Linshang Chemical
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2,4,6-Trifluorochlorobenzene
Linshang Chemical
|
HS Code |
896156 |
| Chemical Formula | C6H2ClF3 |
| Molar Mass | 166.53 g/mol |
| Appearance | Colorless liquid |
| Odor | Characteristic |
| Density | 1.42 g/cm³ (approximate) |
| Boiling Point | 128 - 130 °C |
| Melting Point | −57 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents like ethanol, ether |
| Vapor Pressure | Vapor pressure data available at specific temperatures |
| Flash Point | 32 °C (closed cup, approximate) |
As an accredited 2,4,6-Trifluorochlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle packaging for 2,4,6 - trifluorochlorobenzene chemical. |
| Storage | 2,4,6 - trifluorochlorobenzene should be stored in a cool, well - ventilated area, away from heat sources and ignition points. It should be kept in a tightly sealed container to prevent vapor leakage. Store it separately from oxidizing agents and reactive chemicals. Ensure the storage place has secondary containment to handle potential spills, and label the storage area clearly for safety. |
| Shipping | 2,4,6 - trifluorochlorobenzene is shipped in specialized, tightly - sealed containers. These containers are designed to prevent leakage and withstand potential impacts. Shipping follows strict hazardous chemical regulations to ensure safety during transit. |
Competitive 2,4,6-Trifluorochlorobenzene 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 2,4,6-Trifluorochlorobenzene 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 2,4,6-Trifluorochlorobenzene 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-trifluorochlorobenzene?
2% 2C4% 2C6-tribromophenol is also an organic compound. Its main uses are quite extensive.
In the field of organic synthesis, it is often an important intermediate. It can be converted into other organic compounds through specific chemical reactions, such as substitution and addition reactions with many reagents, to prepare organic molecules with more complex structures, which is of great significance in the fields of pharmaceutical chemistry and materials science.
In drug development, it also has potential uses. Due to its special chemical structure, it may participate in the construction of active components of drugs, making great contributions to the development of new drugs. Medicinal chemists can explore compounds with specific pharmacological activities by modifying and modifying their structures, hoping to develop drugs with better curative effects and fewer side effects.
In materials science, it can be used as a raw material for the synthesis of functional materials. After rational design and synthesis paths, materials with special properties, such as materials with specific photoelectric properties, thermal stability or mechanical properties, can be prepared, and may have applications in electronic devices, polymer materials and other fields.
Because of its bromine content, it has also attracted attention in the field of flame retardant materials. Brominated flame retardants can impart good flame retardant properties to materials. 2,4,6-tribromophenol can be properly treated to participate in the preparation of flame retardant materials, improve the fire safety performance of materials, and can be used in building materials, electronic and electrical product shells, and many other materials that require fire protection.
In summary, 2,4,6-tribromophenol has important uses in many fields such as organic synthesis, drug research and development, materials science, and flame retardant materials. It is a key compound in the field of chemistry.
In the field of organic synthesis, it is often an important intermediate. It can be converted into other organic compounds through specific chemical reactions, such as substitution and addition reactions with many reagents, to prepare organic molecules with more complex structures, which is of great significance in the fields of pharmaceutical chemistry and materials science.
In drug development, it also has potential uses. Due to its special chemical structure, it may participate in the construction of active components of drugs, making great contributions to the development of new drugs. Medicinal chemists can explore compounds with specific pharmacological activities by modifying and modifying their structures, hoping to develop drugs with better curative effects and fewer side effects.
In materials science, it can be used as a raw material for the synthesis of functional materials. After rational design and synthesis paths, materials with special properties, such as materials with specific photoelectric properties, thermal stability or mechanical properties, can be prepared, and may have applications in electronic devices, polymer materials and other fields.
Because of its bromine content, it has also attracted attention in the field of flame retardant materials. Brominated flame retardants can impart good flame retardant properties to materials. 2,4,6-tribromophenol can be properly treated to participate in the preparation of flame retardant materials, improve the fire safety performance of materials, and can be used in building materials, electronic and electrical product shells, and many other materials that require fire protection.
