Xylazine Hydrochloride EP Impurity D CAS 120077-91-0

Description

CATO supplies Xylazine Hydrochloride EP Impurity D (CAS 120077-91-0), a pharmacopoeial impurity reference standard (molecular formula C12H18N2OS, MW 238.35 g/mol) used for the identification and quantification of trace impurities in APIs.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, Xylazine Hydrochloride EP Impurity D is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 238.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

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

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