باب
Salmeterol xinafoate
رقم CAS
108928-81-0
الصيغة الجزيئية
C25H37NO4
وزن جزيئي
415.57
مرادف

1-[4-Hydroxy-3-(hydroxymethyl)phenyl]-2-[[6-(1-methyl-3-phenylpropoxy) hexyl] amino]ethanol; 4-Hydroxy-α1-[[[6-(1-methyl-3-phenylpropoxy)hexyl]amino]methyl]-1,3-benzenedimethanol;4-(1-Hydroxy-2-((6-((4-phenylbutan-2-yl)oxy)hexyl)amino)ethyl)-2-(hydroxymethyl)phenol; Salmeterol-phenyl-2-butoxy; 4-{1-Hydroxy-2-[6-(4-phenylbutan-2-yloxy)hexylamino]ethyl}-2-(hydroxymethyl)phenol

الكلمات الرئيسية
Metabolites.
Pharmaceutical Standards
Impurities
Intermediates
Fine Chemicals
Slide 1.GIF
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.

Salmeterol xinafoate Impurity-E is a certified reference standard used in the quality control and impurity profiling of Salmeterol xinafoate. It supports analytical method validation, stability studies, and regulatory compliance in pharmaceutical development.