Linshang Chemical
PRODUCTS
1-Bromo-2,4,6-Trichlorobenzene
Linshang Chemical
|
HS Code |
327568 |
| Chemical Formula | C6H2BrCl3 |
| Molecular Weight | 271.34 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 258 - 260 °C |
| Melting Point | 19 - 21 °C |
| Density | 1.848 g/cm³ at 20 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents like ethanol, ether |
| Flash Point | 126 °C |
| Vapor Pressure | Low at room temperature |
As an accredited 1-Bromo-2,4,6-Trichlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - bromo - 2,4,6 - trichlorobenzene in 500 - gram bottles for chemical storage. |
| Storage | 1 - Bromo - 2,4,6 - trichlorobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. It should be kept in a tightly sealed container to prevent leakage and vapor release. Store it separately from oxidizing agents, reducing agents, and other reactive chemicals to avoid potential chemical reactions. |
| Shipping | 1 - bromo - 2,4,6 - trichlorobenzene is shipped in sealed, corrosion - resistant containers. These are carefully packaged to prevent leakage. Shipment follows strict hazardous chemical regulations, ensuring safe transport. |
Competitive 1-Bromo-2,4,6-Trichlorobenzene 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-Bromo-2,4,6-Trichlorobenzene in China?
As a trusted 1-Bromo-2,4,6-Trichlorobenzene 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-Bromo-2,4,6-Trichlorobenzene 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 physical properties of 1-bromo-2,4,6-trichlorobenzene?
1-% cyanogen-2,4,6-trifluorobenzene is an organic compound with special physical and chemical properties. Its physical properties are as follows:
In appearance, it is mostly a colorless to light yellow liquid under normal conditions. When it is pure, it is clear and transparent. However, due to differences in impurities or preparation methods, it may have a slight color. This appearance characteristic can be used as a preliminary basis for discrimination in chemical production and product inspection.
In terms of olfaction, the substance emits an irritating odor. If you smell it close, the smell is pungent and it has obvious irritation to the olfactory system. This characteristic warns people to take good protection when operating and avoid inhalation. The melting point of
is about [specific value] ° C. At this temperature, the substance changes from solid to liquid. This property is of great significance for its storage and transportation. If the ambient temperature is close to the melting point, it is necessary to prevent problems such as leakage caused by changes in its state. The boiling point of
is about [specific value] ° C. When this temperature is reached, the substance changes sharply from liquid to gaseous. The boiling point is a key parameter when separating and purifying the substance. Mixtures can be separated according to the difference in boiling point by means of distillation. The density of
is about [specific value] g/cm ³, which means the mass of the substance per unit volume. This data is an important reference in chemical metrology and mixing processes, and is related to the accuracy of the ratio of reactants.
In terms of solubility, 1-% cyanogen-2,4,6-trifluorobenzene has good solubility in organic solvents such as ethanol and ether, but very low solubility in water. This solubility characteristic plays a key role in chemical synthesis, product separation and wastewater treatment. According to the solubility, suitable solvents and treatment methods can be selected.
In addition, its volatility is strong, and it is easy to evaporate from liquid to gaseous state at room temperature and pressure, which increases the concentration in the air and increases the risk of exposure. Therefore, ventilation should be paid attention to when storing and using.
The above physical properties are interrelated and affect their application in chemical, pharmaceutical and other fields. In practice, all properties need to be fully considered to ensure safe and efficient use.
In appearance, it is mostly a colorless to light yellow liquid under normal conditions. When it is pure, it is clear and transparent. However, due to differences in impurities or preparation methods, it may have a slight color. This appearance characteristic can be used as a preliminary basis for discrimination in chemical production and product inspection.
In terms of olfaction, the substance emits an irritating odor. If you smell it close, the smell is pungent and it has obvious irritation to the olfactory system. This characteristic warns people to take good protection when operating and avoid inhalation. The melting point of
is about [specific value] ° C. At this temperature, the substance changes from solid to liquid. This property is of great significance for its storage and transportation. If the ambient temperature is close to the melting point, it is necessary to prevent problems such as leakage caused by changes in its state. The boiling point of
is about [specific value] ° C. When this temperature is reached, the substance changes sharply from liquid to gaseous. The boiling point is a key parameter when separating and purifying the substance. Mixtures can be separated according to the difference in boiling point by means of distillation. The density of
is about [specific value] g/cm ³, which means the mass of the substance per unit volume. This data is an important reference in chemical metrology and mixing processes, and is related to the accuracy of the ratio of reactants.
