3 Pyridinecarboxylic Acid 2 6 Dichloro
pyridine pyrrole pyrazine piperidine piperazine

3-Pyridinecarboxylic acid, 2,6-dichloro-

    Specifications

    HS Code

    790047

    Chemical Formula C6H3Cl2NO2
    Molecular Weight 192.00
    Appearance Solid (presumed, based on similar compounds)
    Solubility In Water Low solubility expected, due to non - polar parts in molecule
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Odor Odorless or mild odor (assumed, based on pyridine - carboxylic acid derivatives)

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    General Information
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    Frequently Asked Questions

    As a leading 3-Pyridinecarboxylic acid, 2,6-dichloro- 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-
    3-Pyridinecarboxylic acid, 2,6-dichloro-This is an organic compound with specific chemical properties. Its appearance may be solid, as for color, crystal form, etc., it often varies according to the preparation and purification status.
    In terms of solubility, it may have a certain solubility in organic solvents such as ethanol and acetone, but its solubility in water may be limited. The molecular structure contains pyridine rings, carboxyl groups and chlorine atoms, resulting in specific polarity, which affects the dissolution in different solvents.
    Its chemical properties are active, and carboxyl groups can participate in many reactions. If it reacts with a base, it can form a corresponding carboxylate, which is a typical reaction of acid-base neutralization. Under acid catalysis, esterification reactions with alcohols may occur to form ester compounds. Pyridine rings are also reactive and can undergo electrophilic substitution reactions due to the uneven distribution of electron cloud density on the ring. Chlorine atoms can be replaced by nucleophiles to achieve molecular structure modification.
    In addition, in view of its chlorine atoms, under certain conditions, or chlorine-related reactions, its chemical properties and reaction paths are greatly affected. Its stability also varies in different environments. In case of high temperature, strong light or specific chemical reagents, it may initiate reactions such as decomposition and rearrangement. This is a summary of the chemical properties of 3-pyridinecarboxylic acid and 2,6-dichloro.
    What are the main uses of 3-Pyridinecarboxylic acid, 2,6-dichloro-
    3-Pyridinecarboxylic acid, 2,6-dichloro-, this substance has a wide range of uses. In the field of medicine, it can be used as an important pharmaceutical intermediate. Due to its structural properties, it can participate in many key steps in drug synthesis. For example, some antibacterial drugs with specific curative effects are synthesized with 3-pyridinecarboxylic acid, 2,6-dichloro- as the starting material, and through a series of delicate chemical reactions, complex drug molecular structures with antibacterial activity are constructed, providing a key basis for drug development against bacterial infections.
    In the field of pesticides, it also plays an important role. It can be used to synthesize some highly efficient and low-toxic pesticides. By reasonably combining and reacting with other chemical substances, the obtained pesticides have a significant repellent effect on specific pests, while having relatively little impact on the environment, contributing to the green and sustainable development of agriculture. For example, for common pests in farmland, such pesticides composed of 3-pyridinecarboxylic acid, 2,6-dichloro-can precisely act on the physiological system of pests and destroy their normal physiological functions, thus achieving the purpose of pest control.
    In addition, in the field of materials science, 3-pyridinecarboxylic acid, 2,6-dichloro-also shows unique value. Can be used as an important component in the synthesis of functional materials. In the preparation of certain polymer materials with special properties, the introduction of this substance can endow the material with specific physical and chemical properties, such as improving the stability and solubility of the material, thereby broadening the application range of the material and meeting the diverse needs of different fields for material properties.
    What are the synthesis methods of 3-Pyridinecarboxylic acid, 2,6-dichloro-
    To prepare 2,6-dichloro-3-pyridinecarboxylic acid, the following ancient method can be used.
    First take the pyridine as the group, and the pyridine has the structure of a six-membered heterocycle, and carboxyl groups and chlorine atoms are introduced into the ring. Pyridine can be oxidized and carboxylated to obtain 3-pyridinecarboxylic acid. In this step, a suitable oxidant, such as potassium permanganate, can be used to carboxylate the 3-position on the pyridine ring under appropriate reaction conditions.
