3-(tert-Butyl)-1-ethyl-4-phenyl-1,4-dihydroindeno[1,2-c]pyrazol-4-ol CAS 56767-27-2

Purity 97%+In StockPharmaceutical Standards
CAS No.56767-27-2
Molecular FormulaC22H24N2O
Molecular Weight332.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(tert-Butyl)-1-ethyl-4-phenyl-1,4-dihydroindeno[1,2-c]pyrazol-4-ol CAS 56767-27-2 chemical structure

Description

CATO supplies 3-(tert-Butyl)-1-ethyl-4-phenyl-1,4-dihydroindeno[1,2-c]pyrazol-4-ol (CAS 56767-27-2), a certified reference material (molecular formula C22H24N2O, MW 332.44 g/mol) for analytical method development and quality control.

Based on its molecular formula C22H24N2O, 3-(tert-Butyl)-1-ethyl-4-phenyl-1,4-dihydroindeno[1,2-c]pyrazol-4-ol contains a steroid core, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 332.44 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

CATO manufactures 3-(tert-Butyl)-1-ethyl-4-phenyl-1,4-dihydroindeno[1,2-c]pyrazol-4-ol under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC22H24N2O
Molecular Weight332.44 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Nitrogen Atoms2

Recommended Standards

Why CATO?