Linshang Chemical
PRODUCTS
1-Nitro-2,3,4-Trichlorobenzene
Linshang Chemical
|
HS Code |
358876 |
| Chemical Formula | C6H2Cl3NO2 |
| Appearance | Solid |
| Solubility In Water | Low |
As an accredited 1-Nitro-2,3,4-Trichlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - nitro - 2,3,4 - trichlorobenzene: 500g in a sealed, corrosion - resistant chemical - grade bottle. |
| Storage | 1 - nitro - 2,3,4 - trichlorobenzene should be stored in a cool, dry, well - ventilated area away from sources of ignition. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, reducing agents, and substances that may react with it to prevent dangerous chemical reactions. |
| Shipping | 1 - nitro - 2,3,4 - trichlorobenzene is a chemical that must be shipped in accordance with strict hazardous materials regulations. It should be packaged securely in appropriate containers to prevent leakage during transit. |
Competitive 1-Nitro-2,3,4-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
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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 1-Nitro-2,3,4-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 chemical properties of 1-nitro-2,3,4-trichlorobenzene?
1 - nitro - 2,3,4 - trichlorobenzene is an organic compound with special chemical properties. It is a light yellow solid, which is relatively stable at room temperature and pressure. When it encounters hot topics, open flames or strong oxidants, it poses a risk of explosion.
In this compound, the nitro group and the chlorine atom give it unique reactivity. The nitro group is a strong electron-absorbing group, which decreases the electron cloud density of the benzene ring, causing its electrophilic substitution activity to decrease, but the nucleophilic substitution activity to increase. For example, under suitable conditions, it can be substituted with nucleophiles, and the nitro group can be replaced by other groups.
The chlorine atom is also an electron-withdrawing group, which further affects the electron cloud distribution of the benzene ring, so that the density of the adjacent and para-site electron clouds on the benzene ring is relatively reduced. Therefore, electrophilic reagents are more likely to attack the intermediate sites. And these chlorine atoms can participate in the substitution reaction and are replaced by other atoms or groups under certain conditions.
1-nitro-2,3,4-trichlorobenzene is insoluble in water, but easily soluble in organic solvents such as ethanol, ether, benzene, etc. This solubility characteristic is related to the polarity of its molecular structure, which is relatively small, so it has good solubility in non-polar or weakly polar organic solvents.
In terms of chemical stability, although it is stable at room temperature and pressure, decomposition or other chemical reactions will occur when high temperature, light or specific catalysts are present. Due to its certain toxicity, it is potentially harmful to human health and the environment. When using and handling, strict safety regulations and environmental protection requirements must be followed to prevent damage to the ecology and human body.
In this compound, the nitro group and the chlorine atom give it unique reactivity. The nitro group is a strong electron-absorbing group, which decreases the electron cloud density of the benzene ring, causing its electrophilic substitution activity to decrease, but the nucleophilic substitution activity to increase. For example, under suitable conditions, it can be substituted with nucleophiles, and the nitro group can be replaced by other groups.
The chlorine atom is also an electron-withdrawing group, which further affects the electron cloud distribution of the benzene ring, so that the density of the adjacent and para-site electron clouds on the benzene ring is relatively reduced. Therefore, electrophilic reagents are more likely to attack the intermediate sites. And these chlorine atoms can participate in the substitution reaction and are replaced by other atoms or groups under certain conditions.
1-nitro-2,3,4-trichlorobenzene is insoluble in water, but easily soluble in organic solvents such as ethanol, ether, benzene, etc. This solubility characteristic is related to the polarity of its molecular structure, which is relatively small, so it has good solubility in non-polar or weakly polar organic solvents.
In terms of chemical stability, although it is stable at room temperature and pressure, decomposition or other chemical reactions will occur when high temperature, light or specific catalysts are present. Due to its certain toxicity, it is potentially harmful to human health and the environment. When using and handling, strict safety regulations and environmental protection requirements must be followed to prevent damage to the ecology and human body.
What are the physical properties of 1-nitro-2,3,4-trichlorobenzene?
1 - nitro - 2,3,4 - trichlorobenzene is an organic compound with unique physical properties. At room temperature and pressure, it is a solid state, like a light yellow crystalline powder. Viewed in sunlight, it shimmers and shines like fine gold sand.
When it comes to the melting point, it is about 55 ° C to 57 ° C, which is very important. Just like winter ice, it melts when it is warm. When heated to a specific temperature, this compound slowly solidifies into a liquid state. The exact melting point allows craftsmen to precisely control the temperature when refining and refining to ensure the purity and quality of the product.
