Category
Safinamide
CAS Number
1000370-27-3
Alternate CAS Number
1000370-30-8(HCl Salt)
Molecular Formula
C₂₄H₂₄F₂N₂O₂
Molecular Weight
410.46 g/mol
Synonym

(S)-2-[[3-(3-Fluorobenzyl)-4-[(3-fluorobenzyl)oxy]benzyl]amino]propanamide; (2S)-2-[[[4-[(3-Fluorophenyl)methoxy]-3-[(3-fluorophenyl)methyl]phenyl]methyl]amino]propanamide; (S)-2-((3-(3-Fluorobenzyl)-4-((3-fluorobenzyl)oxy)benzyl)amino)propanamide; Safinamide Dialkyl Impurity

Keywords
Aromatics
Fine Chemicals
Impurities
Intermediates
Pharmaceutical Standards
Amines
Impurities manufacturer and Suppliers in Hyderabad india
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.

Accelerate your analytical validation and stability testing with premium Safinamide Impurity-1, proudly synthesized and distributed worldwide by Manasa Life Sciences, a trusted pharmaceutical manufacturer and supplier. This critical process-related substance, cross-referenced under CAS number 1000370-27-3, carries the systematic chemical name (S)-2-[[3-(3-Fluorobenzyl)-4-[(3-fluorobenzyl)oxy]benzyl]amino]propanamide, with a defined molecular formula of C₂₄H₂₄F₂N₂O₂ and a molecular weight of 410.46 g/mol. To satisfy the rigorous documentation needs of quality assurance laboratories, every lot is accompanied by a detailed COA and an updated MSDS generated under strict GDP and GMP frameworks. It serves as an indispensable reference tool for forced degradation studies and impurity profiling using advanced instrumentation such as HPLC, LCMS, NMR, and IR profiling. Designed to help pharmaceutical developers successfully meet the stringent threshold and reporting expectations mandated by the USFDA, EMA, ICH, USP, and EP, this impurity standard from Manasa Life Sciences ensures your final API matrices achieve absolute global compliance.