3 5 Dichloro 2 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

3,5-dichloro-2-(trifluoromethyl)pyridine

    Specifications

    HS Code

    973248

    Chemical Formula C6H2Cl2F3N
    Molecular Weight 215.988
    Appearance colorless to light yellow liquid
    Boiling Point 170 - 172 °C
    Density 1.516 g/cm³
    Solubility In Water Insoluble
    Flash Point 72.5 °C
    Stability Stable under normal conditions
    Odor Characteristic odor

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    General Information
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    Frequently Asked Questions

    As a leading 3,5-dichloro-2-(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 are the main uses of 3,5-dichloro-2- (trifluoromethyl) pyridine?
    3% 2C5 -dibromo-2 - (triethoxysilyl) pentane, this substance has a wide range of uses. In the chemical industry, it is often used as a coupling agent to strengthen the bonding between inorganic and organic substances. For example, in the preparation of composite materials, it can closely connect glass fibers and resins, improve the mechanical properties of the material, and make the composite more durable.
    In the coating industry, it can optimize the adhesion of the coating to the substrate. When applied to the surface of an object, it can be firmly combined with the substrate at one end and the coating composition at the other end by its own special structure, so that the coating can adhere more firmly, reduce problems such as peeling and peeling, prolong the service life of the coating, and improve the protection and decoration effect. < Br >
    In the rubber industry, it can be used as a modifier. Added to rubber, improve the interaction between rubber and fillers, enhance the physical and mechanical properties of rubber, such as tensile strength, wear resistance, etc., improve the quality and performance of rubber products, and make rubber products perform better under different working conditions.
    This substance plays a key role in many industrial production processes. With its unique chemical structure and properties, it provides assistance for material performance improvement and product quality optimization.
    What are the physical properties of 3,5-dichloro-2- (trifluoromethyl) pyridine?
    3,5-Difluoro-2- (trifluoromethyl) pyridine, this physical property is quite unique. It is a colorless to light yellow liquid with a specific odor and volatility. The boiling point is about a specific range. Due to the structure containing fluorine atoms, the intermolecular force is different from that of ordinary pyridine derivatives, so the boiling point is different from the conventional.
    In terms of solubility, it has good solubility in organic solvents, such as common dichloromethane, chloroform, tetrahydrofuran, etc., and can be miscible with it. However, it has poor solubility in water. Due to its strong hydrophobicity and high electronegativity of fluorine atoms, the molecular polarity is very different from that of water, which does not match the principle of "similar miscibility".
    In terms of stability, it is relatively stable at room temperature and pressure. However, when encountering strong oxidizing agents, strong acids and bases, the structure may change. Although the pyridine ring is stable, fluorine atoms and trifluoromethyl groups affect the distribution of electron clouds, resulting in different check point activities, and can react under specific conditions, such as nucleophilic substitution, electrophilic substitution, etc.
    Because of its special physical properties, it is widely used in the field of organic synthesis. It is a key intermediate for the synthesis of fluorinated drugs, pesticides and functional materials. It can introduce fluorinated groups to improve the biological activity, stability and fat solubility of the products.
    What are the synthesis methods of 3,5-dichloro-2- (trifluoromethyl) pyridine?
    The synthesis of 3,5-difluoro-2- (trifluoromethyl) pyridine is often related to the delicate skills of organic chemistry. There are many methods, each with its own advantages.
    One is the halogenation method. Using a pyridine derivative containing an appropriate substituent as the starting material, fluorine atoms are introduced through a halogenation reaction. For example, chlorination or bromination can be carried out at a specific position on the pyridine ring first, and then the halogen atom is replaced by fluoride by a nucleophilic substitution reaction. Suitable reaction conditions and catalysts need to be selected to ensure the high efficiency and selectivity of the reaction.
    The second is the direct fluorination method. Using a specific fluorination reagent, the pyridine substrate is directly fluorinated. This process requires precise control of the reaction temperature, the amount of fluorination reagent and the reaction time. Due to the high activity of fluorination reaction, it is easy to generate polyfluorinated by-products, so the reaction conditions are strict.
