3-Hydroxy-1H-inden-1-one CAS 70432-32-5

Purity 97%+In StockPharmaceutical Standards
CAS No.70432-32-5
Molecular FormulaC9H6O2
Molecular Weight146.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Hydroxy-1H-inden-1-one CAS 70432-32-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 146.14 g/mol gives 3-Hydroxy-1H-inden-1-one distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3-Hydroxy-1H-inden-1-one (CAS 70432-32-5), a certified reference material (molecular formula C9H6O2, MW 146.14 g/mol) for analytical method development and quality control.

The molecular framework of 3-Hydroxy-1H-inden-1-one (C9H6O2) 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.

As a certified reference material (CRM), 3-Hydroxy-1H-inden-1-one 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 FormulaC9H6O2
Molecular Weight146.14 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977

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