The boiling point is about 274 ° C to 276 ° C. When the temperature rises to this point, the compound is like a rising mist, changing from liquid to gaseous. This boiling point characteristic is of great significance in the process of distillation separation, which can help separate the components of different boiling points in the mixture and achieve the purpose of purification.
The density of this compound is about 1.72 g/cm ³, which is heavier than common water. If placed in water, it is like a stone sinking to the bottom. This density characteristic plays a key role in the stratification and separation of substances in chemical production.
1 - nitro - 2,3,4 - trichlorobenzene is extremely insoluble in water, just like the incompatibility of oil and water. However, in organic solvents, such as acetone, ether, benzene, etc., it can dissolve well, just like salt in water. This solubility, in organic synthesis, can be used as a solvent or co-solvent to assist the reaction and facilitate the extraction and separation of the product.
In addition, it has a certain volatility and slowly emits an odor in the air. Although it is not pungent and smelly, it should be treated with caution because it evaporates in the environment or has potential effects on the human body and ecology. When storing and using, it should be well ventilated to prevent the accumulation of volatile gases.
When it comes to the melting point, it is about 55 ° C to 57 ° C, which is very important. Just like winter ice, it melts when it is warm. When heated to a specific temperature, this compound slowly solidifies into a liquid state. The exact melting point allows craftsmen to precisely control the temperature when refining and refining to ensure the purity and quality of the product.
The boiling point is about 274 ° C to 276 ° C. When the temperature rises to this point, the compound is like a rising mist, changing from liquid to gaseous. This boiling point characteristic is of great significance in the process of distillation separation, which can help separate the components of different boiling points in the mixture and achieve the purpose of purification.
The density of this compound is about 1.72 g/cm ³, which is heavier than common water. If placed in water, it is like a stone sinking to the bottom. This density characteristic plays a key role in the stratification and separation of substances in chemical production.
1 - nitro - 2,3,4 - trichlorobenzene is extremely insoluble in water, just like the incompatibility of oil and water. However, in organic solvents, such as acetone, ether, benzene, etc., it can dissolve well, just like salt in water. This solubility, in organic synthesis, can be used as a solvent or co-solvent to assist the reaction and facilitate the extraction and separation of the product.
In addition, it has a certain volatility and slowly emits an odor in the air. Although it is not pungent and smelly, it should be treated with caution because it evaporates in the environment or has potential effects on the human body and ecology. When storing and using, it should be well ventilated to prevent the accumulation of volatile gases.
In which fields is 1-nitro-2,3,4-trichlorobenzene used?
1 - nitro - 2,3,4 - trichlorobenzene (1 - nitro - 2,3,4 - trichlorobenzene) is an organic compound, which is used in chemical industry, medicine, agriculture and other fields.
In the chemical industry, it can be used as an intermediate in organic synthesis. The presence of nitro and chlorine atoms in the molecule gives it unique chemical reactivity and can participate in many reactions, such as nucleophilic substitution reactions. With such reactions, chemists can introduce other functional groups into molecules to synthesize organic compounds with more complex structures, which is of great significance for the preparation of fine chemical products. For example, when synthesizing special dyes, 1-nitro-2,3,4-trichlorobenzene can be used as a starting material. The specific structure of the dye molecule is constructed through a series of reactions, which endows the dye with excellent dyeing performance and color fastness.
In the pharmaceutical field, although it is itself or an indirect medicinal ingredient, it is a key intermediate and is crucial for the synthesis of some drugs. By chemically modifying and transforming it, compounds with specific pharmacological activities can be prepared. For example, through a specific reaction path, it can be converted into drug molecules that have therapeutic effects on specific diseases, or as antibacterial drugs, or as drugs for the treatment of cardiovascular diseases, providing an important material basis for pharmaceutical research and development.
In agriculture, 1-nitro-2,3,4-trichlorobenzene can be used to synthesize pesticides. Due to the characteristics of chlorine atoms and nitro groups, synthetic pesticides may have good insecticidal, bactericidal or herbicidal activities. For example, insecticides made from it can effectively act on specific physiological processes of pests, interfere with the growth, reproduction and feeding of pests, so as to achieve the purpose of crop protection and help improve crop yield and quality.
In summary, 1-nitro-2,3,4-trichlorobenzene plays an indispensable role in many industrial fields, providing important material support for the development of various fields.
In the chemical industry, it can be used as an intermediate in organic synthesis. The presence of nitro and chlorine atoms in the molecule gives it unique chemical reactivity and can participate in many reactions, such as nucleophilic substitution reactions. With such reactions, chemists can introduce other functional groups into molecules to synthesize organic compounds with more complex structures, which is of great significance for the preparation of fine chemical products. For example, when synthesizing special dyes, 1-nitro-2,3,4-trichlorobenzene can be used as a starting material. The specific structure of the dye molecule is constructed through a series of reactions, which endows the dye with excellent dyeing performance and color fastness.
