Dosulepin N-Oxide Sulfoxide hydrochloride CAS CATO-C4X-33561

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-33561
Molecular FormulaC19H21NO2S
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Dosulepin N-Oxide Sulfoxide hydrochloride CAS CATO-C4X-33561 chemical structure

Description

CATO supplies Dosulepin N-Oxide Sulfoxide hydrochloride (CAS CATO-C4X-33561), a pharmacopoeial impurity reference standard (molecular formula C19H21NO2SHCl, MW 363.90 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Dosulepin N-Oxide Sulfoxide hydrochloride (C19H21NO2SHCl) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), Dosulepin N-Oxide Sulfoxide hydrochloride 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 FormulaC19H21NO2S HCl
Molecular Weight363.90 g/mol
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 ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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