Linshang Chemical
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Benzene,1-Chloro-4-(Chloromethyl)-
Linshang Chemical
|
HS Code |
772848 |
| Chemical Formula | C7H6Cl2 |
| Molar Mass | 161.03 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Pungent odor |
| Density | 1.25 g/cm³ |
| Boiling Point | 208 - 213 °C |
| Melting Point | -2 °C |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in many organic solvents |
| Vapor Pressure | Low vapor pressure |
| Flash Point | 93 °C |
| Hazardous Nature | Toxic, may cause skin and eye irritation, potential carcinogen |
As an accredited Benzene,1-Chloro-4-(Chloromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 1 - chloro - 4 - (chloromethyl)benzene in sealed, chemical - resistant container. |
| Storage | 1 - Chloro - 4 - (chloromethyl) benzene should be stored in a cool, well - ventilated area, away from heat sources and open flames. It is best stored in a tightly - sealed container made of materials resistant to corrosion, like stainless steel or certain plastics. Keep it separate from oxidizing agents, as it may react. Store in a location with restricted access to prevent unauthorized handling. |
| Shipping | "1 - Chloro - 4-(chloromethyl)benzene is shipped in tightly sealed, corrosion - resistant containers. It follows strict hazardous chemical shipping regulations to prevent leakage, ensuring safety during transit." |
Competitive Benzene,1-Chloro-4-(Chloromethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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What are the chemical properties of 1-chloro-4- (chloromethyl) benzene?
There is no direct description of this substance in "Tiangong Kaiwu", but its chemical properties can be described in ancient forms according to modern chemical knowledge.
1 + -alkane-4- (alkyl methyl) benzene has the commonality of aromatic hydrocarbons. In its molecular structure, the benzene ring is a stable conjugated system, so its chemical properties are different from chain hydrocarbons.
First, it has the property of substitution reaction. Under appropriate conditions, the hydrogen atom on the benzene ring can be replaced by various groups. If it is with halogens, under the action of catalysts, the halogen atom can replace the hydrogen of the benzene ring to produce halogenated aromatic hydrocarbons. The mechanism of this reaction is that the catalyst polarizes the halogen molecule, produces an electrophilic reagent, attacks the electron-rich π electron cloud of the benzene ring, and passes through the intermediate to obtain the replacement product.
Second, an addition reaction can occur. Although the benzene ring is stable, under special conditions and the action of strong reagents, the conjugated system can also be opened for addition. For example, under high temperature, high pressure and catalyst conditions, it can be added with hydrogen to generate saturated alicyclic hydrocarbons. This process reduces the unsaturation of the benzene ring.
Third, it has the characteristics of an oxidation reaction. In the case of strong oxidants, such as acidic potassium permanganate solution, if there is a hydrogen atom on the carbon atom directly connected to the alkyl group and the benzene ring, the alkyl group can be oxidized to a carboxyl group. This reaction shows the sensitivity of its side chain to
Fourth, when burning, due to the high carbon content, the flame is bright and accompanied by thick smoke. The combustion reaction converts the carbon and hydrogen contained in it into carbon dioxide and water, and releases a lot of heat energy at the same time.
In summary, the chemical properties of 1 + -alkane-4- (alkylmethyl) benzene are determined by its benzene ring and alkyl structure, and have important uses and reactivity in organic synthesis, chemical production and other fields.
1 + -alkane-4- (alkyl methyl) benzene has the commonality of aromatic hydrocarbons. In its molecular structure, the benzene ring is a stable conjugated system, so its chemical properties are different from chain hydrocarbons.
First, it has the property of substitution reaction. Under appropriate conditions, the hydrogen atom on the benzene ring can be replaced by various groups. If it is with halogens, under the action of catalysts, the halogen atom can replace the hydrogen of the benzene ring to produce halogenated aromatic hydrocarbons. The mechanism of this reaction is that the catalyst polarizes the halogen molecule, produces an electrophilic reagent, attacks the electron-rich π electron cloud of the benzene ring, and passes through the intermediate to obtain the replacement product.
Second, an addition reaction can occur. Although the benzene ring is stable, under special conditions and the action of strong reagents, the conjugated system can also be opened for addition. For example, under high temperature, high pressure and catalyst conditions, it can be added with hydrogen to generate saturated alicyclic hydrocarbons. This process reduces the unsaturation of the benzene ring.
