4 Chloro 2 3 Dimethylpyridine 1 Oxide
pyridine pyrrole pyrazine piperidine piperazine

4-Chloro-2,3-dimethylpyridine 1-oxide

    Specifications

    HS Code

    515921

    Chemical Formula C7H10ClNO
    Molecular Weight 159.618 g/mol
    Appearance Solid (likely white to off - white powder or crystalline solid)
    Physical State At Room Temperature Solid
    Melting Point Data needed (check relevant literature)
    Boiling Point Data needed (check relevant literature)
    Solubility In Water Low solubility (amine oxides of this type generally have limited water solubility)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, dichloromethane
    Density Data needed (check relevant literature)
    Pka Value Data needed (amine - oxide group can influence acidity; check relevant literature)
    Odor Odorless or with a faint, characteristic odor
    Stability Stable under normal conditions; may be sensitive to strong acids, bases, or oxidizing agents

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    Frequently Asked Questions

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    What are the chemical properties of 4-Chloro-2,3-dimethylpyridine 1-oxide?
    4-Chloro-2,3-dimethylpyridine-1-oxide, this is an organic compound. Its chemical properties are unique and it has a wide range of uses in the field of organic synthesis.
    Let's talk about its physical properties first, usually in a solid state. Due to the orderly arrangement of atoms in the molecule, the intermolecular force keeps it in a solid state at room temperature. As for the melting boiling point, affected by the molecular structure, the polarity introduced by the chlorine atom, the methyl group and the oxygen atom on the pyridine ring increases the intermolecular force, so the melting boiling point is relatively high.
    Regarding chemical properties, after the nitrogen atom of the pyridine ring is oxidized to pyridine-1-oxide, the electron cloud distribution changes and the electrophilicity is enhanced. The chlorine atom on the ring is active and can undergo many substitution reactions, such as nucleophilic substitution. Because of its conjugation with the pyridine ring, the carbon-chlorine bond electron cloud is biased towards the ring, making the chlorine atom vulnerable to attack by nucleophilic reagents, and replacing the chlorine atom with nucleophilic reagents such as cyano and hydroxyl groups, a variety of pyridine derivatives can be prepared.
    Furthermore, the methyl group is attached to the pyridine ring and can participate in the reaction of α-hydrogen. Due to the electron absorption of the pyridine ring, the methyl α-hydrogen acid property is enhanced, and it is easy to leave under the action of a base, which in turn triggers reactions such as alkylation and acylation.
    In addition, the pyridine-1-oxide Under certain conditions, oxygen atoms may be reduced, and the structure of the pyridine ring may change accordingly, playing a key role in some catalytic reactions or synthesis steps.
    Overall, 4-chloro-2,3-dimethylpyridine-1-oxide is of great significance in the fields of medicinal chemistry, materials science and other fields due to its unique chemical properties, providing an effective way for the synthesis of complex organic molecules.
    What are the common synthesis methods of 4-Chloro-2,3-dimethylpyridine 1-oxide?
    The common synthesis methods of 4-chloro-2,3-dimethylpyridine-1-oxide cover the following kinds.
    First, 2,3-dimethylpyridine is used as the starting material, and 2,3-dimethylpyridine-1-oxide is oxidized to obtain 2,3-dimethylpyridine-1-oxide, and then chlorination is carried out. Usually suitable oxidizing agents, such as hydrogen peroxide, peroxyacid, etc., are used to oxidize 2,3-dimethylpyridine to the corresponding pyridine-1-oxide under appropriate reaction conditions. Thereafter, using chlorination reagents, such as phosphorus oxychloride, phosphorus pentachloride, etc., under suitable solvent and temperature conditions, the specific position of pyridine-1-oxide is chlorinated to obtain 4-chloro-2,3-dimethylpyridine-1-oxide. The key to this method is to control the reaction conditions of the oxidation and chlorination steps to ensure that the reaction proceeds smoothly and has good selectivity.
    Second, halogenated pyridine derivatives are used as raw materials. Halogenated pyridine with specific substituents can be selected first, such as 4-halo-2,3-dimethylpyridine containing suitable substituents, and the nitrogen atoms on the pyridine ring can be oxidized into oxide forms by appropriate oxidation means. During the oxidation process, attention should be paid to the activity and selectivity of the oxidizing agent used to avoid unnecessary effects on halogen atoms and other substituents. At the same time, according to the characteristics of the raw materials, the temperature, time and solvent of the reaction should be adjusted reasonably to achieve higher yield and purity.
    Third, with the help of metal-catalyzed reaction pathways. Use suitable metal catalysts, such as palladium, copper and other metal complexes, to catalyze the reaction of specific reaction substrates. For example, a metal-catalyzed coupling reaction can be used to couple a substrate containing a pyridine structure with a chlorine-containing reagent under specific conditions, and at the same time complete the oxidation process of the pyridine ring. This method requires precise regulation of the amount of metal catalyst, the selection of ligands, and the reaction environment to ensure that the reaction efficiently and selectively generates the target product 4-chloro-2,3-dimethylpyridine-1-oxide. Each method has its own advantages and disadvantages. In practical applications, it is necessary to choose the best one according to specific needs and conditions.
    Where is 4-Chloro-2,3-dimethylpyridine 1-oxide used?
