Linshang Chemical
PRODUCTS
Benzene,1,2,3,4,5-Pentachloro-6-(Trifluoromethyl)-
Linshang Chemical
|
HS Code |
174033 |
| Chemical Formula | C7Cl5F3 |
| Molar Mass | 320.33 g/mol |
| Physical State At Stp | Solid (assumed) |
| Solubility In Water | Low (non - polar compound) |
| Solubility In Organic Solvents | Likely soluble in non - polar organic solvents like hexane |
| Vapor Pressure | Low at room temperature |
As an accredited Benzene,1,2,3,4,5-Pentachloro-6-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottle of 1,2,3,4,5 - pentachloro - 6 - (trifluoromethyl)benzene, well - sealed. |
| Storage | Store "Benzene,1,2,3,4,5 - pentachloro - 6 - (trifluoromethyl)-" in a cool, well - ventilated area, away from heat sources and open flames. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials due to its potentially reactive nature. Separate it from oxidizing agents, reducing agents, and incompatible substances to prevent dangerous reactions. |
| Shipping | **Shipping Description for 1,2,3,4,5 - Pentachloro - 6 - (trifluoromethyl)benzene**: This chemical, being hazardous, requires specialized shipping. It must be in sealed, approved containers, transported by carriers compliant with chemical transportation regulations, with proper labeling for safety. |
Competitive Benzene,1,2,3,4,5-Pentachloro-6-(Trifluoromethyl)- 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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What are the chemical properties of Benzene, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) -
Benzene, 1,2,3,4,5 - pentachloro - 6 - (trifluoromethyl) - This substance is an organic halide and the like. Its chemical properties are specific and contain many extraordinary things.
This compound has high chemical stability due to polychlorine and trifluoromethyl. The bond between chlorine atoms and trifluoromethyl is strong, and it requires very high energy to break it. Therefore, under normal environmental conditions, its chemical activity is low and it is not easy to participate in general chemical reactions.
From the perspective of reactivity, the electron cloud density of the benzene ring decreases because the distribution of the surrounding electron cloud is affected by chlorine and trifluoromethyl. This makes it difficult for the electrophilic substitution reaction to occur, because its attraction to electrophilic reagents is greatly reduced. However, in case of strong electrophilic reagents and harsh reaction conditions, electrophilic substitution is still possible.
In terms of physical properties, due to the inclusion of polyhalogen atoms, the intermolecular force is enhanced, resulting in its high boiling point and melting point. Its density is also greater than that of water, and it is difficult to dissolve in water. Due to the increase of molecular polarity of halogen atoms, it is difficult to form effective hydrogen bonds with water molecules.
Furthermore, its fluorine-containing properties endow it with unique chemical properties. Fluorine atoms are extremely electronegative, and the existence of trifluoromethyl groups greatly increases the polarity of molecules, affecting their solubility and reactivity. In some specific reactions, trifluoromethyl can act as an electron-withdrawing group to change the electron cloud distribution of the benzene ring and guide the reaction in a specific direction.
In addition, this compound has potential uses in the field of organic synthesis. Due to its stability and unique electronic effects, it may be used as an intermediate to prepare materials with special properties, such as polymers with high chemical stability and thermal stability. However, due to its polyhalogen atoms, it is difficult to degrade in the environment or pose potential hazards to the ecological environment, so it should be used with caution when using and disposing.
This compound has high chemical stability due to polychlorine and trifluoromethyl. The bond between chlorine atoms and trifluoromethyl is strong, and it requires very high energy to break it. Therefore, under normal environmental conditions, its chemical activity is low and it is not easy to participate in general chemical reactions.
From the perspective of reactivity, the electron cloud density of the benzene ring decreases because the distribution of the surrounding electron cloud is affected by chlorine and trifluoromethyl. This makes it difficult for the electrophilic substitution reaction to occur, because its attraction to electrophilic reagents is greatly reduced. However, in case of strong electrophilic reagents and harsh reaction conditions, electrophilic substitution is still possible.
In terms of physical properties, due to the inclusion of polyhalogen atoms, the intermolecular force is enhanced, resulting in its high boiling point and melting point. Its density is also greater than that of water, and it is difficult to dissolve in water. Due to the increase of molecular polarity of halogen atoms, it is difficult to form effective hydrogen bonds with water molecules.
Furthermore, its fluorine-containing properties endow it with unique chemical properties. Fluorine atoms are extremely electronegative, and the existence of trifluoromethyl groups greatly increases the polarity of molecules, affecting their solubility and reactivity. In some specific reactions, trifluoromethyl can act as an electron-withdrawing group to change the electron cloud distribution of the benzene ring and guide the reaction in a specific direction.
