4 Propanolpyridine
pyridine pyrrole pyrazine piperidine piperazine

4-propanolpyridine

    Specifications

    HS Code

    247496

    Name 4 - propanolpyridine
    Molecular Formula C8H11NO
    Molar Mass 137.18 g/mol
    Appearance Solid (usually)
    Odor Characteristic
    Melting Point Data needed
    Boiling Point Data needed
    Density Data needed
    Solubility In Water Data needed
    Solubility In Organic Solvents Data needed
    Flash Point Data needed
    Vapor Pressure Data needed
    Ph Data needed
    Stability Data needed

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    General Information
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    Frequently Asked Questions

    As a leading 4-propanolpyridine 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 chemical structure of 4-propanolpyridine?
    4-Propanolpyridine is an organic compound whose chemical structure contains a pyridine ring and a propanolyl group is attached to the 4th position of the pyridine ring. The pyridine ring has a six-membered nitrogen-containing heterocyclic structure, which is formed by five carbon atoms and one nitrogen atom connected by a conjugated double bond. It presents a planar structure and has aromatic properties. This structure endows the pyridine ring with certain stability and unique electronic properties. The propanolpyridine group attached to the 4th position of the pyridine ring is a straight-chain alkyl group containing three carbon atoms, with a hydroxyl group (-OH) attached at the end. Hydroxyl groups are polar and can participate in the formation of hydrogen bonds, which has a great impact on the physical and chemical properties of compounds. For example, it enhances its solubility in polar solvents, endows it with certain reactivity, and can occur various chemical reactions such as esterification and oxidation. 4-propanolpyridine exhibits unique physical and chemical properties and reactivity due to the interaction between pyridine ring and propanol group, and may have potential application value in organic synthesis, pharmaceutical chemistry and other fields.
    What are the physical properties of 4-propanolpyridine?
    4-Propanolpyridine is an organic compound with unique physical properties. It is mostly liquid at room temperature, due to the characteristics of intermolecular forces. Looking at its boiling point, because the molecule contains polar groups and a certain carbon chain length, the boiling point is moderate, about 150 ° C - 200 ° C. Due to the need for sufficient energy to overcome intermolecular hydrogen bonds and van der Waals forces, it can be converted from liquid to gaseous.
    On the melting point, the degree of molecular arrangement and intermolecular forces of 4-propanolpyridine determine its melting point, which is roughly in the range of -10 ° C - 10 ° C. At lower temperatures, the molecular motion is suppressed and arranged tightly with each other, so it becomes a solid state. < Br >
    4-propanolpyridine is soluble in some organic solvents, such as ethanol and acetone. Because of its certain polarity, it can be miscible with polar organic solvents according to the principle of similarity and miscibility. In water, although its polar groups can form hydrogen bonds with water, the existence of carbon chains limits its solubility in water and only has certain solubility.
    Furthermore, the density of 4-propanolpyridine is slightly greater than that of water, so it can sink in water. Its refractive index also has a specific value, which can refract light when it propagates in it. This property is often used in material identification and purity analysis.
    In conclusion, the physical properties of 4-propanolpyridine, such as liquid state, specific melting point, solubility, density and refractive index, are of great significance for its applications in organic synthesis, drug development and other fields.
    What are the main uses of 4-propanolpyridine?
    4-Propanolpyridine is 4-propanolpyridine, which has a wide range of uses. In the field of medicine, it is often used as a key intermediate in organic synthesis. Due to the unique chemical activity of the pyridine ring and propanol structure, it can participate in a variety of chemical reactions and help synthesize drug molecules with specific physiological activities. For example, when developing certain drugs for the treatment of cardiovascular diseases or neurological diseases, 4-propanolpyridine can undergo a series of reactions to build the core structure of the drug and lay the foundation for the creation of new drugs.
    In the field of materials science, 4-propanolpyridine also has important uses. In the preparation of functional polymer materials, it can be used as a modifier or crosslinking agent. With the hydroxyl group of propanol and the nitrogen atom of the pyridine ring, it can interact with the polymer chain to change the physical and chemical properties of the material, such as improving the mechanical strength, thermal stability and solubility of the material. When preparing high-performance engineering plastics or special-purpose coatings, adding an appropriate amount of 4-propanol pyridine can significantly optimize the material properties and broaden the material application scenarios.
