2-[(4-chlorophenyl)amino]-2-oxoethyl imidothiocarbamate hydrochloride CAS 1097683-47-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1097683-47-0
Molecular FormulaC9H10ClN3OS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[(4-chlorophenyl)amino]-2-oxoethyl imidothiocarbamate hydrochloride CAS 1097683-47-0 chemical structure

Description

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.

2-[(4-chlorophenyl)amino]-2-oxoethyl imidothiocarbamate hydrochloride (CAS 1097683-47-0) is a high-purity analytical reference standard with the molecular formula C9H10ClN3OSHCl and a molecular weight of 280.17 g/mol.

The molecular framework of 2-[(4-chlorophenyl)amino]-2-oxoethyl imidothiocarbamate hydrochloride (C9H10ClN3OSHCl) 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 the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

Physical & Chemical Properties

Molecular FormulaC9H10ClN3OS HCl
Molecular Weight280.17 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.)1989
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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