4 Chloro 3 Fluoropyridine Hydrochloride 1 1
pyridine pyrrole pyrazine piperidine piperazine

4-chloro-3-fluoropyridine hydrochloride (1:1)

    Specifications

    HS Code

    555754

    Chemical Formula C5H4Cl2FN
    Appearance Solid
    Color Off - white to light yellow
    Solubility In Water Soluble
    Melting Point 170 - 175°C
    Boiling Point Decomposes before boiling
    Purity Typically high purity in commercial products

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    General Information
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    Frequently Asked Questions

    As a leading 4-chloro-3-fluoropyridine hydrochloride (1:1) 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 4-chloro-3-fluoropyridine hydrochloride (1:1)?
    4-Cyanogen-3-fluorocarboxylic acid (1:1) is a class of organic compounds with unique physical properties. When the ratio of the two is 1:1, the appearance is often white to off-white crystalline powder. Viewed under a microscope, its crystal structure is orderly arranged, refracting light, and showing crystal clear texture.
    When it comes to melting point, the melting point range of 4-cyanogen-3-fluorocarboxylic acid (1:1) is about 120-130 ° C. In this temperature range, the material lattice can be overcome by heat energy, and the molecules are freed from the fixed position and gradually melt from the solid state to the liquid state. The melting point can be accurately determined by melting point meter, which is an important indicator to identify the purity and characteristics of the compound. The melting point range of high-purity samples is narrow and close to the theoretical value.
    In terms of solubility, it is slightly soluble in water, because water is a polar strong solvent, and although 4-cyanogen-3-fluorine to its carboxylic acid (1:1) contains polar carboxylic groups, it also has non-polar cyanyl groups and fluorine atoms. The overall polarity is not very high, and the interaction with water is weak. However, it has good solubility in organic solvents such as dichloromethane, N, N-dimethylformamide (DMF). In dichloromethane, the solute and solvent molecules form a homogeneous solution through van der Waals force and dipole-dipole interaction; in DMF, due to the strong polarity and electron-feeding ability of DMF, it interacts with the solute to form hydrogen bonds, which promotes dissolution.
    The density of 4-cyanogen-3-fluorine to its carboxylic acid (1:1) is about 1.4-1.5 g/cm ³, which is higher than that of water. If placed in water, it will sink to the bottom. The density is affected by temperature and pressure, and is usually measured at room temperature and pressure. It is tightly packed in the solid state, with a large mass per unit volume and a relatively high density.
    In addition, the compound has certain stability and can exist stably at room temperature and pressure, but in case of extreme conditions such as strong acid, strong base or high temperature, the molecular structure may change. In case of strong base, the carboxyl group may undergo neutralization reaction, and the cyanyl group may hydrolyze; at high temperature, it may trigger intramolecular rearrangement or decomposition reaction.
    The above physical properties are of great significance for their applications in organic synthesis, drug development and other fields. Understanding the melting point helps to determine the purity and control the reaction process; solubility knowledge guides the selection of appropriate reaction solvents and separation and purification methods; density and stability information provide key references for storage, transportation and practical applications.
    What are the chemical properties of 4-chloro-3-fluoropyridine hydrochloride (1:1)?
    4-Chloro-3-fluorobenzoyl chloride (1:1) is an important compound in organic chemistry. Its chemical properties are quite unique and have many remarkable characteristics.
    First of all, its reactivity. In this compound, the presence of chlorine atoms and fluorine atoms greatly increases its reactivity. Because both chlorine and fluorine are halogen elements, they have strong electronegativity, which can reduce the electron cloud density of the benzene ring, making the benzene ring more vulnerable to attack by electrophilic reagents. For example, in the aromatic electrophilic substitution reaction, it can react with many electrophilic reagents, introduce various functional groups, and then synthesize a variety of organic compounds.
    Second on the characteristics of its acid chloride. The acid chloride functional group is extremely active, and it is very easy to hydrolyze in contact with water to generate corresponding benzoic acid and hydrogen chloride. This hydrolysis reaction rate is quite fast, so when storing this substance, it is necessary to strictly maintain a dry environment to prevent its deterioration. In addition, acid chloride is also easy to react with alcohols, amines, etc. When reacting with alcohols, ester compounds can be formed, which is one of the common methods for preparing esters; when reacting with amines, amides can be formed. This reaction is also widely used in organic synthesis. It can be used to construct compounds containing amide bonds, which is of great significance in pharmaceutical chemistry, materials science and other fields.
    Furthermore, the characteristics of fluorine atoms cannot be ignored. Fluorine atoms have a small radius and large electronegativity. When fluorine atoms are introduced, they can significantly change the physical and chemical properties of compounds. For example, it can enhance the lipophilicity of compounds and improve their absorption and distribution characteristics in living organisms. This is often used in drug development to improve the pharmacokinetic properties of drugs.
    4-Chloro-3-fluorobenzoyl chloride (1:1) plays an important role in many fields such as organic synthesis, pharmaceutical chemistry, and materials science, providing important raw materials and tools for chemists to synthesize various functional compounds.
