Ruxolitinib Impurity 170 CAS CATO-C4X-2058170

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-2058170
Molecular FormulaC17H20N6O
Molecular Weight324.39 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Ruxolitinib Impurity 170 CAS CATO-C4X-2058170 chemical structure

Description

As a certified reference material (CRM), Ruxolitinib Impurity 170 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Ruxolitinib Impurity 170 (CAS CATO-C4X-2058170) is a certified pharmaceutical impurity reference standard with the molecular formula C17H20N6O and a molecular weight of 324.39 g/mol.

The molecular framework of Ruxolitinib Impurity 170 (C17H20N6O) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

Physical & Chemical Properties

Molecular FormulaC17H20N6O
Molecular Weight324.39 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms6

Related Ruxolitinib Standards

Recommended Standards

Why CATO?