Linshang Chemical
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2,3,4-Trichloronitrobenzene
Linshang Chemical
|
HS Code |
932344 |
| Chemical Formula | C6H2Cl3NO2 |
| Molar Mass | 226.44 g/mol |
| Appearance | Yellow - brown solid |
| Melting Point | 68 - 70 °C |
| Boiling Point | 274 - 276 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in benzene, toluene, xylene, etc. |
| Vapor Pressure | Low |
| Density | 1.634 g/cm³ (20 °C) |
| Odor | Pungent |
As an accredited 2,3,4-Trichloronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 - gram bottle packaging for 2,3,4 - trichloronitrobenzene chemical. |
| Storage | 2,3,4 - Trichloronitrobenzene should be stored in a cool, dry, well - ventilated area, away from sources of heat, ignition, and direct sunlight. It must be stored separately from incompatible substances like oxidizing agents, reducing agents, and bases. Keep containers tightly sealed to prevent leakage, and store in a dedicated chemical storage facility with proper labeling for safety. |
| Shipping | 2,3,4 - Trichloronitrobenzene is a hazardous chemical. Shipping must comply with strict regulations. It should be properly packaged in approved containers, labeled clearly, and transported by carriers licensed for such hazardous materials. |
Competitive 2,3,4-Trichloronitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 2,3,4-Trichloronitrobenzene in China?
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Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 2,3,4-Trichloronitrobenzene 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 2,3,4-trichloronitrobenzene?
2% 2C3% 2C4-trihydroxybenzylbenzene has a wide range of main uses. In the field of medicine, this compound may have unique pharmacological activities. In its structure, hydroxyl groups and benzyl groups are combined with each other, or can interact with specific receptors, enzymes, etc. in organisms.
According to modern medical research, many natural products and synthetic compounds have shown therapeutic effects due to their unique chemical structures. 2% 2C3% 2C4-trihydroxybenzylbenzene hydroxyl groups can participate in the formation of hydrogen bonds, combine with biological macromolecules, or regulate their functions. It is, or is expected to be developed into new drugs for the treatment of diseases such as inflammation and tumors.
In the field of materials science, this substance also has potential value. The presence of hydroxyl groups makes the molecule have a certain polarity, or can improve the physical properties such as hydrophilicity and solubility of the material. It can be introduced into polymer materials to improve some properties of the material, such as enhancing the compatibility of the material with other substances, and then expanding the application scenarios of the material.
Furthermore, in the field of chemical synthesis, 2% 2C3% 2C4 -trihydroxybenzylbenzene can be used as a key intermediate. With its unique structure, many compounds with more complex structures can be derived. Chemists can modify and modify it by means of organic synthesis to prepare new compounds with specific functions, which contribute to the development of chemical science. Overall, 2% 2C3% 2C4-trihydroxybenzylbenzene has important potential applications in many fields such as medicine, materials, and chemical synthesis.
According to modern medical research, many natural products and synthetic compounds have shown therapeutic effects due to their unique chemical structures. 2% 2C3% 2C4-trihydroxybenzylbenzene hydroxyl groups can participate in the formation of hydrogen bonds, combine with biological macromolecules, or regulate their functions. It is, or is expected to be developed into new drugs for the treatment of diseases such as inflammation and tumors.
In the field of materials science, this substance also has potential value. The presence of hydroxyl groups makes the molecule have a certain polarity, or can improve the physical properties such as hydrophilicity and solubility of the material. It can be introduced into polymer materials to improve some properties of the material, such as enhancing the compatibility of the material with other substances, and then expanding the application scenarios of the material.
Furthermore, in the field of chemical synthesis, 2% 2C3% 2C4 -trihydroxybenzylbenzene can be used as a key intermediate. With its unique structure, many compounds with more complex structures can be derived. Chemists can modify and modify it by means of organic synthesis to prepare new compounds with specific functions, which contribute to the development of chemical science. Overall, 2% 2C3% 2C4-trihydroxybenzylbenzene has important potential applications in many fields such as medicine, materials, and chemical synthesis.
What are the effects of 2,3,4-trichloronitrobenzene on the environment?