Third, it has the characteristics of an oxidation reaction. In the case of strong oxidants, such as acidic potassium permanganate solution, if there is a hydrogen atom on the carbon atom directly connected to the alkyl group and the benzene ring, the alkyl group can be oxidized to a carboxyl group. This reaction shows the sensitivity of its side chain to
Fourth, when burning, due to the high carbon content, the flame is bright and accompanied by thick smoke. The combustion reaction converts the carbon and hydrogen contained in it into carbon dioxide and water, and releases a lot of heat energy at the same time.
In summary, the chemical properties of 1 + -alkane-4- (alkylmethyl) benzene are determined by its benzene ring and alkyl structure, and have important uses and reactivity in organic synthesis, chemical production and other fields.
What are the physical properties of 1-chloro-4- (chloromethyl) benzene?
1 + -Deuterium-4- (deuterium methyl) naphthalene is one of the organic compounds. Its physical properties are quite unique.
Looking at its shape, under room temperature and pressure, it is mostly in the shape of a solid state. Due to the relatively strong intermolecular forces, the molecules are arranged in an orderly manner and firmly formed. Its color is often white or off-white, and the texture is delicate, just like the frost and snow that falls at the beginning of winter, pure and rustic.
When it comes to the melting point, it is about a specific temperature range. When the external temperature gradually rises to a certain value, the substance will gradually melt from the solid state to the liquid state. The characteristics of this melting point are closely related to its molecular structure. The mode and strength of intermolecular interactions determine the energy required to destroy the solid lattice, which in turn affects the melting point.
As for the boiling point, it needs to be reached at a higher temperature. At that time, the molecule obtains enough energy to break free from the liquid phase and escape into the gas phase. This boiling point reflects the strength of the intermolecular forces, and also highlights its phase transition characteristics at different temperatures.
In terms of solubility, in organic solvents such as ethanol, ether, etc., it exhibits a certain solubility. This is because the molecules of the substance and the organic solvent molecules can form specific forces, such as van der Waals forces, hydrogen bonds, etc., so that they can be uniformly dispersed in the solvent. However, the solubility in water is poor, because the polarity of water is quite different from the molecular polarity of the substance, and the interaction between the two is weak and difficult to dissolve.
Density is also one of its important physical properties. Compared with water, its density may be different. This property determines its positional relationship when it comes into contact with liquids such as water. In related experiments and industrial applications, this property affects the separation, mixing and other operation processes.
In summary, the physical properties of 1 + -deuterium-4- (deuteromethyl) naphthalene are of great significance in chemical research, industrial production and other fields, and help people to understand and use this substance rationally.
Looking at its shape, under room temperature and pressure, it is mostly in the shape of a solid state. Due to the relatively strong intermolecular forces, the molecules are arranged in an orderly manner and firmly formed. Its color is often white or off-white, and the texture is delicate, just like the frost and snow that falls at the beginning of winter, pure and rustic.
When it comes to the melting point, it is about a specific temperature range. When the external temperature gradually rises to a certain value, the substance will gradually melt from the solid state to the liquid state. The characteristics of this melting point are closely related to its molecular structure. The mode and strength of intermolecular interactions determine the energy required to destroy the solid lattice, which in turn affects the melting point.
As for the boiling point, it needs to be reached at a higher temperature. At that time, the molecule obtains enough energy to break free from the liquid phase and escape into the gas phase. This boiling point reflects the strength of the intermolecular forces, and also highlights its phase transition characteristics at different temperatures.
In terms of solubility, in organic solvents such as ethanol, ether, etc., it exhibits a certain solubility. This is because the molecules of the substance and the organic solvent molecules can form specific forces, such as van der Waals forces, hydrogen bonds, etc., so that they can be uniformly dispersed in the solvent. However, the solubility in water is poor, because the polarity of water is quite different from the molecular polarity of the substance, and the interaction between the two is weak and difficult to dissolve.
Density is also one of its important physical properties. Compared with water, its density may be different. This property determines its positional relationship when it comes into contact with liquids such as water. In related experiments and industrial applications, this property affects the separation, mixing and other operation processes.
In summary, the physical properties of 1 + -deuterium-4- (deuteromethyl) naphthalene are of great significance in chemical research, industrial production and other fields, and help people to understand and use this substance rationally.
What are the industrial applications of 1-chloro-4- (chloromethyl) benzene?
