N-(2,4-dimethylphenyl)-1H-pyrazole-3-carboxamide CAS 305346-15-0

Purity 97%+In StockPharmaceutical Standards
CAS No.305346-15-0
Molecular FormulaC12H13N3O
Molecular Weight215.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2,4-dimethylphenyl)-1H-pyrazole-3-carboxamide CAS 305346-15-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 215.25 g/mol gives N-(2,4-dimethylphenyl)-1H-pyrazole-3-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies N-(2,4-dimethylphenyl)-1H-pyrazole-3-carboxamide (CAS 305346-15-0), a certified reference material (molecular formula C12H13N3O, MW 215.25 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, N-(2,4-dimethylphenyl)-1H-pyrazole-3-carboxamide is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 215.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures N-(2,4-dimethylphenyl)-1H-pyrazole-3-carboxamide 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 FormulaC12H13N3O
Molecular Weight215.25 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.)2025
Nitrogen Atoms3

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