باب
Fluvoxamine
رقم CAS
192876-02-1
الصيغة الجزيئية
C₁₄H₁₉F₃N₂O₂
وزن جزيئي
304.31 g/mol
مرادف

(5E)-5-[(2-Aminoethoxy)imino]-5-[4-(trifluoromethyl)phenyl]pentan-1-ol; Fluvoxamino acid ; Desmethyl Fluvoxamine; (E)-5-Hydroxy-1-(4-(trifluoromethyl)phenyl)pentan-1-one O-(2-aminoethyl) Oxime; (1E)-5-Hydroxy-1-[4-(trifluoromethyl)phenyl]-1-pentanone O-(2-Aminoethyl)oxime

الكلمات الرئيسية
Metabolites.
Impurities
Pharmaceutical Standards
Intermediates
Fine Chemicals
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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.

Fluvoxamine EP Impurity G is a related substance of fluvoxamine that may occur as a process-related or degradation-related impurity. It is monitored during pharmaceutical analysis to assess the purity and stability of the fluvoxamine active pharmaceutical ingredient (API). Its control helps ensure consistent product quality and compliance with applicable pharmacopoeial requirements.