In the pharmaceutical field, although it is itself or an indirect medicinal ingredient, it is a key intermediate and is crucial for the synthesis of some drugs. By chemically modifying and transforming it, compounds with specific pharmacological activities can be prepared. For example, through a specific reaction path, it can be converted into drug molecules that have therapeutic effects on specific diseases, or as antibacterial drugs, or as drugs for the treatment of cardiovascular diseases, providing an important material basis for pharmaceutical research and development.
In agriculture, 1-nitro-2,3,4-trichlorobenzene can be used to synthesize pesticides. Due to the characteristics of chlorine atoms and nitro groups, synthetic pesticides may have good insecticidal, bactericidal or herbicidal activities. For example, insecticides made from it can effectively act on specific physiological processes of pests, interfere with the growth, reproduction and feeding of pests, so as to achieve the purpose of crop protection and help improve crop yield and quality.
In summary, 1-nitro-2,3,4-trichlorobenzene plays an indispensable role in many industrial fields, providing important material support for the development of various fields.
What is the production method of 1-nitro-2,3,4-trichlorobenzene?
1 - nitro - 2,3,4 - trichlorobenzene is an organic compound, and the preparation methods are common and have several ends.
First, 2,3,4 - trichloronitrobenzene is used as the starting material and can be prepared by nucleophilic substitution reaction. Under suitable reaction conditions, the starting material is mixed with a specific nucleophilic reagent, and the nucleophilic reagent attacks its specific position. Through the substitution reaction process, 1 - nitro - 2,3,4 - trichlorobenzene is finally obtained. For example, select the appropriate nucleophilic reagent, and the reaction can proceed smoothly under the action of suitable solvents, temperatures and catalysts. Pay attention to the precise regulation of reaction conditions. Too high or too low temperature may affect the reaction rate and product purity.
Second, it can be prepared from benzene through a multi-step reaction. First, benzene is chlorinated, and many chlorinated benzenes are obtained. During the chlorination reaction, depending on the reaction conditions and catalysts, the position and number of chlorine atom substitutions can be controlled to obtain 2,3,4-trichlorobenzene. Subsequently, the polychlorinated benzene is nitrified, and nitro groups are introduced at specific positions to obtain the target product 1-nitro-2,3,4-trichlorobenzene. During the chlorination process, factors such as the amount of chlorine gas introduced, the reaction temperature and time have a great influence on the formation and product distribution of polychlorinated benzene. During the nitration reaction, the concentration, reaction temperature and reaction time of nitric acid are also related to the position and yield of nitro groups introduced.
Third, there are also other related aromatic compounds as starting materials and prepared by a series of functional group conversion reactions. This approach requires careful design of the reaction route according to the structural characteristics of the starting material, reasonable arrangement of the reaction sequence of each step, and gradual construction of the structure of the target molecule through multi-step reactions to achieve the synthesis of 1-nitro-2,3,4-trichlorobenzene. In this process, the selectivity and conversion rate of each step of the reaction need to be carefully considered and regulated to ensure the quality and yield of the final product.
First, 2,3,4 - trichloronitrobenzene is used as the starting material and can be prepared by nucleophilic substitution reaction. Under suitable reaction conditions, the starting material is mixed with a specific nucleophilic reagent, and the nucleophilic reagent attacks its specific position. Through the substitution reaction process, 1 - nitro - 2,3,4 - trichlorobenzene is finally obtained. For example, select the appropriate nucleophilic reagent, and the reaction can proceed smoothly under the action of suitable solvents, temperatures and catalysts. Pay attention to the precise regulation of reaction conditions. Too high or too low temperature may affect the reaction rate and product purity.
Second, it can be prepared from benzene through a multi-step reaction. First, benzene is chlorinated, and many chlorinated benzenes are obtained. During the chlorination reaction, depending on the reaction conditions and catalysts, the position and number of chlorine atom substitutions can be controlled to obtain 2,3,4-trichlorobenzene. Subsequently, the polychlorinated benzene is nitrified, and nitro groups are introduced at specific positions to obtain the target product 1-nitro-2,3,4-trichlorobenzene. During the chlorination process, factors such as the amount of chlorine gas introduced, the reaction temperature and time have a great influence on the formation and product distribution of polychlorinated benzene. During the nitration reaction, the concentration, reaction temperature and reaction time of nitric acid are also related to the position and yield of nitro groups introduced.
