3 Pyridinecarboxylic Acid 2 6 Dichloro Methyl Ester
pyridine pyrrole pyrazine piperidine piperazine

3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester

    Specifications

    HS Code

    211388

    Chemical Formula C7H5Cl2NO2
    Molar Mass 206.026 g/mol
    Appearance Solid (predicted)
    Boiling Point Approx. 293 - 294 °C (estimated)
    Melting Point 68 - 70 °C
    Density 1.492 g/cm³ (estimated)
    Solubility In Water Low solubility in water
    Logp 2.99 (estimated)
    Vapor Pressure Very low vapor pressure
    Flash Point 131.0 °C (estimated)

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    General Information
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    Frequently Asked Questions

    As a leading 3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester 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 chemical properties of 3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester
    3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester, its chemical properties are as follows:
    The appearance of this compound may be colorless to light yellow liquid or solid, depending on the specific conditions. Under normal temperature and pressure, it is relatively stable, but under extreme conditions such as hot topics and open flames, or there is a risk of decomposition, and harmful gases such as chlorine and nitrogen may be released.
    In terms of solubility, it may have a certain solubility in organic solvents such as ethanol, ether, dichloromethane, etc. Because its structure contains ester groups and pyridine rings, it has a certain lipophilicity. However, the solubility in water is relatively small, due to the limited polarity of the whole molecule, and the presence of pyridine rings and chlorine atoms reduces its ability to form hydrogen bonds with water.
    From the perspective of chemical activity, ester groups are an important reaction check point. Hydrolysis can occur, and the hydrolysis rate varies under acidic or alkaline conditions. In alkaline environments, hydrolysis is easier and faster, resulting in corresponding carboxylic salts and methanol; under acidic conditions, hydrolysis is reversible, and heating or appropriate catalysts are required to proceed efficiently.
    Pyridine rings also give the compound unique chemical properties. The pyridine ring is weakly basic and can react with acids to form salts, and the electron cloud density distribution characteristics on the ring enable it to participate in electrophilic substitution reactions, but the reactivity is slightly lower than that of the benzene ring. The substitution check point is mostly at the β position of the pyridine ring (relative to the nitrogen atom), because of its relatively high electron cloud density. In addition, chlorine atoms at the 2,6-position can participate in nucleophilic substitution reactions, and in the presence of appropriate nucleophiles, chlorine atoms can be replaced to form new carbon-heteroatomic bonds.
    What are the main uses of 3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester
    3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester, this is an organic compound with a wide range of uses.
    In the field of medicine, it is often an important intermediate for drug synthesis. Due to the special chemical structure of this compound, it can introduce specific active groups to drug molecules, which helps to develop new drugs with unique pharmacological activities. For example, it may be used to synthesize small molecule inhibitors targeting specific disease targets, which can precisely act on disease-related proteins to regulate cellular physiological processes and achieve the purpose of treating diseases.
    In the field of pesticides, it also plays a key role. It can be used as a raw material for the synthesis of new pesticides. After rational structural modification and modification, it can give pesticides excellent characteristics such as high efficiency, low toxicity, and environmental friendliness. Or it can synthesize high-efficiency insecticides, showing strong killing ability to crop pests, and has little impact on the environment, which is in line with the current needs of green agriculture development.
    In the field of materials science, 3-pyridine carboxylic acid, 2,6-dichloro -, methyl ester or can participate in the preparation of functional materials. For example, in the synthesis of some polymer materials, the introduction of this compound may improve the properties of the material, such as improving the stability and solubility of the material or giving the material special optical and electrical properties, etc., thereby expanding the application of the material in many fields such as electronic devices and optical materials. In addition, in the study of organic synthetic chemistry, this compound is often used as a model substrate due to its unique combination of functional groups to explore novel organic reaction pathways and methods, promote the development of organic synthetic chemistry, and provide new ideas and strategies for the synthesis of more complex organic compounds.
    What is the synthesis method of 3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester
    To make 3-pyridinecarboxylic acid, 2,6-dichloro-, methyl ester, you can follow the following ancient method.
    First take an appropriate amount of pyridine and place it in a clean reactor. The kettle should be made of glass or ceramic to prevent corrosion. Slowly add an appropriate amount of chlorination reagent to the kettle, such as a mixture of phosphorus oxychloride and phosphorus pentachloride. When adding dropwise, the temperature should be strictly controlled, and it should be maintained at a low temperature, between about 0 and 5 degrees Celsius, and constantly stir to make the reaction uniform. This step aims to chlorinate the 2,6 positions of pyridine to generate 2,6-dichloropyridine.
