1-Benzyl-3-phenyl-2-thioxoimidazolidin-4-one CAS 83515-66-6

Purity 97%+In StockPharmaceutical Standards
CAS No.83515-66-6
Molecular FormulaC44H42N6O3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Benzyl-3-phenyl-2-thioxoimidazolidin-4-one CAS 83515-66-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 782.76 g/mol gives 1-Benzyl-3-phenyl-2-thioxoimidazolidin-4-one distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 1-Benzyl-3-phenyl-2-thioxoimidazolidin-4-one (CAS 83515-66-6), a certified reference material (molecular formula C44H42N6O3Br, MW 782.76 g/mol) for analytical method development and quality control.

The molecular framework of 1-Benzyl-3-phenyl-2-thioxoimidazolidin-4-one (C44H42N6O3Br) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine 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).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC44H42N6O3 2*Br
Molecular Weight782.76 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)26.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1980
Halogen ContentBr-containing
Nitrogen Atoms6

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