Pyrazine 2 3 Dichloro 5 Methyl
pyridine pyrrole pyrazine piperidine piperazine

Pyrazine, 2,3-dichloro-5-methyl-

    Specifications

    HS Code

    563424

    Chemical Formula C5H4Cl2N2
    Molecular Weight 163.004 g/mol
    Stability Can be stable under normal conditions, but reactivity may occur with strong oxidizing agents or in specific reaction conditions

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    General Information
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    Frequently Asked Questions

    As a leading Pyrazine, 2,3-dichloro-5-methyl- 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 physical properties of Pyrazine, 2, 3-dichloro-5-methyl-
    2% 2C3-dichloro-5-methylpyrazine, this compound is an organic compound with unique physical properties, which is related to its application in chemical industry.
    Looking at its shape, it is mostly colorless to light yellow liquid under normal conditions, with a clear texture and can be seen flowing. Its smell is specific, although it is not pungent or intolerable, it also has a discernible smell, just like being in a chemical industry, you can feel its unique charm.
    When it comes to boiling point, it is about a certain temperature range. When the external temperature rises to this point, 2% 2C3-dichloro-5-methylpyrazine gradually converts from a liquid state to a gaseous state. This boiling point is crucial in separation and purification and other process steps. Its melting point is also fixed. At low temperatures, it can condense into a solid state, and the morphology changes depending on the temperature.
    In terms of solubility, it has a certain solubility in organic solvents, such as ethanol, ether, etc., and can be melted with it. However, in water, the solubility is poor, similar to the difficulty of combining oil and water. This property determines its behavior in different solvent systems. < Br >
    In terms of density, there is a relatively fixed value. Compared with water, it is either lighter or heavier. In the mixed system, there are layered phenomena due to density differences, which provides a basis for separation operations.
    In addition, its stability is acceptable under general conditions. In case of extreme conditions such as hot topics and open flames, or there is a risk of danger, it needs to be properly stored, away from fire and heat sources, and placed in a cool and ventilated place to ensure safety.
    What are the chemical properties of Pyrazine, 2, 3-dichloro-5-methyl-
    2,3-Dichloro-5-methylpyrazine is an organic compound. It is active and has unique chemical properties.
    On the reactivity, the electron cloud density of pyrazine ring changes due to the presence of chlorine atoms and methyl groups. Chlorine atoms have electron-absorbing properties, which reduce the electron cloud density on the ring and the electrophilic substitution reaction activity. Methyl groups are the power supply groups, which can increase the electron cloud density of adjacent and para-potential to a certain extent, which has an impact on the electrophilic substitution reaction. In general, the electrophilic substitution reaction conditions of 2,3-dichloro-5-methylpyrazine are more severe than that of pyrazine itself.
    In the nucleophilic substitution reaction, the chlorine atom can be used as a leaving group, which is easily attacked by the nucleophilic reagent and undergoes a substitution reaction. Due to the large electronegativity of the chlorine atom, the bond between the carbon atom and the carbon atom is strong in polarity, and it is easy to crack. Nucleophilic reagents such as sodium alcohol and amines can attack the carbon atom connected to the chlorine to generate new compounds.
    From the perspective of redox, 2,3-dichloro-5-methylpyrazine can be reduced, and the nitrogen atom of the pyrazine ring can be partially or completely hydrogenated under the action of a suitable reducing agent to generate corresponding reduction products. At the same time, in case of strong oxidizing agents, some groups in the molecule may be oxidi
    In terms of solubility, because it is an organic compound, it has a certain solubility in organic solvents such as dichloromethane, chloroform, acetone, etc., but has a small solubility in water. Due to its limited molecular polarity, the interaction with water molecules is weak.
    The chemical properties of 2,3-dichloro-5-methylpyrazine are significantly affected by the chlorine atom and methyl group in its structure. In the field of organic synthesis, it can be used as a key intermediate to construct complex organic molecules through various reactions.
    What are the main uses of Pyrazine, 2, 3-dichloro-5-methyl-
    2,3-Dichloro-5-methylpyrazine has a wide range of uses. In the field of medicine, it is an important raw material for traditional Chinese medicine. It can help synthesize drugs with special effects, or play unique pharmacological effects on specific diseases, so as to cure various diseases and contribute to the development of medicine.
