باب
Abacavir
رقم CAS
1443421-67-7
الصيغة الجزيئية
C₁₄H₁₈N₆O
وزن جزيئي
286.34 g/mol
مرادف

[(1R,4R)-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]cyclopent-2-enyl]methanol; (1R,4R)-4-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene-1-methanol; trans-Abacavir; {(1R,4R)-4-[2-Amino-6-(cyclopropylamino)-9H-purin-9-yl]-cyclopent-2-enyl}methanol (USP)

الكلمات الرئيسية
Fine Chemicals
Pharmaceutical Standards
Intermediates
Impurities manufacturer and Suppliers in Hyderabad india
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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.

Abacavir EP Impurity D is a specified impurity associated with Abacavir, an antiretroviral medication used in the treatment of HIV infection. It is monitored during the quality control testing of abacavir drug substances and products according to the European Pharmacopoeia (EP) standards. The impurity is identified and quantified to ensure the purity, safety, and consistency of the final pharmaceutical product. Its presence is controlled within acceptable limits using analytical techniques such as chromatography.