Linshang Chemical
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Benzene, 1-Chloro-4-(1,1-Dimethylethyl)-
Linshang Chemical
|
HS Code |
781297 |
| Chemical Formula | C10H13Cl |
| Molar Mass | 168.667 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 213 - 214 °C |
| Melting Point | -57.8 °C |
| Density | 1.005 g/cm³ |
| Solubility In Water | Insoluble |
| Vapor Pressure | Low |
| Odor | Aromatic odor |
| Flash Point | 83 °C |
As an accredited Benzene, 1-Chloro-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 - chloro - 4 - (1,1 - dimethylethyl)benzene in a tightly - sealed plastic container. |
| Storage | **Storage of 1 - chloro - 4 - (1,1 - dimethylethyl)benzene**: Store this chemical in a cool, well - ventilated area, away from heat, sparks, and open flames as it is flammable. Keep containers tightly closed to prevent vapor release. Store it separately from oxidizing agents, strong acids, and bases to avoid potential reactions. Use appropriate secondary containment to catch any spills. |
| Shipping | "1 - Chloro - 4 - (1,1 - dimethylethyl)benzene is shipped in accordance with strict chemical regulations. Packed in suitable containers, it's transported by specialized carriers ensuring safety during transit to prevent spills and exposure." |
Competitive Benzene, 1-Chloro-4-(1,1-Dimethylethyl)- 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- (1,1-dimethylethyl) benzene
1 + - neon - 4 - (1,1 - dimethylethyl) benzene, that is, p-tert-butyl neon, this substance is composed of neon element and p-tert-butyl phenyl group. Its chemical properties are:
1. ** Stability **: The structure of p-tert-butyl benzene is relatively stable, and the reactivity on the benzene ring is changed due to the steric resistance effect of the tert-butyl group. The benzene ring itself is aromatic, and the electron cloud is highly delocalized, which is not prone to addition reactions, and tends to electrophilic substitution reactions. Neon, as a rare gas, has extremely stable chemical properties, and it is usually difficult to chemically react with other substances. In this compound, neon exists in a special binding way, the overall structure is relatively stable, and it is not easy to decompose under general mild conditions.
2. ** Electrophilic Substitution Reaction **: Due to the high density of the electron cloud of the benzene ring, it is vulnerable to the attack of electrophilic reagents. For example, when encountering a halogenating agent (such as bromine and iron tribromide catalysts), a halogenation reaction occurs, and the electrophilic reagent will replace the hydrogen atom on the benzene ring. Tert-butyl is an electron donor group, and the electron cloud density of the benzene ring is relatively increased through the superconjugation effect, so the electrophilic substitution reaction mainly occurs in the adjacent and para-position of the benzene ring ** Oxidation reaction **: Although the benzene ring is relatively stable, under the action of strong oxidants such as acidic potassium permanganate, if the benzene ring is connected with a side chain of α-hydrogen (such as the tert-butyl here has α-carbon but no α-hydrogen), it is usually not oxidized. If the conditions are extremely severe, the structure of the benzene ring may be destroyed. In addition, the neon element in the whole compound is chemically stable and generally does not participate in the oxidation reaction.
4. ** Reaction tendency under the influence of physical properties **: p-tert-butyl neon has a certain lipid solubility due to the presence of tert-butyl. In some organic solvents, its solubility is better, which will affect its reaction activity and reaction process in solution. At the same time, the presence of neon may affect the physical properties such as the boiling point and melting point of the entire molecule, which in turn has an indirect impact on its chemical reactions at different temperatures.
1. ** Stability **: The structure of p-tert-butyl benzene is relatively stable, and the reactivity on the benzene ring is changed due to the steric resistance effect of the tert-butyl group. The benzene ring itself is aromatic, and the electron cloud is highly delocalized, which is not prone to addition reactions, and tends to electrophilic substitution reactions. Neon, as a rare gas, has extremely stable chemical properties, and it is usually difficult to chemically react with other substances. In this compound, neon exists in a special binding way, the overall structure is relatively stable, and it is not easy to decompose under general mild conditions.