2% 2C3% 2C4-trichlorobenzylbenzene. The effect of this substance on the environment is quite complex, and I will describe it in detail for you.
This substance is quite toxic. If released in the natural environment, it is harmful to all kinds of organisms. It may remain in the soil, hindering the development of plant roots and nutrient absorption, causing plant growth to be trapped, and even wither and die.
In the aquatic environment, 2% 2C3% 2C4-trichlorobenzylbenzene can affect the survival of aquatic organisms. After fish are exposed, they may show breathing difficulties and abnormal behavior. Over time, the population will also decrease. Aquatic plants are also damaged by it, and photosynthesis and metabolism are destroyed, which in turn affects the balance of the entire aquatic ecosystem.
And it is bioaccumulative, transmitted through the food chain, and the concentration in organisms is gradually increasing. If humans ingest contaminated organisms, their health may be seriously threatened, such as causing diseases of the liver, kidneys and other organs, or even teratogenic and carcinogenic risks.
And because of its relatively stable chemical properties, it is difficult to degrade in the environment, can be retained for a long time, and continues to have adverse effects on the environment. Therefore, the control and monitoring of 2% 2C3% 2C4-trichlorobenzylbenzene is extremely important to prevent it from causing irreparable damage to the environment and organisms.
This substance is quite toxic. If released in the natural environment, it is harmful to all kinds of organisms. It may remain in the soil, hindering the development of plant roots and nutrient absorption, causing plant growth to be trapped, and even wither and die.
In the aquatic environment, 2% 2C3% 2C4-trichlorobenzylbenzene can affect the survival of aquatic organisms. After fish are exposed, they may show breathing difficulties and abnormal behavior. Over time, the population will also decrease. Aquatic plants are also damaged by it, and photosynthesis and metabolism are destroyed, which in turn affects the balance of the entire aquatic ecosystem.
And it is bioaccumulative, transmitted through the food chain, and the concentration in organisms is gradually increasing. If humans ingest contaminated organisms, their health may be seriously threatened, such as causing diseases of the liver, kidneys and other organs, or even teratogenic and carcinogenic risks.
And because of its relatively stable chemical properties, it is difficult to degrade in the environment, can be retained for a long time, and continues to have adverse effects on the environment. Therefore, the control and monitoring of 2% 2C3% 2C4-trichlorobenzylbenzene is extremely important to prevent it from causing irreparable damage to the environment and organisms.
What are the preparation methods of 2,3,4-trichloronitrobenzene?
There are several ways to prepare 2% 2C3% 2C4-trifluorobenzene.
One method can be obtained by reacting halogenated benzene with a reagent containing trifluoromethyl through nucleophilic substitution. In a clean reactor, place an appropriate amount of halogenated benzene, prepare a compound with trifluoromethyl, add an appropriate amount of base as a catalyst, and make it fully react at a suitable temperature and pressure. When the reaction is completed, the process of the reaction needs to be closely monitored, and the temperature and pressure should be adjusted in a timely manner to make the reaction proceed smoothly. After the reaction is completed, the impurities can be removed through separation and purification, and pure 2% 2C3% 2C4-trifluorobenzylbenzene can be obtained.
The second method uses benzene derivatives as the starting material and is prepared by multi-step reaction. The benzene derivative undergoes a substitution reaction with a specific reagent to introduce a specific functional group, and then undergoes a fluorination reaction to replace the atoms at the desired position with fluorine atoms. During the fluorination reaction, select an appropriate fluorination reagent and control the reaction conditions to achieve the purpose of selective fluorination. Subsequent to a series of reactions, such as reduction and condensation, the structure of the target molecule is gradually constructed. After each step of the reaction, the product needs to be carefully separated and purified to ensure the purity and quality of the product.
The third method uses the reaction path catalyzed by transition metals. Select suitable transition metal catalysts, such as palladium, nickel, etc., with specific ligands, so that the reactants can be coupled under mild conditions. The benzene-ring-containing substrate and the trifluoromethyl-containing reactant are reacted in an organic solvent under the action of catalysts and ligands. Control the temperature, time and other conditions of the reaction, so that the reaction can efficiently and selectively generate 2% 2C3% 2C4-trifluorobenzylbenzene. At the end of the reaction, the product is separated by extraction, column chromatography and other means to obtain the target compound.
