4 Chloro 2 6 Dimethylpyridine
pyridine pyrrole pyrazine piperidine piperazine

4-Chloro-2,6-dimethylpyridine

    Specifications

    HS Code

    103193

    Name 4-Chloro-2,6-dimethylpyridine
    Molecular Formula C7H8ClN
    Molar Mass 141.598 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 187 - 189 °C
    Melting Point N/A
    Density 1.068 g/mL at 25 °C
    Solubility Insoluble in water, soluble in organic solvents like ethanol, ether
    Flash Point 73 °C
    Odor Characteristic pyridine - like odor
    Purity Typically available in high purity grades (e.g., 95%+)

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    Frequently Asked Questions

    As a leading 4-Chloro-2,6-dimethylpyridine 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 main use of 4-Chloro-2,6-dimethylpyridine?
    4-Chloro-2,6-dimethylpyridine is a crucial compound in the field of organic synthesis. It has a wide range of uses and is often a key intermediate in the synthesis of many drugs in the field of medicinal chemistry. Due to its unique chemical structure, it endows the synthesized drugs with specific pharmacological activity and biocompatibility.
    In the field of pesticide chemistry, 4-chloro-2,6-dimethylpyridine also plays a pivotal role. It can be used to prepare high-efficiency, low-toxicity and environmentally friendly pesticides. Such pesticides can precisely act on pests, effectively inhibit their growth and reproduction, and have little impact on the environment and non-target organisms, meeting the needs of the current green agriculture development.
    Furthermore, in the field of materials science, this compound can be used as a raw material to synthesize polymer materials with special properties. For example, some materials with good thermal stability, mechanical properties or optical properties are widely used in electronics, optics and other industries.
    4-chloro-2,6-dimethylpyridine, with its unique structure and properties, has shown an important role in many fields such as medicine, pesticides, materials, etc., promoting technological innovation and development in various fields.
    What are the physical properties of 4-Chloro-2,6-dimethylpyridine?
    4-Chloro-2,6-dimethylpyridine is one of the organic compounds. It has various physical properties, which are described in detail as follows.
    Looking at its properties, under normal temperature and pressure, it is mostly colorless to light yellow liquid. This is the characteristic of its appearance and can be seen by the naked eye. Its odor is unique and has a certain irritation. If people are close to it, they can feel a pungent smell. The nature of this odor is related to its molecular structure and volatilization characteristics.
    When it comes to the melting point, the melting point is about -48 ° C, that is, the temperature drops to the value of Si, and the substance will gradually change from liquid to solid; the boiling point is about 197-198 ° C. When the temperature rises to Si, the liquid will boil and transform into a gaseous state. The characteristics of this melting point are closely related to the intermolecular forces, such as van der Waals forces, hydrogen bonds, etc., which act on the molecules, causing them to require specific energy to change the state of matter.
    Density is also an important physical property, about 1.06g/cm ³. This value represents the mass of the substance per unit volume, indicating that it is slightly heavier than water, and the density of water is 1g/cm ³. This property is of great significance when it comes to operations such as mixing and separation of substances.
    In terms of solubility, it is slightly soluble in water. Because of its molecular structure, the presence of chlorine atoms, methyl groups, etc., the molecular polarity is limited, and the force between water molecules is difficult to defeat the hydrogen bond of the water molecule itself, so it is insoluble; however, it can be soluble in a variety of organic solvents, such as ethanol, ether, acetone, etc., because the organic solvent and the compound molecule can form similar and soluble forces, such as van der Waals force, dispersion force, etc., so it can be miscible.
    In addition, its vapor pressure, refractive index and other properties also have their own characteristics. Vapor pressure reflects its tendency to evaporate into a gaseous state at a certain temperature; refractive index reflects the degree of refraction when light passes through the substance, both of which are closely related to molecular structure and interaction. This is also the physical properties of 4-chloro-2,6-dimethylpyridine.
    Is 4-Chloro-2,6-dimethylpyridine chemically stable?
    The chemical properties of 4-chloro-2,6-dimethylpyridine are quite stable. Due to its molecular structure, the pyridine ring is aromatic, and the substitution of chlorine atoms with dimethyl groups affects its chemical activity to a certain extent, but also gives it specific stability.
    The pyridine ring has a conjugated system, and the electron cloud is evenly distributed, which reduces the molecular energy and tends to be stable. The 2,6-position methyl group is the power supply group, which can increase the electron cloud density of the pyridine ring, which is beneficial to the stability of the ring. And the steric blocking effect of the methyl group can hinder the attack of external reagents on the pyridine ring, reduce the reaction check point, and further improve its stability.