In addition, this compound has potential uses in the field of organic synthesis. Due to its stability and unique electronic effects, it may be used as an intermediate to prepare materials with special properties, such as polymers with high chemical stability and thermal stability. However, due to its polyhalogen atoms, it is difficult to degrade in the environment or pose potential hazards to the ecological environment, so it should be used with caution when using and disposing.
What are the uses of Benzene, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) -
1,2,3,4,5-pentachloro-6- (trifluoromethyl) benzene, this substance may have many uses in the chemical technology of the past.
In the field of organic synthesis in the past, it can be used as a key intermediate. Due to its special structure, it contains multiple chlorine atoms and trifluoromethyl groups, which give it unique chemical activity. Through carefully designed chemical reactions, chemists can build more complex organic molecular structures. For example, in the case of nucleophilic substitution reactions, chlorine atoms can be replaced by other nucleophilic reagents, and then various required functional groups can be introduced, providing the possibility for the synthesis of special drug molecules, raw materials for high-performance materials, etc.
In the preparation of materials of the past, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) benzene also has a place. The polymer materials involved in the synthesis may have excellent chemical stability, weather resistance and low surface energy due to the presence of trifluoromethyl. These materials may be used in places with strict material performance requirements, such as the aerospace industry, to make parts of aircraft to withstand harsh environmental erosion; or for high-end electronic equipment to provide high-quality insulation and protective materials.
However, it is also necessary to understand that this substance contains chlorine and fluorine elements. If not disposed of properly, it may be difficult to degrade in the environment, and may pose a potential hazard to ecosystems and biological health. Therefore, when using it in the past, it is also necessary to carefully consider its dosage and subsequent treatment methods, and strive to find a balance between its function and environmental protection.
In the field of organic synthesis in the past, it can be used as a key intermediate. Due to its special structure, it contains multiple chlorine atoms and trifluoromethyl groups, which give it unique chemical activity. Through carefully designed chemical reactions, chemists can build more complex organic molecular structures. For example, in the case of nucleophilic substitution reactions, chlorine atoms can be replaced by other nucleophilic reagents, and then various required functional groups can be introduced, providing the possibility for the synthesis of special drug molecules, raw materials for high-performance materials, etc.
In the preparation of materials of the past, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) benzene also has a place. The polymer materials involved in the synthesis may have excellent chemical stability, weather resistance and low surface energy due to the presence of trifluoromethyl. These materials may be used in places with strict material performance requirements, such as the aerospace industry, to make parts of aircraft to withstand harsh environmental erosion; or for high-end electronic equipment to provide high-quality insulation and protective materials.
However, it is also necessary to understand that this substance contains chlorine and fluorine elements. If not disposed of properly, it may be difficult to degrade in the environment, and may pose a potential hazard to ecosystems and biological health. Therefore, when using it in the past, it is also necessary to carefully consider its dosage and subsequent treatment methods, and strive to find a balance between its function and environmental protection.
What is the preparation method of Benzene, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) -
The method of preparing 1,2,3,4,5-pentachloro-6- (trifluoromethyl) benzene requires delicate techniques and suitable materials. Although there is no such exact method in the ancient book "Tiangong Kaiwu", the chemical method described can lead us to think.
To make this product, you can first find suitable raw materials containing fluorine and chlorine. In the method of organic synthesis, choose an appropriate starting reactant, or an aromatic hydrocarbon containing methyl, and introduce chlorine atoms through halogenation. Under suitable temperature, pressure and catalyst, chlorine gas can be used as a halogenating agent to gradually chlorinate specific positions on the benzene ring.
When the chlorine atoms on the benzene ring are introduced to a certain extent, then trifluoromethyl is introduced. This step may require the help of reagents containing trifluoromethyl, such as some active trifluoromethylation reagents, to replace the atom or group at a suitable position on the benzene ring under specific reaction conditions. In this process, the control of reaction conditions is crucial, and temperature, pH, and reaction time will all affect the yield and purity of the product.
During halogenation, if the temperature is too high, or excessive halogenation is caused, the product is complex and difficult to distinguish; if the temperature is too low, the reaction will be slow and take too long. In the trifluoromethylation step, the choice of reagent activity and reaction solvent is also critical. Choosing a suitable solvent can help the reagent dissolve and disperse, which is conducive to the uniform progress of the reaction. And the reaction process must prevent impurities from invading, so as not to affect the quality of the product. So through careful operation in multiple steps, separation and purification, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) benzene can be obtained.
To make this product, you can first find suitable raw materials containing fluorine and chlorine. In the method of organic synthesis, choose an appropriate starting reactant, or an aromatic hydrocarbon containing methyl, and introduce chlorine atoms through halogenation. Under suitable temperature, pressure and catalyst, chlorine gas can be used as a halogenating agent to gradually chlorinate specific positions on the benzene ring.
