Linshang Chemical
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1,2,4,5-Tetrachloro-3-Methoxybenzene
Linshang Chemical
|
HS Code |
641827 |
| Chemical Formula | C7H4Cl4O |
| Molecular Weight | 269.92 g/mol |
| Appearance | Solid (predicted, based on similar compounds) |
| Solubility In Water | Low (aromatic chlorinated compounds are generally hydrophobic) |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone (predicted due to non - polar nature) |
| Vapor Pressure | Low (due to its relatively high molecular weight and solid nature, predicted) |
As an accredited 1,2,4,5-Tetrachloro-3-Methoxybenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram pack of 1,2,4,5 - tetrachloro - 3 - methoxybenzene in airtight chemical - grade container. |
| Storage | 1,2,4,5 - Tetrachloro - 3 - methoxybenzene should be stored in a cool, dry, well - ventilated area, away from sources of heat, ignition, and incompatible substances. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials, to prevent leakage and evaporation. Store it in a dedicated chemical storage facility, segregated from oxidizing agents and reactive chemicals. |
| Shipping | 1,2,4,5 - Tetrachloro - 3 - methoxybenzene is shipped in well - sealed, corrosion - resistant containers. It adheres to strict hazardous chemical shipping regulations, ensuring secure transport to prevent spills and environmental or safety risks. |
Competitive 1,2,4,5-Tetrachloro-3-Methoxybenzene 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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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 1,2,4,5-Tetrachloro-3-Methoxybenzene 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 1,2,4,5-tetrachloro-3-methoxybenzene?
The chemical properties of 1% 2C2% 2C4% 2C5-tetrahydro-3-acetylbenzene are related to the unique properties of this compound. This compound has specific physical and chemical properties.
From the perspective of physical properties, it may have a certain melting point and boiling point. The melting point is the temperature at which a substance changes from a solid state to a liquid state. The boiling point is the temperature at which a substance changes from a liquid state to a gaseous state. These two are crucial for the identification and purification of the compound. It may exhibit a specific aggregate state at room temperature and pressure, or be a solid state or a liquid state, depending on factors such as intermolecular forces.
In terms of chemical properties, 1% 2C2% 2C4% 2C5-tetrahydro-3-acetylbenzene contains an acetyl group, which is a functional group with active chemical activity. The carbon of the carbonyl group in the acetyl group is positively charged and susceptible to attack by nucleophiles. For example, it can undergo a condensation reaction with alcohols to form ester compounds. In this reaction, the hydroxyl oxygen of the alcohol acts as a nucleophile to attack the carbonyl carbon of the acetyl group, and through a series of intermediate steps, a new ester bond is formed.
Furthermore, the phenyl ring structure of the compound is also characteristic. The phenyl ring has a conjugated system and is relatively stable. However, under appropriate conditions, electrophilic substitution reactions can also occur. For example, under the action of a halogenating agent in a catalyst, halogen atoms can be introduced into the benzene ring. This is because the electrophilic reagent is attracted by the electron cloud of the benzene ring, attacks the benzene ring, forms an intermediate, and then completes the reaction through proton transfer and other steps.
In addition, the tetrahydrogen structure also affects its chemical properties. The tetrahydrogen structure changes the spatial configuration of the molecule, which affects the intermolecular force, and then affects its solubility and other properties. Its solubility is different in different solvents, and it behaves differently in polar solvents and non-polar solvents, which is related to the polarity of the molecule.
1% 2C2% 2C4% 2C5-tetrahydro-3-acetylbenzene is rich and diverse in chemical properties, and its functional groups and structures jointly determine its behavior and properties in chemical reactions.
From the perspective of physical properties, it may have a certain melting point and boiling point. The melting point is the temperature at which a substance changes from a solid state to a liquid state. The boiling point is the temperature at which a substance changes from a liquid state to a gaseous state. These two are crucial for the identification and purification of the compound. It may exhibit a specific aggregate state at room temperature and pressure, or be a solid state or a liquid state, depending on factors such as intermolecular forces.
In terms of chemical properties, 1% 2C2% 2C4% 2C5-tetrahydro-3-acetylbenzene contains an acetyl group, which is a functional group with active chemical activity. The carbon of the carbonyl group in the acetyl group is positively charged and susceptible to attack by nucleophiles. For example, it can undergo a condensation reaction with alcohols to form ester compounds. In this reaction, the hydroxyl oxygen of the alcohol acts as a nucleophile to attack the carbonyl carbon of the acetyl group, and through a series of intermediate steps, a new ester bond is formed.
