Linshang Chemical
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1,2,3-Trichloro-4-Nitrobenzene
Linshang Chemical
|
HS Code |
876276 |
| Chemical Formula | C6H2Cl3NO2 |
| Molar Mass | 226.44 g/mol |
| Appearance | Yellow - brown solid |
| Melting Point | 46 - 48 °C |
| Boiling Point | 275 - 277 °C |
| Density | 1.65 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents like benzene, toluene |
| Vapor Pressure | Low vapor pressure |
| Odor | Pungent odor |
| Flash Point | 132 °C |
As an accredited 1,2,3-Trichloro-4-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle of 1,2,3 - trichloro - 4 - nitrobenzene with secure chemical - resistant packaging. |
| Storage | 1,2,3 - Trichloro - 4 - nitrobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from sources of ignition, heat, and incompatible substances like strong oxidizers. Store it in a tightly closed container made of corrosion - resistant material, such as steel or high - density polyethylene, to prevent leakage and contamination. |
| Shipping | 1,2,3 - Trichloro - 4 - nitrobenzene is a hazardous chemical. Shipping must comply with strict regulations. It should be packaged securely in appropriate containers, clearly labeled, and transported by carriers licensed for such hazardous substances. |
Competitive 1,2,3-Trichloro-4-Nitrobenzene 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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As a leading 1,2,3-Trichloro-4-Nitrobenzene 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 1,2,3-trichloro-4-nitrobenzene?
The main uses of 1% 2C2% 2C3-triazepine-4-pyridine are as follows:
1% 2C2% 2C3-triazepine-4-pyridine has important applications in many fields. In the field of medicine, it can be used as a key intermediate for the synthesis of drugs. Due to its specific chemical structure, it can participate in the construction of a variety of drug molecules, providing the possibility for the development of new drugs with unique pharmacological activities. For example, in the synthesis of some antibacterial drugs, it can be combined with other chemical groups through specific chemical reactions, thus giving the drug the antibacterial ability to target specific bacteria and helping medical researchers develop more effective anti-infective drugs.
In materials science, 1% 2C2% 2C3-triazo-4-pyridine can be used to prepare functional materials. With its chemical properties, it can be combined or reacted with other substances, giving materials special properties such as good electrical conductivity and optical properties. For example, when preparing organic optoelectronic materials, introducing them into the material system can optimize the electronic transport performance of the material and improve the application effect of the material in optoelectronic devices, such as improving the photoelectric conversion efficiency of solar cells.
In the field of organic synthesis, 1% 2C2% 2C3-triazo-4-pyridine is an extremely important building block for organic synthesis. It can react with various organic reagents through different chemical reaction paths to construct complex and diverse organic compounds. Synthetic chemists can use its reactivity to achieve precise regulation of the molecular structure of the target compound, and then synthesize organic compounds with specific functions and structures to meet the needs of different fields for special organic compounds.
1% 2C2% 2C3-triazepine-4-pyridine has important applications in many fields. In the field of medicine, it can be used as a key intermediate for the synthesis of drugs. Due to its specific chemical structure, it can participate in the construction of a variety of drug molecules, providing the possibility for the development of new drugs with unique pharmacological activities. For example, in the synthesis of some antibacterial drugs, it can be combined with other chemical groups through specific chemical reactions, thus giving the drug the antibacterial ability to target specific bacteria and helping medical researchers develop more effective anti-infective drugs.
In materials science, 1% 2C2% 2C3-triazo-4-pyridine can be used to prepare functional materials. With its chemical properties, it can be combined or reacted with other substances, giving materials special properties such as good electrical conductivity and optical properties. For example, when preparing organic optoelectronic materials, introducing them into the material system can optimize the electronic transport performance of the material and improve the application effect of the material in optoelectronic devices, such as improving the photoelectric conversion efficiency of solar cells.
In the field of organic synthesis, 1% 2C2% 2C3-triazo-4-pyridine is an extremely important building block for organic synthesis. It can react with various organic reagents through different chemical reaction paths to construct complex and diverse organic compounds. Synthetic chemists can use its reactivity to achieve precise regulation of the molecular structure of the target compound, and then synthesize organic compounds with specific functions and structures to meet the needs of different fields for special organic compounds.
What are the physical properties of 1,2,3-trichloro-4-nitrobenzene?
