Linshang Chemical
PRODUCTS
1-Chloro-4-(Trichloromethyl)Benzene
Linshang Chemical
|
HS Code |
911008 |
| Chemical Formula | C7H4Cl4 |
| Molar Mass | 229.92 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 245 - 247 °C |
| Melting Point | 32 - 34 °C |
| Density | 1.49 g/cm³ |
| Solubility In Water | Insoluble |
| Vapor Pressure | Low |
| Flash Point | 116 °C |
| Odor | Pungent |
As an accredited 1-Chloro-4-(Trichloromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1 - chloro - 4 - (trichloromethyl)benzene packaged in a sealed, chemical - resistant bottle. |
| Storage | 1 - Chloro - 4 - (trichloromethyl)benzene should be stored in a cool, well - ventilated area away from heat sources and ignition points. Keep it in a tightly - sealed container to prevent vapor leakage. Store it separately from oxidizing agents, reducing agents, and incompatible materials. Ensure proper labeling for easy identification and handling, in compliance with safety regulations. |
| Shipping | 1 - chloro - 4 - (trichloromethyl)benzene is a hazardous chemical. Shipping requires compliance with strict regulations. It must be properly packaged, labeled, and transported by carriers authorized for such substances to ensure safety. |
Competitive 1-Chloro-4-(Trichloromethyl)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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 1-Chloro-4-(Trichloromethyl)Benzene in China?
As a trusted 1-Chloro-4-(Trichloromethyl)Benzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
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 1-Chloro-4-(Trichloromethyl)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 chemical properties of 1-chloro-4- (trichloromethyl) benzene?
The chemical properties of 1 + -deuterium-4- (trideuteromethyl) benzene are particularly important and are relevant to the investigation of many chemical fields.
In this substance, the introduction of deuterium atoms makes its properties different from those of ordinary hydrogen-containing congeners. Because the mass of deuterium is greater than that of hydrogen, it causes an isotope effect. First, in terms of chemical reaction rate, the reaction involving the breaking of deuterium-carbon bonds is often slower than that of ordinary hydrogen-carbon bonds. This is because the zero point energy of deuterium-carbon bonds is lower, and more energy is required to break their bonds.
Furthermore, its physical properties are also different. Due to the change in mass, its boiling point, melting point or ordinary benzene derivatives are different. Generally speaking, the boiling point of deuterium-containing compounds is slightly higher than that of hydrogen-containing compounds, and the intermolecular force is slightly enhanced due to the increase in mass.
In terms of stability, 1 + -deuterium-4- (trideuteromethyl) benzene may have an advantage. Due to the stronger deuterium-carbon bond than the hydrogen-carbon bond, the substance may be more difficult to decompose in some bond-breaking environments, exhibiting higher thermal and chemical stability.
And because of its special structure, it can be used as a tracer in organic synthesis. By detecting the whereabouts of deuterium atoms, chemists can gain insight into the reaction mechanism and clarify the specific path of molecular transformation, which is of great value in the study of complex organic reactions.
In addition, in some catalytic reactions, the presence of 1 + -deuterium-4- (trideuteromethyl) benzene may affect the activity and selectivity of the catalyst. Because its structure is different from that of ordinary benzene derivatives, it also interacts with the catalyst surface activity check point differently, thereby altering the catalytic reaction process and product distribution.
In this substance, the introduction of deuterium atoms makes its properties different from those of ordinary hydrogen-containing congeners. Because the mass of deuterium is greater than that of hydrogen, it causes an isotope effect. First, in terms of chemical reaction rate, the reaction involving the breaking of deuterium-carbon bonds is often slower than that of ordinary hydrogen-carbon bonds. This is because the zero point energy of deuterium-carbon bonds is lower, and more energy is required to break their bonds.
Furthermore, its physical properties are also different. Due to the change in mass, its boiling point, melting point or ordinary benzene derivatives are different. Generally speaking, the boiling point of deuterium-containing compounds is slightly higher than that of hydrogen-containing compounds, and the intermolecular force is slightly enhanced due to the increase in mass.
In terms of stability, 1 + -deuterium-4- (trideuteromethyl) benzene may have an advantage. Due to the stronger deuterium-carbon bond than the hydrogen-carbon bond, the substance may be more difficult to decompose in some bond-breaking environments, exhibiting higher thermal and chemical stability.
And because of its special structure, it can be used as a tracer in organic synthesis. By detecting the whereabouts of deuterium atoms, chemists can gain insight into the reaction mechanism and clarify the specific path of molecular transformation, which is of great value in the study of complex organic reactions.
