1-(Naphthalen-2-ylsulfonyl)-4-(5-(trifluoromethyl)pyridin-2-yl)piperazine CAS 556010-07-2

Purity 97%+In StockPharmaceutical Standards
CAS No.556010-07-2
Molecular FormulaC20H18F3N3O2S
Molecular Weight421.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(Naphthalen-2-ylsulfonyl)-4-(5-(trifluoromethyl)pyridin-2-yl)piperazine CAS 556010-07-2 chemical structure

Description

CATO supplies 1-(Naphthalen-2-ylsulfonyl)-4-(5-(trifluoromethyl)pyridin-2-yl)piperazine (CAS 556010-07-2), a certified reference material (molecular formula C20H18F3N3O2S, MW 421.44 g/mol) for analytical method development and quality control.

The molecular framework of 1-(Naphthalen-2-ylsulfonyl)-4-(5-(trifluoromethyl)pyridin-2-yl)piperazine (C20H18F3N3O2S) is characterized by a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

CATO manufactures 1-(Naphthalen-2-ylsulfonyl)-4-(5-(trifluoromethyl)pyridin-2-yl)piperazine 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 FormulaC20H18F3N3O2S
Molecular Weight421.44 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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