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Instruction of 3-Chloro-6-(trifluoromethyl)pyridazine: A Comprehensive Guide for Chemical Industry
3-Chloro-6-(trifluoromethyl)pyridazine, commonly referred to as 3-Cl-6-CF3-Py, is a derivative of pyridazine that has gained significant attention in the chemical industry due to its unique properties and versatile applications.
This compound has been widely used in various fields, including organic synthesis, pharmaceuticals, and materials science.
In this article, we will provide a comprehensive guide to the instruction of 3-Cl-6-CF3-Py, including its synthesis, purification, characterization, storage, transportation, and safety measures.
Synthesis of 3-Cl-6-CF3-Py
The synthesis of 3-Cl-6-CF3-Py can be achieved through various methods, including chemical reactions, electrochemical methods, and organic synthesis.
The chemical reaction method involves the reaction of 3-chloropyridazine with 4-fluoro-6-chloro-s-triazine in the presence of a solvent and a catalyst.
The reaction typically involves heating the mixture at a certain temperature for a specific period of time to yield the desired compound.
The electrochemical method involves the reduction of 4-fluoro-6-chloro-s-triazine using sodium hypophosphite as a reducing agent in a sodium hydroxide solution.
The resulting compound is then treated with chlorine and pyridazine to obtain 3-Cl-6-CF3-Py.
Organic synthesis involves the reaction of 6-chloro-4-fluoro-s-triazine with 3-chloropyridazine in the presence of a solvent and a catalyst.
The reaction is typically carried out at a lower temperature to minimize the formation of unwanted side products.
Purification of 3-Cl-6-CF3-Py
The purification of 3-Cl-6-CF3-Py is typically achieved through several methods, including crystallization, chromatography, and recrystallization.
Crystallization involves the dissolution of the compound in a suitable solvent and allowing it to crystallize out.
The crystals are then collected and dried for further use.
Chromatography involves the separation of the compound from other impurities by passing it through a column packed with a stationary phase.
The compound is then eluted with a suitable solvent to yield pure 3-Cl-6-CF3-Py.
Recrystallization involves the dissolution of the compound in a suitable solvent and allowing it to recrystallize.
The resulting crystals are then collected and dried for further use.
Characterization of 3-Cl-6-CF3-Py
The characterization of 3-Cl-6-CF3-Py is typically achieved through several techniques, including spectroscopy, chromatography, and mass spectrometry.
Spectroscopy involves the analysis of the electronic and vibrational properties of the compound using techniques such as infrared spectroscopy and nuclear magnetic resonance spectroscopy.
Chromatography involves the separation of the compound from other impurities using a suitable column and a suitable solvent.
The eluted compound is then collected and analyzed to determine its purity and identity.
Mass spectrometry involves the analysis of the molecular mass of the compound by ionizing it and fragmenting it in a mass spectrometer.
The resulting mass spectrum provides information on the molecular structure and elemental composition of the compound.
Storage of 3-Cl-6-CF3-Py
The storage of 3-Cl-6-CF3-Py is typically carried out in a cool, dry, and well-ventilated area, away from sources