3-((2-Fluorobenzyl)thio)-6-(pyridin-2-yl)pyridazine CAS 893993-99-2

Purity 97%+In StockPharmaceutical Standards
CAS No.893993-99-2
Molecular FormulaC16H12FN3S
Molecular Weight297.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((2-Fluorobenzyl)thio)-6-(pyridin-2-yl)pyridazine CAS 893993-99-2 chemical structure

Description

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.

3-((2-Fluorobenzyl)thio)-6-(pyridin-2-yl)pyridazine (CAS 893993-99-2), molecular formula C16H12FN3S and molecular weight 297.35 g/mol, is a CATO reference standard with documented purity and traceability.

3-((2-Fluorobenzyl)thio)-6-(pyridin-2-yl)pyridazine (C16H12FN3S) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures 3-((2-Fluorobenzyl)thio)-6-(pyridin-2-yl)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.

Physical & Chemical Properties

Molecular FormulaC16H12FN3S
Molecular Weight297.35 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms3
Sulfur Atoms1

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