2. ** Electrophilic Substitution Reaction **: Due to the high density of the electron cloud of the benzene ring, it is vulnerable to the attack of electrophilic reagents. For example, when encountering a halogenating agent (such as bromine and iron tribromide catalysts), a halogenation reaction occurs, and the electrophilic reagent will replace the hydrogen atom on the benzene ring. Tert-butyl is an electron donor group, and the electron cloud density of the benzene ring is relatively increased through the superconjugation effect, so the electrophilic substitution reaction mainly occurs in the adjacent and para-position of the benzene ring ** Oxidation reaction **: Although the benzene ring is relatively stable, under the action of strong oxidants such as acidic potassium permanganate, if the benzene ring is connected with a side chain of α-hydrogen (such as the tert-butyl here has α-carbon but no α-hydrogen), it is usually not oxidized. If the conditions are extremely severe, the structure of the benzene ring may be destroyed. In addition, the neon element in the whole compound is chemically stable and generally does not participate in the oxidation reaction.
4. ** Reaction tendency under the influence of physical properties **: p-tert-butyl neon has a certain lipid solubility due to the presence of tert-butyl. In some organic solvents, its solubility is better, which will affect its reaction activity and reaction process in solution. At the same time, the presence of neon may affect the physical properties such as the boiling point and melting point of the entire molecule, which in turn has an indirect impact on its chemical reactions at different temperatures.
What are the physical properties of 1-chloro-4- (1,1-dimethylethyl) benzene?
The physical properties of 1 + -neon-4- (1,1-dimethylethyl) benzene are as follows:
neon, which is an atom. Its density is small. Color, odor, chemical properties are determined, and other substances are biochemically reactive. Under normal conditions, neon is low, boiling temperature is low, -246.08 ° C, melting temperature is -248.67 ° C. It has good performance, and it is applied to the discharge tube with high current, which can produce orange light. This property makes it commonly used in the manufacture of neon and other lighting devices.
And (1,1-dimethylethyl) benzene, and tert-butylbenzene. Its color solution is aromatic. The phase density is smaller than that of water, 0.8669 (20 ° C), melting temperature -57.85 ° C, boiling temperature 169 ° C. It is insoluble in water and can be miscible in ethanol, ether, acetone, etc. It can cause an explosion in the face of an open flame and high temperature. Its evaporation can form an explosive mixture, and the explosion is limited to a certain extent. Moreover, the eye and upper respiratory mucosa have a stimulating effect, and high-temperature inhalation can inhibit the reaction. Of the two, one is fixed and the other is flammable aromatic liquid, which is physical.
neon, which is an atom. Its density is small. Color, odor, chemical properties are determined, and other substances are biochemically reactive. Under normal conditions, neon is low, boiling temperature is low, -246.08 ° C, melting temperature is -248.67 ° C. It has good performance, and it is applied to the discharge tube with high current, which can produce orange light. This property makes it commonly used in the manufacture of neon and other lighting devices.
And (1,1-dimethylethyl) benzene, and tert-butylbenzene. Its color solution is aromatic. The phase density is smaller than that of water, 0.8669 (20 ° C), melting temperature -57.85 ° C, boiling temperature 169 ° C. It is insoluble in water and can be miscible in ethanol, ether, acetone, etc. It can cause an explosion in the face of an open flame and high temperature. Its evaporation can form an explosive mixture, and the explosion is limited to a certain extent. Moreover, the eye and upper respiratory mucosa have a stimulating effect, and high-temperature inhalation can inhibit the reaction. Of the two, one is fixed and the other is flammable aromatic liquid, which is physical.
What are the industrial applications of 1-chloro-4- (1,1-dimethylethyl) benzene?
Mercury, commonly known as mercury, is a liquid metal at room temperature. It is widely used in industry and is related to organic mercury compounds such as 1,1-dimethylethylmercury.
Mercury is used in the metallurgical industry and is often used as a medium for extracting precious metals such as gold and silver from ores. Through the amalgamation process, mercury can be combined with metals in ores to separate the target metal. This method has existed since ancient times and is an important means of obtaining precious metals.
In the chemical industry, mercury and its compounds can act as catalysts. Like some organic synthesis reactions in the past, organic mercury compounds such as 1,1-dimethylethylmercury may be used as special catalysts in specific reactions to help the reaction proceed smoothly, but due to their toxicity, their use has been extremely limited today.
