Letermovir impurity 137 CAS CATO-C4X-2915137

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-2915137
Molecular FormulaC22H24FN3O4
Molecular Weight413.44 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Letermovir impurity 137 CAS CATO-C4X-2915137 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 413.44 g/mol gives Letermovir impurity 137 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Letermovir impurity 137 (CAS CATO-C4X-2915137), a pharmacopoeial impurity reference standard (molecular formula C22H24FN3O4, MW 413.44 g/mol) used for the identification and quantification of trace impurities in APIs.

Letermovir impurity 137 (C22H24FN3O4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC22H24FN3O4
Molecular Weight413.44 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentF-containing
Nitrogen Atoms3

Related Letermovir Standards

Recommended Standards

Why CATO?