2-(2-Phenyl-1H-indol-3-yl)ethan-1-ol CAS 92962-52-2

Purity 97%+In StockPharmaceutical Standards
CAS No.92962-52-2
Molecular FormulaC16H15NO
Molecular Weight237.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2-Phenyl-1H-indol-3-yl)ethan-1-ol CAS 92962-52-2 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2-(2-Phenyl-1H-indol-3-yl)ethan-1-ol.

CATO supplies 2-(2-Phenyl-1H-indol-3-yl)ethan-1-ol (CAS 92962-52-2), a certified reference material (molecular formula C16H15NO, MW 237.30 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H15NO, 2-(2-Phenyl-1H-indol-3-yl)ethan-1-ol contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 237.30 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.

As a certified reference material (CRM), 2-(2-Phenyl-1H-indol-3-yl)ethan-1-ol 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 FormulaC16H15NO
Molecular Weight237.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1983
Nitrogen Atoms1

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