    4-Chloro-2,3-dimethylpyridine-1-oxide is used in various fields. In the field of medicine, it is an important intermediate for the synthesis of many drugs. When creating antibacterial drugs, compounds with unique antibacterial activities can be derived from this base. After delicate chemical reactions, structures that fit the target of pathogens can be constructed. By blocking the key metabolic pathways of pathogens or destroying their cellular structures, antibacterial effects can be achieved.
    In the field of pesticides, it is also indispensable. Using this as a starting material can prepare highly efficient and low-toxic pesticide products. After ingenious chemical modification, pesticides can precisely act on the specific physiological links of pests, or interfere with the nervous system of pests, or damage their respiratory system, which has strong killing and control effects on crop pests, and has little harm to the environment. It is in line with the needs of today's green agriculture development.
    In the field of material chemistry, 4-chloro-2,3-dimethylpyridine-1-oxide can participate in the synthesis of special materials. In the process of preparing certain high-performance polymers or functional materials, their unique chemical structure can endow the material with special electrical, optical or mechanical properties, such as enhancing the conductivity of the material, enhancing the fluorescence properties of the material, or improving the mechanical strength and stability of the material, thereby expanding the application of the material in electronic devices, optical displays and other fields.
    With its unique chemical structure, this compound plays a key role in the fields of medicine, pesticides and material chemistry, and helps to promote technological innovation and product optimization in various fields. It is of great significance to promote the development of related industries.
    What are the physical properties of 4-Chloro-2,3-dimethylpyridine 1-oxide
    4-Chloro-2,3-dimethylpyridine-1-oxide is one of the organic compounds. Its physical properties are particularly important, and it is related to its performance in various chemical processes and practical applications.
    First of all, its appearance is usually in the shape of a solid state. Due to the intermolecular force, the molecules are arranged in an orderly manner and maintain the solid-state structure. Its color is often white to light yellow powder or crystal, and this color feature can help to identify it preliminarily.
    Second and melting point, this compound has a specific melting point, which is an important physical constant. The value of the melting point can reflect the strength of the intermolecular force and the stability of the crystal structure. When the temperature rises to the melting point, the molecule is energized enough to overcome the lattice energy and convert from solid to liquid.
    Furthermore, when it comes to solubility, it exhibits a certain solubility in organic solvents, such as ethanol and acetone. This is because the molecular structure of the compound makes it possible to form interactions such as van der Waals force and hydrogen bond with organic solvent molecules, so it can be dissolved in it. However, the solubility in water is poor, because the interaction between water molecules and the compound molecules is weak, it is difficult to break the original intermolecular force and disperse it in water.
    has density, and its density is one of the characteristics of the substance, reflecting the mass contained in the unit volume. This value is crucial for considering the distribution of the compound in a particular system and its behavior when mixed with other substances.
    In addition, its low volatility means that at room temperature and pressure, the compound is more difficult to transition from solid or liquid to gaseous fugitive. This property is due to the relatively strong intermolecular forces that limit the escape of molecules from the condensed phase to the gas phase.
    All these physical properties are the basis for understanding 4-chloro-2,3-dimethylpyridine-1-oxide, and provide an important basis for its synthesis, separation, and application in many fields.
    What is the market price of 4-Chloro-2,3-dimethylpyridine 1-oxide?
    4-Chloro-2,3-dimethylpyridine-1-oxide, the price of this product in the market is difficult to break. The price of this product often changes due to various factors, just like the vagaries of the situation.
    First, the price of raw materials has a huge impact on its cost. If the raw materials required for its preparation change in the origin and output, or are affected by the weather, geographical location, and government orders, and the supply is scarce, the price will rise; on the contrary, if the supply is full, the price may drop.
    Second, the method of preparation is also the key. Sophisticated methods can reduce its cost and make the price easy; if the preparation is difficult and expensive, the price will be high.
    Third, the supply and demand of the city determines the price. If there is a strong demand for this product in the market and the supply is limited, the price will rise; if there is little demand and the supply is excessive, the price will fall.
    Fourth, trade regulations and taxation systems are also involved. In different places, regulations and taxes are different, or the cost may increase or decrease, resulting in different prices.
    Due to the interaction of the above factors, in order to determine the current market price of 4-chloro-2,3-dimethylpyridine-1-oxide, it is necessary to carefully observe the dynamics of the raw material market, the development of preparation processes, changes in supply and demand in the market, and trade regulations and taxes in various places. Only in this way can we have a closer understanding of its price.