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Benzene, 1,2-Dichloro-4-(1,1-Dimethylethyl)-
Linshang Chemical
|
HS Code |
991348 |
| Chemical Formula | C10H12Cl2 |
| Molar Mass | 203.11 g/mol |
| Appearance | colorless to pale yellow liquid |
| Boiling Point | 237 - 239 °C |
| Melting Point | -21.7 °C |
| Density | 1.12 g/cm³ |
| Solubility In Water | insoluble |
| Solubility In Organic Solvents | soluble |
| Vapor Pressure | low |
| Odor | aromatic |
As an accredited Benzene, 1,2-Dichloro-4-(1,1-Dimethylethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1,2 - dichloro - 4 - (1,1 - dimethylethyl)benzene in a sealed, chemical - resistant bottle. |
| Storage | **Storage of 1,2 - dichloro - 4 - (1,1 - dimethylethyl)benzene**: Store in a cool, well - ventilated area away from heat, sparks, and open flames. Keep containers tightly closed to prevent vapor release. It should be separated from oxidizing agents, acids, and bases. Use storage cabinets made of compatible materials to avoid chemical reactions and ensure safety. |
| Shipping | 1,2 - Dichloro - 4 - (1,1 - dimethylethyl)benzene is shipped in containers suitable for hazardous chemicals. It must comply with strict regulations, ensuring proper containment to prevent spills and environmental/health risks during transit. |
Competitive Benzene, 1,2-Dichloro-4-(1,1-Dimethylethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615365006308
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What are the chemical properties of 1,2-dichloro-4- (1,1-dimethylethyl) benzene?
1,2-Dioxo-4- (1,1-dimethylethyl) benzene, this is an organic compound. Its chemical properties are unique, let me go into detail.
Let's talk about the physical properties first. At room temperature or in a liquid state, it has a specific odor, and the physical constants such as density, boiling point, and melting point depend on specific conditions. Because it contains benzene rings and specific substituents, it has a certain solubility to organic solvents.
In terms of chemical properties, benzene rings endow it with aromatic properties and can undergo electrophilic substitution reactions. For example, with halogenating agents under suitable catalysts, halogen atoms can replace hydrogen atoms on benzene rings; in the case of nitrifying reagents, nitrification reactions can occur and nitro groups are introduced; with sulfonating reagents, sulfonation reactions can be achieved.
Its side chain 1,1-dimethylethyl is relatively stable, but under specific conditions such as strong oxidants, it may be oxidized to form corresponding oxygenated compounds.
In addition, the presence of oxygen atoms in this compound may affect its reactivity and selectivity. In some reactions, oxygen atoms can act as electron donors and participate in coordination or chemical reactions. In case of specific reagents, complex reactions such as cyclization and ring opening may be initiated, depending on the reaction conditions and reagent characteristics.
In conclusion, 1,2-dioxy-4- (1,1-dimethylethyl) benzene is rich in chemical properties and has potential applications in organic synthesis, materials science and other fields. It can be used as an intermediate to participate in the preparation of many organic compounds.
Let's talk about the physical properties first. At room temperature or in a liquid state, it has a specific odor, and the physical constants such as density, boiling point, and melting point depend on specific conditions. Because it contains benzene rings and specific substituents, it has a certain solubility to organic solvents.
In terms of chemical properties, benzene rings endow it with aromatic properties and can undergo electrophilic substitution reactions. For example, with halogenating agents under suitable catalysts, halogen atoms can replace hydrogen atoms on benzene rings; in the case of nitrifying reagents, nitrification reactions can occur and nitro groups are introduced; with sulfonating reagents, sulfonation reactions can be achieved.
Its side chain 1,1-dimethylethyl is relatively stable, but under specific conditions such as strong oxidants, it may be oxidized to form corresponding oxygenated compounds.
In addition, the presence of oxygen atoms in this compound may affect its reactivity and selectivity. In some reactions, oxygen atoms can act as electron donors and participate in coordination or chemical reactions. In case of specific reagents, complex reactions such as cyclization and ring opening may be initiated, depending on the reaction conditions and reagent characteristics.
In conclusion, 1,2-dioxy-4- (1,1-dimethylethyl) benzene is rich in chemical properties and has potential applications in organic synthesis, materials science and other fields. It can be used as an intermediate to participate in the preparation of many organic compounds.
What are the physical properties of 1,2-dichloro-4- (1,1-dimethylethyl) benzene
1,2-Dioxy-4- (1,1-dimethylethyl) benzene, the physical properties of this substance are as follows:
It is mostly colorless and transparent to yellowish clear liquid at room temperature, and it has a certain fluidity. In terms of odor, it often emits a special aromatic odor, which can be clearly perceived by the sense of smell.
The value of the boiling point is roughly within a specific range, which makes it transform from liquid to gaseous at the corresponding temperature. The melting point determines the critical temperature for its transition from solid to liquid. When it is lower than the melting point, the substance exists in solid form.
Density is also one of its important physical properties, showing the mass of the substance per unit volume. By comparing with the density of other substances, its position in the mixed system can be understood.
