Glibenclamide trans-4-Hydroxycyclohexyl CAS 23155-00-2

Purity 97%+In StockPharmaceutical Standards
CAS No.23155-00-2
Molecular FormulaC23H28ClN3O6S
Molecular Weight510.00 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Glibenclamide trans-4-Hydroxycyclohexyl CAS 23155-00-2 chemical structure

Description

As a certified reference material (CRM), Glibenclamide trans-4-Hydroxycyclohexyl 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.

Glibenclamide trans-4-Hydroxycyclohexyl (CAS 23155-00-2) is a high-purity analytical reference standard with the molecular formula C23H28ClN3O6S and a molecular weight of 510.00 g/mol.

The molecular framework of Glibenclamide trans-4-Hydroxycyclohexyl (C23H28ClN3O6S) is characterized by a flavonoid core, 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 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).

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.

Physical & Chemical Properties

Molecular FormulaC23H28ClN3O6S
Molecular Weight510.00 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

Related Glibenclamide Standards

Recommended Standards

Why CATO?