2,5-Dimethyl-1-(3-methylphenyl)-1H-pyrrole-3-carboxylic acid CAS 749219-01-0

Purity 97%+In StockPharmaceutical Standards
CAS No.749219-01-0
Molecular FormulaC14H15NO2
Molecular Weight229.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,5-Dimethyl-1-(3-methylphenyl)-1H-pyrrole-3-carboxylic acid CAS 749219-01-0 chemical structure

Description

2,5-Dimethyl-1-(3-methylphenyl)-1H-pyrrole-3-carboxylic acid (C14H15NO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 2,5-Dimethyl-1-(3-methylphenyl)-1H-pyrrole-3-carboxylic acid (CAS 749219-01-0), a certified reference material (molecular formula C14H15NO2, MW 229.27 g/mol) for analytical method development and quality control.

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), 2,5-Dimethyl-1-(3-methylphenyl)-1H-pyrrole-3-carboxylic acid 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 FormulaC14H15NO2
Molecular Weight229.27 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms1

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