3-(4-Fluorophenyl)-6-((pyridin-4-ylmethyl)thio)pyridazine CAS 899740-41-1

Purity 97%+In StockPharmaceutical Standards
CAS No.899740-41-1
Molecular FormulaC16H12FN3S
Molecular Weight297.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Fluorophenyl)-6-((pyridin-4-ylmethyl)thio)pyridazine CAS 899740-41-1 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-(4-Fluorophenyl)-6-((pyridin-4-ylmethyl)thio)pyridazine (CAS 899740-41-1) is a high-purity analytical reference standard with the molecular formula C16H12FN3S and a molecular weight of 297.35 g/mol.

The molecular framework of 3-(4-Fluorophenyl)-6-((pyridin-4-ylmethyl)thio)pyridazine (C16H12FN3S) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, sulfur-containing functionality, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 3-(4-Fluorophenyl)-6-((pyridin-4-ylmethyl)thio)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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