Linshang Chemical
PRODUCTS
2,4,6-Trichlorobromobenzene
Linshang Chemical
|
HS Code |
610743 |
| Chemical Formula | C6H2BrCl3 |
| Molecular Weight | 272.24 |
| Appearance | Solid (Typically) |
| Boiling Point | Around 257 - 260 °C |
| Melting Point | 64 - 67 °C |
| Density | Approx. 1.94 g/cm³ |
| Odor | Characteristic Aromatic Odor |
| Solubility In Water | Very Low Solubility |
| Solubility In Organic Solvents | Soluble in many organic solvents like benzene, toluene |
| Vapor Pressure | Low Vapor Pressure |
| Flash Point | Around 110 °C |
| Hazard Class | Harmful, may cause skin and eye irritation |
As an accredited 2,4,6-Trichlorobromobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 - gram bottle packaging for 2,4,6 - trichlorobromobenzene chemical. |
| Storage | 2,4,6 - Trichlorobromobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store it in a tightly sealed container, preferably made of corrosion - resistant materials like glass, to prevent leakage and potential chemical reactions. Label the storage clearly to avoid confusion. |
| Shipping | 2,4,6 - trichlorobromobenzene, a chemical, is shipped in specialized, leak - proof containers. These are designed to withstand transportation stresses, ensuring safe delivery while following strict hazardous material shipping regulations. |
Competitive 2,4,6-Trichlorobromobenzene 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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Where to Buy 2,4,6-Trichlorobromobenzene in China?
As a trusted 2,4,6-Trichlorobromobenzene manufacturer, we deliver:
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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-Trichlorobromobenzene 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 chemical properties of 2,4,6-trichlorobromobenzene?
2% 2C4% 2C6-trifluorobromobenzene is one of the organic compounds. Its chemical properties are unique and have many important characteristics.
In this compound, the presence of halogen atoms such as fluorine and bromine endows it with specific chemical activities. Fluorine atoms have strong electronegativity, which can change the distribution of molecular electron clouds, resulting in active chemical properties. For example, in nucleophilic substitution reactions, its halogen atoms can be replaced by nucleophilic reagents. Due to the high electronegativity of fluorine atoms, strong C-F bond energy, and special reaction conditions, specific catalysts and reaction environments are required to carry out the substitution reaction smoothly.
Because of its bromine atoms, bromine atoms can participate in some reactions, such as bromine atoms can be removed by reduction reactions, or under appropriate conditions, addition reactions with other reagents can occur. In some organic synthesis pathways, 2% 2C4% 2C6-trifluorobromobenzene can be used as a key intermediate. Through rational design of reaction steps, the activity of its halogen atoms can be used to construct complex organic molecular structures.
Furthermore, the stability of 2% 2C4% 2C6-trifluorobrobenzene is also affected by halogen atoms. Although fluorine atoms enhance molecular stability, their active chemical properties can lead to reactions under specific conditions. The solubility of this compound in organic solvents is acceptable, and a suitable organic solvent can be selected to help it participate in the reaction according to the principle of similar miscibility. When storing and using, pay attention to its chemical properties and avoid contact with strong oxidizing agents, strong reducing agents and other substances to avoid accidental chemical reactions.
In this compound, the presence of halogen atoms such as fluorine and bromine endows it with specific chemical activities. Fluorine atoms have strong electronegativity, which can change the distribution of molecular electron clouds, resulting in active chemical properties. For example, in nucleophilic substitution reactions, its halogen atoms can be replaced by nucleophilic reagents. Due to the high electronegativity of fluorine atoms, strong C-F bond energy, and special reaction conditions, specific catalysts and reaction environments are required to carry out the substitution reaction smoothly.
Because of its bromine atoms, bromine atoms can participate in some reactions, such as bromine atoms can be removed by reduction reactions, or under appropriate conditions, addition reactions with other reagents can occur. In some organic synthesis pathways, 2% 2C4% 2C6-trifluorobromobenzene can be used as a key intermediate. Through rational design of reaction steps, the activity of its halogen atoms can be used to construct complex organic molecular structures.
