1-(4-Butylphenyl)-1H-pyrazole-4-carbaldehyde CAS 1015845-98-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1015845-98-3
Molecular FormulaC14H16N2O
Molecular Weight228.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Butylphenyl)-1H-pyrazole-4-carbaldehyde CAS 1015845-98-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 228.29 g/mol gives 1-(4-Butylphenyl)-1H-pyrazole-4-carbaldehyde distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-(4-Butylphenyl)-1H-pyrazole-4-carbaldehyde (CAS 1015845-98-3) is a high-purity analytical reference standard with the molecular formula C14H16N2O and a molecular weight of 228.29 g/mol.

The molecular framework of 1-(4-Butylphenyl)-1H-pyrazole-4-carbaldehyde (C14H16N2O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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-Butylphenyl)-1H-pyrazole-4-carbaldehyde 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 FormulaC14H16N2O
Molecular Weight228.29 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.)1988
Nitrogen Atoms2

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