1-(1-Tert-butyl-3,5-dimethyl-1h-pyrazol-4-yl)-2,2,2-trifluoroethan-1-one CAS 1315366-32-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1315366-32-5
Molecular FormulaC11H15F3N2O
Molecular Weight248.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(1-Tert-butyl-3,5-dimethyl-1h-pyrazol-4-yl)-2,2,2-trifluoroethan-1-one CAS 1315366-32-5 chemical structure

Description

As a certified reference material (CRM), 1-(1-Tert-butyl-3,5-dimethyl-1h-pyrazol-4-yl)-2,2,2-trifluoroethan-1-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.

1-(1-Tert-butyl-3,5-dimethyl-1h-pyrazol-4-yl)-2,2,2-trifluoroethan-1-one (CAS 1315366-32-5) is a high-purity analytical reference standard with the molecular formula C11H15F3N2O and a molecular weight of 248.24 g/mol.

1-(1-Tert-butyl-3,5-dimethyl-1h-pyrazol-4-yl)-2,2,2-trifluoroethan-1-one (C11H15F3N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; 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.

Physical & Chemical Properties

Molecular FormulaC11H15F3N2O
Molecular Weight248.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms2

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