1-(4-aminophenyl)-N-methyl-1H-pyrazole-3-carboxamide CAS 1155164-75-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1155164-75-2
Molecular FormulaC11H12N4O
Molecular Weight216.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-aminophenyl)-N-methyl-1H-pyrazole-3-carboxamide CAS 1155164-75-2 chemical structure

Description

The occurrence of 1-(4-aminophenyl)-N-methyl-1H-pyrazole-3-carboxamide is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 1-(4-aminophenyl)-N-methyl-1H-pyrazole-3-carboxamide (CAS 1155164-75-2), a certified reference material (molecular formula C11H12N4O, MW 216.24 g/mol) for analytical method development and quality control.

1-(4-aminophenyl)-N-methyl-1H-pyrazole-3-carboxamide (C11H12N4O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its physicochemical properties are representative of its class; 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).

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), 1-(4-aminophenyl)-N-methyl-1H-pyrazole-3-carboxamide 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 FormulaC11H12N4O
Molecular Weight216.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Nitrogen Atoms4

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