Furthermore, the stability of 2% 2C4% 2C6-trifluorobrobenzene is also affected by halogen atoms. Although fluorine atoms enhance molecular stability, their active chemical properties can lead to reactions under specific conditions. The solubility of this compound in organic solvents is acceptable, and a suitable organic solvent can be selected to help it participate in the reaction according to the principle of similar miscibility. When storing and using, pay attention to its chemical properties and avoid contact with strong oxidizing agents, strong reducing agents and other substances to avoid accidental chemical reactions.
What are the physical properties of 2,4,6-trichlorobromobenzene?
2% 2C4% 2C6-trifluorobromobenzene, that is, 1,3,5-trifluoro-2-bromobenzene, this material has special physical and chemical properties and is widely used in the field of chemical industry and scientific research. The following details its physical properties:
- ** Appearance and Properties **: Under normal conditions, 2,4,6-trifluorobromobenzene is a colorless to light yellow transparent liquid, which is clear and free of impurities. Its appearance characteristics are conducive to observation and identification in practical applications. In the chemical production process, its purity and reaction process can be preliminarily judged by its appearance.
- ** Melting Point and Boiling Point **: The melting point is about -19 ° C, and the boiling point is between 142-144 ° C. The low melting point indicates that it is liquid at room temperature and pressure, making it easy to use. The boiling point determines the operating conditions such as distillation and separation. In the chemical separation and purification process, it is necessary to precisely control the temperature within this boiling point range to achieve separation from other substances.
- ** Density and solubility **: The density is about 1.72 g/cm ³, which is heavier than water, so it will sink to the bottom when mixed with water. It is slightly soluble in water, but can be miscible with most organic solvents, such as ethanol, ether, acetone, etc. in any ratio. This solubility characteristic makes it often used as a solvent in organic synthesis reactions, providing a homogeneous environment for the reaction and promoting the reaction.
- ** Vapor Pressure and Volatility **: With a certain vapor pressure, it will evaporate at room temperature. In a poorly ventilated environment, its vapor is easy to accumulate. When using volatile, pay attention to the ventilation of the operating environment to avoid safety and health problems caused by high vapor concentration.
- ** Odor and irritation **: There is a special odor and it has a certain irritation. Direct contact and inhalation should be avoided during operation, as it may irritate the eyes, respiratory tract and skin. In case of inadvertent contact, correct treatment measures should be taken in time.
The physical properties of 2,4,6-trifluorobromobenzene have a significant impact on its storage, transportation and use. In actual operation, reasonable safety measures and operating specifications should be formulated based on these properties to ensure the safe and efficient application process.
- ** Appearance and Properties **: Under normal conditions, 2,4,6-trifluorobromobenzene is a colorless to light yellow transparent liquid, which is clear and free of impurities. Its appearance characteristics are conducive to observation and identification in practical applications. In the chemical production process, its purity and reaction process can be preliminarily judged by its appearance.
- ** Melting Point and Boiling Point **: The melting point is about -19 ° C, and the boiling point is between 142-144 ° C. The low melting point indicates that it is liquid at room temperature and pressure, making it easy to use. The boiling point determines the operating conditions such as distillation and separation. In the chemical separation and purification process, it is necessary to precisely control the temperature within this boiling point range to achieve separation from other substances.
- ** Density and solubility **: The density is about 1.72 g/cm ³, which is heavier than water, so it will sink to the bottom when mixed with water. It is slightly soluble in water, but can be miscible with most organic solvents, such as ethanol, ether, acetone, etc. in any ratio. This solubility characteristic makes it often used as a solvent in organic synthesis reactions, providing a homogeneous environment for the reaction and promoting the reaction.
