Linshang Chemical
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2,4,6-Trichloronitro Benzene
Linshang Chemical
|
HS Code |
820829 |
| Chemical Formula | C6H2Cl3NO2 |
| Molar Mass | 226.44 g/mol |
| Appearance | Yellow - brown crystals |
| Odor | Pungent |
| Melting Point | 46 - 48 °C |
| Boiling Point | 284 - 286 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in benzene, toluene, chloroform, etc. |
| Density | 1.69 g/cm³ |
| Stability | Stable under normal conditions, but can decompose on heating |
| Toxicity | Toxic, harmful if swallowed, inhaled or in contact with skin |
As an accredited 2,4,6-Trichloronitro Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - kg pack of 2,4,6 - trichloronitro benzene in sealed, chemical - resistant container. |
| Storage | 2,4,6 - trichloronitrobenzene should be stored in a cool, dry, well - ventilated area, away from heat and ignition sources. It must be separated from oxidizing agents, reducing agents, and substances that could react with it. Store in a tightly - sealed container made of compatible materials, like steel drums or specific plastic containers, to prevent leakage and exposure. |
| Shipping | 2,4,6 - trichloronitrobenzene is a hazardous chemical. Shipping requires proper classification, use of specialized containers compliant with regulations, and strict documentation to ensure safe transport and prevent environmental and safety risks. |
Competitive 2,4,6-Trichloronitro Benzene 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
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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 2,4,6-Trichloronitro Benzene 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 2,4,6-trichloronitrobenzene?
2% 2C4% 2C6-trifluorobenzylbenzene is also an organic compound. Its main use is quite wide, in the field of medicinal chemistry, it is often a key intermediate for the creation of new drugs. It can be combined with other compounds through specific chemical reaction steps to build a molecular structure with specific pharmacological activities, which helps to develop drugs against various diseases.
In the field of materials science, it also has extraordinary performance. Its unique chemical structure gives the material special properties, such as improving the stability, heat resistance or chemical resistance of the material. For example, adding this compound to polymer materials may improve the weather resistance and corrosion resistance of the material, making it suitable for more harsh environments.
In the field of pesticide chemistry, it is also an important component. With its chemical properties, pesticides with high insecticidal, bactericidal or herbicidal effects can be designed and synthesized. Because it can precisely act on the specific physiological processes of pests, it can achieve good control effects, and has a relatively small impact on the environment.
In addition, in the study of organic synthetic chemistry, 2% 2C4% 2C6-trifluorobenzylbenzene provides an important structural unit for the construction of complex organic molecules. Chemists can expand the structural diversity of organic molecules by manipulating their reactivity and functional groups, and promote the development and innovation of organic synthetic chemistry. In fact, compounds are also of key value in many scientific and industrial fields.
In the field of materials science, it also has extraordinary performance. Its unique chemical structure gives the material special properties, such as improving the stability, heat resistance or chemical resistance of the material. For example, adding this compound to polymer materials may improve the weather resistance and corrosion resistance of the material, making it suitable for more harsh environments.
In the field of pesticide chemistry, it is also an important component. With its chemical properties, pesticides with high insecticidal, bactericidal or herbicidal effects can be designed and synthesized. Because it can precisely act on the specific physiological processes of pests, it can achieve good control effects, and has a relatively small impact on the environment.
In addition, in the study of organic synthetic chemistry, 2% 2C4% 2C6-trifluorobenzylbenzene provides an important structural unit for the construction of complex organic molecules. Chemists can expand the structural diversity of organic molecules by manipulating their reactivity and functional groups, and promote the development and innovation of organic synthetic chemistry. In fact, compounds are also of key value in many scientific and industrial fields.
What are the environmental hazards of 2,4,6-trichloronitrobenzene?
2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF%E8%83%BD%E6%9C%89%E5%A4%A7%E5%8D%B1%E4%BA%8E%E5%A4%A9%E5%9C%B0%E3%80%82
This substance is called 2,4,6-trichloroaniline, which is a toxic and harmful chemical. It persists in the environment for a long time and can accumulate in organisms.