Third, there are also other related aromatic compounds as starting materials and prepared by a series of functional group conversion reactions. This approach requires careful design of the reaction route according to the structural characteristics of the starting material, reasonable arrangement of the reaction sequence of each step, and gradual construction of the structure of the target molecule through multi-step reactions to achieve the synthesis of 1-nitro-2,3,4-trichlorobenzene. In this process, the selectivity and conversion rate of each step of the reaction need to be carefully considered and regulated to ensure the quality and yield of the final product.
What is the environmental impact of 1-nitro-2,3,4-trichlorobenzene?
1-Nitro-2,3,4-trichlorobenzene (1-nitro-2,3,4-trichlorobenzene) is an organic compound that has a complex impact on the environment and cannot be ignored.
First, in the atmosphere, 1-nitro-2,3,4-trichlorobenzene has a certain volatility. If it is released, it will participate in photochemical reactions. Its molecular structure contains chlorine and nitro groups. During the photolysis process, chlorine atoms will escape, catalyzing the destruction of the ozone layer, resulting in the depletion of the ozone layer, weakening its shielding function against ultraviolet rays, and then affecting the earth's ecological balance and human health. And in photochemical reactions, it may generate secondary pollutants such as nitro radicals, which can react with other components in the atmosphere to generate fine particulate matter (PM2.5, etc.) and ozone and other pollutants, aggravating air pollution and harming the human respiratory system.
Second, in the aquatic environment, 1-nitro-2,3,4-trichlorobenzene is insoluble in water, but it is easily adsorbed on suspended particulate matter. When it migrates with water flow, it will accumulate in the sediment. Because of its bioaccumulation, aquatic organisms will accumulate in the body after ingestion, pass and amplify along the food chain. For example, small fish swallow plankton containing this substance, large fish eat small fish, and eventually humans eat contaminated fish, the substance will enter the human body and endanger health. Moreover, it can interfere with the normal physiological functions of aquatic organisms, such as affecting the reproduction and development of fish, resulting in decreased reproductive capacity and larval deformity.
Third, the soil environment is also affected by it. After 1-nitro-2,3,4-trichlorobenzene enters the soil, it is difficult to be rapidly degraded by microorganisms due to its stable chemical properties, and will remain for a long time. This not only changes the physical and chemical properties of the soil, but also affects the aeration and water retention of the soil, and also inhibits the growth and metabolic activities of beneficial microorganisms in the soil, destroying the balance of the soil ecosystem. After the plant root system absorbs this substance, it will affect its own growth and development, reduce the yield and quality of crops, and pass through the food chain, threatening human food safety.
In conclusion, 1-nitro-2,3,4-trichlorobenzene poses a potential threat to the atmosphere, water, soil and other environmental factors, and human production and life need to be treated with caution to reduce its negative impact on the environment.
First, in the atmosphere, 1-nitro-2,3,4-trichlorobenzene has a certain volatility. If it is released, it will participate in photochemical reactions. Its molecular structure contains chlorine and nitro groups. During the photolysis process, chlorine atoms will escape, catalyzing the destruction of the ozone layer, resulting in the depletion of the ozone layer, weakening its shielding function against ultraviolet rays, and then affecting the earth's ecological balance and human health. And in photochemical reactions, it may generate secondary pollutants such as nitro radicals, which can react with other components in the atmosphere to generate fine particulate matter (PM2.5, etc.) and ozone and other pollutants, aggravating air pollution and harming the human respiratory system.
Second, in the aquatic environment, 1-nitro-2,3,4-trichlorobenzene is insoluble in water, but it is easily adsorbed on suspended particulate matter. When it migrates with water flow, it will accumulate in the sediment. Because of its bioaccumulation, aquatic organisms will accumulate in the body after ingestion, pass and amplify along the food chain. For example, small fish swallow plankton containing this substance, large fish eat small fish, and eventually humans eat contaminated fish, the substance will enter the human body and endanger health. Moreover, it can interfere with the normal physiological functions of aquatic organisms, such as affecting the reproduction and development of fish, resulting in decreased reproductive capacity and larval deformity.
Third, the soil environment is also affected by it. After 1-nitro-2,3,4-trichlorobenzene enters the soil, it is difficult to be rapidly degraded by microorganisms due to its stable chemical properties, and will remain for a long time. This not only changes the physical and chemical properties of the soil, but also affects the aeration and water retention of the soil, and also inhibits the growth and metabolic activities of beneficial microorganisms in the soil, destroying the balance of the soil ecosystem. After the plant root system absorbs this substance, it will affect its own growth and development, reduce the yield and quality of crops, and pass through the food chain, threatening human food safety.
In conclusion, 1-nitro-2,3,4-trichlorobenzene poses a potential threat to the atmosphere, water, soil and other environmental factors, and human production and life need to be treated with caution to reduce its negative impact on the environment.
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