n-Phenyl-1,3-thiazolidine-4-carboxamide hydrochloride CAS 1078162-97-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1078162-97-6
Molecular FormulaC10H12N2OS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-Phenyl-1,3-thiazolidine-4-carboxamide hydrochloride CAS 1078162-97-6 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution, n-Phenyl-1,3-thiazolidine-4-carboxamide hydrochloride is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 244.74 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

n-Phenyl-1,3-thiazolidine-4-carboxamide hydrochloride (CAS 1078162-97-6), molecular formula C10H12N2OSHCl and molecular weight 244.74 g/mol, is a CATO reference standard with documented purity and traceability.

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 manufactures n-Phenyl-1,3-thiazolidine-4-carboxamide 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 FormulaC10H12N2OS HCl
Molecular Weight244.74 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.)1988
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

Recommended Standards

Why CATO?