2 Hydroxy 3 Trifluoromethylpyridine
pyridine pyrrole pyrazine piperidine piperazine

2-hydroxy-3-trifluoromethylpyridine

    Specifications

    HS Code

    959330

    Chemical Formula C6H4F3NO
    Molecular Weight 163.097
    Appearance Colorless to light yellow liquid
    Boiling Point 176 - 178 °C
    Density Around 1.402 g/cm³
    Flash Point 72 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Pka Approx. 2.85
    Vapor Pressure Low at room temperature
    Odor Characteristic pyridine - like odor

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    General Information
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    Frequently Asked Questions

    As a leading 2-hydroxy-3-trifluoromethylpyridine 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 physical properties of 2-hydroxy-3-trifluoromethylpyridine?
    2-Hydroxy-3-trifluoromethylpyridine is one of the organic compounds. Its physical properties are quite unique, and they are described in detail today.
    First of all, its appearance, under normal conditions, is mostly white to light yellow crystalline powder, this appearance is clearly recognizable, like fine sand particles agglomerate, fine texture, and it looks quite textured.
    As for the melting point, it is about 132-134 ° C. When the temperature gradually rises, the substance slowly converts from solid to liquid, just like ice and snow melting. This melting point characteristic is of great significance in the identification and purification of the substance.
    Its solubility also has characteristics. It is slightly soluble in water, but soluble in organic solvents such as ethanol, ether, chloroform, etc. In water, it can only dissolve in a small amount, just like oil drops into water, and it is difficult to dissolve; in organic solvents, it can be better dispersed, just like fish entering water, swimming freely. This difference in solubility provides a variety of options for it in different chemical reactions and separation operations.
    Furthermore, the stability of this substance is also worthy of attention. Under normal conditions, its properties are still stable, but when it encounters strong oxidizing agents, strong acids, strong bases, etc., it is prone to chemical reactions and its stability is broken.
    In terms of density, although there is no exact universal value, its density is similar to that of common organic compounds. In specific chemical processes and product designs, this density characteristic also affects the mixing and separation of materials.
    In addition, 2-hydroxy-3-trifluoromethyl pyridine has certain fat-solubility and hydrophobicity due to the fluorine atoms in its molecular structure. This property makes it a unique advantage in the design and synthesis of compounds with specific physiological activities in the fields of medicinal chemistry, pesticide chemistry, etc.
    Looking at its physical properties, each property is interrelated and plays an important role in many fields such as organic synthesis, pharmaceutical research and development, materials science, etc., laying a solid foundation for related research and applications.
    What are the chemical properties of 2-hydroxy-3-trifluoromethylpyridine?
    2-Hydroxy-3-trifluoromethyl pyridine is one of the organic compounds. Its chemical properties are unique and worth exploring.
    This compound is weakly acidic, and its hydroxyl group can ionize a small amount of hydrogen ions. Under specific conditions, the hydroxyl group can participate in many reactions, such as esterification reactions. When confronted with suitable acids and catalysts, the hydrogen atom in the hydroxyl group can be replaced by other groups to form new ester compounds.
    Furthermore, its pyridine ring also has certain activity. The nitrogen atom on the pyridine ring is rich in solitary pairs of electrons, which can be used as an electron donor to participate in coordination reactions and form complexes with metal ions. Moreover, the pyridine ring can undergo electrophilic substitution reaction. Due to the electronegativity of nitrogen atoms, the electron cloud density at different positions on the pyridine ring varies, which in turn determines the position of the electrophilic agent attack.
    In addition, the existence of trifluoromethyl greatly changes the properties of the molecule. Trifluoromethyl has strong electron-absorbing properties, which can redistribute the electron cloud density of the whole molecule, affecting the stability and reactivity of the compound. It can enhance the lipid solubility of the molecule and have an effect on the solubility of the compound in different solvents. In some reactions, trifluoromethyl can be used as a stable functional group to improve the chemical stability and thermal stability of the product.
    In the field of organic synthesis, 2-hydroxy-3-trifluoromethylpyridine is often used as a key intermediate. With its diverse reactivity, it can be used to construct complex organic molecules, and has important application prospects in many fields such as medicinal chemistry and materials science.
    What are the main uses of 2-hydroxy-3-trifluoromethylpyridine?
    2-Hydroxy-3-trifluoromethylpyridine is widely used in the field of chemical medicine. It is first used in the creation of drugs and is an essential material for pharmaceutical synthesis. Here, it can be used as an intermediate to prepare new drugs with special curative effects. For example, in the synthesis of some antibacterial and anti-inflammatory drugs, 2-hydroxy-3-trifluoromethylpyridine participates in the construction of key structures, so that the drug has better biological activity and targeting.