Furthermore, mercury is also used in the electrical industry. The traditional mercury lamp uses mercury vapor discharge to emit light. Mercury lamps have the advantages of high luminous efficiency and unique spectral characteristics, and have been widely used in lighting, optical instruments and other fields.
However, it should be emphasized that organic mercury compounds such as 1,1-dimethylethylmercury are extremely toxic and pose great harm to organisms. With the growing awareness of the dangers of mercury, many industrial applications have gradually abandoned mercury and its toxic compounds in favor of more environmentally friendly and safer alternatives. However, mercury and its related compounds have indeed played an important role in many fields in the history of industrial development in the past.
Mercury is used in the metallurgical industry and is often used as a medium for extracting precious metals such as gold and silver from ores. Through the amalgamation process, mercury can be combined with metals in ores to separate the target metal. This method has existed since ancient times and is an important means of obtaining precious metals.
In the chemical industry, mercury and its compounds can act as catalysts. Like some organic synthesis reactions in the past, organic mercury compounds such as 1,1-dimethylethylmercury may be used as special catalysts in specific reactions to help the reaction proceed smoothly, but due to their toxicity, their use has been extremely limited today.
Furthermore, mercury is also used in the electrical industry. The traditional mercury lamp uses mercury vapor discharge to emit light. Mercury lamps have the advantages of high luminous efficiency and unique spectral characteristics, and have been widely used in lighting, optical instruments and other fields.
However, it should be emphasized that organic mercury compounds such as 1,1-dimethylethylmercury are extremely toxic and pose great harm to organisms. With the growing awareness of the dangers of mercury, many industrial applications have gradually abandoned mercury and its toxic compounds in favor of more environmentally friendly and safer alternatives. However, mercury and its related compounds have indeed played an important role in many fields in the history of industrial development in the past.
What are the preparation methods of 1-chloro-4- (1,1-dimethylethyl) benzene?
The method of making soda has been known for a long time. To obtain the soda of 1 + -4- (1,1-dimethylethyl) ether, the method is as follows:
First, the acid of the phase can be used to reverse soda 1,1-dimethylethyl ether. Take the soda amount of acid, such as soda acid, sulfuric acid, etc., and put it into a container containing 1,1-dimethylethyl ether. Under the appropriate soda mixing element, it can be fully reacted. The soda in the acid can combine with the oxygen atoms in the soda to form a phase. It should be noted that the soda should not be high, and the soda should not be high. If it is not high or the side soda is introduced, the soda will not cause soda.
Second, the soda can be mixed with soda by soda. The acid ether is used to communicate with the lipid. First, the acid solution is used to treat the lipid, so that the active group of the lipid is in the shape of the lipid. The 1,1-dimethyl ethyl ether is passed through the treated lipid column. The ether interaction on the lipid can be set to generate the target. The main purpose of this method is that the operating phase is convenient, and the lipid can be used in a follow-up manner, which can effectively reduce the cost.
Third, if there is a phase of lipid, and the target can be formed into 1,1-dimethyl ethyl ether, the decomposition reaction method can also be used. Take the target, dissolve it in the suitable solution, add 1,1-dimethyl ethyl ether, and react under certain conditions. Through the control of the reverse parts, such as the degree of resistance, the degree of resistance, etc., to promote the reverse direction of the formation of the object. After the reverse process is completed, the required speed can be obtained.
The above methods have their own shortcomings, and they need to be used according to the situation, such as the availability of raw materials, cost considerations, and the requirements of the degree of resistance, etc., to obtain 1 + -4- (1,1-dimethyl ethyl) ether.
First, the acid of the phase can be used to reverse soda 1,1-dimethylethyl ether. Take the soda amount of acid, such as soda acid, sulfuric acid, etc., and put it into a container containing 1,1-dimethylethyl ether. Under the appropriate soda mixing element, it can be fully reacted. The soda in the acid can combine with the oxygen atoms in the soda to form a phase. It should be noted that the soda should not be high, and the soda should not be high. If it is not high or the side soda is introduced, the soda will not cause soda.
