(1H-indol-3-yl)(phenyl)methanone CAS 15224-25-6

Purity 97%+In StockPharmaceutical Standards
CAS No.15224-25-6
Molecular FormulaC15H11NO
Molecular Weight221.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(1H-indol-3-yl)(phenyl)methanone CAS 15224-25-6 chemical structure

Description

The occurrence of (1H-indol-3-yl)(phenyl)methanone is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

(1H-indol-3-yl)(phenyl)methanone (CAS 15224-25-6) is a high-purity analytical reference standard with the molecular formula C15H11NO and a molecular weight of 221.25 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, (1H-indol-3-yl)(phenyl)methanone is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 221.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), (1H-indol-3-yl)(phenyl)methanone 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 FormulaC15H11NO
Molecular Weight221.25 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Nitrogen Atoms1

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