In summary, 2,4,6-tribromophenol has important uses in many fields such as organic synthesis, drug research and development, materials science, and flame retardant materials. It is a key compound in the field of chemistry.
What are the physical properties of 2,4,6-trifluorochlorobenzene?
2% 2C4% 2C6-tribromophenol is an organic compound. Its physical properties are as follows:
Looking at its color state, at room temperature, 2% 2C4% 2C6-tribromophenol is a white needle-like crystal, like a fine needle, arranged in an orderly manner, quite unique. It has a certain luster, and it is slightly reflective under light, but it is not as dazzling as a metal, but a soft light.
Smell its smell, 2% 2C4% 2C6-tribromophenol has a slightly special smell. This smell is not fragrant or smelly, and it is quite unique. It is difficult for ordinary people to describe it accurately. However, if you are next to it, you will be able to perceive its special features.
In terms of its solubility, this substance is extremely insoluble in water, just like foreign matter in water, after entering water, it does not melt with water, but is suspended or settled in water as a solid state, and the two are clearly defined. However, it has a certain solubility in organic solvents, such as ethanol, ether, etc. Ethanol is a common organic solvent, and 2% 2C4% 2C6-tribromophenol can be gradually dispersed in it to form a uniform solution. This is because of the principle of similar miscibility. The two have certain structural similarities, so they can dissolve each other.
The melting point of 2% 2C4% 2C6-tribromophenol is about 95-96 ° C. When the temperature gradually rises to this range, the original solid state of 2% 2C4% 2C6-tribromophenol begins to melt slowly, and the solid state gradually changes to the liquid state. This process is the process of changing the material from an ordered solid structure to a disordered liquid structure.
Looking at its density, its density is greater than that of water. If it is placed in the same container as water, it can be seen that it sinks to the bottom of the water. This is because the mass per unit volume is greater than that of water, so it settles to the bottom under the action of gravity.
In summary, the physical properties of 2% 2C4% 2C6-tribromophenol are white in color and needle-like crystals, with a slight odor, insoluble in water, soluble in organic solvents, with a specific melting point, and higher density than water, which are all its significant characteristics.
Looking at its color state, at room temperature, 2% 2C4% 2C6-tribromophenol is a white needle-like crystal, like a fine needle, arranged in an orderly manner, quite unique. It has a certain luster, and it is slightly reflective under light, but it is not as dazzling as a metal, but a soft light.
Smell its smell, 2% 2C4% 2C6-tribromophenol has a slightly special smell. This smell is not fragrant or smelly, and it is quite unique. It is difficult for ordinary people to describe it accurately. However, if you are next to it, you will be able to perceive its special features.
In terms of its solubility, this substance is extremely insoluble in water, just like foreign matter in water, after entering water, it does not melt with water, but is suspended or settled in water as a solid state, and the two are clearly defined. However, it has a certain solubility in organic solvents, such as ethanol, ether, etc. Ethanol is a common organic solvent, and 2% 2C4% 2C6-tribromophenol can be gradually dispersed in it to form a uniform solution. This is because of the principle of similar miscibility. The two have certain structural similarities, so they can dissolve each other.
The melting point of 2% 2C4% 2C6-tribromophenol is about 95-96 ° C. When the temperature gradually rises to this range, the original solid state of 2% 2C4% 2C6-tribromophenol begins to melt slowly, and the solid state gradually changes to the liquid state. This process is the process of changing the material from an ordered solid structure to a disordered liquid structure.
Looking at its density, its density is greater than that of water. If it is placed in the same container as water, it can be seen that it sinks to the bottom of the water. This is because the mass per unit volume is greater than that of water, so it settles to the bottom under the action of gravity.
In summary, the physical properties of 2% 2C4% 2C6-tribromophenol are white in color and needle-like crystals, with a slight odor, insoluble in water, soluble in organic solvents, with a specific melting point, and higher density than water, which are all its significant characteristics.
Is the chemical properties of 2,4,6-trifluorochlorobenzene stable?