    In the field of organic synthetic chemistry, 4-propanol pyridine is a characteristic organic reagent and is often used to catalyze specific chemical reactions. The alkalinity of its pyridine ring and the nucleophilicity of propanol make it play a catalytic role in nucleophilic substitution, addition and other reactions, and improve the reaction rate and yield. For example, in the synthesis of some fine chemicals, 4-propanolpyridine can effectively promote the reaction, simplify the synthesis steps, and improve production efficiency. In short, 4-propanolpyridine plays an important role in many fields, promoting the development and progress of related fields.
    What are the synthesis methods of 4-propanolpyridine?
    4-Propanolpyridine is 4-pyridyl-propanol, and there are many synthesis methods, which are described in detail today.
    First, pyridyl is used as the starting material. Pyridyl is first added to acrylonitrile under suitable catalyst and reaction conditions to form pyridyl-4-acetonitrile derivatives. This process requires strict control of the reaction temperature and catalyst dosage to ensure the smooth progress of the reaction. Subsequently, the derivative is reduced to propanolyl group under the action of strong reducing agents such as lithium aluminum hydride to obtain 4-pyridyl-propanol. However, lithium aluminum hydride is active in nature, and special attention should be paid to safety during operation. It is carried out in an anhydrous and oxygen-free environment.
    Second, it can be started from 4-methylpyridine. 4-methylpyridine is first oxidized by side chain, and the methyl is oxidized to carboxyl group with a suitable oxidant, such as potassium permanganate or potassium dichromate, etc., to obtain 4-pyridinecarboxylic acid. Then, 4-pyridinecarboxylic acid and ethanol are esterified under the catalysis of concentrated sulfuric acid to form 4-ethyl pyridinecarboxylate. Finally, 4-pyridinecarboxylate ethyl ester is reduced to propanol group in the reduction system composed of metal sodium and ethanol, and 4-pyridinecarboxylic alcohol is successfully synthesized. However, this method is a little complicated, and the reaction products in each step need to be carefully separated and purified to prevent the accumulation of impur
    Third, 4-pyridyl formaldehyde is used as raw material. 4-pyridyl formaldehyde and malonic acid are catalyzed by organic bases such as pyridine, and the condensation reaction is carried out by Knoevenagel to generate 4-pyridyl acrylic intermediates. Subsequently, the intermediate is catalyzed by hydrogenation in the presence of palladium carbon and other catalysts, and the double bond and carboxyl group are reduced to obtain 4-pyridyl propanol. The conditions of this route are relatively mild, but the cost of the catalyst is high, and cost-effectiveness needs to be considered.
    The above synthesis methods have their own advantages and disadvantages. In practical application, the appropriate synthesis path should be carefully selected according to factors such as raw material availability, cost, and product purity requirements.
    What are the precautions for using 4-propanolpyridine?
    In the case of 4-propanol pyridine, the agent used in the chemical is also used. When using it, all the important items should not be ignored.
    First, it is related to safety. This substance may be flammable and irritating, and it must be kept away from fire and heat sources when using it. Keep it in a cool and ventilated place. When handling, use protective equipment, such as gloves, goggles, etc., to prevent it from touching the body and entering the eyes, causing skin and eye injuries. If you accidentally touch it, rinse it with a lot of water quickly, and seek medical treatment for those who are serious.
    Second, it involves storage. Existence must be sealed to avoid moisture, oxygen, and deterioration. The degree of temperature and humidity must also be paid attention to. According to its nature, it should be controlled in a suitable area to ensure the stability of its quality.
    Third, about use. Before use, study its properties and methods of use in detail, and operate according to regulations. Dissolve the liquid, choose the appropriate agent, and observe its dissolution. In the opposite direction, control the temperature, time, and amount of agent to obtain good results. And after use, the rest should be handled according to regulations, do not discard it indiscriminately, and avoid pollution.
    Fourth, discuss the measurement. In the middle, it is appropriate to measure its concentration and change in nature, and ensure stability. If there is any abnormality in the measurement, stop the operation quickly and check the cause.
    In summary, 4-propanol pyridine is used as the first priority, and it should be carefully stored, used, and tested before it can be effective in avoiding risks.