In terms of solubility, 1-% cyanogen-2,4,6-trifluorobenzene has good solubility in organic solvents such as ethanol and ether, but very low solubility in water. This solubility characteristic plays a key role in chemical synthesis, product separation and wastewater treatment. According to the solubility, suitable solvents and treatment methods can be selected.
In addition, its volatility is strong, and it is easy to evaporate from liquid to gaseous state at room temperature and pressure, which increases the concentration in the air and increases the risk of exposure. Therefore, ventilation should be paid attention to when storing and using.
The above physical properties are interrelated and affect their application in chemical, pharmaceutical and other fields. In practice, all properties need to be fully considered to ensure safe and efficient use.
What are the chemical properties of 1-bromo-2,4,6-trichlorobenzene?
1-Bromo-2,4,6-trifluorobenzene is one of the organic compounds. Its chemical properties are unique and valuable for investigation.
Looking at the properties of its halogen atoms, bromine atoms and fluorine atoms coexist on the benzene ring. Fluorine atoms have strong electronegativity, which can reduce the electron cloud density of the benzene ring and reduce the electrophilic substitution activity of the benzene ring. Because of the significant electron-absorbing induction effect of fluorine atoms, the electron cloud on the benzene ring can be biased towards the fluorine atom, causing the benzene ring to lack electrons, making it difficult to react with electrophilic reagents.
And its bromine atoms, although affected by fluorine atoms, still have certain reactivity. Under appropriate conditions, nucleophilic substitution reactions can occur. For example, when encountering nucleophilic reagents, bromine atoms can be replaced by nucleophilic groups. This is because the C-Br bond has a certain polarity, and bromine atoms are slightly positively charged, making them vulnerable to attack by nucleophilic reagents.
Furthermore, the physical properties of this compound are also different due to the presence of fluorine atoms. The introduction of fluorine atoms can improve the stability and fat solubility of the compound. In some organic synthesis reactions, 1-bromo-2,4,6-trifluorobenzene is often used as a key intermediate. Due to its unique structure, it can construct complex organic molecular structures through various reactions, and is widely used in pharmaceutical chemistry, materials science and other fields.
In conclusion, 1-bromo-2,4,6-trifluorobenzene plays an important role in the research and practical application of organic chemistry due to its unique chemical properties, providing assistance for the development of many fields.
Looking at the properties of its halogen atoms, bromine atoms and fluorine atoms coexist on the benzene ring. Fluorine atoms have strong electronegativity, which can reduce the electron cloud density of the benzene ring and reduce the electrophilic substitution activity of the benzene ring. Because of the significant electron-absorbing induction effect of fluorine atoms, the electron cloud on the benzene ring can be biased towards the fluorine atom, causing the benzene ring to lack electrons, making it difficult to react with electrophilic reagents.
And its bromine atoms, although affected by fluorine atoms, still have certain reactivity. Under appropriate conditions, nucleophilic substitution reactions can occur. For example, when encountering nucleophilic reagents, bromine atoms can be replaced by nucleophilic groups. This is because the C-Br bond has a certain polarity, and bromine atoms are slightly positively charged, making them vulnerable to attack by nucleophilic reagents.
Furthermore, the physical properties of this compound are also different due to the presence of fluorine atoms. The introduction of fluorine atoms can improve the stability and fat solubility of the compound. In some organic synthesis reactions, 1-bromo-2,4,6-trifluorobenzene is often used as a key intermediate. Due to its unique structure, it can construct complex organic molecular structures through various reactions, and is widely used in pharmaceutical chemistry, materials science and other fields.
In conclusion, 1-bromo-2,4,6-trifluorobenzene plays an important role in the research and practical application of organic chemistry due to its unique chemical properties, providing assistance for the development of many fields.
What are the main uses of 1-bromo-2,4,6-trichlorobenzene?
1-% hydrazine-2,4,6-trinitrobenzene, also known as hydrazine picrate, has specific uses in many fields.
In the military field, hydrazine picrate has high explosive properties and can be used as an explosive component. In the past war years, military craftsmen found that hydrazine picrate can release huge energy under specific conditions in order to find powerful explosives. After repeated trials, they found that hydrazine picrate can release huge energy under specific conditions, so they used it in artillery shells, bombs and other weapons to enhance the damage effect of weapons and cause serious damage to enemy fortifications and equipment.
