Category
Carfilzomib
CAS Number
NA
Molecular Formula
C40H59N5O8
Molecular Weight
737.9 g/mol
Synonym

N-(1-((1,2-dihydroxy-2,6-dimethyl-3-oxoheptan-4-yl)amino)-1-oxo-3-phenylpropan-2-yl)-4-methyl-2-(2-(2-morpholinoacetamido)-4-phenylbutanamido)pentanamide;

Keywords
Pharmaceutical Standards
Impurities
Metabolites.
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.

Carfilzomib Impurity 104 is a process- or degradation-related impurity formed during the synthesis or storage of Carfilzomib. It is monitored in impurity profiling, stability studies, and quality control to ensure the drug’s purity, safety, and regulatory compliance.