamino)-9H-purin-9- yl]cyclopentyl]methanol; Dihydro Abacavir; [(1R,3S)-3-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]cyclopentyl] methanol; (1R,3S)-3-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]cyclopentanemethanol; ((1R,3S)-3-(2-amino-6-(cyclopropylamino)-9H-purin-9-yl)cyclopentyl)methanol

الكلمات الرئيسية
Intermediates
Enzyme inhibitors
Fine Chemicals
bases and related reagents
Nucleotides
Impurities
Pharmaceutical Standards
slide.1
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.

Abacavir EP Impurity E is a specified impurity in the European Pharmacopoeia (EP) for abacavir, an antiretroviral drug used to treat HIV. It may form during the manufacturing process or storage and is monitored to ensure the quality, safety, and purity of the active pharmaceutical ingredient.