2 Hydroxy 5 Trifluoromethylpyridine
pyridine pyrrole pyrazine piperidine piperazine

2-hydroxy-5-trifluoromethylpyridine

    Specifications

    HS Code

    751257

    Chemical Formula C6H4F3NO
    Appearance Typically a colorless to light - yellow liquid or solid
    Boiling Point Approximately 190 - 195 °C
    Melting Point Data may vary, but around -20 to - 10 °C
    Density Around 1.4 - 1.5 g/cm³
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
    Pka Value Indicative of its acidic or basic nature in solution, data around 3 - 4
    Odor May have a characteristic pyridine - like odor
    Flash Point Caution in handling due to flammability, flash point around 70 - 80 °C

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    Frequently Asked Questions

    As a leading 2-hydroxy-5-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 main uses of 2-hydroxy-5-trifluoromethylpyridine?
    2-% hydroxymethyl-5-trifluoromethyl pyridine is a crucial chemical intermediate in the field of organic synthesis, and is widely used in many fields such as medicinal chemistry, pesticide chemistry, and materials science. The details are as follows:
    - ** Medicinal chemistry field **: Because its structure contains fluorine atoms and pyridine rings, it endows the compound with unique physical and chemical properties, such as enhancing lipophilicity, making it easier for the drug to pass through the biofilm and improve bioavailability. And the introduction of fluorine atoms can change the distribution of molecular electron clouds, enhance metabolic stability, and prolong the action time of drugs. For example, in some innovative drug development for the treatment of cardiovascular diseases and nervous system diseases, 2-% hydroxymethyl-5-trifluoromethylpyridine is used as a key intermediate to chemically modify complex active molecular structures to achieve targeted therapy and high efficiency and low toxicity.
    - ** Pesticide Chemistry Field **: With its unique structural characteristics, high efficiency, low toxicity and environmentally friendly pesticide products can be developed. Pyridine ring structure has certain biological activity to insects, fungi, etc. The introduction of fluorine atoms can enhance its affinity and inhibition to specific targets. For example, some new insecticides and fungicides, using 2-% hydroxymethyl-5-trifluoromethyl pyridine as the starting material, can be synthesized through multi-step reaction, which can effectively control crop diseases and pests, while reducing the impact on the environment and non-target organisms, in line with the development needs of modern green agriculture.
    - ** Material Science Field **: It can be used to prepare functional materials with special properties. For example, in organic optoelectronic materials, the introduction of this structure can adjust the electronic transport properties and fluorescence properties of the material. By combining with other conjugated structural units, an organic Light Emitting Diode (OLED) material with high fluorescence quantum yield, good thermal stability and chemical stability can be prepared. It is used in the field of display technology to improve display effect and device life. In addition, in terms of polymer material modification, it can participate in the polymerization reaction as a functional monomer, endowing the polymer material with special properties, such as corrosion resistance and UV resistance.
    What are the physical properties of 2-hydroxy-5-trifluoromethylpyridine?
    2-% fluoro-5-trifluoromethyl pyridine is an organic compound with special physical properties, which has attracted much attention in the fields of chemical industry and medicine. Its physical properties are as follows:
    - ** Appearance and Properties **: At room temperature and pressure, it is mostly colorless to light yellow liquid, pure and transparent. In specific experimental or industrial scenarios, white solid forms can also be seen. Due to the relatively low melting point of the compound, changes in external conditions can easily cause phase changes.
    - ** Melting Boiling Point **: The melting point is about -20 ° C, and the boiling point is between 140 and 145 ° C. This kind of melting and boiling point characteristic allows the compound to exist stably in a liquid state in a conventional temperature environment, and then when heated to near the boiling point, it quickly vaporizes into a gaseous state. This property is crucial for the temperature regulation of organic synthesis reactions, which is conducive to the phase conversion and separation and purification of compounds during the reaction process.
    - ** Solubility **: It exhibits good solubility in organic solvents, such as common dichloromethane, chloroform, toluene, etc., which can be miscible with 2-fluoro-5-trifluoromethyl pyridine in any ratio. Due to the similar chemical properties of the compound molecular structure and organic solvents, it follows the principle of "similar miscibility"; but it has poor solubility in water because of its large difference in molecular polarity and water molecules, limiting its application in aqueous systems. However, it has an advantage in organic phase reaction systems and can participate in organic reactions efficiently. < Br > - ** Density **: The density is about 1.4 g/cm ³, which is slightly higher than that of water, causing it to settle at the bottom when mixed with water, forming an obvious stratification phenomenon, which provides convenience for the separation of the mixed system containing the compound. By simple liquid separation operation, the compound and the aqueous substance can be preliminarily separated.
    - ** Volatility and odor **: It has a certain volatility and emits a special odor in the air. Although it is difficult to describe accurately, it has a unique identification. It is similar to a slightly irritating odor. The operation needs to be carried out in a well-ventilated environment to avoid excessive inhalation and harm to the human body.
    What are the synthesis methods of 2-hydroxy-5-trifluoromethylpyridine?
    There are many methods for the synthesis of 2-% pentyl-5-trifluoromethyl pyridine, which are described in ancient methods. I hope it will be helpful.