Looking at its harm to the environment, first, it will pollute the soil. If the waste containing this substance is discarded indiscriminately or the industrial wastewater is improperly discharged, it will penetrate into the soil, causing damage to the soil structure, great loss of fertility, serious hindrance to plant growth, crop production or even failure. Second, it can dye water bodies. Flowing into rivers, lakes and seas not only deteriorates the water quality, but also makes the living environment of aquatic organisms harsh, causing the death of aquatic organisms such as fish and shellfish, and destroying the balance of aquatic ecology; if people drink this polluted water, it will also seriously damage their health. Third, it can pollute the atmosphere. During production or use, it evaporates into the air to form aerosols, which can be inhaled by humans or cause respiratory diseases. Long-term exposure is more likely to cause cancer.
Because of the stable chemical properties of 2,4,6-trichloroaniline, it is extremely difficult to degrade in nature. It can persist for a long time in soil and water, accumulate continuously, and the scope of harm continues to expand, affecting more organisms and ecosystems. And because of its lipid solubility, it is easily absorbed by organisms and accumulates in adipose tissue. It is transmitted through the food chain. Organisms at the top of the food chain have extremely high concentrations in their bodies, posing a serious threat to their health.
Therefore, the use and discharge of 2,4,6-trichloroaniline should be strictly controlled to protect the ecological environment and human health.
This substance is called 2,4,6-trichloroaniline, which is a toxic and harmful chemical. It persists in the environment for a long time and can accumulate in organisms.
Looking at its harm to the environment, first, it will pollute the soil. If the waste containing this substance is discarded indiscriminately or the industrial wastewater is improperly discharged, it will penetrate into the soil, causing damage to the soil structure, great loss of fertility, serious hindrance to plant growth, crop production or even failure. Second, it can dye water bodies. Flowing into rivers, lakes and seas not only deteriorates the water quality, but also makes the living environment of aquatic organisms harsh, causing the death of aquatic organisms such as fish and shellfish, and destroying the balance of aquatic ecology; if people drink this polluted water, it will also seriously damage their health. Third, it can pollute the atmosphere. During production or use, it evaporates into the air to form aerosols, which can be inhaled by humans or cause respiratory diseases. Long-term exposure is more likely to cause cancer.
Because of the stable chemical properties of 2,4,6-trichloroaniline, it is extremely difficult to degrade in nature. It can persist for a long time in soil and water, accumulate continuously, and the scope of harm continues to expand, affecting more organisms and ecosystems. And because of its lipid solubility, it is easily absorbed by organisms and accumulates in adipose tissue. It is transmitted through the food chain. Organisms at the top of the food chain have extremely high concentrations in their bodies, posing a serious threat to their health.
Therefore, the use and discharge of 2,4,6-trichloroaniline should be strictly controlled to protect the ecological environment and human health.
What are the physical properties of 2,4,6-trichloronitrobenzene?
2% 2C4% 2C6 -trifluorobenzylbenzene, this substance is an organic compound. Its physical properties are quite unique.
Under normal temperature, it is mostly colorless to light yellow liquid, with pure and clear texture, no obvious impurities and precipitation, and it has a transparent texture.
When it comes to smell, it emits a special aromatic smell, but this aroma is not strong and pungent, but slowly diffuses in the air, giving people a unique feeling.
The boiling point is also one of its important physical properties. Its boiling point is in a specific temperature range, at standard atmospheric pressure, about [X] degrees Celsius. At this temperature, the substance rapidly converts from a liquid state to a gaseous state, which is crucial in chemical operations such as distillation and separation.
In terms of melting point, when the temperature drops to [X] degrees Celsius, the substance will solidify from a liquid state to a solid state, showing a crystalline-like shape with a tight and regular crystal structure.
The solubility should not be underestimated. In organic solvents, such as ethanol and ether, it exhibits good solubility and can be miscible with these solvents in a certain proportion to form a uniform and stable solution. However, in water, its solubility is poor, which is related to the polarity of its molecular structure. Due to the strong polarity of water molecules, and the relatively weak polarity of this substance, it is difficult to dissolve in water.
Density is also an important physical property parameter. Its density is slightly higher than that of water. When mixed with water, it will sink to the bottom of the water. This property can be used in separation operations.
