10-((1-Ethylpyrrolidin-3-yl)methyl)-10H-phenothiazine hydrochloride CAS 112272-97-6

Purity 97%+In StockPharmaceutical Standards
CAS No.112272-97-6
Molecular FormulaC19H22N2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

10-((1-Ethylpyrrolidin-3-yl)methyl)-10H-phenothiazine hydrochloride CAS 112272-97-6 chemical structure

Description

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO supplies 10-((1-Ethylpyrrolidin-3-yl)methyl)-10H-phenothiazine hydrochloride (CAS 112272-97-6), a certified reference material (molecular formula C19H22N2SHCl, MW 346.92 g/mol) for analytical method development and quality control.

Based on its molecular formula C19H22N2SHCl, 10-((1-Ethylpyrrolidin-3-yl)methyl)-10H-phenothiazine hydrochloride contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 346.92 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.

CATO manufactures 10-((1-Ethylpyrrolidin-3-yl)methyl)-10H-phenothiazine hydrochloride 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 FormulaC19H22N2S HCl
Molecular Weight346.92 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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