Category
Ribociclib
CAS Number
1331847-17-6
Molecular Formula
C₁₄H₁₉N₅O
Molecular Weight
273.3 g/mol
Synonym

2-Amino-7-cyclopentyl-N,N-dimethyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxamide ; 7H-Pyrrolo[2,3-d]pyrimidine-6-carboxamide, 2-amino-7-cyclopentyl-N,N-dimethyl; 2-Amino-7-cyclopentyl-N,N-dimethyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxamide;2-Amino-7-cyclopentyl-N,N-dimethyl-7H-pyrrolo[2,3-d]pyrimidine-6-carboxamide ; 

Keywords
High-Quality Pharmaceutical Reference Standards
Intermediates
Impurities
Metabolites.
Pharmaceutical Standards
Fine Chemicals
Impurities Manufacturer in India
Impurities manufacturer 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.

Ribociclib Amine Impurity (CAS No. 1331847-17-6), with a Molecular Formula of C₁₄H₁₉N₅O and Molecular Weight of 273.30 g/mol, is a Ribociclib-related impurity reference standard used for Ribociclib API impurity profiling, process-related impurity identification, related substances analysis, analytical method development, and pharmaceutical quality control testing. This Ribociclib Amine Impurity Reference Standard supports analytical applications including HPLC, LC-MS/MS, NMR spectroscopy, impurity characterization, and stability-indicating method validation in anticancer pharmaceutical research.

Manasa Life Sciences, a pharmaceutical impurity reference standards manufacturer and supplier in India, offers Ribociclib Amine Impurity CAS 1331847-17-6 for oncology API manufacturers, pharmaceutical companies, CROs, CDMOs, and analytical testing laboratories. Our Ribociclib-related compounds, anticancer API impurity standards, pharmaceutical process impurity reference materials, and HPLC analytical standards support pharmaceutical research and quality control requirements. Product-specific documentation, including Certificate of Analysis (COA), SDS/MSDS, HPLC chromatograms, and spectral characterization reports, may be available upon request, subject to availability.