3-(4-aminophenyl)-1-phenyl-1H-pyrazole-4-carboxylic acid CAS 1017526-20-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1017526-20-3
Molecular FormulaC16H13N3O2
Molecular Weight279.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-aminophenyl)-1-phenyl-1H-pyrazole-4-carboxylic acid CAS 1017526-20-3 chemical structure

Description

3-(4-aminophenyl)-1-phenyl-1H-pyrazole-4-carboxylic acid (CAS 1017526-20-3) is a high-purity analytical reference standard with the molecular formula C16H13N3O2 and a molecular weight of 279.29 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 3-(4-aminophenyl)-1-phenyl-1H-pyrazole-4-carboxylic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 279.29 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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-(4-aminophenyl)-1-phenyl-1H-pyrazole-4-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 FormulaC16H13N3O2
Molecular Weight279.29 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms3

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