One method can be obtained by reacting halogenated benzene with a reagent containing trifluoromethyl through nucleophilic substitution. In a clean reactor, place an appropriate amount of halogenated benzene, prepare a compound with trifluoromethyl, add an appropriate amount of base as a catalyst, and make it fully react at a suitable temperature and pressure. When the reaction is completed, the process of the reaction needs to be closely monitored, and the temperature and pressure should be adjusted in a timely manner to make the reaction proceed smoothly. After the reaction is completed, the impurities can be removed through separation and purification, and pure 2% 2C3% 2C4-trifluorobenzylbenzene can be obtained.
The second method uses benzene derivatives as the starting material and is prepared by multi-step reaction. The benzene derivative undergoes a substitution reaction with a specific reagent to introduce a specific functional group, and then undergoes a fluorination reaction to replace the atoms at the desired position with fluorine atoms. During the fluorination reaction, select an appropriate fluorination reagent and control the reaction conditions to achieve the purpose of selective fluorination. Subsequent to a series of reactions, such as reduction and condensation, the structure of the target molecule is gradually constructed. After each step of the reaction, the product needs to be carefully separated and purified to ensure the purity and quality of the product.
The third method uses the reaction path catalyzed by transition metals. Select suitable transition metal catalysts, such as palladium, nickel, etc., with specific ligands, so that the reactants can be coupled under mild conditions. The benzene-ring-containing substrate and the trifluoromethyl-containing reactant are reacted in an organic solvent under the action of catalysts and ligands. Control the temperature, time and other conditions of the reaction, so that the reaction can efficiently and selectively generate 2% 2C3% 2C4-trifluorobenzylbenzene. At the end of the reaction, the product is separated by extraction, column chromatography and other means to obtain the target compound.
What are the physical properties of 2,3,4-trichloronitrobenzene?
2%2C3%2C4-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E5%A6%82%E4%B8%8B%EF%BC%9A
This substance is often colorless to light yellow liquid, its appearance characteristics are obvious, and it exists stably under normal temperature and pressure. Looking at its properties, it has a certain fluidity, just like smart water, but it has unique characteristics.
Its density is different from common substances. Under specific conditions, the density value shows uniqueness. In many reactions and practical applications, this density characteristic has a great impact.
Furthermore, the boiling point is also one of its important physical properties. In a specific pressure environment, when it reaches a certain temperature, it will boil and transform into a gaseous state. This boiling point value provides a key basis for chemical production, separation and purification processes. In terms of solubility, in organic solvents, it shows good solubility and can dissolve with some organic solvents to form a uniform and stable system. In water, the solubility is poor, and this difference plays a key role in operations such as substance separation and extraction.
Volatility cannot be ignored. Under appropriate temperatures and environments, it has a certain degree of volatility and will gradually diffuse into the air. This characteristic needs to be properly considered during storage and use to avoid loss and safety hazards.
2%2C3%2C4-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%9A%84%E8%BF%99%E7%A7%8D%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E7%AD%89%E7%89%B9%E6%80%A7%EF%BC%8C%E4%B8%BA%E5%85%B6%E5%9C%A8%E5%88%86%E6%9E%90%E5%8C%96%E5%B7%A5%E3%80%81%E5%8C%96%E5%B7%A5%E7%94%9F%E4%BA%A7%E7%AD%89%E9%9D%A2%E9%9D%A2%E9%9D%A2%E7%9A%84%E5%BA%94%E7%94%A8%E6%8F%90%E4%BE%9B%E4%BA%86%E9%87%8D%E8%A6%81%E7%9A%84%E5%9F%BA%E7%A1%80%E6%95%B0%E6%8D%AE%E4%B8%8E%E5%8F%82%E8%80%83%E3%80%82
This substance is often colorless to light yellow liquid, its appearance characteristics are obvious, and it exists stably under normal temperature and pressure. Looking at its properties, it has a certain fluidity, just like smart water, but it has unique characteristics.
