Nebivolol Impurity 51(SS+RR+RS+SR) CAS CATO-C4X-196851

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-196851
Molecular Formula4*C19H22FNO2
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Nebivolol Impurity 51(SS+RR+RS+SR) CAS CATO-C4X-196851 chemical structure

Description

CATO supplies Nebivolol Impurity 51(SS+RR+RS+SR) (CAS CATO-C4X-196851), a pharmacopoeial impurity reference standard (molecular formula C19H22FNO2, MW 315.39 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C19H22FNO2, Nebivolol Impurity 51(SS+RR+RS+SR) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 315.39 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

CATO manufactures Nebivolol Impurity 51(SS+RR+RS+SR) under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular Formula4*C19H22FNO2
Molecular Weight315.39 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentF-containing
Nitrogen Atoms1

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