    Furthermore, although the 4-position chlorine atom is an electron-withdrawing group, it will reduce the electron cloud density of the pyridine ring, but it will enhance the polarity of the molecule to a certain extent. Although this polarity change will affect its reactivity with some reagents, the conjugation effect formed between the chlorine atom and the pyridine ring also helps to disperse the charge and stabilize the molecular structure.
    Under normal conditions, 4-chloro-2,6-dimethylpyridine can maintain a relatively stable state at room temperature and in common environments. In the absence of specific reaction conditions, such as high temperature and catalyst, the molecular structure of common acid-base and oxidative reductant is difficult to change significantly. However, in specific organic synthesis reactions, by reasonably selecting reaction conditions and reagents, it can participate in various reactions, such as nucleophilic substitution reactions, etc., demonstrating its value as an intermediate in organic synthesis. Overall, 4-chloro-2,6-dimethyl pyridine is chemically stable under normal conditions, but under appropriate conditions, it can also exhibit corresponding reactivity.
    What are the synthesis methods of 4-Chloro-2,6-dimethylpyridine?
    The synthesis method of 4-chloro-2,6-dimethylpyridine has been explored by many scholars in the past, but now it is Jun Chen.
    First, 2,6-dimethylpyridine is used as the starting material and prepared by chlorination reaction. In this method, it is often necessary to choose a suitable chlorination reagent, such as chlorine gas, sulfuryl chloride, etc. Taking chlorine gas as an example, chlorine gas is introduced into a specific reaction vessel, and the reaction temperature, pressure and time are controlled at the same time. If the temperature is too high, it may cause side reactions to increase and the product is impure; if the temperature is too low, the reaction rate will be delayed. And appropriate catalysts are often added to the reaction system to promote the smooth progress of the reaction. < Br >
    Second, synthesized by 2,6-dimethyl-4-hydroxypyridine as an intermediate. First prepare 2,6-dimethyl-4-hydroxypyridine, and then react with suitable chlorination reagents to replace the hydroxyl group with a chlorine atom. In this approach, the preparation steps of 2,6-dimethyl-4-hydroxypyridine also need to be carefully controlled. From the selection of raw materials to the setting of reaction conditions, the yield and purity of the final product are all related.
    Third, a specific pyridine derivative is used as the starting material to construct the target molecule through a multi-step reaction. This process involves many organic reaction steps such as substitution reaction and condensation reaction. Each step requires fine operation to ensure that the reaction proceeds in the desired direction and reduce the occurrence of side reactions.
    All synthesis methods have their own advantages and disadvantages. In practical application, when considering factors such as the availability of raw materials, the difficulty of controlling the reaction conditions, and the purity and yield requirements of the product, the choice should be made carefully.
    What are the precautions for 4-Chloro-2,6-dimethylpyridine during storage and transportation?
    4-Chloro-2,6-dimethylpyridine is an important raw material for organic synthesis. During storage and transportation, many matters should be paid attention to.
    First, about storage. This substance should be placed in a cool, dry and well-ventilated place. Cover because of its certain chemical activity, if it is exposed to high temperature and humidity, it may cause chemical reactions and cause it to deteriorate. If it is in a hot and humid place, it may interact with water vapor and affect its chemical properties. And it needs to be kept away from fire and heat sources. Because the substance may be flammable, it is easy to be dangerous in case of open flames and hot topics. Therefore, smoking and fire are strictly prohibited in the storage area. Furthermore, it should be stored separately from oxidants, acids, alkalis, etc., to prevent mutual reaction. For example, if it coexists with strong oxidants, or a violent oxidation reaction occurs, it endangers safety.
    Second, it is related to transportation. Be sure to ensure that the packaging is complete and sealed before transportation. If the packaging is damaged, 4-chloro-2,6-dimethyl pyridine leaks, which not only pollutes the environment, but also poses a hazard to transporters. During transportation, the speed should not be too fast, nor should it brake suddenly to prevent packaging damage due to vibration and collision. And the transportation vehicle should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In case of leakage, it can be dealt with in time to avoid greater disasters. At the same time, transportation personnel need to undergo specialized training to be familiar with the properties of the substance and emergency treatment methods in order to ensure safe transportation.