In terms of solubility, 1,2-dioxy-4- (1,1-dimethylethyl) benzene has good solubility in some organic solvents and can be miscible with it to form a uniform system; however, in water, its solubility is poor, and it will mostly exhibit stratification with water.
In addition, its refractive index also has a specific value. When light passes through the substance, optical phenomena such as refraction will occur. This refractive index can be used as an important reference in material identification and purity analysis. These physical properties are interrelated and together describe the unique physical properties of 1,2-dioxy-4- (1,1-dimethylethyl) benzene, laying the foundation for its application and research in many fields.
It is mostly colorless and transparent to yellowish clear liquid at room temperature, and it has a certain fluidity. In terms of odor, it often emits a special aromatic odor, which can be clearly perceived by the sense of smell.
The value of the boiling point is roughly within a specific range, which makes it transform from liquid to gaseous at the corresponding temperature. The melting point determines the critical temperature for its transition from solid to liquid. When it is lower than the melting point, the substance exists in solid form.
Density is also one of its important physical properties, showing the mass of the substance per unit volume. By comparing with the density of other substances, its position in the mixed system can be understood.
In terms of solubility, 1,2-dioxy-4- (1,1-dimethylethyl) benzene has good solubility in some organic solvents and can be miscible with it to form a uniform system; however, in water, its solubility is poor, and it will mostly exhibit stratification with water.
In addition, its refractive index also has a specific value. When light passes through the substance, optical phenomena such as refraction will occur. This refractive index can be used as an important reference in material identification and purity analysis. These physical properties are interrelated and together describe the unique physical properties of 1,2-dioxy-4- (1,1-dimethylethyl) benzene, laying the foundation for its application and research in many fields.
What are the industrial uses of 1,2-dichloro-4- (1,1-dimethylethyl) benzene?
1,2-Dioxy-4- (1,1-dimethylethyl) benzene, which is widely used in industry.
In the theory of "Tiangong Kaiji", although this specific chemical is not directly described, it is deduced from the ancient process principles, and its principles are similar. Among this compound, the dioxy structure is connected to the benzene ring, and the side chain is dimethylethyl, which gives it unique physical and chemical properties, so it has many applications in industry.
First, because of its structural characteristics, it is often an important intermediate in the field of organic synthesis. The art of organic synthesis is like a craftsman building a building, and every step needs to be precise. Due to its stable structure and modifiable check point, this compound can introduce other functional groups through various chemical reactions to build more complex organic molecules, such as the preparation of polymers with special functions, pharmaceutical intermediates, etc.
Second, in materials science, or can be a modification aid. The properties of materials are related to the advantages and disadvantages of industrial products. Adding this compound to a specific material may change the solubility, melting point, mechanical properties of the material. If added to some polymer materials, its processing performance and performance can be optimized, making the material more suitable for different industrial scenarios.
Third, in the coating and adhesive industry, it also has potential value. The coating needs to be firmly adhered and durable, and the adhesive needs to have strong adhesion. This compound can improve the performance of coatings and adhesives by virtue of its chemical properties, such as enhancing its adhesion to different substrates, improving film formation and weather resistance, and improving the appearance and protective performance of industrial products.
All of these can be seen in 1,2-dioxy-4- (1,1-dimethylethyl) benzene for industrial use, which cannot be ignored.
In the theory of "Tiangong Kaiji", although this specific chemical is not directly described, it is deduced from the ancient process principles, and its principles are similar. Among this compound, the dioxy structure is connected to the benzene ring, and the side chain is dimethylethyl, which gives it unique physical and chemical properties, so it has many applications in industry.
First, because of its structural characteristics, it is often an important intermediate in the field of organic synthesis. The art of organic synthesis is like a craftsman building a building, and every step needs to be precise. Due to its stable structure and modifiable check point, this compound can introduce other functional groups through various chemical reactions to build more complex organic molecules, such as the preparation of polymers with special functions, pharmaceutical intermediates, etc.
Second, in materials science, or can be a modification aid. The properties of materials are related to the advantages and disadvantages of industrial products. Adding this compound to a specific material may change the solubility, melting point, mechanical properties of the material. If added to some polymer materials, its processing performance and performance can be optimized, making the material more suitable for different industrial scenarios.
Third, in the coating and adhesive industry, it also has potential value. The coating needs to be firmly adhered and durable, and the adhesive needs to have strong adhesion. This compound can improve the performance of coatings and adhesives by virtue of its chemical properties, such as enhancing its adhesion to different substrates, improving film formation and weather resistance, and improving the appearance and protective performance of industrial products.
All of these can be seen in 1,2-dioxy-4- (1,1-dimethylethyl) benzene for industrial use, which cannot be ignored.
What are the environmental effects of 1,2-dichloro-4- (1,1-dimethylethyl) benzene?
The environmental impact of 1,2-dioxy-4- (1,1-dimethylethyl) benzene is quite complex and crucial, so let me analyze it in detail.
In this compound, the dioxy structure has certain chemical activity. In the atmospheric environment, if it encounters light, free radicals and other conditions, it may participate in a series of photochemical reactions. This reaction may cause secondary pollutants, such as some oxidizing substances, which affect air quality, or even form photochemical smog and other hazards, affecting visibility and causing damage to the biological respiratory system.