In addition, in some catalytic reactions, the presence of 1 + -deuterium-4- (trideuteromethyl) benzene may affect the activity and selectivity of the catalyst. Because its structure is different from that of ordinary benzene derivatives, it also interacts with the catalyst surface activity check point differently, thereby altering the catalytic reaction process and product distribution.
What are the industrial applications of 1-chloro-4- (trichloromethyl) benzene?
1 + -Bromo-4- (tribromomethyl) benzene, which is widely used in industry.
In the field of organic synthesis, it is often used as a key intermediate. It can be derived from other types of organic compounds with special functions through many reactions. For example, by nucleophilic substitution reaction, bromine atoms on the benzene ring can be replaced by other functional groups, such as hydroxyl groups, amino groups, etc., so that a variety of organic materials containing different functional groups can be prepared, providing raw materials for pharmaceutical chemistry, materials science and other fields.
In the field of materials science, 1 + -bromo-4- (tribromomethyl) benzene is involved in the synthesis of polymer materials, showing excellent flame retardant properties. Due to its rich content of bromine in the molecule, when such materials encounter fire sources, bromine will play a role, effectively blocking the combustion process by trapping free radicals and other mechanisms, thereby improving the fire safety level of materials. It is widely used in the manufacture of products with strict flame retardant requirements such as building materials, electronic and electrical shells.
In pharmaceutical research and development, this compound also plays an important role. Due to its special chemical structure, it can be used as a starting material or key intermediate for the synthesis of specific drug molecules. Through a series of chemical modifications and reactions, biologically active drug molecules can be constructed, providing the possibility for the creation of new drugs.
In addition, in the field of fine chemicals, 1 + -bromo-4- (tribromomethyl) benzene can be used to synthesize high-end pigments, dyes and other fine chemicals, providing products with excellent color performance and stability, and enhancing product quality and added value.
In the field of organic synthesis, it is often used as a key intermediate. It can be derived from other types of organic compounds with special functions through many reactions. For example, by nucleophilic substitution reaction, bromine atoms on the benzene ring can be replaced by other functional groups, such as hydroxyl groups, amino groups, etc., so that a variety of organic materials containing different functional groups can be prepared, providing raw materials for pharmaceutical chemistry, materials science and other fields.
In the field of materials science, 1 + -bromo-4- (tribromomethyl) benzene is involved in the synthesis of polymer materials, showing excellent flame retardant properties. Due to its rich content of bromine in the molecule, when such materials encounter fire sources, bromine will play a role, effectively blocking the combustion process by trapping free radicals and other mechanisms, thereby improving the fire safety level of materials. It is widely used in the manufacture of products with strict flame retardant requirements such as building materials, electronic and electrical shells.
In pharmaceutical research and development, this compound also plays an important role. Due to its special chemical structure, it can be used as a starting material or key intermediate for the synthesis of specific drug molecules. Through a series of chemical modifications and reactions, biologically active drug molecules can be constructed, providing the possibility for the creation of new drugs.
In addition, in the field of fine chemicals, 1 + -bromo-4- (tribromomethyl) benzene can be used to synthesize high-end pigments, dyes and other fine chemicals, providing products with excellent color performance and stability, and enhancing product quality and added value.
What are the environmental effects of 1-chloro-4- (trichloromethyl) benzene?
The impact of 1-bromo-4- (tribromo-methyl) benzene on the environment is an important matter and should be analyzed in detail.
1-bromo-4- (tribromo-methyl) benzene has unique chemical properties and can undergo various processes in the environment, resulting in various effects. The first to bear the brunt is its effect on the water environment. If this substance accidentally flows into rivers, lakes and seas and other waters, it has certain chemical stability or is difficult to degrade rapidly. It is soluble in water, although its solubility is limited, it can still diffuse in water, causing water pollution. Aquatic organisms, such as fish, shellfish, etc., may accumulate this substance in the body due to ingestion of this contaminated water. Over time, it may affect their physiological functions, such as reproduction, immune systems, etc., resulting in a decrease in the number of biological populations and a disruption of ecological balance.
In the soil environment, 1-bromo-4- (tribromomethyl) benzene can also cause problems. It can adsorb on soil particles, hindering the normal circulation and exchange of nutrients in the soil. When plant roots ingest nutrients, they may be disturbed by this substance, causing plant growth and development to be stunted. In severe cases, plants may wither and die, affecting the vegetation cover and biodiversity of terrestrial ecosystems.
