3 Chloro 2 Chloromethyl 6 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3-chloro-2-(chloromethyl)-6-(trifluoromethyl)pyridine

    Specifications

    HS Code

    796189

    Chemical Formula C7H4Cl2F3N
    Molar Mass 229.994 g/mol
    Appearance likely a solid or liquid (no definite color given, often colorless to pale yellow in related compounds)
    Physical State state may vary depending on temperature, typically solid or liquid at room conditions
    Boiling Point no standard value found (but boiling points of similar pyridine derivatives can range from 150 - 300 °C)
    Melting Point no standard value found
    Solubility soluble in organic solvents like dichloromethane, chloroform; likely insoluble in water
    Density no standard value found (but similar halogen - containing pyridines have densities around 1.4 - 1.6 g/cm³)
    Flash Point no standard value found
    Vapor Pressure no standard value found (but lower for solids and higher for liquids, usually in the range of 10^-5 - 10^-1 mmHg at room temperature for similar compounds)
    Pka no standard value found (but pyridine derivatives typically have pKa values around 5 - 6 for the pyridinium ion formation)

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    General Information
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    Frequently Asked Questions

    As a leading 3-chloro-2-(chloromethyl)-6-(trifluoromethyl)pyridine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the main use of 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine
    3-Chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine is a crucial compound in the field of organic synthesis. Its main uses are widely found in various industries such as medicine and pesticides.
    In the field of medicine, this compound is often used as a key intermediate to synthesize various specific drugs. Due to its unique chemical structure, the prepared drug has excellent biological activity and pharmacological properties. Through a carefully designed organic synthesis path, it can be skillfully converted into therapeutic drugs for specific diseases, such as antibacterial and antiviral drugs, which contribute greatly to human health and well-being.
    In the pesticide industry, 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine also plays a pivotal role. Often used as an important raw material for the synthesis of high-efficiency pesticides, the pesticides produced have excellent insecticidal and herbicidal properties. Due to its structural characteristics, it can effectively act on specific physiological targets of pests, accurately combat pests and diseases, and has a relatively slight impact on the environment, which is in line with the needs of the development of modern green agriculture.
    In addition, in the fields of materials science, this compound is also occasionally used. With its special chemical properties, it can participate in the synthesis of materials with special properties, providing new opportunities for innovation and development in related fields.
    In summary, 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine has shown indispensable value in many industries due to its unique structure and properties. It is indeed a widely used and significant compound in the field of organic chemistry.
    What are the synthesis methods of 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine
    The synthesis method of 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine covers various routes. The first method is to start from the compound containing the pyridine structure and introduce chlorine atoms through halogenation reaction. First, take an appropriate pyridine derivative, and under specific reaction conditions, such as in a suitable solvent, use a specific halogenating agent, such as thionyl chloride, phosphorus oxychloride, etc. to interact with it. Control the reaction temperature, time and reagent dosage, so that chlorine atoms are successfully introduced at specific positions on the pyridine ring, that is, at positions 3 and 2-chloromethyl, and trifluoromethyl is introduced at positions 6. This process requires fine regulation of the reaction conditions. Due to the high activity of halogenation reaction, if you are not careful, there will be a lot of side reactions.
    Another method can be used to construct a pyridine ring through multi-step reaction. First, a suitable organic small molecule is used as the raw material, and the pyridine ring skeleton is formed through condensation, cyclization and other reactions. For example, in the presence of a catalyst, a condensation reaction occurs under a certain temperature and pressure conditions to initially form a pyridine ring structure. Then, through halogenation, substitution and other reactions, chlorine atoms and trifluoromethyl groups are precisely introduced into the pyridine ring at the designated position. Although this approach has many steps, it can precisely control the position and quantity of each substituent in the pyridine ring, and improve the purity and yield of the product.
    In addition, transition metal catalysis is also used. Transition metal catalysts, such as palladium, copper and other complexes, are used to catalyze the coupling reaction of halogenated aromatics with fluorine and chlorine-containing alkenes or alkynes to construct pyridine rings and introduce the desired substituents at the same time. This method has relatively mild reaction conditions and good selectivity, but requires high catalyst requirements. Appropriate ligands and reaction conditions need to be screened to optimize reaction efficiency and product selectivity.
    All synthetic methods have their own advantages and disadvantages. In practical application, it is necessary to comprehensively consider factors such as raw material availability, cost, product purity and yield, and choose the optimal method to prepare 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine.