    First, pyridine is used as a group, and a halogenation reaction is carried out to introduce a halogen atom, such as bromine or chlorine, at a specific position in the pyridine ring. This step requires selecting a suitable halogenation reagent, such as N-bromosuccinimide (NBS) or a halogen elemental substance catalyzed by iron halide. Subsequently, a Grignard reagent is made from a metal reagent, such as magnesium, or reacted with a lithium reagent to generate a corresponding organometallic intermediate. This intermediate is highly active and can react with reagents containing trifluoromethyl, such as trifluoromethyl halide magnesium or trifluoromethyl sul At the same time, through the alkylation reaction, the halogenated pentane interacts with the base, and the pentyl group is introduced at another position of the pyridine ring, which can promote the reaction through a phase transfer catalyst and improve the yield.
    Second, the heterocyclic synthesis method is adopted. Nitrogen-containing and suitable carbon chain precursors, such as 2-amino-3-pentyl pyridine derivatives and trifluoromethyl-containing β-dicarbonyl compounds, are condensed under acidic or basic catalysis to construct the pyridine ring. P-toluenesulfonic acid can be used for acidic conditions, and potassium carbonate can be used for alkaline conditions. This process requires controlling the reaction temperature and time to obtain the target product. After the reaction, it is separated and purified, such as column chromatography, to obtain pure 2-pentyl-5-trifluoromethyl pyridine.
    Third, the coupling reaction is catalyzed by transition metals. Halogenated pyridine derivatives, which contain both halogen atoms, are conducive to the introduction of trifluoromethyl groups, and have suitable substituents to be connected to amyl groups. In the presence of transition metal catalysts and ligands such as palladium or nickel, it is coupled with trifluoromethylborate or trifluoromethyltin reagents to introduce trifluoromethyl groups. At the same time, or successively with reagents such as amyl borate, through similar coupling reactions, the amyl group is connected at another position. This method requires precise control of catalyst dosage, reaction solvent and reaction atmosphere. Anhydrous and anaerobic conditions are often the key to ensure the smooth progress of the reaction and improve the purity and yield of the product.
    What are the precautions for storing and transporting 2-hydroxy-5-trifluoromethylpyridine?
    2-%E7%BE%9F%E5%9F%BA - 5-%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%E5%90%A1%E5%95%B6%E7%94%A8%E4%BA%8E%E5%82%A8%E5%AD%98%E4%B8%8E%E8%BF%90%E8%BE%93%E8%BF%87%E7%A8%8B%E6%97%B6, you need to pay attention to the following things:
    First, this object has special properties and is quite picky in the storage environment. It should be placed in a cool, dry and well-ventilated place, and must not be near fire or heat sources to prevent it from changing due to excessive temperature. If it is in a humid place, it is easy to cause it to come into contact with water vapor or undergo biological changes, which will damage its quality and efficiency.
    Second, when handling, be sure to handle it with care. Because of its structure or fragile, if it is violently vibrated or collided, it may cause damage to the internal structure, which will affect subsequent use. The person handling should be cautious and follow the correct method to ensure its integrity.
    Third, when storing, it should be placed separately from other chemicals. Because of its unique chemical properties, if it coexists with inappropriate chemicals or reacts chemically, it will not only destroy itself, but also may cause dangerous conditions, such as fire, explosion, etc., endangering the safety of the surrounding.
    Fourth, pay close attention to its storage period. Every time, its quality may change, beyond a specific time limit, its performance may not meet expectations. Therefore, it needs to be checked regularly, and its use should be reasonably arranged according to its condition and duration to avoid adverse consequences caused by the use of expired materials.
    Fifth, during the entire storage and transportation process, relevant personnel need to be familiar with the characteristics and precautions of this material. Through training, make them understand how to deal with emergencies, such as leaks, fires, etc. Prepare corresponding emergency equipment and materials so that they can be dealt with quickly and properly at the beginning of the accident to minimize harm.
    What are the effects of 2-hydroxy-5-trifluoromethylpyridine on the environment and human health?
    Fu2-cyano-5-trifluoromethylpyridine is a kind of organic compound. Its impact on the environment and human health cannot be ignored.
    As far as the environment is concerned, if this compound is released in nature, it may disturb the ecology of soil and water. In soil, or change the structure and function of soil microbial community. Microorganisms play a great role in soil material circulation and nutrient transformation. The existence of this compound may inhibit the growth and reproduction of some beneficial microorganisms, causing damage to soil fertility and affecting plant growth. In water, or bring bad luck to aquatic organisms. Fish, plankton, etc. are very sensitive to chemicals in water. It may interfere with the physiological processes of aquatic organisms, such as respiration, reproduction, etc., and even cause a decrease in population and damage the balance of aquatic ecology.
    As for human health, it also has potential threats. If ingested through respiration, skin contact or diet, it may affect the normal physiological functions of the human body. In the nervous system, it may interfere with the transmission of neurotransmitters, causing headaches, vertigo, fatigue, etc. In the immune system, or weaken the immune function, making people susceptible to diseases. And long-term exposure to this compound environment may increase the risk of cancer. Because some of these structures may have mutagenic effects, causing cell gene mutations and carcinogenesis. < Br >
    Therefore, the use and discharge of 2-cyano-5-trifluoromethylpyridine should be treated with caution. Strict supervision and proper handling are required to reduce its harm to the environment and human health, and to maintain ecological harmony and human health.