Furthermore, in the atmospheric environment, if 1-bromo-4- (tribromo-methyl) benzene enters the air due to volatilization and other reasons, it may participate in photochemical reactions. This will not only change the atmospheric composition, affect the air quality, but also generate secondary pollutants, or cause more serious harm to human health and the environment. If it can form photochemical smog, stimulate the human respiratory tract, and cause many diseases.
1-bromo-4- (tribromo-methyl) benzene migrates in the environment, which has adverse effects on water, soil and air, disrupting the ecological balance, endangering biological survival and human health. Therefore, during its production and use, it is necessary to exercise caution to reduce its harm to the environment.
1-bromo-4- (tribromo-methyl) benzene has unique chemical properties and can undergo various processes in the environment, resulting in various effects. The first to bear the brunt is its effect on the water environment. If this substance accidentally flows into rivers, lakes and seas and other waters, it has certain chemical stability or is difficult to degrade rapidly. It is soluble in water, although its solubility is limited, it can still diffuse in water, causing water pollution. Aquatic organisms, such as fish, shellfish, etc., may accumulate this substance in the body due to ingestion of this contaminated water. Over time, it may affect their physiological functions, such as reproduction, immune systems, etc., resulting in a decrease in the number of biological populations and a disruption of ecological balance.
In the soil environment, 1-bromo-4- (tribromomethyl) benzene can also cause problems. It can adsorb on soil particles, hindering the normal circulation and exchange of nutrients in the soil. When plant roots ingest nutrients, they may be disturbed by this substance, causing plant growth and development to be stunted. In severe cases, plants may wither and die, affecting the vegetation cover and biodiversity of terrestrial ecosystems.
Furthermore, in the atmospheric environment, if 1-bromo-4- (tribromo-methyl) benzene enters the air due to volatilization and other reasons, it may participate in photochemical reactions. This will not only change the atmospheric composition, affect the air quality, but also generate secondary pollutants, or cause more serious harm to human health and the environment. If it can form photochemical smog, stimulate the human respiratory tract, and cause many diseases.
1-bromo-4- (tribromo-methyl) benzene migrates in the environment, which has adverse effects on water, soil and air, disrupting the ecological balance, endangering biological survival and human health. Therefore, during its production and use, it is necessary to exercise caution to reduce its harm to the environment.
What are the methods for preparing 1-chloro-4- (trichloromethyl) benzene?
To prepare 1-bromo-4- (tribromomethyl) benzene, the method is as follows:
First take toluene, and act with an appropriate amount of bromine and a catalyst. In this reaction, the methyl hydrogen atom of toluene is active, and bromine can replace the hydrogen atom on the methyl group under the condition of light or heating and the presence of an initiator. Temperature control and bromine dosage are required to make it a bromogenic product to obtain benzyl bromide.
Then, bromine atoms are reintroduced into benzyl bromide. The activity of the hydrogen atom on the benzyl carbon in benzyl bromide can be used to further react benzyl bromide with bromine under suitable reaction conditions, such as with suitable solvents, catalysts and temperatures, etc., and the hydrogen atom on the benzyl group is gradually replaced to obtain (tribromomethyl) bromobenzene.
Then use (tribromomethyl) bromobenzene as raw material, in a suitable reaction system, such as with a suitable catalyst, at a specific temperature and solvent environment, and react with a brominating agent to introduce bromine atoms at the 4th position on the benzene ring. This step requires the selection of a catalyst and conditions that have a better positioning effect on the 4 position of the benzene ring to increase the yield of 1-bromo-4- (tribromo-methyl) benzene.
Or first brominate the benzene, and in the presence of a suitable catalyst, such as iron filings or iron tribromide, react the benzene with bromine to obtain bromobenzene. The side chain of bromobenzene is then brominated, and through a multi-step reaction, similar to the above method of preparing (tribromo-methyl) bromobenzene from toluene, the side chain of bromobenzene is introduced into tribromo-methyl, and then the target product 1-bromo-4- (tribromo-methyl) benzene is During the reaction process, each step requires fine control of the reaction conditions to achieve higher yield and purity.
First take toluene, and act with an appropriate amount of bromine and a catalyst. In this reaction, the methyl hydrogen atom of toluene is active, and bromine can replace the hydrogen atom on the methyl group under the condition of light or heating and the presence of an initiator. Temperature control and bromine dosage are required to make it a bromogenic product to obtain benzyl bromide.
