Category
Aprepitant
CAS Number
2348441-62-1
Molecular Formula
C₂₉H₂₅F₇N₄O₃
Molecular Weight
610.5 g/mol
Synonym

5-[[(2R,3S)-2-[(1R)-1-[3,5-Bis(trifluoromethyl)phenyl]ethoxy]-3-(4′-fluorobiphenyl-3-yl)morpholin-4-yl]methyl]-1,2-dihydro-3H-1,2,4-triazol-3-one ( as per EP) ; 

Keywords
Fine Chemicals
Aromatics
Pharmaceutical Standards
Heterocycles
Intermediates
High-Quality Pharmaceutical Reference Standards
Impurities Manufacturer in India
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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.

Aprepitant EP Impurity B (CAS No. 2348441-62-1; Molecular Formula: C₂₉H₂₅F₇N₄O₃; Molecular Weight: 610.50 g/mol) is a high-purity Aprepitant impurity marker and pharmaceutical analytical reference material intended for drug substance characterization, impurity identification, process-related substance monitoring, degradation pathway assessment, chromatographic impurity determination, specification analysis, and stability-indicating testing. Manasa Life Sciences, a trusted pharmaceutical impurity reference material manufacturer and supplier in Hyderabad, India, offers Aprepitant EP Impurity B standards, Aprepitant related substance materials, process impurity markers, degradation impurity references, chromatographic control standards, pharmaceutical testing materials, and API characterization compounds for pharmaceutical development, quality assurance, QC laboratories, CROs, and analytical research worldwide. Products are supported with COA, MSDS, SDS, and relevant technical documentation, with quality and distribution practices aligned with applicable GMP, GDP, ICH, USFDA, USP, EP, and EMA requirements.