1% 2C2% 2C3 is one, two, and three, which are common numbers. In the world, it is often used for counting and sorting.
And "trichlorine", this is the related title of chemical substances. Trichlorine substances, many of which have special physical and chemical properties. It may be a liquid, with a certain volatility, and some of them have a pungent smell. In the field of chemistry, it is often used as a solvent to dissolve many organic compounds. However, many of them are toxic. If they are accidentally exposed to the human body, they may cause skin burns, respiratory damage, etc.
As for "4-cyanopyridine", it is also a chemical substance. Its appearance is often white to light yellow crystalline powder. In chemical synthesis, it is an important intermediate and can be used to prepare a variety of drugs, pesticides and functional materials. Because its structure contains a cyanide group and a pyridine ring, it has both chemical activities. Its physical properties, such as melting point and boiling point, have specific values, and their solubility varies in different solvents. In chemical reactions, cyanide groups can undergo hydrolysis, addition and other reactions, and pyridine rings can also participate in electrophilic substitution and other reactions. With these properties, it plays a key role in the field of organic synthesis.
And "trichlorine", this is the related title of chemical substances. Trichlorine substances, many of which have special physical and chemical properties. It may be a liquid, with a certain volatility, and some of them have a pungent smell. In the field of chemistry, it is often used as a solvent to dissolve many organic compounds. However, many of them are toxic. If they are accidentally exposed to the human body, they may cause skin burns, respiratory damage, etc.
As for "4-cyanopyridine", it is also a chemical substance. Its appearance is often white to light yellow crystalline powder. In chemical synthesis, it is an important intermediate and can be used to prepare a variety of drugs, pesticides and functional materials. Because its structure contains a cyanide group and a pyridine ring, it has both chemical activities. Its physical properties, such as melting point and boiling point, have specific values, and their solubility varies in different solvents. In chemical reactions, cyanide groups can undergo hydrolysis, addition and other reactions, and pyridine rings can also participate in electrophilic substitution and other reactions. With these properties, it plays a key role in the field of organic synthesis.
What are the environmental effects of 1,2,3-trichloro-4-nitrobenzene?
The impact of 1% 2C2% 2C3-trifluoro-4-cyanopyridine on the environment is actually the key to ecological balance and the survival of all things.
If this substance is released in the natural environment, the first person to bear the brunt is the aquatic ecology. It may dissolve into rivers, lakes and seas, causing poisoning to aquatic organisms. For example, fish, their gills and body surfaces come into contact with water bodies containing this substance, which can cause respiratory disorders, physiological disorders, and juvenile fish and eggs are more susceptible to it, or cause a sharp decrease in population. Aquatic plants are also difficult to escape, and their physiological processes such as photosynthesis and nutrient absorption may be disturbed, destroying the basic food chain of aquatic ecology and triggering an ecological chain reaction.
In the soil environment, the substance or residue accumulates, affecting the activity of soil microorganisms. Soil microorganisms are crucial in the decomposition of organic matter and nutrient circulation, and their activity is inhibited, which will reduce soil fertility and affect plant growth. Plant roots absorb soil nutrients containing this substance, which not only hinders their own development, but also deteriorates fruit quality, and may be transmitted through the food chain, endangering organisms that feed on plants.
In the atmospheric environment, if the substance volatilizes to form gaseous pollutants, it will affect air quality. Humans inhale air containing this pollutant, and organs such as the respiratory tract and lungs may be damaged, causing health problems such as cough and asthma. Flying animals such as birds will also be affected by it, or their flight ability and reproductive ability will be reduced.
In summary, 1% 2C2% 2C3-trifluoro-4-cyanopyridine is harmful to the environment. During its production, use and disposal, it is necessary to take precautions to reduce its threat to the ecological environment and biological health, and maintain the harmony and stability of the earth's ecology.
If this substance is released in the natural environment, the first person to bear the brunt is the aquatic ecology. It may dissolve into rivers, lakes and seas, causing poisoning to aquatic organisms. For example, fish, their gills and body surfaces come into contact with water bodies containing this substance, which can cause respiratory disorders, physiological disorders, and juvenile fish and eggs are more susceptible to it, or cause a sharp decrease in population. Aquatic plants are also difficult to escape, and their physiological processes such as photosynthesis and nutrient absorption may be disturbed, destroying the basic food chain of aquatic ecology and triggering an ecological chain reaction.