    What are the main uses of 4-chloro-3-fluoropyridine hydrochloride (1:1)?
    4-3-methoxybenzoic acid (1:1), also known as vanillic acid, is a common compound in nature. Its main uses are universal, and I will describe them here.
    First and foremost, in the field of vanillic acid, vanillic acid has shown excellent efficacy. Studies have shown that it has antioxidant properties, which can effectively scavenge human free radicals, oxidize cells, and delay aging. And it also has a certain anti-inflammatory effect, can inhibit the release of inflammatory factors, and is beneficial for the prevention and treatment of multiple inflammatory diseases. In addition, vanillic acid also has benefits in the cardiovascular system, or can reduce blood lipids and inhibit platelet aggregation, which is of great help to cardiovascular health.
    Furthermore, in the food industry, vanillic acid can be used as a food additive. Because of its special fragrance, it can add a special taste to food and improve the taste and taste of food. At the same time, its antioxidant properties can prevent food oxidation, prolong the shelf life of food, and ensure the freshness and safety of food.
    And in the chemical industry, vanilic acid also has a place. Based on its antioxidant and anti-inflammatory properties, it is widely used in food products. It can help the muscle resist external environmental damage, reduce the damage, reduce the growth of pigmentation, and promote the new generation of skin, so that the skin can maintain the quality of light, so it is the best for those who are researched by chemical products.
    Therefore, 4-3-methoxybenzoic acid (1:1) plays an important role in many industries, such as food, chemical products, etc., due to its unique chemical properties, and contributes to the well-being of people's lives.
    What is the synthesis method of 4-chloro-3-fluoropyridine hydrochloride (1:1)?
    To prepare 4-cyanogen-3-fluorobenzoic acid (1:1), you can follow the following ancient method.
    First take an appropriate amount of 3-fluorobenzoic acid as the starting material, which is the root material. Place it in a suitable reaction vessel, which needs to be clean and able to withstand the conditions required for the reaction. Then, a specific reagent is slowly added to it, so that the cyanide group is introduced at a specific position of the benzoic acid. In this process, the ratio of reagents and the rate of addition need to be carefully controlled.
    The introduction of cyanobenzoic acid is often by means of a specific chemical reaction. Nucleophilic substitution can be used to select suitable cyanide reagents, such as potassium cyanide. However, potassium cyanide is highly toxic, and the operation must be carried out with caution, in a well-ventilated environment, and under comprehensive protective measures. In the reaction system, the hydrogen atom at the carboxyl ortho-position of 3-fluorobenzoic acid can be replaced by cyanide due to its special chemical environment. In order to promote the smooth occurrence of this reaction, it is necessary to adjust the temperature, pH and other conditions of the reaction.
    Temperature control is quite critical. Usually, the reaction needs to be carried out under moderate heating. However, the heating should not be excessive to prevent the growth of side reactions. The reaction system can be heated evenly by water bath heating or oil bath heating. As for the pH, it can be adjusted with the help of reagents such as buffer solutions to create an acid-base environment suitable for the reaction.
    After the reaction has been carried out for a period of time, the product needs to be separated and purified. This step is also challenging because there may be impurities such as unreacted raw materials and by-products in the reaction system. The reaction mixture can be extracted with a suitable solvent to initially separate the product and impurities. Then column chromatography and other means are used to further purify to obtain high-purity 4-cyano3-fluorobenzoic acid (1:1).
    The entire synthesis process is like a delicate display of skills. From the selection of raw materials, the control of reaction conditions to the purification of the product, it is necessary to be rigorous. If there is a slight difference, it is difficult to obtain the ideal product.
    What are the precautions for storing and transporting 4-chloro-3-fluoropyridine hydrochloride (1:1)?
    4-Alkane-3-ene to its carboxylic anhydride (1:1) during storage and transportation, pay attention to many matters. Both are organic compounds with active properties. When storing, they should be placed in a cool, dry and well-ventilated place. Because the carboxylic anhydride is quite sensitive to water vapor in the air and is prone to hydrolysis, it is necessary to take sealing measures to prevent contact with water vapor. And 4-alkane-3-ene may also deteriorate due to environmental factors, affecting its quality.
    When transporting, it is necessary to strictly abide by the relevant regulations on the transportation of hazardous chemicals. These two may be flammable, irritating, or even toxic. Transportation vehicles should be equipped with complete fire fighting equipment and emergency treatment equipment to prevent accidents. At the same time, transportation personnel also need to undergo professional training, familiar with the characteristics of the transported goods and emergency disposal methods.
    In addition, storage and transportation places should be equipped with obvious warning signs to indicate the danger of the goods. Fireworks are strictly prohibited. Avoid mixing with strong oxidants, strong acids, strong alkalis and other substances to prevent severe chemical reactions from occurring and causing serious consequences. Detailed records of storage and transportation processes are also required, including time, location, quantity, handling personnel and other information for traceability and management. Only in this way can the purpose of safe storage and transportation of 4-alkane-3-ene and its carboxylic anhydride (1:1) be achieved.