N-((3-Chloro-2-hydroxy-5-nitrophenyl)carbamothioyl)benzamide CAS 53501-41-0

Purity 97%+In StockPharmaceutical Standards
CAS No.53501-41-0
Molecular FormulaC14H10ClN3O4S
Molecular Weight351.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((3-Chloro-2-hydroxy-5-nitrophenyl)carbamothioyl)benzamide CAS 53501-41-0 chemical structure

Description

The molecular framework of N-((3-Chloro-2-hydroxy-5-nitrophenyl)carbamothioyl)benzamide (C14H10ClN3O4S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

N-((3-Chloro-2-hydroxy-5-nitrophenyl)carbamothioyl)benzamide (CAS 53501-41-0) is a high-purity analytical reference standard with the molecular formula C14H10ClN3O4S and a molecular weight of 351.76 g/mol.

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-((3-Chloro-2-hydroxy-5-nitrophenyl)carbamothioyl)benzamide 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 FormulaC14H10ClN3O4S
Molecular Weight351.76 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1972
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

Related N Standards

Recommended Standards

Why CATO?