Linshang Chemical
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2,3,5,6-Tetrachlorobenzene-1,4-Dicarboxylate
Linshang Chemical
|
HS Code |
854470 |
| Chemical Formula | C8H2Cl4O4 |
| Molar Mass | 303.91 g/mol |
| Appearance | Solid (likely white or off - white) |
| Solubility In Water | Low solubility |
| Solubility In Organic Solvents | Soluble in some organic solvents like chloroform, benzene |
| Boiling Point | Decomposes before boiling in normal conditions |
| Melting Point | Relatively high melting point (exact value depends on isomer and purity) |
| Density | Higher than water density |
| Odor | May have a faint, characteristic chlorinated odor |
| Stability | Stable under normal conditions but can react under strong acidic or basic conditions |
As an accredited 2,3,5,6-Tetrachlorobenzene-1,4-Dicarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram pack of 2,3,5,6 - tetrachlorobenzene - 1,4 - dicarboxylate in air - tight container. |
| Storage | 2,3,5,6 - tetrachlorobenzene - 1,4 - dicarboxylate should be stored in a cool, dry, well - ventilated area. Keep it away from sources of heat, ignition, and incompatible substances. Store in tightly closed containers to prevent moisture and air exposure, which could potentially cause decomposition or reactivity issues. Label containers clearly for easy identification. |
| Shipping | 2,3,5,6 - tetrachlorobenzene - 1,4 - dicarboxylate is shipped in well - sealed containers, following strict chemical transportation regulations. Packaging ensures no leakage during transit to safeguard the environment and handlers. |
Competitive 2,3,5,6-Tetrachlorobenzene-1,4-Dicarboxylate prices that fit your budget—flexible terms and customized quotes for every order.
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What are the main uses of 2,3,5,6-tetrachlorobenzene-1,4-dicarboxylate?
Tetrazines of dicyandiamine, triazine, pentazine, and hexazine, the main uses of one and tetradiaminoguanidine are in many fields such as chemical industry, medicine, and agriculture.
In chemical industry, tetrazines can be used as key raw materials for the synthesis of new energetic materials. Energetic materials have high energy density and are of great significance in explosives, propellants, etc. Tetrazines can give better properties to energetic materials due to their special chemical structure, such as improving energy output and stability.
In the field of medicine, diaminoguanidine and its derivatives have biological activity. Or can participate in the design and synthesis of drug molecules, or can play a therapeutic effect on specific diseases. After research and exploration, it is expected to develop new specific drugs to deal with refractory diseases such as cardiovascular diseases and tumors.
In the field of agriculture, such compounds may be active ingredients that can be used as pesticides. Its unique chemical properties may show the ability to inhibit or kill specific pests and pathogens, thereby providing protection for crops and improving yield and quality. And compared with traditional pesticides, it may be more selective and environmentally friendly, reducing the impact on non-target organisms and environmental residues.
In addition, it also has potential application value in other fields such as materials science. For example, in the synthesis of functional materials, such compounds may be introduced to endow materials with special optical, electrical and other properties, expanding the scope of material applications.
In summary, tetrazine, dicyanodiamine, triazine, pentazine, hexazine, and tetrazine are widely used in many fields, with great research and development potential, and provide important assistance for promoting the development of various industries.
In chemical industry, tetrazines can be used as key raw materials for the synthesis of new energetic materials. Energetic materials have high energy density and are of great significance in explosives, propellants, etc. Tetrazines can give better properties to energetic materials due to their special chemical structure, such as improving energy output and stability.
In the field of medicine, diaminoguanidine and its derivatives have biological activity. Or can participate in the design and synthesis of drug molecules, or can play a therapeutic effect on specific diseases. After research and exploration, it is expected to develop new specific drugs to deal with refractory diseases such as cardiovascular diseases and tumors.
In the field of agriculture, such compounds may be active ingredients that can be used as pesticides. Its unique chemical properties may show the ability to inhibit or kill specific pests and pathogens, thereby providing protection for crops and improving yield and quality. And compared with traditional pesticides, it may be more selective and environmentally friendly, reducing the impact on non-target organisms and environmental residues.
In addition, it also has potential application value in other fields such as materials science. For example, in the synthesis of functional materials, such compounds may be introduced to endow materials with special optical, electrical and other properties, expanding the scope of material applications.
In summary, tetrazine, dicyanodiamine, triazine, pentazine, hexazine, and tetrazine are widely used in many fields, with great research and development potential, and provide important assistance for promoting the development of various industries.
