N-(pyridin-2-ylmethyl)thiazolidine-4-carboxamide hydrochloride CAS 1572243-26-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1572243-26-5
Molecular FormulaC10H13N3OS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(pyridin-2-ylmethyl)thiazolidine-4-carboxamide hydrochloride CAS 1572243-26-5 chemical structure

Description

N-(pyridin-2-ylmethyl)thiazolidine-4-carboxamide hydrochloride (CAS 1572243-26-5) is a high-purity analytical reference standard with the molecular formula C10H13N3OSHCl and a molecular weight of 259.75 g/mol.

The molecular framework of N-(pyridin-2-ylmethyl)thiazolidine-4-carboxamide hydrochloride (C10H13N3OSHCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

As a certified reference material (CRM), N-(pyridin-2-ylmethyl)thiazolidine-4-carboxamide 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 FormulaC10H13N3OS HCl
Molecular Weight259.75 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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