    After the chlorination reaction is completed, pour the reaction solution into an appropriate amount of ice water to stop the reaction. Subsequently, the reaction mixture is separated and treated. The extraction method can be used to extract the product with an organic solvent such as dichloromethane, extract several times, combine the organic phases, and then dry it with anhydrous sodium sulfate to remove the moisture.
    Next, the dried organic phase is distilled to recover the organic solvent to obtain pure 2,6-dichloropyridine. Take this 2,6-dichloropyridine and place it in another reactor. Add an appropriate amount of carbon dioxide and a suitable catalyst, such as a palladium-based catalyst, and then add an appropriate amount of basic substances, such as potassium carbonate. When the reaction temperature rises to a certain level, about 100 to 120 degrees Celsius, and the reaction number under a certain pressure, this makes it carboxylated to obtain 2,6-dichloro-3-pyridinecarboxylic acid.
    After the reaction is completed, the reaction system is cooled, and the pH value is adjusted to be acidic with dilute acid, so that the product is precipitated. The precipitated solids are filtered and collected, washed with water several times, and dried to obtain pure 2,6-dichloro-3-pyridinecarboxylic acid.
    In the last step, 2,6-dichloro-3-pyridinecarboxylic acid is placed in a reaction kettle, and an appropriate amount of methanol and a catalyst, such as concentrated sulfuric acid, are added. When the reflux reaction is heated, this is an esterification reaction, so that 2,6-dichloro-3-pyridinecarboxylic acid is converted into 3-pyridinecarboxylic acid, 2,6-dichloro-methyl ester. After the reaction is completed, the reaction solution is cooled, poured into an appropriate amount of water, extracted with an organic solvent, and then distilled and dried to obtain pure target products 3-pyridinecarboxylic acid, 2,6-dichloro-methyl ester. The whole process needs to be handled with caution and attention to the conditions of each step of the reaction in order to obtain satisfactory results.
    What is the market price of 3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester
    I don't know the market price of 3 - Pyridinecarboxylic acid, 2,6 - dichloro -, methyl ester (methyl 2,6 - dichloronicotinate). This is a chemical in the field of fine chemicals, and its price often varies due to many factors.
    First, the cost of raw materials has a great impact. If the price of the basic raw materials for preparing this methyl ester, such as pyridine, chlorine source, methanol, etc., fluctuates, the price of methyl 2,6 - dichloronicotinate will also fluctuate. The shortage of raw materials or the increase in production costs can cause its price to rise.
    Second, the production process is also key. Efficient and advanced processes can reduce costs. If the process is complex and energy consumption is high, the cost will increase accordingly. Technological innovation can optimize the production process, or the price can be changed.
    Third, the market supply and demand relationship determines the price. If the market demand for this product is strong, but the supply is limited, the price will rise; conversely, if the demand is weak and the supply is excessive, the price will easily drop. The development of downstream industries such as pharmaceuticals and pesticides has a huge impact on their demand. If new drugs with this as a key intermediate are developed in the pharmaceutical field, the demand may increase sharply, which will affect the price.
    Fourth, the brand of the manufacturer is also related to the quality of the product. Well-known manufacturers, high-quality products, or relatively high prices due to quality assurance and good reputation.
    To know the exact market price, consult relevant chemical product suppliers, distributors, or refer to chemical product trading platforms and industry information for the latest and accurate price information.
    3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester in the process of use
    3-Pyridinecarboxylic acid, 2,6-dichloro-, methyl ester, when using this substance, many matters need to be paid attention to.
    Bearing the brunt of it, safety precautions are essential. This is a chemical substance, or it may be toxic and irritating to a certain extent. When taking it, be sure to wear complete protective equipment, such as gloves, goggles, protective clothing, etc., to prevent it from coming into direct contact with the skin and eyes, and to beware of inhaling its volatile aerosol. In case of accidental contact, rinse with plenty of water immediately. If the situation is serious, seek medical attention immediately.
    Furthermore, storage should not be ignored. It should be stored in a cool, dry and well-ventilated place, away from fire, heat and oxidants. Due to its active chemical nature, improper storage or dangerous reactions should be caused. At the same time, it should be stored separately from other chemicals to avoid accidents caused by mixed storage.
    During use, accurate control of the dosage is extremely critical. According to experimental or production requirements, carefully calculate and measure the appropriate dose to prevent too much or too little dosage from affecting the effect, and to avoid waste and potential danger caused by excessive use.
    In addition, the operating environment needs to be well ventilated. This helps to disperse volatile harmful gases in time, reduce the concentration of harmful substances in the air, and protect the health of operators.
    And, after use, properly dispose of the remaining substances and waste. Do not discard at will, follow relevant environmental regulations, and dispose of in an appropriate manner to avoid pollution to the environment.
    In short, when using 3-pyridinecarboxylic acid, 2,6-dichloro -, methyl ester, from safety protection to storage, use, ventilation and waste disposal, all aspects must be treated with caution, not sloppy at all, so as to ensure safe and smooth operation.