باب
Salmeterol xinafoate
رقم CAS
1391052-04-2
الصيغة الجزيئية
C34H47NO7
وزن جزيئي
581.76
مرادف

1-[4-[2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethoxy]-3-(hydroxymethyl)phenyl]-2-[[6-(4-phenylbutoxy)hexyl]amino]ethanol; 3-Benzenedimethanol, 4-[2-hydroxy-2-[4-hydroxy-3-(hydroxymethyl)phenyl]ethoxy]-α1-[[[6-(4-phenylbutoxy)hexyl]amino]methyl]-; Salmeterol-O-alkyl; 4-(1-Hydroxy-2-(4-(1-hydroxy-2-((6-(4-phenylbutoxy)hexyl)amino)ethyl)-2-(hydroxymethyl)phenoxy)ethyl)-2-(hydroxymethyl)phenol

الكلمات الرئيسية
Pharmaceutical Standards
Aromatic
Amines
Fine Chemicals
Intermediates
Impurities
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-D 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.