What are the physical properties of 2,3,5,6-tetrachlorobenzene-1,4-dicarboxylate
Fudicyanotriazine pentazine hexazine is a class of nitrogen-containing compounds. Its monocyanide and tetracyanide also have their own characteristics.
The physical properties of guanidine dicyanate, first of all, in its appearance, are often white crystalline solid, with a more delicate texture. This is due to its regular molecular structure and orderly arrangement of crystal forms. Looking at its solubility, it has a certain solubility in water. Because the molecule contains polar groups, it can interact with water molecules to form hydrogen bonds, etc. However, the solubility is not very high and is still moderate. As for the melting point, it is in a relatively moderate range, which is determined by the intermolecular force. There are hydrogen bonds and other effects between molecules, as well as van der Waals forces, which jointly maintain its solid structure and heat to a specific temperature before it can destroy the structure and melt.
Furthermore, its density also has a certain value. Compared with common organic solvents, the density is slightly higher. This is due to the type and quantity of atoms in its molecular composition. The atomic accumulation is relatively close, resulting in high density.
The stability of guanidine dicyanate is also an important physical property. Under normal temperature and pressure, it is quite stable and can be stored for a long time without significant chemical changes. However, under extreme conditions such as high temperature, strong acid, and strong base, its molecular structure can be damaged, decomposed, or other chemical reactions occur.
These are the general physical properties of guanidine dicyanate, which are interrelated and determined by its molecular structure. Applications in many fields such as chemical industry and materials also depend on these properties.
The physical properties of guanidine dicyanate, first of all, in its appearance, are often white crystalline solid, with a more delicate texture. This is due to its regular molecular structure and orderly arrangement of crystal forms. Looking at its solubility, it has a certain solubility in water. Because the molecule contains polar groups, it can interact with water molecules to form hydrogen bonds, etc. However, the solubility is not very high and is still moderate. As for the melting point, it is in a relatively moderate range, which is determined by the intermolecular force. There are hydrogen bonds and other effects between molecules, as well as van der Waals forces, which jointly maintain its solid structure and heat to a specific temperature before it can destroy the structure and melt.
Furthermore, its density also has a certain value. Compared with common organic solvents, the density is slightly higher. This is due to the type and quantity of atoms in its molecular composition. The atomic accumulation is relatively close, resulting in high density.
The stability of guanidine dicyanate is also an important physical property. Under normal temperature and pressure, it is quite stable and can be stored for a long time without significant chemical changes. However, under extreme conditions such as high temperature, strong acid, and strong base, its molecular structure can be damaged, decomposed, or other chemical reactions occur.
These are the general physical properties of guanidine dicyanate, which are interrelated and determined by its molecular structure. Applications in many fields such as chemical industry and materials also depend on these properties.
What are the environmental effects of 2,3,5,6-tetrachlorobenzene-1,4-dicarboxylate?
2% 2C3% 2C5% 2C6 refers to tetrabromobenzene, and 1% 2C4 refers to dichlorobenzoic acid, both of which can cause significant effects in the environment.
Tetrabromobenzene has unique chemical properties due to its bromine-containing structure. In the natural environment, it is easy to retain for a long time due to its difficult-to-degrade characteristics. When released into water bodies, it can migrate with water flow and can produce bioaccumulation effects through the food chain. After biological ingestion, it may interfere with the normal physiological functions of organisms, in aquatic organisms, or destroy their endocrine systems, affect reproduction and development, and cause population changes. In the soil environment, or adsorbed on soil particles, it affects the activity of soil microorganisms and disrupts the material cycle and energy flow of soil ecosystems.
Dichlorobenzoic acid also poses certain environmental risks. It is highly stable in the environment and difficult to be rapidly decomposed by microorganisms. If it enters the soil, or changes the pH of the soil, it will affect the availability of nutrients in the soil, hinder the absorption of nutrients by plant roots, and then affect plant growth and development. In water bodies, it can affect water quality, change the chemical properties of water bodies, cause damage to the living environment of aquatic organisms, or cause the death of some aquatic organisms, and destroy the ecological balance of water. And if the two volatilize into the atmosphere, or participate in atmospheric chemical reactions, affect air quality and pose a potential threat to human health and the ecological environment. In short, these two types of substances can have many negative effects on the physical, chemical and biological characteristics of the environment, and must be paid attention to and controlled to ensure the safety of the ecological environment.