    In the field of pesticides, it also has extraordinary uses. It can be used as an active ingredient to make pesticides to remove pests, protect the growth of crops, vegetables and fruits, and ensure the hope of a bumper harvest. Because of its unique chemical structure, it can affect the physiological function of pests, prevent their reproduction, feeding, etc., and achieve the effect of pest control.
    In the fragrance industry, 2,3-dichloro-5-methylpyrazine also has a place. It can add a unique smell to the fragrance or add a unique flavor to the fragrance. In the preparation of daily flavors and food flavors, its unique smell increases the richness and layering of the fragrance, making the product smell more attractive and catering to the diverse needs of people for aroma.
    From this perspective, 2,3-dichloro-5-methylpyrazine is of great value in the pharmaceutical, pesticide, fragrance and other industries, and has made great contributions to promoting the development of various industries.
    What is the preparation method of Pyrazine, 2, 3-dichloro-5-methyl-
    To prepare 2,3-dichloro-5-methylpyrazine, the following ancient methods can be used.
    First take the appropriate starting material, often with methyl-containing pyrazine derivatives as the starting point. If 5-methylpyrazine is the basis, this is the base choice. Because its structure already has the required methyl group, it can lay the foundation for subsequent reactions.
    In the reaction system, add an appropriate amount of chlorination reagents. Common chlorination reagents, such as chlorine ($Cl_2 $), thionyl chloride ($SOCl_2 $) or phosphorus oxychloride ($POCl_3 $), etc. If chlorine is used, the reaction can proceed smoothly under suitable reaction conditions, such as light or the presence of a catalyst. Light can initiate a free radical reaction, which prompts chlorine atoms to replace hydrogen atoms on the pyrazine ring. If you choose thionyl chloride or phosphorus oxychloride, you often need to have appropriate catalysts, such as Lewis acid (such as $AlCl_3 $, $FeCl_3 $, etc.). Lewis acid can interact with chlorination reagents to enhance its electrophilicity, which is conducive to the attack of chlorine atoms on specific positions on the pyrazine ring.
    Control of reaction temperature and time is also critical. The reaction temperature should not be too high to avoid excessive chlorination or other side reactions. Generally speaking, the reaction process can be observed before the lower temperature, and then the temperature can be fine-tuned according to the actual situation. The reaction time depends on the rate of the reaction and the monitoring results. The reaction process can be monitored in real time by means of thin layer chromatography (TLC). When the raw material point disappears and the product point reaches the expected ratio, the reaction can be regarded as basically completed.
    After the reaction is completed, the product needs to be separated and purified. Usually, the product is extracted with an organic solvent to enrich the organic phase. Then it is further purified by distillation, column chromatography and other methods. Distillation can separate the product according to the difference in boiling point between the product and the impurity. Column chromatography uses the different distribution coefficients of different substances between the stationary phase and the mobile phase to achieve effective separation of the product and the impurity, and finally obtains a pure 2,3-dichloro-5-methylpyrazine.
    What impact does Pyrazine, 2, 3-dichloro-5-methyl- have on the environment?
    2% 2C3-dichloro-5-methylpyrazine, the impact on the environment cannot be ignored. The chemical properties of this substance are different, and it may cause various changes in the natural environment.
    Looking at its structure, chlorine and methyl are attached to the pyrazine ring, resulting in its active properties. It reacts chemically in the atmosphere or with various substances, affecting air quality. If it enters the water body, it has a certain solubility and may disturb the aquatic ecology. Exposure of aquatic organisms to it may cause abnormal physiological functions, hinder development and reproduction, and even endanger survival, disrupting the balance of water ecology.
    In the soil environment, it may be adsorbed by soil particles, changing the physical and chemical properties of the soil, hindering the uptake of nutrients and water by plant roots, causing poor plant growth. And this substance may be enriched through the food chain, gradually accumulating in high-rise organisms from lower organisms, and eventually endangering human health.
    In addition, its decomposition or transformation products should not be underestimated, or have more toxicity and environmental persistence. In the long run, the potential threat to the environment is profound. Therefore, such chemicals should be handled with caution and closely monitored to prevent them from causing serious harm to the environment and maintain the harmony and stability of the natural ecology.