N'-(1-(phenylsulfonyl)piperidin-4-ylidene)-3-(trifluoromethyl)benzohydrazide CAS 478248-22-5

Purity 97%+In StockPharmaceutical Standards
CAS No.478248-22-5
Molecular FormulaC19H18F3N3O3S
Molecular Weight425.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N'-(1-(phenylsulfonyl)piperidin-4-ylidene)-3-(trifluoromethyl)benzohydrazide CAS 478248-22-5 chemical structure

Description

As a certified reference material (CRM), N'-(1-(phenylsulfonyl)piperidin-4-ylidene)-3-(trifluoromethyl)benzohydrazide 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.

CATO supplies N'-(1-(phenylsulfonyl)piperidin-4-ylidene)-3-(trifluoromethyl)benzohydrazide (CAS 478248-22-5), a certified reference material (molecular formula C19H18F3N3O3S, MW 425.42 g/mol) for analytical method development and quality control.

N'-(1-(phenylsulfonyl)piperidin-4-ylidene)-3-(trifluoromethyl)benzohydrazide (C19H18F3N3O3S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC19H18F3N3O3S
Molecular Weight425.42 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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