1 + -Deuterium-4- (deuterium methyl) silicon is mostly used in semiconductor manufacturing, photovoltaic industry and organic synthesis in industry. This silicide has great functions in the field of semiconductor manufacturing. Due to its unique properties, the cover can optimize the performance of semiconductor materials, such as improving the electron mobility, making the operation of semiconductor devices more efficient and agile, just like a good horse with a saddle, which complements each other. The processing speed of the chip is significantly increased, and the power consumption is also reduced. In the process of miniaturization and high performance of electronic devices, it plays a major role.
As for the photovoltaic industry, 1 + -deuterium-4- (deuterium methyl) silicon is also indispensable. It can be used as a key raw material for the preparation of silicon wafers for photovoltaic cells. With its participation in the production of silicon wafers, the photoelectric conversion efficiency is quite high, which can more effectively convert solar energy into electricity, just like a skilled craftsman who makes good use of good materials, which greatly improves the efficiency of photovoltaic power generation and contributes to the development of clean energy.
In the field of organic synthesis, this silicide is like a magic key, which can open the door to the synthesis of many complex organic compounds. Because of its specific reactivity and selectivity, chemists can use it to ingeniously design reaction paths to synthesize organic molecules with novel structures and unique properties, which are used in medicine, materials and many other fields. For example, when creating new drug molecules, 1 + -deuterium-4- (deuterium methyl) silicon can help build a key molecular framework, providing a powerful tool for the development of new drugs.
As for the photovoltaic industry, 1 + -deuterium-4- (deuterium methyl) silicon is also indispensable. It can be used as a key raw material for the preparation of silicon wafers for photovoltaic cells. With its participation in the production of silicon wafers, the photoelectric conversion efficiency is quite high, which can more effectively convert solar energy into electricity, just like a skilled craftsman who makes good use of good materials, which greatly improves the efficiency of photovoltaic power generation and contributes to the development of clean energy.
In the field of organic synthesis, this silicide is like a magic key, which can open the door to the synthesis of many complex organic compounds. Because of its specific reactivity and selectivity, chemists can use it to ingeniously design reaction paths to synthesize organic molecules with novel structures and unique properties, which are used in medicine, materials and many other fields. For example, when creating new drug molecules, 1 + -deuterium-4- (deuterium methyl) silicon can help build a key molecular framework, providing a powerful tool for the development of new drugs.
What are the methods for preparing 1-chloro-4- (chloromethyl) benzene?
The preparation methods of 1 + -alkane-4- (alkyl methyl) benzene are numerous due to chemical synthesis methods, each depending on the required conditions and raw materials.
First, the corresponding halogenated alkane and benzene can be prepared by Fu-g alkylation under the catalysis of Lewis acid such as aluminum trichloride. The method is as follows: In the clean reactor, first put an appropriate amount of benzene, slowly add anhydrous aluminum trichloride, stir well to create a suitable catalytic environment. Subsequently, the halogenated alkanes (such as 4-halogenated-1-alkane) are slowly dropped into the kettle to control the dripping speed, while paying attention to the reaction temperature and maintaining it in an appropriate range. This reaction temperature often depends on the type of halogenated alkanes and the reactivity, usually at tens of degrees Celsius. During the reaction process, continuous stirring is used to fully contact the reactants to accelerate the reaction process. After the reaction is completed, a pure target product 1 + -alkane-4- (alkyl methyl) benzene can be obtained through subsequent operations such as hydrolysis, liquid separation, and distillation.
Second, alkenyl alkanes and benzene can also be used as raw materials, and under appropriate catalyst and reaction conditions, prepared by addition reaction. First, benzene and alkenyl alkanes are mixed in a reaction vessel in a certain proportion, and specific catalysts, such as some transition metal complexes, are added. During the reaction, the temperature and pressure are adjusted to promote the addition of alkenyl alkanes and benzene to form 1 + -alkane-4- (alkyl methyl) benzene. After the reaction is completed, the unreacted raw materials and by-products are separated and purified, and the product can be obtained.
Third, it can also be converted from a specific aromatic compound through a multi-step reaction. For example, select a benzene derivative with a suitable substituent, introduce a specific group through a substitution reaction, and then gradually build the structure of the target molecule through a series of reactions such as reduction and rearrangement, and finally obtain 1 + -alkane-4- (alkyl methyl) benzene. Although this method is complicated, it can flexibly design the reaction route according to the needs, which is advantageous for the preparation of special structures or high-purity products.
