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1,1'-Disulfanediylbis(Pentachlorobenzene)
Linshang Chemical
|
HS Code |
117064 |
| Chemical Formula | C12Cl10S2 |
| Molecular Weight | 545.73 g/mol |
| Appearance | Solid (presumably, based on similar organochlorine compounds) |
| Solubility In Water | Very low (expected due to high chlorine content and non - polar nature) |
| Solubility In Organic Solvents | Soluble in non - polar organic solvents like benzene, toluene (expected behavior) |
| Vapor Pressure | Very low (expected for a high - molecular - weight, non - volatile compound) |
| Stability | Stable under normal conditions, but may decompose under high heat or in the presence of strong oxidizing agents |
As an accredited 1,1'-Disulfanediylbis(Pentachlorobenzene) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaging: 1 kg of 1,1'-disulfanediylbis(pentachlorobenzene) in sealed chemical - grade containers. |
| Storage | 1,1'-Disulfanediylbis(pentachlorobenzene) should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, ignition sources, and incompatible substances. Store in a tightly closed container, preferably made of corrosion - resistant materials, to prevent leakage and exposure, as it is likely hazardous. |
| Shipping | 1,1'-Disulfanediylbis(pentachlorobenzene) is a chemical. Shipping must follow strict hazardous material regulations. It should be properly packaged to prevent leakage and transported by carriers licensed for such chemicals. |
Competitive 1,1'-Disulfanediylbis(Pentachlorobenzene) prices that fit your budget—flexible terms and customized quotes for every order.
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What is the chemical structure of 1,1 '-disulfanediylbis (pentachlorobenzene)?
1% 2C1% 27 - disulfanediylbis (pentachlorobenzene), its chemical structure is quite interesting. This is one of the organic compounds. Looking at its name, it can be seen that it is composed of two parts of pentachlorobenzene connected by a disulfide group.
For pentachlorobenzene, there are pentachlorine atoms attached to the benzene ring. The benzene ring has a hexagonal structure, and the carbon and carbon are connected by a covalent bond to form a stable conjugated system. The chlorine atom replaces the hydrogen atom of the benzene ring, each occupying a different position in the benzene ring.
And the disulfide group is a group where two sulfur atoms are connected by a covalent bond. This disulfide is based on the molecule, like a bridge, connecting the two The outer electronic structure of the sulfur atom allows it to form bonds with other atoms. In this molecule, sulfur is connected to the carbon atom of pentachlorobenzene, forming the overall structure of 1% 2C1% 27-disulfanediylbis (pentachlorobenzene).
The unique structure of its structure affects its physical and chemical properties. For example, due to the large number of chlorine atoms, it has a high polarity, which affects its solubility, melting point, boiling point and other physical properties. And because its structure contains benzene ring and disulfide group, it can exhibit the aromatization-related reactions of benzene ring and the characteristic reactions of disulfide bond in chemical reactions. It may have unique uses in organic synthesis, materials science and other fields.
For pentachlorobenzene, there are pentachlorine atoms attached to the benzene ring. The benzene ring has a hexagonal structure, and the carbon and carbon are connected by a covalent bond to form a stable conjugated system. The chlorine atom replaces the hydrogen atom of the benzene ring, each occupying a different position in the benzene ring.
And the disulfide group is a group where two sulfur atoms are connected by a covalent bond. This disulfide is based on the molecule, like a bridge, connecting the two The outer electronic structure of the sulfur atom allows it to form bonds with other atoms. In this molecule, sulfur is connected to the carbon atom of pentachlorobenzene, forming the overall structure of 1% 2C1% 27-disulfanediylbis (pentachlorobenzene).
The unique structure of its structure affects its physical and chemical properties. For example, due to the large number of chlorine atoms, it has a high polarity, which affects its solubility, melting point, boiling point and other physical properties. And because its structure contains benzene ring and disulfide group, it can exhibit the aromatization-related reactions of benzene ring and the characteristic reactions of disulfide bond in chemical reactions. It may have unique uses in organic synthesis, materials science and other fields.
