4-(Cyclohexylmethylene)-3-methyl-1H-pyrazol-5(4H)-one CAS 834898-54-3

Purity 97%+In StockPharmaceutical Standards
CAS No.834898-54-3
Molecular FormulaC11H16N2O
Molecular Weight192.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Cyclohexylmethylene)-3-methyl-1H-pyrazol-5(4H)-one CAS 834898-54-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 192.26 g/mol gives 4-(Cyclohexylmethylene)-3-methyl-1H-pyrazol-5(4H)-one distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-(Cyclohexylmethylene)-3-methyl-1H-pyrazol-5(4H)-one (CAS 834898-54-3), molecular formula C11H16N2O and molecular weight 192.26 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 4-(Cyclohexylmethylene)-3-methyl-1H-pyrazol-5(4H)-one (C11H16N2O) 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 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), 4-(Cyclohexylmethylene)-3-methyl-1H-pyrazol-5(4H)-one 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 FormulaC11H16N2O
Molecular Weight192.26 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms2

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