Furthermore, the phenyl ring structure of the compound is also characteristic. The phenyl ring has a conjugated system and is relatively stable. However, under appropriate conditions, electrophilic substitution reactions can also occur. For example, under the action of a halogenating agent in a catalyst, halogen atoms can be introduced into the benzene ring. This is because the electrophilic reagent is attracted by the electron cloud of the benzene ring, attacks the benzene ring, forms an intermediate, and then completes the reaction through proton transfer and other steps.
In addition, the tetrahydrogen structure also affects its chemical properties. The tetrahydrogen structure changes the spatial configuration of the molecule, which affects the intermolecular force, and then affects its solubility and other properties. Its solubility is different in different solvents, and it behaves differently in polar solvents and non-polar solvents, which is related to the polarity of the molecule.
1% 2C2% 2C4% 2C5-tetrahydro-3-acetylbenzene is rich and diverse in chemical properties, and its functional groups and structures jointly determine its behavior and properties in chemical reactions.
What are the main uses of 1,2,4,5-tetrachloro-3-methoxybenzene?
1% 2C2% 2C4% 2C5 refers to carbon tetrachloride. Carbon tetrachloride has a wide range of uses. In the past, it was often used as a fire extinguishing agent. Because of its non-flammability and density greater than air, it can cover the flame, isolate the air, and extinguish the flame. However, due to its destructive effect on the ozone layer, it is now less used for this purpose.
Furthermore, carbon tetrachloride is an excellent organic solvent. Many organic compounds have good solubility in it, and are often used in chemical experiments and industrial production to dissolve and extract substances. For example, in organic synthesis experiments, it can be used to dissolve reactants to make the reaction easier to proceed; in industry, it can be used to extract specific components from mixtures.
3 refers to ethanol, and ethanol has many uses. In the medical field, it is often used as a disinfectant. Ethanol at an appropriate concentration can effectively kill bacteria and other microorganisms, and ensure the hygiene of the medical environment and equipment. In the food industry, it is the main ingredient of alcoholic beverages. Alcohol products with different alcohol levels can be obtained through fermentation processes. In addition, ethanol can also be used as a fuel and mixed with gasoline to make ethanol gasoline, which relieves energy pressure to a certain extent and is more environmentally friendly.
As for "acetylaniline", it is mainly used as a medicine (such as paracetamol), a dye intermediate, and a rubber vulcanization accelerator. In pharmaceutical synthesis, it is a key raw material for the preparation of a variety of antipyretic and analgesic drugs; in the dye industry, it provides an important intermediate for the synthesis of specific color dyes; in the rubber industry, it can accelerate the vulcanization rate of rubber and improve the performance of rubber products.
Furthermore, carbon tetrachloride is an excellent organic solvent. Many organic compounds have good solubility in it, and are often used in chemical experiments and industrial production to dissolve and extract substances. For example, in organic synthesis experiments, it can be used to dissolve reactants to make the reaction easier to proceed; in industry, it can be used to extract specific components from mixtures.
3 refers to ethanol, and ethanol has many uses. In the medical field, it is often used as a disinfectant. Ethanol at an appropriate concentration can effectively kill bacteria and other microorganisms, and ensure the hygiene of the medical environment and equipment. In the food industry, it is the main ingredient of alcoholic beverages. Alcohol products with different alcohol levels can be obtained through fermentation processes. In addition, ethanol can also be used as a fuel and mixed with gasoline to make ethanol gasoline, which relieves energy pressure to a certain extent and is more environmentally friendly.
As for "acetylaniline", it is mainly used as a medicine (such as paracetamol), a dye intermediate, and a rubber vulcanization accelerator. In pharmaceutical synthesis, it is a key raw material for the preparation of a variety of antipyretic and analgesic drugs; in the dye industry, it provides an important intermediate for the synthesis of specific color dyes; in the rubber industry, it can accelerate the vulcanization rate of rubber and improve the performance of rubber products.
What are the environmental effects of 1,2,4,5-tetrachloro-3-methoxybenzene?
1% 2C2% 2C4% 2C5 is the impact of 1,2,4,5-tetrahydro-3-methoxyphenyl on the environment, which is related to the many levels of chemicals in the environment. Let me tell you one by one.
First of all, such chemicals enter natural water bodies, which may disturb the ecological balance of aquatic organisms. If they accumulate in water bodies, fish, shellfish and other aquatic organisms may cause physiological disorders after ingestion. For example, it may affect the reproductive ability of fish, reduce the hatching rate of fish eggs, deform the development of juvenile fish, and in the long run, may reduce the number of aquatic organisms.
