4-Amino-4-(2-chlorobenzyl)tetrahydro-2h-thiopyran 1,1-dioxide hydrochloride CAS 1992957-13-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1992957-13-7
Molecular FormulaC12H16ClNO2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Amino-4-(2-chlorobenzyl)tetrahydro-2h-thiopyran 1,1-dioxide hydrochloride CAS 1992957-13-7 chemical structure

Description

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

CATO supplies 4-Amino-4-(2-chlorobenzyl)tetrahydro-2h-thiopyran 1,1-dioxide hydrochloride (CAS 1992957-13-7), a certified reference material (molecular formula C12H16ClNO2SHCl, MW 310.23 g/mol) for analytical method development and quality control.

The molecular framework of 4-Amino-4-(2-chlorobenzyl)tetrahydro-2h-thiopyran 1,1-dioxide hydrochloride (C12H16ClNO2SHCl) 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 its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

As a certified reference material (CRM), 4-Amino-4-(2-chlorobenzyl)tetrahydro-2h-thiopyran 1,1-dioxide 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 FormulaC12H16ClNO2S HCl
Molecular Weight310.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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