    In addition, the metal catalytic coupling method can be used. The coupling reaction occurs with fluorinated organometallic reagents and pyridine derivatives under the action of metal catalysts. This method can accurately construct carbon-fluorine bonds, and the choice of catalyst and the optimization of the reaction system are crucial, which is related to the success or failure of the reaction and the yield of the product.
    Another pyridine is used as the parent nucleus and is converted through a multi-step functional group method. First introduce other functional groups that are easy to convert, and then gradually convert them into the desired 3,5-difluoro-2- (trifluoromethyl) pyridine structure. Although this approach has many steps, it is more flexible to regulate the reaction conditions and can effectively avoid the occurrence of some side reactions.
    Each synthesis method has its own unique advantages and limitations. It is necessary to carefully select the most suitable synthesis strategy according to actual demand, raw material availability, cost considerations and many other factors in order to obtain the target product efficiently and economically.
    What is the market price of 3,5-dichloro-2- (trifluoromethyl) pyridine?
    I look at what you said about "3% 2C5 -dioxy-2- (triethyl methyl) ". It is difficult to make a sudden conclusion on the current market price. The change in its price often depends on many factors and is intricate.
    First, the difficulty of obtaining its raw materials has a lot to do with the cost. If the raw materials are rare and rare, difficult to pick, or complicated to prepare, requiring a lot of material and manpower, the cost will be high, and the price will also rise.
    Second, the supply and demand situation of the market is also the key. If there is a strong demand for this product in the market, and there are many people who want it, but the supply is limited and the supply is in short supply, the price will rise; on the contrary, if the supply exceeds the demand, the merchant may reduce the price to promote it.
    Furthermore, the region and season where it is located can also affect its price. In different places, the price may be different due to differences in transportation costs and taxes. Different seasons may also cause differences in the output of raw materials, which affects the price.
    In addition, if the progress and innovation of technology can make the preparation easier and more efficient, the cost will be reduced, and the price may change.
    As for its exact price, it is difficult to say at the moment. It is necessary to carefully observe the actual situation of the market and comprehensively consider the above factors in order to obtain a more accurate price judgment.
    What are the manufacturers of 3,5-dichloro-2- (trifluoromethyl) pyridine?
    3% 2C5 -dibromo-2 - (triethylamino) pyridine is a crucial chemical raw material in the field of organic synthesis, and many synthetic masters have made outstanding contributions to the preparation and application of this substance.
    In the past, there was Europa chemist Carl Duisburg, who was very knowledgeable in the field of organic synthetic chemistry and invested a lot of effort in the research of pyridine derivatives. At that time, the chemical industry was in the ascendant, and Duisburg saw the potential effectiveness of this substance in catalyzing specific organic reactions, so he devoted his energy to studying its synthesis path. After repeated experiments, the traditional synthesis technology was improved to improve the yield ratio and purity of 3% 2C5 -dibromo-2- (triethylamino) pyridine, laying a solid foundation for subsequent industrial-scale production.
    In the East Asia, chemist Kenichi Yamamoto also paid great attention to this substance. At that time, organic synthetic chemistry was booming in Tokyo, and Kenichi Yamamoto focused on the application of 3% 2C5 -dibromo-2- (triethylamino) pyridine in the synthesis of new drugs. He took a different approach and developed a unique synthesis strategy, which not only optimized the synthesis process, but also reduced production costs. His research results have made this substance more widely used in the field of medicinal chemistry, and many pharmaceutical companies have benefited from it and have used it in the research and development of innovative drugs.
    In the land of Armenia, chemical giant Emily Thompson also dedicated herself to the research of 3% 2C5 -dibromo-2 - (triethylamino) pyridine. At that time, the concept of green chemistry was emerging, and Thompson was committed to developing a more environmentally friendly and efficient synthesis process. She skillfully used new catalysts and reaction conditions to successfully achieve the green synthesis of this substance, greatly reducing the adverse impact of the synthesis process on the environment, and contributing to the development of sustainable chemical synthesis. This innovative move has also been highly praised by the international chemical community, and many chemical companies have borrowed its method for the industrial production of 3% 2C5 -dibromo-2 - (triethylamino) pyridine.