4 Chloro 2 Chloromethyl 3 5 Dimethylpyridine Hydrochloride 1 1
pyridine pyrrole pyrazine piperidine piperazine

4-Chloro-2-(chloromethyl)-3,5-dimethylpyridine hydrochloride (1:1)

    Specifications

    HS Code

    503625

    Name 4-Chloro-2-(chloromethyl)-3,5-dimethylpyridine hydrochloride (1:1)
    Molecular Formula C8H10Cl2N.ClH
    Molecular Weight 224.54 g/mol
    Appearance Typically a solid (but appearance can vary based on purity and preparation)
    Melting Point Data may vary, check specific literature for exact value
    Solubility Solubility characteristics would depend on the solvent, likely has some solubility in polar solvents
    Chemical Structure Pyridine ring with chloro, chloromethyl and dimethyl substituents, plus a hydrochloride salt
    Odor May have a characteristic odor, details would require experimental determination
    Density Density data specific to this compound needs to be sourced from relevant literature
    Purity Purity can range widely depending on source and preparation method

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    General Information
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    Frequently Asked Questions

    As a leading 4-Chloro-2-(chloromethyl)-3,5-dimethylpyridine 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 chemical properties of 4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1)
    4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1) is one of the organic compounds. It is active and has unique chemical properties.
    In this compound, the chlorine atom is connected to the structure of chloromethyl and dimethylpyridine, and the state of hydrochloride adds to its chemical properties. In terms of its physical properties, it is mostly solid and can have certain solubility in specific solvents.
    In terms of chemical activity, both chlorine atoms and chloromethyl groups are active reaction check points. Chlorine atoms can participate in nucleophilic substitution reactions. Due to the certain electronegativity of chlorine, the connected carbon atoms can be partially positively charged and vulnerable to attack by nucleophilic reagents, resulting in substitution and the introduction of new functional groups.
    Chloromethyl chloride is also highly active, and can be replaced by nucleophilic reagents or participate in some reactions to build carbon-carbon bonds under suitable conditions to expand the molecular structure.
    Furthermore, the nitrogen atom of the pyridine ring has lone pairs of electrons, which can be used as electron donors to participate in coordination reactions or combine with protons to form hydrochloride salts in acidic environments, changing its physical and chemical properties and affecting its reactivity and solubility.
    It has a wide range of uses in the field of organic synthesis, or is an intermediary for the synthesis of complex organic molecules. With its active check point, it can gradually build the required molecular structure, and has potential application value in many fields such as medicinal chemistry and materials chemistry.
    What are the main uses of 4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1)
    4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1) is widely used in the chemical and pharmaceutical fields.
    In the field of chemical industry, it is often a key intermediate in organic synthesis. It can combine with many reagents through a specific reaction path to construct more complex organic compounds. With its unique chemical structure, it can participate in various reactions such as nucleophilic substitution and condensation, and assist in the synthesis of materials with specific properties and functions, such as monomer synthesis of some polymer polymers, laying the foundation for the development of new materials.
    In the field of medicine, this compound is also of great value. It may be an important raw material for the synthesis of specific drugs. The chlorine atoms, chloromethyl groups and pyridine rings in its structure can interact with specific targets in organisms. After reasonable structural modification and optimization, the synthesized drugs may exhibit antibacterial, anti-inflammatory, anti-tumor and other pharmacological activities, providing novel lead compounds for pharmaceutical research and development, and is expected to promote the birth of innovative drugs to solve the difficulties of many diseases and benefit patients.
    In summary, 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1) occupies a key position in both chemical and pharmaceutical fields, and plays an indispensable role in the development of related industries.
    What is the synthesis method of 4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1)
    To prepare 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1), you can do it according to the following method.
    Take 3,5-dimethylpyridine first and place it in an appropriate reaction vessel. Cool it at low temperature and slowly add an appropriate amount of chlorinated reagents, such as sulfonyl chloride. During the reaction, the temperature should be carefully controlled to avoid side reactions caused by excessive temperature. This step aims to introduce chlorine atoms into the fourth position of the pyridine ring to generate 4-chloro-3,5-dimethylpyridine.
    Wait for 4-chloro-3,5-dimethylpyridine to be obtained and move it to another reaction system. In this system, formaldehyde and hydrogen chloride gas are added, and appropriate catalysts such as zinc salts are added. The reaction is carried out at moderate temperature and pressure, formaldehyde interacts with hydrogen chloride, and chloromethyl is introduced into the second position of the pyridine ring to obtain 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine.
    Finally, 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine is dissolved in an organic solvent, such as ethanol, and hydrogen chloride gas is introduced. Hydrogen chloride is combined with 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine in a ratio of 1:1 to obtain the crystallization of 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1). After filtration, washing, drying and other operations, a pure product can be obtained. After each step of the reaction, suitable analytical methods, such as gas chromatography, nuclear magnetic resonance, etc. are required to detect the purity and structure of the product to ensure that the reaction is smooth and the product is correct.
    What is the market price of 4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1)
    4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1), the market price of this product is difficult to determine due to various reasons. Looking at the chemical products of the past, the price is often affected by the abundance of raw materials, the simplicity of the process, and the amount of supply and demand.
    If the raw materials are discussed, the various materials required for their synthesis, if the supply is smooth, the price may be stable; however, if the raw materials are scarce, they need to be tossed around, and the price will rise. The process is also the main reason. If the synthesis method is complicated, it requires exquisite utensils and exquisite techniques, and it consumes a huge amount of energy, the cost will be high, and the price will follow.
    Changes in market supply and demand affect its price. If this product is in the market, there are many seekers and few suppliers, merchants will raise its price to seek a big profit; on the contrary, if the supply exceeds the demand, in order to sell inventory, the price may drop.
    Furthermore, industry competition, policies and decrees also have an impact. There may be competition in the same industry, or there may be those who seek the market at a price; if the decree is regulated, it is related to production and circulation, and the price fluctuates. Therefore, in order to know the exact market price of 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1), it is necessary to study the raw material market, process progress, supply and demand situation in detail, and change over time.
    4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1) What are the precautions in storage and transportation
    4-Chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1), there are several ends that need to be paid attention to during storage and transportation.
    This compound has certain chemical activity, and it must be placed in a dry place when storing. Because moisture can easily lead to adverse reactions such as hydrolysis, its quality will be damaged. In the warehouse, the humidity should be strictly controlled within a suitable range, and it must not be allowed to be damp.
    Temperature is also the key. It should be stored in a cool place to avoid hot topics. Under high temperature, the compound may decompose, polymerize and other reactions, causing its chemical structure to be damaged and its properties to change. Therefore, the storage environment temperature should be maintained at a specific range to ensure its stability.
    Furthermore, its packaging must be tight. To prevent contact with air, oxidation or other gas-phase reactions. Packaging materials should also be selected carefully, must be resistant to the corrosion of the compound, and have good sealing performance.
    When transporting, also strictly abide by relevant specifications. The inside of the vehicle should be clean and dry, and there should be no impurities that may react with it. And during transportation, try to avoid bumps and vibrations to prevent package damage and leakage of compounds.
    If there is a leak, immediately start emergency response. Relevant personnel must wear protective equipment and clean it up quickly to prevent its spread from causing harm to the environment and people. In conclusion, during the storage and transportation of 4-chloro-2- (chloromethyl) -3,5-dimethylpyridine hydrochloride (1:1), comprehensive consideration must be taken from environmental control to packaging protection to ensure the quality and safety of the compound.