What are the main uses of 1,1 '-disulfanediylbis (pentachlorobenzene)?
1% 2C1% 27-dithioalkyl bis (pentachlorobenzene), this is an organic compound. Its use is quite extensive and has been recorded in many ancient books.
First, in the agricultural field, this compound is often used as a special pesticide. Looking at the past agricultural practices, pests often caused crop failure, while 1% 2C1% 27-dithioalkyl bis (pentachlorobenzene), with its unique chemical properties, can effectively repel and kill insects, and ensure the growth of crops. Because it can interfere with the physiological metabolism of pests, making it difficult for pests to survive and multiply, it is often applied in the field to protect the hope of a bumper harvest.
Second, in the industrial field, it also has important functions. In the production process of some special materials, 1% 2C1% 27-dithioalkylbis (pentachlorobenzene) can be used as an additive. By adding this compound, the properties of the material can be improved, such as enhancing the stability and durability of the material. When manufacturing high-end plastic products or special rubber products, adding an appropriate amount of this compound can make the product more resistant to external environmental erosion, prolong its service life, and contribute greatly to industrial production.
Third, in the process of scientific research and exploration, 1% 2C1% 27-dithioalkylbis (pentachlorobenzene) is also an important research object. Scientists often study its chemical structure and reaction properties to explore new chemical synthesis paths or explore its potential new uses. Using it as a cornerstone may develop more efficient compounds, promote the progress of chemistry, and bring more practical results to the world.
First, in the agricultural field, this compound is often used as a special pesticide. Looking at the past agricultural practices, pests often caused crop failure, while 1% 2C1% 27-dithioalkyl bis (pentachlorobenzene), with its unique chemical properties, can effectively repel and kill insects, and ensure the growth of crops. Because it can interfere with the physiological metabolism of pests, making it difficult for pests to survive and multiply, it is often applied in the field to protect the hope of a bumper harvest.
Second, in the industrial field, it also has important functions. In the production process of some special materials, 1% 2C1% 27-dithioalkylbis (pentachlorobenzene) can be used as an additive. By adding this compound, the properties of the material can be improved, such as enhancing the stability and durability of the material. When manufacturing high-end plastic products or special rubber products, adding an appropriate amount of this compound can make the product more resistant to external environmental erosion, prolong its service life, and contribute greatly to industrial production.
Third, in the process of scientific research and exploration, 1% 2C1% 27-dithioalkylbis (pentachlorobenzene) is also an important research object. Scientists often study its chemical structure and reaction properties to explore new chemical synthesis paths or explore its potential new uses. Using it as a cornerstone may develop more efficient compounds, promote the progress of chemistry, and bring more practical results to the world.
What is the environmental impact of 1,1 '-disulfanediylbis (pentachlorobenzene)?
1% 2C1% 27 -dithiobis (pentachlorobenzene), the impact of this substance on the environment should not be underestimated. It may be harmful in the environment.
Let's talk about water bodies first. If this substance enters rivers, lakes and seas, it will remain for a long time due to its chemical properties and is difficult to degrade. It will cause water quality deterioration and poison aquatic organisms. Aquatic plants may be inhibited as a result, photosynthesis is blocked, and the ecological balance of water bodies is affected. Aquatic animals such as fish, or inhaling or ingesting this substance, cause damage to physiological functions, abnormal reproduction and development, and a sharp decrease in population numbers.
Let's talk about soil. If contaminated with this substance, it will change the physical and chemical properties of the soil and reduce soil fertility. It affects the absorption of nutrients by plant roots, causing poor plant growth and reduced crop yield. And it may accumulate in the soil, further polluting the surrounding environment.
In the atmospheric environment, although its volatilization may be limited, it may also enter the atmosphere through volatilization. If inhaled by humans, it may cause health problems such as respiratory tract and lungs.