In summary, the physical properties of 2% 2C4% 2C6-trifluorobenzene are of great significance in many fields such as chemical industry and scientific research, laying the foundation for its synthesis, separation and application.
Under normal temperature, it is mostly colorless to light yellow liquid, with pure and clear texture, no obvious impurities and precipitation, and it has a transparent texture.
When it comes to smell, it emits a special aromatic smell, but this aroma is not strong and pungent, but slowly diffuses in the air, giving people a unique feeling.
The boiling point is also one of its important physical properties. Its boiling point is in a specific temperature range, at standard atmospheric pressure, about [X] degrees Celsius. At this temperature, the substance rapidly converts from a liquid state to a gaseous state, which is crucial in chemical operations such as distillation and separation.
In terms of melting point, when the temperature drops to [X] degrees Celsius, the substance will solidify from a liquid state to a solid state, showing a crystalline-like shape with a tight and regular crystal structure.
The solubility should not be underestimated. In organic solvents, such as ethanol and ether, it exhibits good solubility and can be miscible with these solvents in a certain proportion to form a uniform and stable solution. However, in water, its solubility is poor, which is related to the polarity of its molecular structure. Due to the strong polarity of water molecules, and the relatively weak polarity of this substance, it is difficult to dissolve in water.
Density is also an important physical property parameter. Its density is slightly higher than that of water. When mixed with water, it will sink to the bottom of the water. This property can be used in separation operations.
In summary, the physical properties of 2% 2C4% 2C6-trifluorobenzene are of great significance in many fields such as chemical industry and scientific research, laying the foundation for its synthesis, separation and application.
What are the chemical properties of 2,4,6-trichloronitrobenzene?
2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF%E7%9A%84%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E5%A6%82%E4%B8%8B%EF%BC%9A
This substance is a white crystalline powder with a special odor. Its melting point is relatively clear, about a certain temperature range, this property enables it to exhibit stable phase changes under specific conditions. In terms of solubility, it shows a certain tendency to dissolve in common organic solvents, but it is relatively limited in water. This solubility is related to the ratio of polar and non-polar parts in its molecular structure.
2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF has strong chemical activity. From the perspective of the reaction type, in the nucleophilic substitution reaction, the halogen atom on its benzene ring can be effectively replaced by nucleophilic reagents, introducing rich structural changes for organic synthesis. In the process of oxidation reaction, the substance exhibits the property that it can be oxidized by a specific oxidant to generate corresponding oxidation products, and the degree of oxidation is closely related to the type of oxidant and the reaction conditions.
From the perspective of stability, 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF under normal temperature and pressure without special chemical environment interference, the structure is stable; but in case of high temperature, strong acid and base or specific catalytic conditions, it is prone to structural changes or chemical reactions.
Its spectral properties are also quite characteristic. In the infrared spectrum, specific functional groups correspond to specific absorption peaks, providing a strong basis for structure identification. In the nuclear magnetic resonance spectrum, hydrogen or carbon atoms in different chemical environments show unique chemical shifts, which further assist in the accurate analysis of their molecular structures. With these chemical properties, 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF has important applications in many fields such as organic synthesis and drug development.
This substance is a white crystalline powder with a special odor. Its melting point is relatively clear, about a certain temperature range, this property enables it to exhibit stable phase changes under specific conditions. In terms of solubility, it shows a certain tendency to dissolve in common organic solvents, but it is relatively limited in water. This solubility is related to the ratio of polar and non-polar parts in its molecular structure.
2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF has strong chemical activity. From the perspective of the reaction type, in the nucleophilic substitution reaction, the halogen atom on its benzene ring can be effectively replaced by nucleophilic reagents, introducing rich structural changes for organic synthesis. In the process of oxidation reaction, the substance exhibits the property that it can be oxidized by a specific oxidant to generate corresponding oxidation products, and the degree of oxidation is closely related to the type of oxidant and the reaction conditions.
From the perspective of stability, 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF under normal temperature and pressure without special chemical environment interference, the structure is stable; but in case of high temperature, strong acid and base or specific catalytic conditions, it is prone to structural changes or chemical reactions.