    What are the physical properties of 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine
    3-Chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine, this is an organic compound. Its physical properties are as follows:
    Looking at its properties, it is either a colorless to light yellow liquid or a crystalline solid under normal conditions, depending on the ambient temperature and pressure. Its color is closely related to its purity. The higher the purity, the closer the color is to colorless.
    When it comes to the melting point, there is no exact literature that accurately specifies the melting point value of this specific compound. However, it can be speculated from the structural characteristics that, in view of the presence of groups such as chlorine atoms, chloromethyl and trifluoromethyl in the molecule, these groups interact with each other, or cause intermolecular forces to increase, thereby increasing the melting point.
    In terms of boiling point, similarly, there is no conclusive literature data. However, due to the existence of many halogen atoms in the molecule, the electronegativity of the halogen atom is large, which enhances the polarity of the molecule and increases the intermolecular force, so the boiling point may be relatively high.
    Solubility is also an important property. From the structural analysis, the compound contains a pyridine ring, which has a certain polarity, and chlorine atoms, chloromethyl and trifluoromethyl also affect the molecular polarity. Therefore, it may have a certain solubility in polar organic solvents such as methanol, ethanol, acetone, etc.; while in non-polar solvents such as n-hexane and cyclohexane, the solubility may be relatively small.
    In terms of density, due to the relatively large atomic mass of elements such as chlorine and fluorine, its density may be greater than that of water.
    In terms of volatility, due to the relatively large intermolecular force, volatility or weak, it is difficult to volatilize into the air at room temperature and pressure.
    The above physical properties have a profound impact on their application in chemical synthesis, drug development and other fields. In chemical synthesis, the melting point and boiling point are related to the separation and purification operation; solubility determines the choice of reaction solvent. In drug development, these properties affect the pharmacokinetic properties such as drug absorption and distribution.
    What are the precautions for 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine in storage and transportation?
    3-Chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine is an important chemical substance in the field of organic synthesis. When storing and transporting this substance, many key precautions must be observed.
    The first priority is to choose the storage environment. This substance should be stored in a cool, dry and well-ventilated place. Due to the fact that the substance is exposed to heat or humidity, it may cause decomposition or other chemical reactions that may damage the quality. Therefore, strict control of temperature and humidity is essential. Warehouse temperature should be maintained within a specific range, humidity must also be constant, and the warehouse should be kept away from fire and heat sources to avoid accidents.
    Furthermore, packaging should not be ignored. Sealed packaging must be used to prevent it from coming into contact with air, oxidation or other reactions. The selection of packaging materials is also crucial, and good corrosion resistance is required to resist the possible erosion of the substance and ensure the integrity of the packaging.
    During transportation, it is necessary to ensure that the container does not leak, collapse, fall or damage. Because of its certain danger, the transportation vehicle must be equipped with corresponding emergency treatment equipment and protective equipment. When transporting, follow the specified route and do not stop in densely populated areas and open flames to prevent serious harm to the surrounding people and the environment in the event of a leakage accident.
    When handling this substance, operators should strictly follow the operating procedures and wear appropriate protective equipment, such as gas masks, protective gloves, etc., to avoid direct contact with the substance to prevent harm to the body.
    When storing and transporting 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine, all details of the environment, packaging, transportation and operation should be carefully considered and handled to ensure its safety and stability.
    What is the market price of 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine?
    I don't know where the market is for 3-chloro-2- (chloromethyl) -6- (trifluoromethyl) pyridine. This compound is uncommon, and its cost is affected by many factors.
    First, the location is very important. If it is well-made and the raw materials are easy to obtain, the cost may be slightly reduced; if it is self-biased and the raw materials are not obtained, the cost will increase.
    Second, the cost will be very large. Those with high cost, the degree of improvement will be high, and the technology used will be fine, and the price will naturally be high; those with low cost will be cheap.
    Third, the market supply and demand will be high. If the demand is strong and the supply is limited, the price must be low; if the demand is low, the supply is sufficient, and the price may be reduced.
    Fourth, the amount of batch also plays a role. If the batch is low, the company may benefit, and the price will be reduced; if a small amount is low, the price will be high.
    Because I do not know the above factors, I will determine the market price. If you want to know about it, you can use the chemical products trading platform, the supplier, or you can get it.