This substance is difficult to decompose in the environment and will be transmitted and enriched along the food chain. After ingestion by lower organisms, it accumulates through the food chain layer by layer. Organisms at the top of the food chain may have extremely high concentrations in their bodies, posing a serious threat to biodiversity and ecosystem stability. Therefore, 1% 2C1% 27-dithiobis (pentachlorobenzene) needs to be strictly controlled to prevent it from causing greater harm to the environment.
Let's talk about water bodies first. If this substance enters rivers, lakes and seas, it will remain for a long time due to its chemical properties and is difficult to degrade. It will cause water quality deterioration and poison aquatic organisms. Aquatic plants may be inhibited as a result, photosynthesis is blocked, and the ecological balance of water bodies is affected. Aquatic animals such as fish, or inhaling or ingesting this substance, cause damage to physiological functions, abnormal reproduction and development, and a sharp decrease in population numbers.
Let's talk about soil. If contaminated with this substance, it will change the physical and chemical properties of the soil and reduce soil fertility. It affects the absorption of nutrients by plant roots, causing poor plant growth and reduced crop yield. And it may accumulate in the soil, further polluting the surrounding environment.
In the atmospheric environment, although its volatilization may be limited, it may also enter the atmosphere through volatilization. If inhaled by humans, it may cause health problems such as respiratory tract and lungs.
This substance is difficult to decompose in the environment and will be transmitted and enriched along the food chain. After ingestion by lower organisms, it accumulates through the food chain layer by layer. Organisms at the top of the food chain may have extremely high concentrations in their bodies, posing a serious threat to biodiversity and ecosystem stability. Therefore, 1% 2C1% 27-dithiobis (pentachlorobenzene) needs to be strictly controlled to prevent it from causing greater harm to the environment.
What is the preparation method of 1,1 '-disulfanediylbis (pentachlorobenzene)?
1% 2C1% 27-dithiobis (pentachlorobenzene), although the preparation method is not detailed in ancient books, it can be deduced based on the principles of modern chemistry, or it can be as follows.
First take pentachlorobenzene as the base material, this substance has unique properties and is often an important angle in organic synthesis. To obtain 1% 2C1% 27-dithiobis (pentachlorobenzene), pentachlorobenzene can interact with sulfur-containing reagents. Common sulfur-containing reagents, such as sodium hydrosulfide (NaHS) or thiourea, etc.
If sodium hydrosulfide is used, pentachlorobenzene can be dissolved in suitable organic solvents, such as dichloromethane and tetrahydrofuran. Such solvents can disperse the reactants evenly and facilitate the reaction. Under the condition of low temperature and stirring, slowly add the solution of sodium hydrosulfide dropwise. At low temperature, the reaction can be stable and side reactions can be avoided; if stirred, the reactants can be fully contacted.
During the reaction, the sulfur atom in sodium hydrosulfide combines with the specific position of pentachlorobenzene, and through a series of complex chemical changes, gradually generates a sulfur-containing intermediate. Subsequently, under appropriate conditions, such as changing the temperature, adding a catalyst, etc., an intermolecular reaction occurs, so that the two sulfur-containing intermediates are connected via sulfur atoms, resulting in 1% 2C1% 27-dithiobis (pentachlorobenzene).
If thiourea is used, pentachlorobenzene and thiourea are first placed in a suitable reaction system, or supplemented with basic reagents to adjust the pH of the reaction to facilitate the progress of the reaction. After multi-step reaction, the sulfur element of thiourea gradually enters the product structure and eventually forms the target. However, no matter what method, it is necessary to carefully control the reaction conditions, such as temperature, time, and the proportion of reactants, etc., in order to increase the yield and purify the product.
First take pentachlorobenzene as the base material, this substance has unique properties and is often an important angle in organic synthesis. To obtain 1% 2C1% 27-dithiobis (pentachlorobenzene), pentachlorobenzene can interact with sulfur-containing reagents. Common sulfur-containing reagents, such as sodium hydrosulfide (NaHS) or thiourea, etc.
