1-(4-Hydroxy-2,3-dimethylphenyl)ethanone CAS 5384-57-6

Purity 97%+In StockPharmaceutical Standards
CAS No.5384-57-6
Molecular FormulaC10H12O2
Molecular Weight164.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Hydroxy-2,3-dimethylphenyl)ethanone CAS 5384-57-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 164.20 g/mol gives 1-(4-Hydroxy-2,3-dimethylphenyl)ethanone distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 1-(4-Hydroxy-2,3-dimethylphenyl)ethanone (CAS 5384-57-6), a certified reference material (molecular formula C10H12O2, MW 164.20 g/mol) for analytical method development and quality control.

The molecular framework of 1-(4-Hydroxy-2,3-dimethylphenyl)ethanone (C10H12O2) 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 its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 1-(4-Hydroxy-2,3-dimethylphenyl)ethanone 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 FormulaC10H12O2
Molecular Weight164.20 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958

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