In the industrial field, hydrazine picrate can be used in the manufacture of fireworks. In the fireworks required for festivals, some of the colorful and unique fireworks have the "credit" of hydrazine picrate. It can produce a bright flame or a special color light through a specific reaction, bringing a visual feast to the public.
In the field of scientific research, hydrazine picrate, as an energetic material, has become the object of research for researchers with its unique chemical properties and explosive properties. By exploring its structure, reaction mechanism, explosion process, etc., scholars hope to gain a deeper understanding of the properties of energetic materials, so as to promote the development of energetic materials, lay the foundation for the research and development of new materials, and help materials science continue to move forward.
In the military field, hydrazine picrate has high explosive properties and can be used as an explosive component. In the past war years, military craftsmen found that hydrazine picrate can release huge energy under specific conditions in order to find powerful explosives. After repeated trials, they found that hydrazine picrate can release huge energy under specific conditions, so they used it in artillery shells, bombs and other weapons to enhance the damage effect of weapons and cause serious damage to enemy fortifications and equipment.
In the industrial field, hydrazine picrate can be used in the manufacture of fireworks. In the fireworks required for festivals, some of the colorful and unique fireworks have the "credit" of hydrazine picrate. It can produce a bright flame or a special color light through a specific reaction, bringing a visual feast to the public.
In the field of scientific research, hydrazine picrate, as an energetic material, has become the object of research for researchers with its unique chemical properties and explosive properties. By exploring its structure, reaction mechanism, explosion process, etc., scholars hope to gain a deeper understanding of the properties of energetic materials, so as to promote the development of energetic materials, lay the foundation for the research and development of new materials, and help materials science continue to move forward.
What are the synthesis methods of 1-bromo-2,4,6-trichlorobenzene?
The synthesis method of 1-bromo-2,4,6-trifluorobenzene is described in ancient books, and it is very delicate.
First, 2,4,6-trifluoroaniline is used as the starting material, and can be obtained through diazotization and bromination reactions. In this way, 2,4,6-trifluoroaniline is first reacted with sodium nitrite under acidic conditions to form diazonium salts. The key to diazotization lies in the control of temperature, and it should be carried out at low temperature to prevent the decomposition of diazonium salts. Then, the diazonium salt is reacted with brominated reagents such as cuprous bromide to achieve the substitution of bromine atoms to obtain 1-bromo-2,4,6-trifluorobenzene. This process requires precise regulation of the reaction conditions in order to increase the yield.
Second, 1,3,5-trifluorobenzene is used as raw material and prepared by bromination reaction. This reaction usually uses liquid bromine as brominating reagent. Under the action of catalysts such as ferric chloride, bromine atoms selectively replace hydrogen atoms on the benzene ring. The amount of catalyst, reaction temperature and time all have a great impact on the reaction. If there are too many catalysts, although the reaction rate increases, it may lead to an increase in polybromination by-products; if the temperature is too high, it will also trigger side reactions and affect the purity of the product. Therefore, careful weighing is required to find the best reaction parameters.
Third, aromatic hydrocarbon derivatives containing fluorine and bromine are used as raw materials and synthesized through a series of reactions such as deprotecting groups. This method is more complicated, but it may be applicable to specific needs. The reaction route needs to be rationally designed according to the characteristics of the raw materials, and each step of the reaction needs to be carefully operated to achieve the synthesis purpose.
Synthesis of 1-bromo-2,4,6-trifluorobenzene has various methods, each with advantages and disadvantages. In practical applications, it is necessary to carefully select the appropriate synthesis path according to factors such as raw material availability, cost, yield and purity requirements, so as to achieve twice the desired synthesis effect with half the effort.
First, 2,4,6-trifluoroaniline is used as the starting material, and can be obtained through diazotization and bromination reactions. In this way, 2,4,6-trifluoroaniline is first reacted with sodium nitrite under acidic conditions to form diazonium salts. The key to diazotization lies in the control of temperature, and it should be carried out at low temperature to prevent the decomposition of diazonium salts. Then, the diazonium salt is reacted with brominated reagents such as cuprous bromide to achieve the substitution of bromine atoms to obtain 1-bromo-2,4,6-trifluorobenzene. This process requires precise regulation of the reaction conditions in order to increase the yield.
Second, 1,3,5-trifluorobenzene is used as raw material and prepared by bromination reaction. This reaction usually uses liquid bromine as brominating reagent. Under the action of catalysts such as ferric chloride, bromine atoms selectively replace hydrogen atoms on the benzene ring. The amount of catalyst, reaction temperature and time all have a great impact on the reaction. If there are too many catalysts, although the reaction rate increases, it may lead to an increase in polybromination by-products; if the temperature is too high, it will also trigger side reactions and affect the purity of the product. Therefore, careful weighing is required to find the best reaction parameters.