If sodium hydrosulfide is used, pentachlorobenzene can be dissolved in suitable organic solvents, such as dichloromethane and tetrahydrofuran. Such solvents can disperse the reactants evenly and facilitate the reaction. Under the condition of low temperature and stirring, slowly add the solution of sodium hydrosulfide dropwise. At low temperature, the reaction can be stable and side reactions can be avoided; if stirred, the reactants can be fully contacted.
During the reaction, the sulfur atom in sodium hydrosulfide combines with the specific position of pentachlorobenzene, and through a series of complex chemical changes, gradually generates a sulfur-containing intermediate. Subsequently, under appropriate conditions, such as changing the temperature, adding a catalyst, etc., an intermolecular reaction occurs, so that the two sulfur-containing intermediates are connected via sulfur atoms, resulting in 1% 2C1% 27-dithiobis (pentachlorobenzene).
If thiourea is used, pentachlorobenzene and thiourea are first placed in a suitable reaction system, or supplemented with basic reagents to adjust the pH of the reaction to facilitate the progress of the reaction. After multi-step reaction, the sulfur element of thiourea gradually enters the product structure and eventually forms the target. However, no matter what method, it is necessary to carefully control the reaction conditions, such as temperature, time, and the proportion of reactants, etc., in order to increase the yield and purify the product.
What are the physical and chemical properties of 1,1 '-disulfanediylbis (pentachlorobenzene)?
1% 2C1% 27 -dithialkyl bis (pentachlorobenzene), this is an organic compound. Its physical and chemical properties are quite important, and it is related to its application in various fields.
Let's talk about the physical properties first. This substance may be a solid under normal conditions, because it contains a large number of chlorine atoms and has strong intermolecular forces. Melting point or higher, the edge chlorine atom increases the molecular mass and intermolecular van der Waals force. Its appearance may be white to light yellow powder, due to the structural characteristics of benzene ring and chlorine atom, it shows this color under the action of light. It is difficult to dissolve in water. Due to the small polarity of the molecule, it is very different from the polarity of water. According to the principle of "similar miscibility", it is difficult to dissolve with water.
Let's talk about chemical properties. Because it contains disulfide bonds, it has certain chemical activity. In case of strong oxidants, disulfide bonds may break, triggering oxidation reactions and causing changes in structure and properties. The chlorine atoms on the benzene ring are active, and under suitable conditions, nucleophilic substitution reactions can occur. For example, when interacting with nucleophilic reagents, chlorine atoms are replaced to form new organic compounds. Because of its polychlorinated benzene structure, it has certain stability and certain tolerance to heat and light, but under high temperature and strong light, the structure or gradual change occurs, and decomposition and other reactions occur. And because of chlorine, harmful gases containing chlorine may be produced during combustion, such as hydrogen chloride.
Let's talk about the physical properties first. This substance may be a solid under normal conditions, because it contains a large number of chlorine atoms and has strong intermolecular forces. Melting point or higher, the edge chlorine atom increases the molecular mass and intermolecular van der Waals force. Its appearance may be white to light yellow powder, due to the structural characteristics of benzene ring and chlorine atom, it shows this color under the action of light. It is difficult to dissolve in water. Due to the small polarity of the molecule, it is very different from the polarity of water. According to the principle of "similar miscibility", it is difficult to dissolve with water.
Let's talk about chemical properties. Because it contains disulfide bonds, it has certain chemical activity. In case of strong oxidants, disulfide bonds may break, triggering oxidation reactions and causing changes in structure and properties. The chlorine atoms on the benzene ring are active, and under suitable conditions, nucleophilic substitution reactions can occur. For example, when interacting with nucleophilic reagents, chlorine atoms are replaced to form new organic compounds. Because of its polychlorinated benzene structure, it has certain stability and certain tolerance to heat and light, but under high temperature and strong light, the structure or gradual change occurs, and decomposition and other reactions occur. And because of chlorine, harmful gases containing chlorine may be produced during combustion, such as hydrogen chloride.
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