باب
Carvedilol
رقم CAS
1391052-16-6
الصيغة الجزيئية
C39H39N3O6
وزن جزيئي
645.8 g/mol
مرادف

1-[9-[3-(9H-carbazol-4-yloxy)-2-hydroxypropyl]carbazol-4-yl]oxy-3-[2-(2-methoxyphenoxy)ethylamino]propan-2-ol; 1-(9H-Carbazol-4-yloxy)-3-[4-[2-hydroxy-3-[[2-(2-methoxyphenoxy)ethyl]amino]propoxy]-9H-carbazol-9-yl]propan-2-ol; [3-(9H-Carbazol-4-yloxy)-2-hydroxy]propyl Carvedilol; (9H-Carbazol-4-yloxy)-3-[4-[2-hydroxy-3-[[2-(2-methoxyphenoxy)ethyl]amino]propoxy]-9H-carbazol-9-yl]propan-2-ol;α-[(9H-Carbazol-4-yloxy)methyl]-4-[2-hydroxy-3-[[2-(2-methoxyphenoxy)ethyl]amino]propoxy]-9H-carbazole-9-ethanol

الكلمات الرئيسية
Aromatics
Heterocycles
Impurities
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.

Carvedilol EP Impurity D is a European Pharmacopoeia reference impurity used for the identification and quantification of a specified related impurity in carvedilol, ensuring quality control and compliance with pharmacopeial requirements.