First, the corresponding halogenated alkane and benzene can be prepared by Fu-g alkylation under the catalysis of Lewis acid such as aluminum trichloride. The method is as follows: In the clean reactor, first put an appropriate amount of benzene, slowly add anhydrous aluminum trichloride, stir well to create a suitable catalytic environment. Subsequently, the halogenated alkanes (such as 4-halogenated-1-alkane) are slowly dropped into the kettle to control the dripping speed, while paying attention to the reaction temperature and maintaining it in an appropriate range. This reaction temperature often depends on the type of halogenated alkanes and the reactivity, usually at tens of degrees Celsius. During the reaction process, continuous stirring is used to fully contact the reactants to accelerate the reaction process. After the reaction is completed, a pure target product 1 + -alkane-4- (alkyl methyl) benzene can be obtained through subsequent operations such as hydrolysis, liquid separation, and distillation.
Second, alkenyl alkanes and benzene can also be used as raw materials, and under appropriate catalyst and reaction conditions, prepared by addition reaction. First, benzene and alkenyl alkanes are mixed in a reaction vessel in a certain proportion, and specific catalysts, such as some transition metal complexes, are added. During the reaction, the temperature and pressure are adjusted to promote the addition of alkenyl alkanes and benzene to form 1 + -alkane-4- (alkyl methyl) benzene. After the reaction is completed, the unreacted raw materials and by-products are separated and purified, and the product can be obtained.
Third, it can also be converted from a specific aromatic compound through a multi-step reaction. For example, select a benzene derivative with a suitable substituent, introduce a specific group through a substitution reaction, and then gradually build the structure of the target molecule through a series of reactions such as reduction and rearrangement, and finally obtain 1 + -alkane-4- (alkyl methyl) benzene. Although this method is complicated, it can flexibly design the reaction route according to the needs, which is advantageous for the preparation of special structures or high-purity products.
What are the effects of 1-chloro-4- (chloromethyl) benzene on the environment and humans?
1 + -Tritium-4- (tritium-methyl) benzene, the impact of this substance on the environment and human body is quite important, let me explain in detail.
Tritium is a radioactive isotope of hydrogen. Tritium-containing compounds, such as 1 + -tritium-4- (tritium-methyl) benzene, if scattered in the environment, its radioactivity may cause many problems. In the atmosphere, it can be dispersed with air currents, causing a wider range of pollution. If it settles into the soil, it may be absorbed by plant roots and enter the food chain. Similarly, if it flows into water bodies, aquatic organisms will also be harmed. Through biological enrichment, it will have a great impact on the balance of the ecosystem.
As for the impact on the human body, it should not be underestimated. If people ingest these tritium-containing compounds through breathing, diet or skin contact, the radioactivity of tritium can cause damage to human cells. It can cause molecular structural mutations in cells, especially damage to DNA. If DNA is damaged, it may cause genetic mutations, increasing the risk of cancer. And radioactive substances also have adverse effects on the human immune system and reproductive system. Impaired immune system, the body's ability to resist diseases will decline; affected reproductive system, it may affect fertility, resulting in fetal malformation and other serious consequences. Therefore, tritium-containing compounds such as 1 + -tritium-4- (tritium-methyl) benzene pose great potential hazards to the environment and human body, and should be treated with caution and their production, use and discharge should be strictly controlled to protect the ecological environment and human health.
Tritium is a radioactive isotope of hydrogen. Tritium-containing compounds, such as 1 + -tritium-4- (tritium-methyl) benzene, if scattered in the environment, its radioactivity may cause many problems. In the atmosphere, it can be dispersed with air currents, causing a wider range of pollution. If it settles into the soil, it may be absorbed by plant roots and enter the food chain. Similarly, if it flows into water bodies, aquatic organisms will also be harmed. Through biological enrichment, it will have a great impact on the balance of the ecosystem.
As for the impact on the human body, it should not be underestimated. If people ingest these tritium-containing compounds through breathing, diet or skin contact, the radioactivity of tritium can cause damage to human cells. It can cause molecular structural mutations in cells, especially damage to DNA. If DNA is damaged, it may cause genetic mutations, increasing the risk of cancer. And radioactive substances also have adverse effects on the human immune system and reproductive system. Impaired immune system, the body's ability to resist diseases will decline; affected reproductive system, it may affect fertility, resulting in fetal malformation and other serious consequences. Therefore, tritium-containing compounds such as 1 + -tritium-4- (tritium-methyl) benzene pose great potential hazards to the environment and human body, and should be treated with caution and their production, use and discharge should be strictly controlled to protect the ecological environment and human health.
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