Third, aromatic hydrocarbon derivatives containing fluorine and bromine are used as raw materials and synthesized through a series of reactions such as deprotecting groups. This method is more complicated, but it may be applicable to specific needs. The reaction route needs to be rationally designed according to the characteristics of the raw materials, and each step of the reaction needs to be carefully operated to achieve the synthesis purpose.
Synthesis of 1-bromo-2,4,6-trifluorobenzene has various methods, each with advantages and disadvantages. In practical applications, it is necessary to carefully select the appropriate synthesis path according to factors such as raw material availability, cost, yield and purity requirements, so as to achieve twice the desired synthesis effect with half the effort.
What are the environmental effects of 1-bromo-2,4,6-trichlorobenzene?
The impact of 1-% hydrazine-2,4,6-trifluorobenzene on the environment is related to ecological balance and the survival of all things, which cannot be ignored.
If this substance escapes in the atmosphere, it interacts with various components in the air, or produces complex chemical changes. Hydrazine has strong reducing properties and is easy to react with oxidants such as oxygen to produce secondary pollutants such as nitrogen oxides. The presence of fluorine atoms in 2,4,6-trifluorobenzene makes its chemical properties stable and volatile, and can be retained in the atmosphere for a long time, or diffused with airflow, affecting the regional and even global atmospheric environment.
As for water bodies, once 1-% hydrazine-2,4,6-trifluorobenzene enters, hydrazine can change the redox potential of water bodies and affect the living environment of aquatic organisms. And 2,4,6-trifluorobenzene has strong hydrophobicity, or is adsorbed on suspended particles and settles to the bottom of the water, causing harm to benthic organisms. At the same time, it is difficult to degrade in water, or enriched through the food chain, from aquatic microorganisms to fish and shrimp, and then to humans, threatening human health.
The soil environment is also affected by it. 1-% hydrazine-2,4,6-trifluorobenzene enters the soil, or affects the structure and function of soil microbial community. Microorganisms are essential for soil nutrient cycling and decomposition of organic matter. If they are inhibited or mutated, they will cause soil fertility to decrease and affect plant growth. After plant roots absorb this substance, they may affect their own physiological metabolism, resulting in crop yield reduction, quality reduction, and transmission through the food chain, which is even more harmful. Therefore, 1-% hydrazine-2,4,6-trifluorobenzene has a wide and far-reaching impact on the environment, from the atmosphere, water to soil, and is disturbed by it, threatening ecological security and human well-being. Therefore, it must be treated with caution to prevent it from polluting the environment.
If this substance escapes in the atmosphere, it interacts with various components in the air, or produces complex chemical changes. Hydrazine has strong reducing properties and is easy to react with oxidants such as oxygen to produce secondary pollutants such as nitrogen oxides. The presence of fluorine atoms in 2,4,6-trifluorobenzene makes its chemical properties stable and volatile, and can be retained in the atmosphere for a long time, or diffused with airflow, affecting the regional and even global atmospheric environment.
As for water bodies, once 1-% hydrazine-2,4,6-trifluorobenzene enters, hydrazine can change the redox potential of water bodies and affect the living environment of aquatic organisms. And 2,4,6-trifluorobenzene has strong hydrophobicity, or is adsorbed on suspended particles and settles to the bottom of the water, causing harm to benthic organisms. At the same time, it is difficult to degrade in water, or enriched through the food chain, from aquatic microorganisms to fish and shrimp, and then to humans, threatening human health.
The soil environment is also affected by it. 1-% hydrazine-2,4,6-trifluorobenzene enters the soil, or affects the structure and function of soil microbial community. Microorganisms are essential for soil nutrient cycling and decomposition of organic matter. If they are inhibited or mutated, they will cause soil fertility to decrease and affect plant growth. After plant roots absorb this substance, they may affect their own physiological metabolism, resulting in crop yield reduction, quality reduction, and transmission through the food chain, which is even more harmful. Therefore, 1-% hydrazine-2,4,6-trifluorobenzene has a wide and far-reaching impact on the environment, from the atmosphere, water to soil, and is disturbed by it, threatening ecological security and human well-being. Therefore, it must be treated with caution to prevent it from polluting the environment.
Scan to WhatsApp