- ** Vapor Pressure and Volatility **: With a certain vapor pressure, it will evaporate at room temperature. In a poorly ventilated environment, its vapor is easy to accumulate. When using volatile, pay attention to the ventilation of the operating environment to avoid safety and health problems caused by high vapor concentration.
- ** Odor and irritation **: There is a special odor and it has a certain irritation. Direct contact and inhalation should be avoided during operation, as it may irritate the eyes, respiratory tract and skin. In case of inadvertent contact, correct treatment measures should be taken in time.
The physical properties of 2,4,6-trifluorobromobenzene have a significant impact on its storage, transportation and use. In actual operation, reasonable safety measures and operating specifications should be formulated based on these properties to ensure the safe and efficient application process.
What are the main uses of 2,4,6-trichlorobromobenzene?
2%2C4%2C6-%E4%B8%89%E6%B0%AF%E6%BA%B4%E8%8B%AF%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E5%9C%A8%E5%8D%8E%E4%B8%BA%E7%94%9F%E5%8C%96%E3%80%81%E8%8D%AF%E7%89%A9%E5%88%86%E5%B8%83%E3%80%81%E6%B0%B4%E5%A4%84%E7%90%86%E3%80%81%E7%89%A9%E7%90%86%E5%8C%96%E5%AD%A6%E5%AE%9E%E9%AA%8C%E3%80%81%E8%87%AA%E7%84%B6%E7%A7%91%E5%AD%A6%E7%AD%94%E8%AF%95%E7%AD%94%E6%A1%88%E3%80%81%E5%88%B6%E8%8D%AF%E5%8F%8A%E6%9C%89%E6%9C%BA%E5%8C%96%E5%AD%A6%E5%88%86%E6%9E%90%E7%AD%89%E9%9D%A2%E3%80%82
"Tiangong Kaiwu" says: "All things metamorphose, and each has its own use." 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E6%BA%B4%E8%8B%AF%E4%B8%93%E6%B3%A2%E7%89%A9%E4%B9%8B%E7%94%A8%E5%85%89%E5%B9%B2%E7%94%A8%E4%B9%8B%E5%A4%A7%E8%80%85%E5%85%B6%E5%A6%82%E4%B8%8B%E3%80%82
One is in the field of biochemistry. This substance is often used as a reagent for biochemical reactions, which can help chemists understand the mysteries of the microscopic world, so that biochemical reactions occur in an orderly manner according to a specific path. It is like a delicate craftsman manipulating silk threads, guiding the direction of reactions, helping to analyze the basic composition and complex mechanism of life, and paving the way for the development of life science.
Second, the distribution level of medicine. Due to its unique chemical properties, it can precisely prepare drug ingredients in drug development and manufacturing to ensure the stability and effectiveness of drugs. Just like a swordsmith carefully quenching, so that drugs have ideal pharmacological properties and bring hope for recovery to patients.
Third, the use of water treatment. 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E6%BA%B4%E8%8B%AF%E5%8F%AF%E4%BD%9C%E6%B0%B4%E5%A4%84%E7%90%86%E5%89%82%E4%B9%8B%E4%B8%80%EF%BC%8C%E6%91%A9%E5%8A%A0%E6%B0%B4%E4%B8%AD%E6%B7%98%E8%99%AB%E7%89%A9%E7%9A%84%E6%B7%BB%E5%8A%A0%E9%80%9F%E5%BA%A6%EF%BC%8C%E5%8D%8A%E5%81%87%E6%B0%B4%E4%B8%8A%E4%B8%8B%E6%B5%81%E5%88%86%E7%A4%BA%E5%88%97%E7%9A%84%E6%B5%81%E9%80%9F%E4%B8%8D%E5%90%8C%EF%BC%8C%E6%9D%A5%E6%B8%85%E6%B8%8A%E6%B0%B4%E4%B8%AD%E6%9D%80%E6%B6%88%E7%89%A9%E8%83%BD%E5%8A%9B%E3%80%82
Fourth, physical and chemical experiments. Provide key condition control elements for experimenters. In exploring the phase changes and surface properties of substances, it is like a beacon of navigation, guiding the direction of research, and helping scientists reveal the deep-seated physical and chemical laws of substances.