    Then, 3-pyridinecarboxylic acid is chlorinated. The method of chlorination can use chlorine gas as a chlorination agent, and in the presence of suitable catalysts, such as iron powder or ferric chloride, the chlorination reaction occurs at the 2,6-position. During the reaction, temperature control and pressure control are required, and attention is paid to the reaction process. Due to the electron cloud distribution characteristics of the pyridine ring, chlorine atoms are more likely to be replaced at the 2,6-position.
    Or first chlorinate the pyridine to obtain 2,6-dichloropyridine, and then oxidize and carboxylate the 2,6-dichloropyridine to obtain the target product. In this chlorination process, chlorine gas and pyridine under the action of the catalyst are formed into 2-chloropyridine, and then further chlorinated under suitable conditions to obtain 2,6-dichloropyridine. In the oxidation and carboxylation step, a suitable strong oxidizing agent can be selected, and the 3-position of 2,6-dichloropyridine can be introduced into the carboxyl group under appropriate solvent and temperature conditions.
    When operating, it is necessary to be careful, strictly control the temperature and time, and properly handle the reaction products. After separation and purification, such as recrystallization, column chromatography, etc., to obtain pure 2,6-dichloro-3-pyridinecarboxylic acid.
    3-Pyridinecarboxylic acid, 2,6-dichloro - what are the precautions in storage and transportation
    3-Pyridinecarboxylic acid, 2,6-dichloro-Many things need to be paid attention to when storing and transporting this substance.
    First, when storing, be sure to choose a dry, cool and well-ventilated place. If this substance is placed in a humid place, it is susceptible to water vapor erosion or changes in its properties, which affects its quality. And if the temperature is too high, it may also cause chemical reactions, so a cool environment is essential. Good ventilation can prevent the accumulation of harmful gases and ensure the safety of storage.
    Second, the packaging must be strong and tight during transportation. Because the substance may be corrosive or irritating, if the packaging is damaged and leaks, it will not only pollute the surrounding environment, but also cause harm to transporters.
    Furthermore, whether it is storage or transportation, it should be separated from oxidizing agents, reducing agents, acids, alkalis and other substances. When these substances come into contact with them, it is very likely to cause violent chemical reactions and even cause dangerous accidents.
    At the same time, the storage and transportation areas should be equipped with corresponding emergency treatment equipment and suitable containment materials. In the event of an unexpected situation such as leakage, emergency treatment can be carried out quickly to minimize the harm. Professional training is also required for relevant operators to make them familiar with the characteristics of the substance and emergency treatment methods to ensure the safety of storage and transportation.
    3-Pyridinecarboxylic acid, 2,6-dichloro - what are the effects on the environment and human health
    The effects of 3-pyridinecarboxylic acid, 2,6-dichloro-this substance on the environment and human health are related to many aspects. In terms of the environment, after it enters the natural water body, it may interfere with the aquatic ecosystem. Aquatic organisms have different sensitivities to it, or cause some biological physiological functions to be disturbed, such as affecting the respiration and reproduction of fish. In the soil environment, or change the structure and function of soil microbial communities, affecting soil nutrient cycling and decomposition of organic matter, and then affecting plant growth.
    As for human health, if inhaled through the respiratory tract, or irritating the respiratory mucosa, causing cough, asthma and other discomfort. After skin contact, some people may have allergic reactions, such as skin redness, swelling, itching. If accidentally ingested, or damage the digestive system, causing nausea, vomiting, abdominal pain and other symptoms. Long-term exposure to the environment containing this substance may also pose a potential carcinogenic risk, because some chlorine-containing organic compounds have been proven to be associated with cancer.
    In summary, such substances should be handled and used with caution, and their content in the environment should be monitored to protect the ecological environment and human health.