In the soil environment, the substance or residue accumulates, affecting the activity of soil microorganisms. Soil microorganisms are crucial in the decomposition of organic matter and nutrient circulation, and their activity is inhibited, which will reduce soil fertility and affect plant growth. Plant roots absorb soil nutrients containing this substance, which not only hinders their own development, but also deteriorates fruit quality, and may be transmitted through the food chain, endangering organisms that feed on plants.
In the atmospheric environment, if the substance volatilizes to form gaseous pollutants, it will affect air quality. Humans inhale air containing this pollutant, and organs such as the respiratory tract and lungs may be damaged, causing health problems such as cough and asthma. Flying animals such as birds will also be affected by it, or their flight ability and reproductive ability will be reduced.
In summary, 1% 2C2% 2C3-trifluoro-4-cyanopyridine is harmful to the environment. During its production, use and disposal, it is necessary to take precautions to reduce its threat to the ecological environment and biological health, and maintain the harmony and stability of the earth's ecology.
What are the preparation methods of 1,2,3-trichloro-4-nitrobenzene?
To obtain 1%, 2%, 3% of triol, and 4-hydroxybenzaldehyde, the method is as follows:
First, the preparation of triol. To obtain 1%, 2%, 3% of triol, can be proportionally proportioned. First take an appropriate amount of alcohol raw materials and measure them with accurate measuring instruments. If 1% of triol is prepared, take a certain amount of triol solute and dissolve it in 100 parts of solvent. If water is used as a solvent, if one gram of triol is taken, when it is dissolved in 99 grams of water, stir well to make the solute evenly dispersed in the solvent to obtain a 1% triol solution. In the same way, make 2% of triol, take two grams of triol, and dissolve it in ninety-eight grams of water; make 3% of triol, take three grams of triol, and dissolve it in ninety-seven grams of water. In this way, according to the proportion of the preparation, the required concentration of triol can be obtained.
As for the preparation of 4-hydroxybenzaldehyde, the ancient method may be based on its raw material characteristics and reaction principle. Or take a suitable aromatic compound and obtain it through several steps of reaction. First, benzene is used as the starting material, and a suitable substituent is introduced through a substitution reaction. Benzene and halogenated hydrocarbons can be alkylated by Fu-g under the action of a catalyst, and an alkyl group can be introduced. Then through an oxidation step, the alkyl group is oxidized to an aldehyde However, this oxidation process requires a suitable oxidizing agent, such as a mild oxidizing agent, to avoid excessive oxidation. Then, through the hydroxylation reaction, a hydroxyl group is introduced at a specific position of the benzene ring, which can be achieved by a specific electrophilic substitution reaction. During the reaction process, it is necessary to control the temperature and time, and pay attention to the changes in the reaction conditions to ensure that the reaction proceeds in the direction of generating 4-hydroxybenzaldehyde. After the reaction is completed, pure 4-hydroxybenzaldehyde can be obtained by separation and purification methods, such as distillation and recrystallization.
In this way, according to the above method, 1%, 2%, 3% triol and 4-hydroxybenzaldehyde can be obtained.
First, the preparation of triol. To obtain 1%, 2%, 3% of triol, can be proportionally proportioned. First take an appropriate amount of alcohol raw materials and measure them with accurate measuring instruments. If 1% of triol is prepared, take a certain amount of triol solute and dissolve it in 100 parts of solvent. If water is used as a solvent, if one gram of triol is taken, when it is dissolved in 99 grams of water, stir well to make the solute evenly dispersed in the solvent to obtain a 1% triol solution. In the same way, make 2% of triol, take two grams of triol, and dissolve it in ninety-eight grams of water; make 3% of triol, take three grams of triol, and dissolve it in ninety-seven grams of water. In this way, according to the proportion of the preparation, the required concentration of triol can be obtained.