Fifth, natural science answer cases. In academic research to answer questions, 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E6%BA%B4%E8%8B%AF%E4%B8%8E%E5%85%B6%E7%94%A8%E9%80%94%E5%B8%B8%E6%88%90%E4%B8%BA%E5%88%86%E6%9E%90%E4%B8%8E%E8%A7%A3%E7%AD%94%E7%9A%84%E9%87%8D%E8%A6%81%E7%94%B0%E7%9A%84%EF%BC%8C%E4%B8%BA%E5%AD%A6%E8%80%85%E6%8F%90%E4%BE%9B%E4%B8%80%E7%A7%8D%E5%85%B7%E4%BD%93%E7%9A%84%E7%A7%91%E5%AD%A6%E5%85%88%E4%BE%8B%EF%BC%8C%E4%BD%BF%E5%85%B6%E6%98%BE%E7%A4%BA%E7%9A%84%E7%90%86%E8%AE%BA%E5%92%8C%E6%96%B9%E6%B3%95%E6%9B%B4%E5%8A%A8%E6%84%8F%E4%B9%8B%E7%94%A8%E3%80%82
Sixth, pharmaceutical and organic chemistry analysis. In the pharmaceutical industry, it escorts the precise synthesis of drug molecules, such as fine screens, to screen out effective reaction paths and products. In the field of organic chemistry analysis, it provides powerful tools for analyzing the structure and properties of complex organic compounds, providing insight into the subtle differences between molecules, and promoting the vigorous development of organic chemistry.
"Tiangong Kaiwu" says: "All things metamorphose, and each has its own use." 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E6%BA%B4%E8%8B%AF%E4%B8%93%E6%B3%A2%E7%89%A9%E4%B9%8B%E7%94%A8%E5%85%89%E5%B9%B2%E7%94%A8%E4%B9%8B%E5%A4%A7%E8%80%85%E5%85%B6%E5%A6%82%E4%B8%8B%E3%80%82
One is in the field of biochemistry. This substance is often used as a reagent for biochemical reactions, which can help chemists understand the mysteries of the microscopic world, so that biochemical reactions occur in an orderly manner according to a specific path. It is like a delicate craftsman manipulating silk threads, guiding the direction of reactions, helping to analyze the basic composition and complex mechanism of life, and paving the way for the development of life science.
Second, the distribution level of medicine. Due to its unique chemical properties, it can precisely prepare drug ingredients in drug development and manufacturing to ensure the stability and effectiveness of drugs. Just like a swordsmith carefully quenching, so that drugs have ideal pharmacological properties and bring hope for recovery to patients.
Third, the use of water treatment. 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E6%BA%B4%E8%8B%AF%E5%8F%AF%E4%BD%9C%E6%B0%B4%E5%A4%84%E7%90%86%E5%89%82%E4%B9%8B%E4%B8%80%EF%BC%8C%E6%91%A9%E5%8A%A0%E6%B0%B4%E4%B8%AD%E6%B7%98%E8%99%AB%E7%89%A9%E7%9A%84%E6%B7%BB%E5%8A%A0%E9%80%9F%E5%BA%A6%EF%BC%8C%E5%8D%8A%E5%81%87%E6%B0%B4%E4%B8%8A%E4%B8%8B%E6%B5%81%E5%88%86%E7%A4%BA%E5%88%97%E7%9A%84%E6%B5%81%E9%80%9F%E4%B8%8D%E5%90%8C%EF%BC%8C%E6%9D%A5%E6%B8%85%E6%B8%8A%E6%B0%B4%E4%B8%AD%E6%9D%80%E6%B6%88%E7%89%A9%E8%83%BD%E5%8A%9B%E3%80%82
Fourth, physical and chemical experiments. Provide key condition control elements for experimenters. In exploring the phase changes and surface properties of substances, it is like a beacon of navigation, guiding the direction of research, and helping scientists reveal the deep-seated physical and chemical laws of substances.