In the soil environment, 1,2,4,5-tetrahydro-3-methoxyphenyl may change the soil microbial community structure. Soil microorganisms are essential for soil fertility and material cycling. The presence of this chemical substance may inhibit the growth of some beneficial microorganisms, such as azobacterium, thereby affecting the soil nitrogen cycle, reducing soil fertility, and affecting plant growth.
In the atmospheric environment, if the substance evaporates into the atmosphere, or participates in photochemical reactions. Under sunlight exposure, it interacts with other pollutants to generate secondary pollutants, such as ozone. Elevated ozone concentrations not only endanger human health and cause respiratory diseases, but also cause damage to plant leaves, affect plant photosynthesis, and then affect the energy flow and material cycle of the ecosystem.
In addition, this chemical also poses a potential threat to biodiversity. Its spread in the environment may lead to the extinction of some sensitive species, destroying the species richness and stability of the ecosystem. Some rare plants may gradually disappear due to poor tolerance to this chemical, disrupting the food chain and food network of the ecosystem, causing a chain reaction.
In summary, 1,2,4,5-tetrahydro-3-methoxybenzene has a wide range of effects in the environment and needs to be treated with caution, and monitoring and control should be strengthened to ensure the stability and safety of the ecological environment.
First of all, such chemicals enter natural water bodies, which may disturb the ecological balance of aquatic organisms. If they accumulate in water bodies, fish, shellfish and other aquatic organisms may cause physiological disorders after ingestion. For example, it may affect the reproductive ability of fish, reduce the hatching rate of fish eggs, deform the development of juvenile fish, and in the long run, may reduce the number of aquatic organisms.
In the soil environment, 1,2,4,5-tetrahydro-3-methoxyphenyl may change the soil microbial community structure. Soil microorganisms are essential for soil fertility and material cycling. The presence of this chemical substance may inhibit the growth of some beneficial microorganisms, such as azobacterium, thereby affecting the soil nitrogen cycle, reducing soil fertility, and affecting plant growth.
In the atmospheric environment, if the substance evaporates into the atmosphere, or participates in photochemical reactions. Under sunlight exposure, it interacts with other pollutants to generate secondary pollutants, such as ozone. Elevated ozone concentrations not only endanger human health and cause respiratory diseases, but also cause damage to plant leaves, affect plant photosynthesis, and then affect the energy flow and material cycle of the ecosystem.
In addition, this chemical also poses a potential threat to biodiversity. Its spread in the environment may lead to the extinction of some sensitive species, destroying the species richness and stability of the ecosystem. Some rare plants may gradually disappear due to poor tolerance to this chemical, disrupting the food chain and food network of the ecosystem, causing a chain reaction.
In summary, 1,2,4,5-tetrahydro-3-methoxybenzene has a wide range of effects in the environment and needs to be treated with caution, and monitoring and control should be strengthened to ensure the stability and safety of the ecological environment.
What is the preparation method of 1,2,4,5-tetrachloro-3-methoxybenzene?
The four substances referred to in 1% 2C2% 2C4% 2C5 are important raw materials for the preparation of 3-acetoxy acetophenone. The preparation method, let me explain in detail.
First, you need to take an appropriate amount of 1. This 1 may be a specific starting reactant with a unique chemical structure and activity, which lays the foundation for the reaction. After mixing 2 with it, 2 can be used in the reaction system as a catalyst or as a key reagent to initiate the reaction, causing specific changes in the chemical bonds of 1.
Subsequently, 4, 4 are added or to provide the necessary reaction environment, such as pH adjustment, or to provide a specific reaction check point for the reaction to guide the reaction in the direction of generating 3-acetoxyacetophenone.
The addition of 5 is also crucial. 5 or in the later stage of the reaction to stabilize the intermediate product, promote the formation of the final product, or assist in the separation and purification of the product, so that the resulting 3-acetoxyacetophenone is more pure.
During the reaction process, it is necessary to precisely control the temperature, time and other conditions. If the temperature is too high, the reaction may be out of control and too many by-products will be formed; if the temperature is too low, the reaction rate will be delayed and take a long time. The control of time should not be underestimated. If it is too short, the reaction will not be complete and the product will be impure; if it is too long, it will cause a secondary reaction of the product and reduce the yield.
After the reaction is completed, a series of separation and purification steps, such as distillation, extraction, recrystallization, etc., are required to obtain high-purity 3-acetoxyacetophenone. In this way, the method of preparing 3-acetoxyacetophenone.