As for the preparation of 4-hydroxybenzaldehyde, the ancient method may be based on its raw material characteristics and reaction principle. Or take a suitable aromatic compound and obtain it through several steps of reaction. First, benzene is used as the starting material, and a suitable substituent is introduced through a substitution reaction. Benzene and halogenated hydrocarbons can be alkylated by Fu-g under the action of a catalyst, and an alkyl group can be introduced. Then through an oxidation step, the alkyl group is oxidized to an aldehyde However, this oxidation process requires a suitable oxidizing agent, such as a mild oxidizing agent, to avoid excessive oxidation. Then, through the hydroxylation reaction, a hydroxyl group is introduced at a specific position of the benzene ring, which can be achieved by a specific electrophilic substitution reaction. During the reaction process, it is necessary to control the temperature and time, and pay attention to the changes in the reaction conditions to ensure that the reaction proceeds in the direction of generating 4-hydroxybenzaldehyde. After the reaction is completed, pure 4-hydroxybenzaldehyde can be obtained by separation and purification methods, such as distillation and recrystallization.
In this way, according to the above method, 1%, 2%, 3% triol and 4-hydroxybenzaldehyde can be obtained.
What should I pay attention to when storing and transporting 1,2,3-trichloro-4-nitrobenzene?
1% 2C2% 2C3 is mono-, di-, and triol. 4-Cyanopyridine needs to pay attention to many key matters when storing and transporting.
One is related to storage conditions. Both should be stored in a cool, dry and well-ventilated place. Because mono-, di-, and triol are flammable, if placed in a high temperature or humid place, there may be a risk of fire, and humid environments may also cause them to deteriorate. 4-Cyanopyridine has no flammability concerns, but humid environments may make it deliquescent and affect quality. Furthermore, both should be kept away from fire, heat sources, and direct sunlight. One, two, and three alcohols are easy to burn and explode when exposed to open flames and hot topics; 4-cyanopyridine is heated or decomposed to produce toxic fumes. At the same time, it should be stored separately from oxidants, acids, and bases. One, two, and three alcohols are mixed with oxidants or react violently. 4-cyanopyridine encounters acid and alkali or reacts chemically, which damages its purity and properties.
Second, transportation should not be ignored. When transporting one, two, and three alcohols, it is necessary to ensure that the container does not leak, collapse, fall, or damage. Because it is a flammable liquid, the transportation vehicle needs to be equipped with corresponding fire equipment and leakage emergency treatment equipment. It should be transported in the morning and evening in summer to prevent danger caused by high temperature. When transporting 4-cyanopyridine, it is also necessary to ensure that the packaging is complete and that there is no leakage during transportation. Because of its toxicity, transporters need to be familiar with protection knowledge and emergency treatment measures. In the event of leakage, they can deal with it quickly and correctly to avoid harm to the environment and people.
In short, whether it is 1% 2C2% 2C3-triol or 4-cyanopyridine, during storage and transportation, it is necessary to strictly follow the relevant regulations and operating procedures, and must not slack off to ensure the safety of personnel and the integrity of materials.
One is related to storage conditions. Both should be stored in a cool, dry and well-ventilated place. Because mono-, di-, and triol are flammable, if placed in a high temperature or humid place, there may be a risk of fire, and humid environments may also cause them to deteriorate. 4-Cyanopyridine has no flammability concerns, but humid environments may make it deliquescent and affect quality. Furthermore, both should be kept away from fire, heat sources, and direct sunlight. One, two, and three alcohols are easy to burn and explode when exposed to open flames and hot topics; 4-cyanopyridine is heated or decomposed to produce toxic fumes. At the same time, it should be stored separately from oxidants, acids, and bases. One, two, and three alcohols are mixed with oxidants or react violently. 4-cyanopyridine encounters acid and alkali or reacts chemically, which damages its purity and properties.
Second, transportation should not be ignored. When transporting one, two, and three alcohols, it is necessary to ensure that the container does not leak, collapse, fall, or damage. Because it is a flammable liquid, the transportation vehicle needs to be equipped with corresponding fire equipment and leakage emergency treatment equipment. It should be transported in the morning and evening in summer to prevent danger caused by high temperature. When transporting 4-cyanopyridine, it is also necessary to ensure that the packaging is complete and that there is no leakage during transportation. Because of its toxicity, transporters need to be familiar with protection knowledge and emergency treatment measures. In the event of leakage, they can deal with it quickly and correctly to avoid harm to the environment and people.
In short, whether it is 1% 2C2% 2C3-triol or 4-cyanopyridine, during storage and transportation, it is necessary to strictly follow the relevant regulations and operating procedures, and must not slack off to ensure the safety of personnel and the integrity of materials.
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