Category
Baricitinib
CAS Number
NA
Molecular Formula
C₁₄H₁₂N₈O
Molecular Weight
308.3 g/mol
Synonym

2-(3-(4-(7H-Pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl)-1-nitrosoazetidin-3-yl)acetonitrile; Baricitinib Nitroso Impurity 4

Keywords
Pharmaceutical Standards
Amines
Nitrosamine
N-Nitrosamines Impurities manufacturers and Suppliers in Hyderabad 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.

Baricitinib Nitroso Impurity A is a process- or degradation-related impurity of Baricitinib, formed when a nitroso (–NO) group is introduced into the molecule, usually during synthesis or storage under certain conditions. Its presence is strictly controlled under pharmaceutical guidelines to ensure the drug’s safety, purity, and stability remain within acceptable limits.