Its spectral properties are also quite characteristic. In the infrared spectrum, specific functional groups correspond to specific absorption peaks, providing a strong basis for structure identification. In the nuclear magnetic resonance spectrum, hydrogen or carbon atoms in different chemical environments show unique chemical shifts, which further assist in the accurate analysis of their molecular structures. With these chemical properties, 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E7%A1%9D%E5%9F%BA%E8%8B%AF has important applications in many fields such as organic synthesis and drug development.
What is the preparation method of 2,4,6-trichloronitrobenzene?
The preparation method of 2% 2C4% 2C6-trifluorobenzyl benzene is a key technique in chemical technology. The method can be done in several ways, and is described below.
First, the nucleophilic substitution reaction is carried out with halogenated aromatics and trifluorobenzyl halides as raw materials under appropriate catalyst and reaction conditions. For example, select a suitable base, such as potassium carbonate, sodium carbonate, etc., in an organic solvent such as N, N-dimethylformamide (DMF), acetonitrile, heat and stir, and the halogen atom of the halogenated aromatics can be replaced by trifluorobenzyl to obtain the target product. This reaction requires precise temperature control. If the temperature is too high or the side reactions increase, if it is too low, the reaction rate will be slow.
Second, by the Grignard reagent method. First prepare Grignard reagents such as trifluorobenzyl magnesium halide, and then react with the corresponding aryl halides or aryl carbonyl compounds. During the reaction, it needs to be operated in an anhydrous and oxygen-free environment to avoid adverse reactions between Grignard reagents and water and oxygen. Anhydrous ether or tetrahydrofuran are often selected as solvents, which are beneficial to the stability of Grignard reagents. During the reaction process, strict control of the proportion of reactive materials can improve the yield and purity of the product.
Third, the coupling reaction catalyzed by transition metals is used. Using transition metal complexes such as palladium and nickel as catalysts, the selection of ligands is also crucial, which can enhance the activity and selectivity of the catalyst. Under basic conditions, the organic halide containing trifluorobenzyl is coupled to aryl boronic acid or its esters. This method has relatively mild conditions, wide adaptability to substrates, and can effectively construct carbon-carbon bonds of target molecules. However, the cost of catalysts is higher, or industrial production is limited.
Preparation of 2% 2C4% 2C6-trifluorobenzene requires weighing the advantages and disadvantages of each method according to the actual situation, and selecting the optimal process route to achieve the purpose of efficient, economical and environmentally friendly preparation.
First, the nucleophilic substitution reaction is carried out with halogenated aromatics and trifluorobenzyl halides as raw materials under appropriate catalyst and reaction conditions. For example, select a suitable base, such as potassium carbonate, sodium carbonate, etc., in an organic solvent such as N, N-dimethylformamide (DMF), acetonitrile, heat and stir, and the halogen atom of the halogenated aromatics can be replaced by trifluorobenzyl to obtain the target product. This reaction requires precise temperature control. If the temperature is too high or the side reactions increase, if it is too low, the reaction rate will be slow.
Second, by the Grignard reagent method. First prepare Grignard reagents such as trifluorobenzyl magnesium halide, and then react with the corresponding aryl halides or aryl carbonyl compounds. During the reaction, it needs to be operated in an anhydrous and oxygen-free environment to avoid adverse reactions between Grignard reagents and water and oxygen. Anhydrous ether or tetrahydrofuran are often selected as solvents, which are beneficial to the stability of Grignard reagents. During the reaction process, strict control of the proportion of reactive materials can improve the yield and purity of the product.
Third, the coupling reaction catalyzed by transition metals is used. Using transition metal complexes such as palladium and nickel as catalysts, the selection of ligands is also crucial, which can enhance the activity and selectivity of the catalyst. Under basic conditions, the organic halide containing trifluorobenzyl is coupled to aryl boronic acid or its esters. This method has relatively mild conditions, wide adaptability to substrates, and can effectively construct carbon-carbon bonds of target molecules. However, the cost of catalysts is higher, or industrial production is limited.
Preparation of 2% 2C4% 2C6-trifluorobenzene requires weighing the advantages and disadvantages of each method according to the actual situation, and selecting the optimal process route to achieve the purpose of efficient, economical and environmentally friendly preparation.
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