Fifth, natural science answer cases. In academic research to answer questions, 2%2C4%2C6-%E4%B8%89%E6%B0%AF%E6%BA%B4%E8%8B%AF%E4%B8%8E%E5%85%B6%E7%94%A8%E9%80%94%E5%B8%B8%E6%88%90%E4%B8%BA%E5%88%86%E6%9E%90%E4%B8%8E%E8%A7%A3%E7%AD%94%E7%9A%84%E9%87%8D%E8%A6%81%E7%94%B0%E7%9A%84%EF%BC%8C%E4%B8%BA%E5%AD%A6%E8%80%85%E6%8F%90%E4%BE%9B%E4%B8%80%E7%A7%8D%E5%85%B7%E4%BD%93%E7%9A%84%E7%A7%91%E5%AD%A6%E5%85%88%E4%BE%8B%EF%BC%8C%E4%BD%BF%E5%85%B6%E6%98%BE%E7%A4%BA%E7%9A%84%E7%90%86%E8%AE%BA%E5%92%8C%E6%96%B9%E6%B3%95%E6%9B%B4%E5%8A%A8%E6%84%8F%E4%B9%8B%E7%94%A8%E3%80%82
Sixth, pharmaceutical and organic chemistry analysis. In the pharmaceutical industry, it escorts the precise synthesis of drug molecules, such as fine screens, to screen out effective reaction paths and products. In the field of organic chemistry analysis, it provides powerful tools for analyzing the structure and properties of complex organic compounds, providing insight into the subtle differences between molecules, and promoting the vigorous development of organic chemistry.
What are the synthesis methods of 2,4,6-trichlorobromobenzene?
2% 2C4% 2C6-trichlorotoluene is also an organic compound. The synthesis method has been studied by many parties in the past, and the important ones are listed as follows:
First, it starts with toluene and is obtained by chlorination. The toluene is placed in a special device, filled with an appropriate amount of chlorine, and introduced by light or a specific catalyst to make the chlorine react with toluene one by one. First get monochlorotoluene, then dichloro, and finally get 2% 2C4% 2C6-trichlorotoluene. However, in this way, the temperature and amount of chlorine of the reaction need to be well controlled, otherwise the side effects will be clustered and the yield will be difficult to be high.
Second, take p-chlorotoluene as the base. p-Chlorotoluene is also chlorinated first. In suitable conditions, chlorine gradually enters the benzene ring, and the target 2% 2C4% 2C6-trichlorotoluene can be obtained. Compared with the former, the side reaction or slightly reduced, but the reaction conditions are also strictly controlled. The choice of temperature, pressure and catalyst is all about success or failure.
Third, m-chlorotoluene is used as the starting material. The chlorination of m-chlorotoluene can also reach 2% 2C4% 2C6-trichlorotoluene by a reasonable method. However, this raw material is relatively rare, and its chlorination process is also difficult, so the application is slightly narrower.
Fourth, benzoic acid is used as the starting material. Benzoic acid first forms an acyl chloride, and then introduces chlorine atoms through a specific method, and then through a series of transformations, it is also expected to obtain 2% 2C4% 2C6-trichlorotoluene. Although this path is difficult, in some situations, it may have unique advantages.
All these synthetic methods have their own advantages and disadvantages. Fang family should make a careful choice according to the materials used, the effect to be achieved, the economic calculation and other factors, in order to achieve good results.
First, it starts with toluene and is obtained by chlorination. The toluene is placed in a special device, filled with an appropriate amount of chlorine, and introduced by light or a specific catalyst to make the chlorine react with toluene one by one. First get monochlorotoluene, then dichloro, and finally get 2% 2C4% 2C6-trichlorotoluene. However, in this way, the temperature and amount of chlorine of the reaction need to be well controlled, otherwise the side effects will be clustered and the yield will be difficult to be high.