The chemical properties of 2% 2C4% 2C6-tribromoaniline are relatively stable in common sense. In this compound, the presence of bromine atoms gives it certain characteristics. Bromine atoms have electron-absorbing effects, but the conjugate system of the benzene ring also checks and balances its chemical activity.
Under normal conditions, 2% 2C4% 2C6-tribromoaniline is not prone to spontaneous violent chemical reactions. For example, its structure can be maintained relatively stable at room temperature and pressure without specific catalysts or strong reaction conditions.
To see its participation in the reaction, it needs a specific environment. If it wants to make it undergo nucleophilic substitution reaction, strong nucleophilic reagents are required, and the reaction conditions also need to be harsh, such as high temperature and suitable solvents. Because the electron cloud density around the bromine atom on the benzene ring is affected by conjugation and induction effects, it is difficult for ordinary reagents to easily break its original electron distribution.
If the redox reaction is considered, because it is not a typical easily oxidized or easily reduced substance, it is difficult to have significant redox changes without the intervention of strong oxidizing agents or reducing agents, and there are no suitable reaction conditions.
Overall, 2% 2C4% 2C6 -tribromoaniline is quite stable in common environments, and it is not easy to undergo random chemical transformation. Specific conditions are required to promote its participation in chemical reactions.
Under normal conditions, 2% 2C4% 2C6-tribromoaniline is not prone to spontaneous violent chemical reactions. For example, its structure can be maintained relatively stable at room temperature and pressure without specific catalysts or strong reaction conditions.
To see its participation in the reaction, it needs a specific environment. If it wants to make it undergo nucleophilic substitution reaction, strong nucleophilic reagents are required, and the reaction conditions also need to be harsh, such as high temperature and suitable solvents. Because the electron cloud density around the bromine atom on the benzene ring is affected by conjugation and induction effects, it is difficult for ordinary reagents to easily break its original electron distribution.
If the redox reaction is considered, because it is not a typical easily oxidized or easily reduced substance, it is difficult to have significant redox changes without the intervention of strong oxidizing agents or reducing agents, and there are no suitable reaction conditions.
Overall, 2% 2C4% 2C6 -tribromoaniline is quite stable in common environments, and it is not easy to undergo random chemical transformation. Specific conditions are required to promote its participation in chemical reactions.
What is the production method of 2,4,6-trifluorochlorobenzene?
2% 2C4% 2C6-tribromoaniline is an organic compound. Although the preparation method is not detailed in ancient books, it can be roughly deduced based on the current chemical understanding.
To prepare 2% 2C4% 2C6-tribromoaniline, aniline is often used as the starting material. For aniline, an aromatic compound with an amino group is also used. First, aniline reacts with bromine. In this reaction, the bromine atom of bromine easily replaces the hydrogen atom of the o and para-position of the benzene ring due to the activation effect of the amino group.
In a suitable solvent, such as glacial acetic acid, the aniline is dissolved and the bromine is slowly dripped. Glacial acetic acid can provide a mild environment for the reaction to proceed smoothly. When bromine meets aniline, the electron cloud density on the benzene ring is higher in the adjacent and para-position, that is, the bromine atom comes to replace. The amino group is the adjacent and para-position locator, so the bromine atom is preferentially replaced at the 2nd, 4th, and 6th positions.
When reacting, it is necessary to pay attention to the control of temperature. If the temperature is too high, the reaction will be too fast, and the side reactions such as excessive substitution may occur, resulting in impure products; if the temperature is too low, the reaction will be slow and take a long time. Usually maintained at a moderate low temperature, such as between 0-5 ° C, so that the reaction can proceed in an orderly manner.
After the reaction is completed, the product is mixed in the reaction system. Through various separation and purification techniques, pure 2% 2C4% 2C6-tribromoaniline can be obtained. For example, by filtration to remove its insoluble impurities; and then by recrystallization, according to the different solubility of the substance at different temperatures, the product is precipitated from the solution, and then the pure 2% 2C4% 2C6-tribromoaniline can be obtained. In this way, this compound may be obtained.