    Furthermore, it also has outstanding performance in the field of pesticide creation. Based on this, high-efficiency and low-toxicity pesticides can be developed to help agricultural pest control. Due to its special structure, the pesticides produced may have strong insecticidal and bactericidal properties, and are environmentally friendly, with less residues, can protect ecological balance, and ensure the quality and safety of agricultural products.
    In addition, in the field of materials science, 2-hydroxy-3-trifluoromethylpyridine is also useful. It can be used to synthesize special polymer materials, giving materials unique properties, such as enhancing the corrosion resistance and heat resistance of materials, broadening their application scenarios, and showing their strengths in high-end fields such as aerospace and electronics.
    In summary, 2-hydroxy-3-trifluoromethylpyridine, with its special chemical structure, is an indispensable raw material in many fields such as medicine, pesticides, and materials, promoting technological innovation and development in various fields.
    What are 2-hydroxy-3-trifluoromethylpyridine synthesis methods?
    The synthesis method of 2-hydroxy-3-trifluoromethyl pyridine can be achieved by various paths. First, 3-trifluoromethyl pyridine is used as the starting material, and hydroxyl groups are introduced into the 2-position of the pyridine ring through oxidation reaction. This process requires careful selection of suitable oxidizing agents, such as hydrogen peroxide, peroxyacid, etc. The reaction conditions also need to be carefully controlled, and the temperature, reaction time, and proportion of reactants are all related to success or failure. If the temperature is too high, it may cause a cluster of side reactions; if it is too low, the reaction rate will be slow and take a long time.
    Furthermore, the structure of 2-hydroxy-3-trifluoromethyl pyridine can be constructed by nucleophilic substitution reaction starting from pyridine derivatives containing specific substituents. For example, 3-trifluoromethyl-2-halogenated pyridine is used as a substrate to react with nucleophiles, such as alkoxides and phenols, under suitable conditions. In this pathway, the halogen atom activity of halogenated pyridine, the nucleophilic property of nucleophilic reagents, and the properties of the reaction solvent are all key elements. If the halogen atom is highly active, the reaction is easy to proceed; the nucleophilic reagent has strong nucleophilic property, which is also conducive to the advancement of the reaction. Suitable solvents can both dissolve the reactants and promote the reaction. For example, polar aprotic solvents are often the best choice for such reactions.
    Or, the coupling reaction strategy of metal catalysis is adopted. Pyridine derivatives containing 2-position activity check point and reagents containing trifluoromethyl are coupled under the action of metal catalysts, and then trifluoromethyl is introduced, and then through appropriate conversion reactions, hydroxyl groups are formed at the 2-position. Among these, the choice of metal catalysts is of paramount importance. Common metal catalysts such as palladium and nickel have different catalytic activities and selectivity. And the factors such as ligands and bases in the reaction system also have a profound impact on the reaction. The ligand can adjust the electron cloud density and steric resistance of the metal catalyst, which in turn affects the catalytic activity and selectivity; the base participates in the reaction mechanism and affects the reaction process.
    There are many ways to synthesize 2-hydroxy-3-trifluoromethylpyridine. However, in order to achieve high-efficiency and high-selectivity synthesis, it is necessary to carefully consider each reaction element according to the specific situation, and carefully select the appropriate synthesis path.
    2-hydroxy-3-trifluoromethylpyridine to pay attention to when storing and transporting
    2-Hydroxy-3-trifluoromethyl pyridine is an important raw material for organic synthesis. When storing and transporting, many key matters need to be paid attention to to to ensure its quality and safety.
    First, the storage place must be dry and well ventilated. This substance is easy to absorb moisture, and humid environment will cause it to deteriorate, which will affect subsequent use. Therefore, a dry place should be selected, and ventilation can disperse volatile gases that may accumulate in time, reducing safety risks.
    Second, temperature control is crucial. It should be stored in a cool place to avoid high temperature. High temperature will accelerate its chemical reaction, cause decomposition or polymerization, and reduce its active ingredients. Usually, the suitable storage temperature is between 2-8 ° C, depending on the product characteristics and instructions.
    Third, the packaging should be tight. Use suitable packaging materials, such as glass bottles or specific plastic containers, to prevent leakage. Leakage not only causes material loss, but also may pollute the environment and cause safety accidents.
    Fourth, be firmly fixed during transportation. Avoid violent vibration and collision, as it may cause damage to the package. The transportation tool also needs to be clean and dry, and there are no other substances that may react with it.
    Fifth, strictly distinguish between storage and transportation. This substance should be separated from oxidants, acids, etc. Contact between the two can easily cause dangerous chemical reactions, such as combustion and explosion.
    Sixth, follow the regulations. Storage and transportation must be strictly in accordance with regulations, personnel should have professional knowledge and skills, and take protective measures, such as wearing protective gloves, glasses, etc.
    Only by paying attention to the above items can we ensure the safety and quality of 2-hydroxy-3-trifluoromethylpyridine during storage and transportation, and avoid accidents and losses.