Second, the soda can be mixed with soda by soda. The acid ether is used to communicate with the lipid. First, the acid solution is used to treat the lipid, so that the active group of the lipid is in the shape of the lipid. The 1,1-dimethyl ethyl ether is passed through the treated lipid column. The ether interaction on the lipid can be set to generate the target. The main purpose of this method is that the operating phase is convenient, and the lipid can be used in a follow-up manner, which can effectively reduce the cost.
Third, if there is a phase of lipid, and the target can be formed into 1,1-dimethyl ethyl ether, the decomposition reaction method can also be used. Take the target, dissolve it in the suitable solution, add 1,1-dimethyl ethyl ether, and react under certain conditions. Through the control of the reverse parts, such as the degree of resistance, the degree of resistance, etc., to promote the reverse direction of the formation of the object. After the reverse process is completed, the required speed can be obtained.
The above methods have their own shortcomings, and they need to be used according to the situation, such as the availability of raw materials, cost considerations, and the requirements of the degree of resistance, etc., to obtain 1 + -4- (1,1-dimethyl ethyl) ether.
What are the effects of 1-chloro-4- (1,1-dimethylethyl) benzene on the environment and human health?
Boron is unique in nature and has various effects on the environment and the human body.
Boron exists in the environment, and its impact is quite complex. In the soil, an appropriate amount of boron is necessary for plant growth. If the amount of boron is appropriate, it can help plant roots develop and promote their reproductive growth. The germination of pollen and the elongation of pollen tubes depend on it. Make crops flower and bear, and the fruit is full, improving yield and quality. However, if the boron content is too high, the soil will be boron-poisoned, and many plants will be hindered from growth, abnormal leaf color, and even wither and die. In water, the content of boron also affects. An appropriate amount of boron can maintain the physiological balance of aquatic organisms, but in excess it will harm the aquatic ecosystem, causing some aquatic organisms to aberrate and inhibit reproduction.
As for the human body, boron is also of great significance. An appropriate amount of boron is beneficial to bone health, can enhance bone density, help calcium, magnesium and other elements absorb, and prevent osteoporosis. In the nervous system, boron can maintain normal nerve conduction and has a positive effect on the cognitive function and memory formation of the brain. And boron also has a regulatory effect on the metabolism of the human body, participating in a variety of enzymatic reactions to ensure the orderly operation of various functions of the body. However, excessive intake of boron can also cause health problems, such as gastrointestinal discomfort, nausea, vomiting, diarrhea, etc. In severe cases, the nervous system and reproductive system will also be damaged, affecting people's normal life and fertility.
Therefore, boron needs to be maintained in an appropriate amount in both the environment and the human body in order to exert its benefits, avoid its harm, and maintain ecological and human health.
Boron exists in the environment, and its impact is quite complex. In the soil, an appropriate amount of boron is necessary for plant growth. If the amount of boron is appropriate, it can help plant roots develop and promote their reproductive growth. The germination of pollen and the elongation of pollen tubes depend on it. Make crops flower and bear, and the fruit is full, improving yield and quality. However, if the boron content is too high, the soil will be boron-poisoned, and many plants will be hindered from growth, abnormal leaf color, and even wither and die. In water, the content of boron also affects. An appropriate amount of boron can maintain the physiological balance of aquatic organisms, but in excess it will harm the aquatic ecosystem, causing some aquatic organisms to aberrate and inhibit reproduction.
As for the human body, boron is also of great significance. An appropriate amount of boron is beneficial to bone health, can enhance bone density, help calcium, magnesium and other elements absorb, and prevent osteoporosis. In the nervous system, boron can maintain normal nerve conduction and has a positive effect on the cognitive function and memory formation of the brain. And boron also has a regulatory effect on the metabolism of the human body, participating in a variety of enzymatic reactions to ensure the orderly operation of various functions of the body. However, excessive intake of boron can also cause health problems, such as gastrointestinal discomfort, nausea, vomiting, diarrhea, etc. In severe cases, the nervous system and reproductive system will also be damaged, affecting people's normal life and fertility.
Therefore, boron needs to be maintained in an appropriate amount in both the environment and the human body in order to exert its benefits, avoid its harm, and maintain ecological and human health.
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