To prepare 2% 2C4% 2C6-tribromoaniline, aniline is often used as the starting material. For aniline, an aromatic compound with an amino group is also used. First, aniline reacts with bromine. In this reaction, the bromine atom of bromine easily replaces the hydrogen atom of the o and para-position of the benzene ring due to the activation effect of the amino group.
In a suitable solvent, such as glacial acetic acid, the aniline is dissolved and the bromine is slowly dripped. Glacial acetic acid can provide a mild environment for the reaction to proceed smoothly. When bromine meets aniline, the electron cloud density on the benzene ring is higher in the adjacent and para-position, that is, the bromine atom comes to replace. The amino group is the adjacent and para-position locator, so the bromine atom is preferentially replaced at the 2nd, 4th, and 6th positions.
When reacting, it is necessary to pay attention to the control of temperature. If the temperature is too high, the reaction will be too fast, and the side reactions such as excessive substitution may occur, resulting in impure products; if the temperature is too low, the reaction will be slow and take a long time. Usually maintained at a moderate low temperature, such as between 0-5 ° C, so that the reaction can proceed in an orderly manner.
After the reaction is completed, the product is mixed in the reaction system. Through various separation and purification techniques, pure 2% 2C4% 2C6-tribromoaniline can be obtained. For example, by filtration to remove its insoluble impurities; and then by recrystallization, according to the different solubility of the substance at different temperatures, the product is precipitated from the solution, and then the pure 2% 2C4% 2C6-tribromoaniline can be obtained. In this way, this compound may be obtained.
What are the precautions for storing and transporting 2,4,6-trifluorochlorobenzene?
2% 2C4% 2C6-tribromophenol, when storing and transporting, be sure to pay attention to many matters.
One is related to storage. This substance should be stored in a cool and ventilated warehouse. Because it has certain chemical activity, high temperature or its properties change, so a cool environment is essential. The relative humidity of the warehouse should be maintained in an appropriate range to prevent chemical reactions caused by moisture. And it needs to be kept away from fires and heat sources. Because tribromophenol is flammable, it is easy to cause combustion hazards in case of open flames and hot topics. At the same time, it should be stored separately from oxidants and acids to avoid mixed storage.
Second, as for transportation. Be sure to ensure that the packaging is complete and sealed before transportation. Packaging materials need to be able to effectively prevent the leakage of tribromophenol. Common packaging should be sturdy and have certain protective properties. During transportation, ensure that the container does not leak, collapse, fall, or be damaged. Transportation vehicles should be equipped with corresponding types and quantities of fire-fighting equipment and leakage emergency treatment equipment. During driving, it should be protected from exposure to the sun, rain, and high temperature. If transported by rail, it should be strictly in accordance with the dangerous goods assembly table in the "Dangerous Goods Transportation Rules" of the Ministry of Railways.
All storage and transportation involving 2% 2C4% 2C6-tribromophenol should be handled with caution and follow relevant procedures to ensure the safety of personnel and the environment.
One is related to storage. This substance should be stored in a cool and ventilated warehouse. Because it has certain chemical activity, high temperature or its properties change, so a cool environment is essential. The relative humidity of the warehouse should be maintained in an appropriate range to prevent chemical reactions caused by moisture. And it needs to be kept away from fires and heat sources. Because tribromophenol is flammable, it is easy to cause combustion hazards in case of open flames and hot topics. At the same time, it should be stored separately from oxidants and acids to avoid mixed storage.
Second, as for transportation. Be sure to ensure that the packaging is complete and sealed before transportation. Packaging materials need to be able to effectively prevent the leakage of tribromophenol. Common packaging should be sturdy and have certain protective properties. During transportation, ensure that the container does not leak, collapse, fall, or be damaged. Transportation vehicles should be equipped with corresponding types and quantities of fire-fighting equipment and leakage emergency treatment equipment. During driving, it should be protected from exposure to the sun, rain, and high temperature. If transported by rail, it should be strictly in accordance with the dangerous goods assembly table in the "Dangerous Goods Transportation Rules" of the Ministry of Railways.
All storage and transportation involving 2% 2C4% 2C6-tribromophenol should be handled with caution and follow relevant procedures to ensure the safety of personnel and the environment.
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