First, you need to take an appropriate amount of 1. This 1 may be a specific starting reactant with a unique chemical structure and activity, which lays the foundation for the reaction. After mixing 2 with it, 2 can be used in the reaction system as a catalyst or as a key reagent to initiate the reaction, causing specific changes in the chemical bonds of 1.
Subsequently, 4, 4 are added or to provide the necessary reaction environment, such as pH adjustment, or to provide a specific reaction check point for the reaction to guide the reaction in the direction of generating 3-acetoxyacetophenone.
The addition of 5 is also crucial. 5 or in the later stage of the reaction to stabilize the intermediate product, promote the formation of the final product, or assist in the separation and purification of the product, so that the resulting 3-acetoxyacetophenone is more pure.
During the reaction process, it is necessary to precisely control the temperature, time and other conditions. If the temperature is too high, the reaction may be out of control and too many by-products will be formed; if the temperature is too low, the reaction rate will be delayed and take a long time. The control of time should not be underestimated. If it is too short, the reaction will not be complete and the product will be impure; if it is too long, it will cause a secondary reaction of the product and reduce the yield.
After the reaction is completed, a series of separation and purification steps, such as distillation, extraction, recrystallization, etc., are required to obtain high-purity 3-acetoxyacetophenone. In this way, the method of preparing 3-acetoxyacetophenone.
What are the precautions for storing and transporting 1,2,4,5-tetrachloro-3-methoxybenzene?
1% 2C2% 2C4% 2C5-tetrahydro-3-methoxybenzene Based on the storage and transportation process, there are several key considerations that must not be taken lightly.
First, this physical property is sensitive and easily disturbed by the surrounding temperature and humidity. Under high temperature, it may cause its chemical structure to change and damage its quality and efficacy. Therefore, the storage place should be kept at a constant temperature within a specific range, and the humidity should also be strictly controlled. It should be maintained in a dry state to prevent the risk of moisture dissolution.
Second, when transporting, the packaging must be strong and well sealed. Due to its certain chemical activity, if the packaging is slightly negligent, comes into contact with external substances, or has a chemical reaction, it will not only endanger the safety of transportation, but also damage the substance itself. And during the handling process, the operation should be careful and gentle to avoid violent vibration and collision, and avoid package damage.
Third, due to its chemical properties, storage and transportation places should be kept away from fire sources, heat sources and various oxidants. These substances are in danger of explosion in case of fire or oxidants, endangering the safety of personnel and the environment. Proper fire and emergency equipment should be prepared in the place, just in case.
Fourth, the label must be clearly and accurately marked. Indicate its chemical name, nature, hazard warning and emergency treatment methods, etc., so that the contact can be clear at a glance, the operation is well-documented, and in case of emergency, it can also respond quickly and respond correctly.
In short, the storage and transportation of 1% 2C2% 2C4% 2C5-tetrahydro-3-methoxyphenyl requires strict treatment in terms of temperature and humidity, packaging, ignition source oxidant isolation and label marking to ensure the safety of the whole process.
First, this physical property is sensitive and easily disturbed by the surrounding temperature and humidity. Under high temperature, it may cause its chemical structure to change and damage its quality and efficacy. Therefore, the storage place should be kept at a constant temperature within a specific range, and the humidity should also be strictly controlled. It should be maintained in a dry state to prevent the risk of moisture dissolution.
Second, when transporting, the packaging must be strong and well sealed. Due to its certain chemical activity, if the packaging is slightly negligent, comes into contact with external substances, or has a chemical reaction, it will not only endanger the safety of transportation, but also damage the substance itself. And during the handling process, the operation should be careful and gentle to avoid violent vibration and collision, and avoid package damage.
Third, due to its chemical properties, storage and transportation places should be kept away from fire sources, heat sources and various oxidants. These substances are in danger of explosion in case of fire or oxidants, endangering the safety of personnel and the environment. Proper fire and emergency equipment should be prepared in the place, just in case.
Fourth, the label must be clearly and accurately marked. Indicate its chemical name, nature, hazard warning and emergency treatment methods, etc., so that the contact can be clear at a glance, the operation is well-documented, and in case of emergency, it can also respond quickly and respond correctly.
In short, the storage and transportation of 1% 2C2% 2C4% 2C5-tetrahydro-3-methoxyphenyl requires strict treatment in terms of temperature and humidity, packaging, ignition source oxidant isolation and label marking to ensure the safety of the whole process.
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