Second, take p-chlorotoluene as the base. p-Chlorotoluene is also chlorinated first. In suitable conditions, chlorine gradually enters the benzene ring, and the target 2% 2C4% 2C6-trichlorotoluene can be obtained. Compared with the former, the side reaction or slightly reduced, but the reaction conditions are also strictly controlled. The choice of temperature, pressure and catalyst is all about success or failure.
Third, m-chlorotoluene is used as the starting material. The chlorination of m-chlorotoluene can also reach 2% 2C4% 2C6-trichlorotoluene by a reasonable method. However, this raw material is relatively rare, and its chlorination process is also difficult, so the application is slightly narrower.
Fourth, benzoic acid is used as the starting material. Benzoic acid first forms an acyl chloride, and then introduces chlorine atoms through a specific method, and then through a series of transformations, it is also expected to obtain 2% 2C4% 2C6-trichlorotoluene. Although this path is difficult, in some situations, it may have unique advantages.
All these synthetic methods have their own advantages and disadvantages. Fang family should make a careful choice according to the materials used, the effect to be achieved, the economic calculation and other factors, in order to achieve good results.
How stable is 2,4,6-trichlorobromobenzene in the environment?
2% 2C4% 2C6-trifluorobromobenzene is in the environment, and its stability is related to many aspects. This substance contains a special atomic structure, and the fluorine atom has a high electronegativity, which forms a strong covalent bond with the benzene ring, which greatly affects its stability. The strong electron-absorbing effect of fluorine atoms reduces the electron cloud density of the benzene ring, stabilizes the benzene ring structure, and enhances the resistance to external action.
From the analysis of chemical bond energy, C-F bond energy is large, and high energy is required for fracture. Under common environmental conditions, it is difficult to provide enough energy to break the C-F bond, so 2% 2C4% 2C6-trifluorobrobenzene can maintain a relatively stable state. However, in certain extreme environments, such as high temperature, strong radiation, or the presence of special catalysts, its stability may be challenged. High temperatures can give molecules enough kinetic energy to accelerate the vibration of chemical bonds. When the energy reaches the dissociation energy of C-F bonds or other related chemical bonds, the bonds will break, triggering material decomposition or reaction. Strong radiation can provide high-energy photons, which interact with molecules to cause chemical bonds to ionize or excite, thereby affecting stability. Special catalysts can reduce the activation energy of the reaction, prompting 2% 2C4% 2C6-trifluorobromobenzene to participate in the reaction and change its stable state. In general, in the conventional environment, 2% 2C4% 2C6-trifluorobromobenzene fluoride has certain stability due to its atomic properties and chemical bond energy factors; but under extreme conditions, its stability will be significantly affected.
From the analysis of chemical bond energy, C-F bond energy is large, and high energy is required for fracture. Under common environmental conditions, it is difficult to provide enough energy to break the C-F bond, so 2% 2C4% 2C6-trifluorobrobenzene can maintain a relatively stable state. However, in certain extreme environments, such as high temperature, strong radiation, or the presence of special catalysts, its stability may be challenged. High temperatures can give molecules enough kinetic energy to accelerate the vibration of chemical bonds. When the energy reaches the dissociation energy of C-F bonds or other related chemical bonds, the bonds will break, triggering material decomposition or reaction. Strong radiation can provide high-energy photons, which interact with molecules to cause chemical bonds to ionize or excite, thereby affecting stability. Special catalysts can reduce the activation energy of the reaction, prompting 2% 2C4% 2C6-trifluorobromobenzene to participate in the reaction and change its stable state. In general, in the conventional environment, 2% 2C4% 2C6-trifluorobromobenzene fluoride has certain stability due to its atomic properties and chemical bond energy factors; but under extreme conditions, its stability will be significantly affected.
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