باب
Nevirapine
رقم CAS
129618-40-2
الصيغة الجزيئية
C15H14N4O
وزن جزيئي
266.8 g/mol
مرادف

2-cyclopropyl-7-methyl-2,4,9,15-tetrazatricyclo[9.4.0.03,8]pentadeca-1(11),3,5,7,12,14-hexaen-10-one; 11-Cyclopropyl-4-methyl-5,11-dihydro-6H-dipyrido [3,2-b:2′,3′-e][1,4]diazepin-6-one; 11-Cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2′,3′-e][1,4]diazepin-6-one

الكلمات الرئيسية
antiviral agents
Enzyme inhibitors
Non nucleoside reverse transcriptase inhibitors
Pharmaceutical Standards
Intermediates
Fine Chemicals
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.

Nevirapine Standard is a certified reference material used in pharmaceutical and analytical testing to ensure the identity, purity, and potency of nevirapine in drug formulations. It provides a reliable benchmark for methods like HPLC, enabling accurate peak identification, quantification, and compliance with pharmacopeial quality standards.