When the chlorine atoms on the benzene ring are introduced to a certain extent, then trifluoromethyl is introduced. This step may require the help of reagents containing trifluoromethyl, such as some active trifluoromethylation reagents, to replace the atom or group at a suitable position on the benzene ring under specific reaction conditions. In this process, the control of reaction conditions is crucial, and temperature, pH, and reaction time will all affect the yield and purity of the product.
During halogenation, if the temperature is too high, or excessive halogenation is caused, the product is complex and difficult to distinguish; if the temperature is too low, the reaction will be slow and take too long. In the trifluoromethylation step, the choice of reagent activity and reaction solvent is also critical. Choosing a suitable solvent can help the reagent dissolve and disperse, which is conducive to the uniform progress of the reaction. And the reaction process must prevent impurities from invading, so as not to affect the quality of the product. So through careful operation in multiple steps, separation and purification, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) benzene can be obtained.
Benzene, 1, 2, 3, 4, 5-pentachloro-6- (trifluoromethyl) - what impact does it have on the environment
Benzene, 1,2,3,4,5 - pentachloro-6 - (trifluoromethyl) - This substance has many effects on the environment. It is highly toxic and, once released into the environment, easily accumulates in soil and water bodies. In soil, it can interfere with the normal activities of microorganisms, destroy soil ecological balance, reduce soil fertility, affect plant root absorption of nutrients, hinder plant growth and development, and reduce crop yield. In water bodies, it can poison aquatic organisms, such as fish, shellfish, etc., causing damage to their physiological functions and even death, thereby destroying the food chain of aquatic ecosystems.
This substance is also persistent, difficult to degrade rapidly in the natural environment, and can be retained for a long time, accumulating continuously, and continuously harming the environment. Moreover, it has low volatility, is not easy to dilute through atmospheric diffusion, and is easy to accumulate in local areas, increasing the harm to the surrounding environment.
In addition, its chemical structure is stable, and it is difficult to chemically react into harmless substances under conventional environmental conditions. It is extremely difficult to treat and remove, and requires complex and expensive technical means. Once the environment is polluted, it will threaten the safety of the ecological environment and biological health for a long time, causing serious damage to the structure and function of the entire ecosystem.
This substance is also persistent, difficult to degrade rapidly in the natural environment, and can be retained for a long time, accumulating continuously, and continuously harming the environment. Moreover, it has low volatility, is not easy to dilute through atmospheric diffusion, and is easy to accumulate in local areas, increasing the harm to the surrounding environment.
In addition, its chemical structure is stable, and it is difficult to chemically react into harmless substances under conventional environmental conditions. It is extremely difficult to treat and remove, and requires complex and expensive technical means. Once the environment is polluted, it will threaten the safety of the ecological environment and biological health for a long time, causing serious damage to the structure and function of the entire ecosystem.
What are the safety precautions for Benzene, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) -?
"Tiangong Kaiwu" says: "Those who have benzene are also organic compounds. Today, this substance, 1,2,3,4,5-pentachloro-6- (trifluoromethyl) -benzene, has different properties and is related to the way of safety and cannot be ignored."
This substance is toxic and will hurt the body if exposed. When using and storing, strictly follow the procedures. When placed in a cool and ventilated place, away from fire and heat sources, do not mix with oxidants, food chemicals, etc.
When operating, make sure that workers wear protective clothing and gas masks to prevent it from invading the human body through the respiratory tract and skin. If you accidentally touch it, rinse it with plenty of water quickly and seek medical attention if necessary.
In addition, the risk of ignition and explosion of this object also exists. Its vapor and air can form an explosive mixture, which can cause combustion and explosion in case of open flame and high heat energy. Therefore, fire extinguishers should be prepared in the workplace, and fireworks are strictly prohibited.
Furthermore, the waste of this object should not be discarded at will. It must be properly disposed of in accordance with environmental protection regulations, so as not to pollute the soil, water sources, and harm all living things. In this way, personal safety and environmental peace can be ensured.
This substance is toxic and will hurt the body if exposed. When using and storing, strictly follow the procedures. When placed in a cool and ventilated place, away from fire and heat sources, do not mix with oxidants, food chemicals, etc.
When operating, make sure that workers wear protective clothing and gas masks to prevent it from invading the human body through the respiratory tract and skin. If you accidentally touch it, rinse it with plenty of water quickly and seek medical attention if necessary.
In addition, the risk of ignition and explosion of this object also exists. Its vapor and air can form an explosive mixture, which can cause combustion and explosion in case of open flame and high heat energy. Therefore, fire extinguishers should be prepared in the workplace, and fireworks are strictly prohibited.
Furthermore, the waste of this object should not be discarded at will. It must be properly disposed of in accordance with environmental protection regulations, so as not to pollute the soil, water sources, and harm all living things. In this way, personal safety and environmental peace can be ensured.
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