1-(Furan-2-yl)prop-2-en-1-one CAS 14123-26-3

Purity 97%+In StockPharmaceutical Standards
CAS No.14123-26-3
Molecular FormulaC7H6O2
Molecular Weight122.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(Furan-2-yl)prop-2-en-1-one CAS 14123-26-3 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 1-(Furan-2-yl)prop-2-en-1-one.

CATO supplies 1-(Furan-2-yl)prop-2-en-1-one (CAS 14123-26-3), a certified reference material (molecular formula C7H6O2, MW 122.12 g/mol) for analytical method development and quality control.

The molecular framework of 1-(Furan-2-yl)prop-2-en-1-one (C7H6O2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC7H6O2
Molecular Weight122.12 g/mol
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961

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