Then, bromine atoms are reintroduced into benzyl bromide. The activity of the hydrogen atom on the benzyl carbon in benzyl bromide can be used to further react benzyl bromide with bromine under suitable reaction conditions, such as with suitable solvents, catalysts and temperatures, etc., and the hydrogen atom on the benzyl group is gradually replaced to obtain (tribromomethyl) bromobenzene.
Then use (tribromomethyl) bromobenzene as raw material, in a suitable reaction system, such as with a suitable catalyst, at a specific temperature and solvent environment, and react with a brominating agent to introduce bromine atoms at the 4th position on the benzene ring. This step requires the selection of a catalyst and conditions that have a better positioning effect on the 4 position of the benzene ring to increase the yield of 1-bromo-4- (tribromo-methyl) benzene.
Or first brominate the benzene, and in the presence of a suitable catalyst, such as iron filings or iron tribromide, react the benzene with bromine to obtain bromobenzene. The side chain of bromobenzene is then brominated, and through a multi-step reaction, similar to the above method of preparing (tribromo-methyl) bromobenzene from toluene, the side chain of bromobenzene is introduced into tribromo-methyl, and then the target product 1-bromo-4- (tribromo-methyl) benzene is During the reaction process, each step requires fine control of the reaction conditions to achieve higher yield and purity.
What are the precautions for storing and transporting 1-chloro-4- (trichloromethyl) benzene?
"Tiangong Kaiwu" says: Mercury is also mercury. This 1 + -mercury-4- (trimercury methyl) benzene substance has several things to pay attention to during storage and transportation.
First, it is related to toxicity. Mercury and its compounds are highly toxic and can invade the human body through the respiratory tract, skin and digestive tract, harming the nervous system, kidneys and many other organs. Therefore, when storing and transporting, it is necessary to take comprehensive protection measures. When the storage place is well ventilated, it is strictly forbidden for unrelated people to approach it; during transportation, escorts also need to wear professional protective equipment to prevent mercury leakage from human contact.
Second, about volatility. Mercury is volatile and forms mercury vapor, which is also toxic. When storing, it should be placed in a well-sealed container to prevent mercury from escaping. The material of the container should be resistant to mercury corrosion, such as special glass bottles or metal cans. When transporting, also make sure that the container is airtight and the ambient temperature should not be too high to prevent mercury volatilization from intensifying.
Third, deal with leaks. If a leak unfortunately occurs, do not panic. Immediately evacuate the surrounding people to avoid more people coming into contact with mercury. At the same time, take prompt measures to clean up. You can use sulfur powder to cover mercury droplets, which react to form mercury sulfide. This is a relatively stable and less toxic substance, and then collect and dispose of it properly.
Fourth, follow regulations. The storage and transportation of mercury are regulated by many regulations. It is necessary to strictly follow the relevant national and local regulations, complete permits and procedures to ensure the legal compliance of the whole process. In this way, the safety of storage and transportation can be guaranteed, and people and the environment can be protected from mercury damage.
First, it is related to toxicity. Mercury and its compounds are highly toxic and can invade the human body through the respiratory tract, skin and digestive tract, harming the nervous system, kidneys and many other organs. Therefore, when storing and transporting, it is necessary to take comprehensive protection measures. When the storage place is well ventilated, it is strictly forbidden for unrelated people to approach it; during transportation, escorts also need to wear professional protective equipment to prevent mercury leakage from human contact.
Second, about volatility. Mercury is volatile and forms mercury vapor, which is also toxic. When storing, it should be placed in a well-sealed container to prevent mercury from escaping. The material of the container should be resistant to mercury corrosion, such as special glass bottles or metal cans. When transporting, also make sure that the container is airtight and the ambient temperature should not be too high to prevent mercury volatilization from intensifying.
Third, deal with leaks. If a leak unfortunately occurs, do not panic. Immediately evacuate the surrounding people to avoid more people coming into contact with mercury. At the same time, take prompt measures to clean up. You can use sulfur powder to cover mercury droplets, which react to form mercury sulfide. This is a relatively stable and less toxic substance, and then collect and dispose of it properly.
Fourth, follow regulations. The storage and transportation of mercury are regulated by many regulations. It is necessary to strictly follow the relevant national and local regulations, complete permits and procedures to ensure the legal compliance of the whole process. In this way, the safety of storage and transportation can be guaranteed, and people and the environment can be protected from mercury damage.
Scan to WhatsApp