Its density is different from common substances. Under specific conditions, the density value shows uniqueness. In many reactions and practical applications, this density characteristic has a great impact.
Furthermore, the boiling point is also one of its important physical properties. In a specific pressure environment, when it reaches a certain temperature, it will boil and transform into a gaseous state. This boiling point value provides a key basis for chemical production, separation and purification processes. In terms of solubility, in organic solvents, it shows good solubility and can dissolve with some organic solvents to form a uniform and stable system. In water, the solubility is poor, and this difference plays a key role in operations such as substance separation and extraction.
Volatility cannot be ignored. Under appropriate temperatures and environments, it has a certain degree of volatility and will gradually diffuse into the air. This characteristic needs to be properly considered during storage and use to avoid loss and safety hazards.
2%2C3%2C4-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%9A%84%E8%BF%99%E7%A7%8D%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E7%AD%89%E7%89%B9%E6%80%A7%EF%BC%8C%E4%B8%BA%E5%85%B6%E5%9C%A8%E5%88%86%E6%9E%90%E5%8C%96%E5%B7%A5%E3%80%81%E5%8C%96%E5%B7%A5%E7%94%9F%E4%BA%A7%E7%AD%89%E9%9D%A2%E9%9D%A2%E9%9D%A2%E7%9A%84%E5%BA%94%E7%94%A8%E6%8F%90%E4%BE%9B%E4%BA%86%E9%87%8D%E8%A6%81%E7%9A%84%E5%9F%BA%E7%A1%80%E6%95%B0%E6%8D%AE%E4%B8%8E%E5%8F%82%E8%80%83%E3%80%82
What are the chemical properties of 2,3,4-trichloronitrobenzene?
2% 2C3% 2C4-trifluorobenzyl benzene has unique chemical properties. This substance has a certain stability, and it is relatively stable at room temperature and pressure. However, under specific conditions, such as high temperature and strong oxidant environment, it will also show activity.
Its physical form is often a liquid, with a specific boiling point and melting point. Because of its fluorine atom, the intermolecular forces are different, which affects the melting boiling point. And its solubility also has characteristics. It has good solubility in some organic solvents such as toluene and dichloromethane, but it is difficult to dissolve in water. This difference in solubility is due to the different polarities of molecules. Fluorine-containing groups change the polarity of molecules, making it difficult to dissolve due to the large difference in polarity from water.
In terms of chemical activity, the benzyl moiety has a certain reactivity. The hydrogen atom on the benzyl carbon can participate in the substitution reaction, and under appropriate catalyst and reaction conditions, it can be replaced by other groups to derive a variety of compounds. At the same time, the conjugate structure of the benzene ring makes it possible to undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. And because of the large electronegativity of the fluorine atom, it affects the distribution of the electron cloud of the benzene ring, which in turn affects the position and activity of the electrophilic substitution reaction. The presence of fluorine atoms enhances the stability and chemical inertness of the molecule, so that the substance exhibits special reactivity and selectivity in
Its physical form is often a liquid, with a specific boiling point and melting point. Because of its fluorine atom, the intermolecular forces are different, which affects the melting boiling point. And its solubility also has characteristics. It has good solubility in some organic solvents such as toluene and dichloromethane, but it is difficult to dissolve in water. This difference in solubility is due to the different polarities of molecules. Fluorine-containing groups change the polarity of molecules, making it difficult to dissolve due to the large difference in polarity from water.
In terms of chemical activity, the benzyl moiety has a certain reactivity. The hydrogen atom on the benzyl carbon can participate in the substitution reaction, and under appropriate catalyst and reaction conditions, it can be replaced by other groups to derive a variety of compounds. At the same time, the conjugate structure of the benzene ring makes it possible to undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. And because of the large electronegativity of the fluorine atom, it affects the distribution of the electron cloud of the benzene ring, which in turn affects the position and activity of the electrophilic substitution reaction. The presence of fluorine atoms enhances the stability and chemical inertness of the molecule, so that the substance exhibits special reactivity and selectivity in
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