2 Chloro 6 Isopropylpyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Chloro-6-Isopropylpyridine

    Specifications

    HS Code

    468256

    Chemical Formula C8H10ClN
    Molecular Weight 155.62
    Appearance A colorless to light yellow liquid
    Boiling Point Around 208 - 210 °C
    Density Approx. 1.06 g/cm³
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
    Odor Characteristic pyridine - like odor
    Flash Point Approx. 87 °C
    Stability Stable under normal conditions but may react with strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 2-Chloro-6-Isopropylpyridine 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 main uses of 2-Chloro-6-Isopropylpyridine?
    2-Chloro-6-isopropylpyridine is widely used in the chemical and pharmaceutical fields.
    In the chemical industry, it is often a key intermediate in organic synthesis. Using it as a starting material, through halogenation reaction, other halogen atoms can be introduced into the pyridine ring to enrich the structure of compounds, which is crucial in the synthesis of organic molecules with special electronic effects or spatial structures. Nucleophilic substitution reactions are also common pathways, in which chlorine atoms are highly active and can be replaced by many nucleophiles, such as alkoxides and amines, to construct a wide variety of pyridine derivatives, which are widely used in the creation of new materials and functional additives.
    In the field of medicine, its role should not be underestimated. In many drug molecular designs, 2-chloro-6-isopropylpyridine structural units are often included. Due to the specific electron distribution and spatial configuration of the pyridine ring and substituent, it can interact with specific targets in organisms. After modification, the synthesized derivatives may have antibacterial, anti-inflammatory, anti-tumor and other pharmacological activities. For example, some compounds derived from this structure have been found to have inhibitory effects on the growth of specific tumor cell lines, which brings hope for the development of new anticancer drugs; some derivatives have shown good antibacterial properties and may become candidates for new antibacterial drugs.
    In summary, 2-chloro-6-isopropylpyridine is a valuable compound in the fields of chemical synthesis and pharmaceutical research and development due to its structural properties, promoting continuous innovation and development in related fields.
    What are the physical properties of 2-Chloro-6-Isopropylpyridine?
    2-Chloro-6-isopropylpyridine is one of the organic compounds. Its physical properties are particularly important, and it is related to the application of this compound in various scenarios.
    First of all, under normal temperature and pressure, 2-chloro-6-isopropylpyridine is often colorless to light yellow liquid, with no obvious impurities. This property makes it easy to operate and handle in many chemical reactions and industrial processes, because its liquid state is easy to mix, transport and participate in various reaction systems.
    Furthermore, the melting point and boiling point are also key properties. Its melting point is relatively low, but the specific value varies slightly depending on the preparation method and purity. The boiling point varies according to the external pressure. In the atmospheric pressure environment, the boiling point is in a certain temperature range. This boiling point characteristic, in the process of separation and purification, can be effectively separated from the mixture by distillation and other means to obtain high purity.
    Solubility is also a property that cannot be ignored. 2-Chloro-6-isopropylpyridine is soluble in many organic solvents, such as ethanol, ethyl ether, dichloromethane, etc. This good solubility makes it very useful in the field of organic synthesis. It can be used as a reactant or solvent to participate in the construction of complex organic molecules. In a specific reaction system, the selection of suitable solvents can greatly promote the reaction, improve the reaction rate and yield.
    Density is also one of the important physical properties of this compound. Its density is different from that of water, and this property is crucial when it comes to operations such as liquid-liquid separation. Depending on the density difference, liquid separation and other methods can be used to achieve effective separation from other liquids.
    In addition, 2-chloro-6-isopropylpyridine has a certain degree of volatility. Although the volatility is not extremely strong, it will gradually evaporate under open systems or specific temperature conditions. This property should be paid attention to when storing and using. It should be ensured that the storage environment is well sealed to prevent its volatilization loss and avoid environmental pollution or safety hazards due to volatilization.
    In summary, the physical properties of 2-chloro-6-isopropylpyridine, from its properties, melting point, solubility, density to volatility, play a pivotal role in its application in chemical synthesis, industrial production and scientific research. In-depth understanding and good use of these properties can better exert the effectiveness of this compound.
    What is the chemistry of 2-Chloro-6-Isopropylpyridine?
    2-Chloro-6-isopropylpyridine is a member of the family of organic compounds. Its chemical properties are interesting and unique.
    In this compound, the chlorine atom is attached to the pyridine ring, and the chlorine atom has electron-withdrawing properties, which can affect the electron cloud density of the pyridine ring. Under this influence, the reactivity of the pyridine ring may change. For example, in nucleophilic substitution reactions, chlorine atoms can provide a check point for the attack of nucleophiles. Due to its electron-withdrawing properties, the electron cloud density on the pyridine ring decreases, making it easier for nucleophiles to react with it.
