Crizotinib Impurity 62 CAS CATO-C4X-102562

Purity ≥95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-102562
Molecular FormulaC16H24N6
Molecular Weight300.40 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Crizotinib Impurity 62 CAS CATO-C4X-102562 chemical structure

Description

CATO supplies Crizotinib Impurity 62 (CAS CATO-C4X-102562), a pharmacopoeial impurity reference standard (molecular formula C16H24N6, MW 300.40 g/mol) used for the identification and quantification of trace impurities in APIs.

Crizotinib Impurity 62 (C16H24N6) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its physicochemical properties are representative of its class; 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).

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

As a certified reference material (CRM), Crizotinib Impurity 62 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.

Physical & Chemical Properties

Molecular FormulaC16H24N6
Molecular Weight300.40 g/mol
AppearancePale yellow to yellow crystalline powder
Purity≥95%
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms6

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