Category
Ribociclib
CAS Number
1374639-77-6
Molecular Formula
C₁₂H₁₄ClN₃O
Molecular Weight
251.71 g/mol
Synonym

(2-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidin-6-yl)methanol ; 

Keywords
High-Quality Pharmaceutical Reference Standards
Miscellaneous compounds
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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 Chloro Hydroxy Impurity (CAS No. 1374639-77-6), with a Molecular Formula of C₁₂H₁₄ClN₃O and Molecular Weight of 251.70 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, method validation, and pharmaceutical quality control testing. Manasa Life Sciences, a pharmaceutical impurity reference standards manufacturer and supplier in India, offers Ribociclib Chloro Hydroxy Impurity Reference Standard for analytical research involving HPLC, UHPLC, LC-MS, NMR, FTIR, and pharmaceutical impurity characterization.

As a Ribociclib Chloro Hydroxy Impurity Manufacturer and Supplier in India, Manasa Life Sciences supports API manufacturers, oncology pharmaceutical companies, CROs, CDMOs, and analytical testing laboratories with Ribociclib related compounds, anticancer API impurity standards, process impurity reference materials, and pharmaceutical analytical reference standards. Product-specific documentation, including Certificate of Analysis (COA), SDS/MSDS, HPLC chromatograms, and spectral characterization reports, may be available upon request. Our Ribociclib Chloro Hydroxy Impurity CAS 1374639-77-6 Reference Standard supports pharmaceutical analytical testing aligned with applicable ICH Q3A, ICH Q3B, ICH Q2, USP, and EP guidelines, serving pharmaceutical research and quality control requirements across India, UAE, GCC countries, Asia, Europe, and Africa.