In the aquatic environment, 1,2-dioxo-4- (1,1-dimethylethyl) benzene may be adsorbed on suspended particles due to its structural characteristics, or insoluble in water. If it is transported and transformed in the water body for a long time, it may have toxic effects on aquatic organisms. Or interfere with the physiological processes of aquatic organisms, such as affecting their growth, reproduction, metabolism and other functions, destroying the balance of aquatic ecosystems.
In the soil environment, the compound may change due to adsorption, degradation and other processes. Microorganisms in the soil may have limited ability to degrade them. If they accumulate for a long time, they may change the physical and chemical properties of the soil, which will affect the nutrient cycle in the soil and the absorption of nutrients by plant roots, and then affect the growth of vegetation.
In addition, the volatility of 1,2-dioxy-4- (1,1-dimethylethyl) benzene should not be underestimated. Its volatilization to the atmosphere not only affects air quality, but also can be transported to distant places through the atmosphere, expanding its influence range.
In general, the migration and transformation of 1,2-dioxy-4- (1,1-dimethylethyl) benzene between various environmental media pose latent risks to ecological environment and biological health, and need to be closely monitored and properly disposed of.
In this compound, the dioxy structure has certain chemical activity. In the atmospheric environment, if it encounters light, free radicals and other conditions, it may participate in a series of photochemical reactions. This reaction may cause secondary pollutants, such as some oxidizing substances, which affect air quality, or even form photochemical smog and other hazards, affecting visibility and causing damage to the biological respiratory system.
In the aquatic environment, 1,2-dioxo-4- (1,1-dimethylethyl) benzene may be adsorbed on suspended particles due to its structural characteristics, or insoluble in water. If it is transported and transformed in the water body for a long time, it may have toxic effects on aquatic organisms. Or interfere with the physiological processes of aquatic organisms, such as affecting their growth, reproduction, metabolism and other functions, destroying the balance of aquatic ecosystems.
In the soil environment, the compound may change due to adsorption, degradation and other processes. Microorganisms in the soil may have limited ability to degrade them. If they accumulate for a long time, they may change the physical and chemical properties of the soil, which will affect the nutrient cycle in the soil and the absorption of nutrients by plant roots, and then affect the growth of vegetation.
In addition, the volatility of 1,2-dioxy-4- (1,1-dimethylethyl) benzene should not be underestimated. Its volatilization to the atmosphere not only affects air quality, but also can be transported to distant places through the atmosphere, expanding its influence range.
In general, the migration and transformation of 1,2-dioxy-4- (1,1-dimethylethyl) benzene between various environmental media pose latent risks to ecological environment and biological health, and need to be closely monitored and properly disposed of.
What are the methods for preparing 1,2-dichloro-4- (1,1-dimethylethyl) benzene?
For the method of making 1,2-dioxy-4- (1,1-dimethylethyl) benzene, please refer to the method of "Tiangong Wuwu". According to the ancient method, there are also new methods.
In the ancient method, or take natural things, and extract them in an appropriate way. Its natural source, or a certain plant, or a stone. First, if the plant is good, wash it and fry it in a kettle. After a long time, take the liquid, and then use the method of If you seek it from the stone, first break the stone and break the particles, use fire to calcine, so that the things in it are melted, and then rinse them with water, take them and dissolve them in water, steam, crystals, etc., can also be obtained.
Today's new research, based on the principle of chemistry, is mainly based on the method of synthesis. Or use other chemical raw materials, under specific conditions, such as controlling the degree and force, adding appropriate catalysts, so that the material can be transformed and reversed. For example, in a high-temperature and high-temperature reactor with a certain gold catalyst, the molecules can be gradually reduced. Reverse, by means of separation, extraction, etc., to remove the unreversed matter and by-products, we can obtain high-grade 1,2-dioxy-4- (1,1-dimethyl ethyl) benzene. And today's technology can be used with precision tools to reverse the process. The ancient method is more precise and efficient, and can obtain more materials in a shorter time with less raw materials.
In the ancient method, or take natural things, and extract them in an appropriate way. Its natural source, or a certain plant, or a stone. First, if the plant is good, wash it and fry it in a kettle. After a long time, take the liquid, and then use the method of If you seek it from the stone, first break the stone and break the particles, use fire to calcine, so that the things in it are melted, and then rinse them with water, take them and dissolve them in water, steam, crystals, etc., can also be obtained.
Today's new research, based on the principle of chemistry, is mainly based on the method of synthesis. Or use other chemical raw materials, under specific conditions, such as controlling the degree and force, adding appropriate catalysts, so that the material can be transformed and reversed. For example, in a high-temperature and high-temperature reactor with a certain gold catalyst, the molecules can be gradually reduced. Reverse, by means of separation, extraction, etc., to remove the unreversed matter and by-products, we can obtain high-grade 1,2-dioxy-4- (1,1-dimethyl ethyl) benzene. And today's technology can be used with precision tools to reverse the process. The ancient method is more precise and efficient, and can obtain more materials in a shorter time with less raw materials.
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