3-(bromomethyl)-6-(trifluoromethyl)pyridazine CAS 1173897-85-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1173897-85-2
Molecular FormulaC6H4BrF3N2
Molecular Weight241.01 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(bromomethyl)-6-(trifluoromethyl)pyridazine CAS 1173897-85-2 chemical structure

Description

CATO manufactures 3-(bromomethyl)-6-(trifluoromethyl)pyridazine 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.

CATO supplies 3-(bromomethyl)-6-(trifluoromethyl)pyridazine (CAS 1173897-85-2), a certified reference material (molecular formula C6H4BrF3N2, MW 241.01 g/mol) for analytical method development and quality control.

The molecular framework of 3-(bromomethyl)-6-(trifluoromethyl)pyridazine (C6H4BrF3N2) is characterized by a nitrile group, fluorine/bromine substitution, an aromatic ring system. 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.

Physical & Chemical Properties

Molecular FormulaC6H4BrF3N2
Molecular Weight241.01 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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.)1989
Halogen ContentF/Br-containing
Nitrogen Atoms2

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