    And the 6-position isopropyl group is an alkyl substituent. Alkyl groups usually exhibit electron-donating effects. Although it can increase the electron cloud density of the pyridine ring to a certain extent, it checks and balances the electron-withdrawing effect of the chlorine atom. This structural feature causes 2-chloro-6-isopropyl pyridine to exhibit unique activities in chemical reactions.
    In terms of acidity and alkalinity, the lone pair electrons on the nitrogen atom of the pyridine ring make it alkaline. However, the electron-withdrawing effect of the chlorine atom and the steric resistance of the isopropyl group may affect its alkalinity. < Br >
    In the redox reaction, the compound may exhibit certain redox properties due to the existence of the pyridine ring. The pyridine ring can participate in the electron transfer process under specific conditions, exhibiting a unique redox behavior.
    From the perspective of stability, its stability is restricted by the interaction between atoms in the molecule. The bond energy between the chlorine atom and the pyridine ring, as well as the connection mode between the isopropyl group and the pyridine ring, all affect the stability of the compound. If the external conditions are suitable, some reactions involving bond breaking and formation may occur, thereby changing its chemical structure.
    In summary, the chemical properties of 2-chloro-6-isopropylpyridine are determined by its molecular structure, and it exhibits diverse characteristics in different chemical reactions, which has potential application value in organic synthesis and other fields.
    What is 2-Chloro-6-Isopropylpyridine production method?
    The preparation method of 2-chloro-6-isopropylpyridine is based on the number-following method in the past.
    First, pyridine is used as the starting material. First, under specific conditions, pyridine interacts with chlorinated reagents such as chlorine gas and phosphorus trichloride, and chlorine atoms are introduced into the pyridine ring to obtain chloropyridine-containing derivatives. Later, the derivative and isopropylation reagents, such as isopropyl halide and isopropyl alcohol, undergo nucleophilic substitution in the presence of suitable catalysts, so that the isopropyl group is attached to the appropriate position of the pyridine ring, thereby obtaining 2-chloro-6-isopropylpyridine. In this pathway, the conditions for the reaction of pyridine with chlorinated reagents are quite critical. Temperature, reaction time, and the proportion of reactants all affect the selectivity and yield of chlorinated products. In the subsequent isopropylation step, the type and amount of catalyst also have an important impact on the reaction process and product purity.
    Second, suitable pyridine derivatives can be used. For example, a pyridine compound with some desired substituents is selected, and the target product is prepared by the transformation and modification of a specific functional group. For example, a pyridine derivative containing a convertible group is first chemically converted into a chlorine atom, and then isopropyl is introduced through another series of reactions. This method requires a precise design of the structure of the starting pyridine derivative, and each step of the reaction needs to be properly planned to ensure the structure and purity of the final product.
    Or use the Grignard reagent method. Using halogenated pyridine as raw material, the corresponding Grignard reagent is first prepared, and then reacted with isopropyl halide or other suitable isopropyl sources to achieve the introduction of isopropyl. At the same time, the chlorine atom is introduced by a suitable halogenation step, and the final product is 2-chloro-6-isopropyl pyridine. In this process, the preparation conditions of Grignard's reagent are extremely strict, requiring an anhydrous and oxygen-free environment, and the subsequent reaction with the isopropyl source also needs to be carefully regulated to avoid the occurrence of side reactions and improve the yield and purity of the product.
    2-Chloro-6-Isopropylpyridine to pay attention to when storing and transporting
    2-Chloro-6-isopropylpyridine is also an organic compound. When storing and transporting it, many matters must be paid attention to.
    First words storage. This compound should be placed in a cool, dry and well-ventilated place. Cover because of its nature has the characteristics of heat and moisture fear, high temperature and humid environment may cause its properties to change, and even chemical reactions and deterioration. In the warehouse, the temperature should be controlled within a specific range, and the humidity should not be too high, and suitable equipment should be used to maintain environmental stability. At the same time, it should be kept away from fire and heat sources to prevent the risk of fire or explosion. Because it may be flammable or may react dangerously with fire and heat contact. And it should be stored separately from oxidants, acids, alkalis, etc., to avoid mixed storage. Due to its active chemical properties, contact with their substances is prone to chemical reactions, resulting in safety accidents.
    As for transportation, make sure that the packaging is complete and sealed. The transportation container must be able to withstand a certain pressure to prevent leakage. During transportation, the speed of the vehicle should not be too fast to avoid sudden braking and violent vibration to prevent damage to the packaging. Transportation vehicles should also be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. If a leak occurs during transportation, drivers and passengers should take prompt measures to evacuate the surrounding people, isolate the leaked pollution area, and strictly restrict access. Emergency personnel must wear appropriate protective equipment to avoid skin and respiratory tract contact with leaks. For a small amount of leakage, inert materials such as sand and vermiculite can be used to absorb it; for a large amount of leakage, it is necessary to build a dike or dig a pit to contain it, transfer it to a special collector with a pump, recycle it or transport it to a waste treatment site for disposal. In this way, it is necessary to ensure the safety of 2-chloro-6-isopropylpyridine during storage and transportation, so as to avoid disasters.