Tetrabromobenzene has unique chemical properties due to its bromine-containing structure. In the natural environment, it is easy to retain for a long time due to its difficult-to-degrade characteristics. When released into water bodies, it can migrate with water flow and can produce bioaccumulation effects through the food chain. After biological ingestion, it may interfere with the normal physiological functions of organisms, in aquatic organisms, or destroy their endocrine systems, affect reproduction and development, and cause population changes. In the soil environment, or adsorbed on soil particles, it affects the activity of soil microorganisms and disrupts the material cycle and energy flow of soil ecosystems.
Dichlorobenzoic acid also poses certain environmental risks. It is highly stable in the environment and difficult to be rapidly decomposed by microorganisms. If it enters the soil, or changes the pH of the soil, it will affect the availability of nutrients in the soil, hinder the absorption of nutrients by plant roots, and then affect plant growth and development. In water bodies, it can affect water quality, change the chemical properties of water bodies, cause damage to the living environment of aquatic organisms, or cause the death of some aquatic organisms, and destroy the ecological balance of water. And if the two volatilize into the atmosphere, or participate in atmospheric chemical reactions, affect air quality and pose a potential threat to human health and the ecological environment. In short, these two types of substances can have many negative effects on the physical, chemical and biological characteristics of the environment, and must be paid attention to and controlled to ensure the safety of the ecological environment.
What is the production method of 2,3,5,6-tetrachlorobenzene-1,4-dicarboxylate?
The manufacturing methods of dicyanodiamine, melamine, and cyanuric acid are quite complicated and need to be explained in detail according to the ancient method.
For dicyanodiamine, the method of making it often starts with lime nitrogen and water. First hydrolyze lime nitrogen to obtain cyanamide, and then polymerize cyanamide to form dicyanodiamine. Its chemical changes are orderly. As the ancient saying goes: "Take an appropriate amount of lime nitrogen, put it in various vessels, slowly inject it with water, and hydrolyze it, and cyanamide is produced. Remelamine, and then dicyanodiamine is obtained." Among them, the temperature of hydrolysis and the time of polymerization are all important and need to be carefully observed and controlled.
The production of melamine is mostly derived from urea. Under specific temperature and pressure, and with the help of catalysts, urea decomposes and polymerizes, and finally forms melamine. If the ancients did it, they would say: "Choose pure urea, put it in the kettle, adjust its temperature and pressure, and add a catalyst to make urea dissolve first, then polymerize, and melamine is obtained." The degree of temperature, pressure, and the amount of catalyst are all related to success or failure, so be careful.
The production of cyanuric acid is mostly obtained from the pyrolysis of urea. When urea is heated, it is converted into cyanuric acid through a series of changes. The ancient workers said, "Take urea, heat it with fire, control its heat, and make urea gradually pyrolyze. After various changes, cyanuric acid is formed." The process of pyrolysis also requires careful inspection of temperature and time to ensure that the reaction is appropriate.
Although the manufacture of these three is derived from basic things, the method is subtle, temperature, pressure, time, catalyst, etc., all need to be carefully reviewed and well managed, in order to obtain its pure quality and use it for everything.
For dicyanodiamine, the method of making it often starts with lime nitrogen and water. First hydrolyze lime nitrogen to obtain cyanamide, and then polymerize cyanamide to form dicyanodiamine. Its chemical changes are orderly. As the ancient saying goes: "Take an appropriate amount of lime nitrogen, put it in various vessels, slowly inject it with water, and hydrolyze it, and cyanamide is produced. Remelamine, and then dicyanodiamine is obtained." Among them, the temperature of hydrolysis and the time of polymerization are all important and need to be carefully observed and controlled.
The production of melamine is mostly derived from urea. Under specific temperature and pressure, and with the help of catalysts, urea decomposes and polymerizes, and finally forms melamine. If the ancients did it, they would say: "Choose pure urea, put it in the kettle, adjust its temperature and pressure, and add a catalyst to make urea dissolve first, then polymerize, and melamine is obtained." The degree of temperature, pressure, and the amount of catalyst are all related to success or failure, so be careful.
The production of cyanuric acid is mostly obtained from the pyrolysis of urea. When urea is heated, it is converted into cyanuric acid through a series of changes. The ancient workers said, "Take urea, heat it with fire, control its heat, and make urea gradually pyrolyze. After various changes, cyanuric acid is formed." The process of pyrolysis also requires careful inspection of temperature and time to ensure that the reaction is appropriate.
Although the manufacture of these three is derived from basic things, the method is subtle, temperature, pressure, time, catalyst, etc., all need to be carefully reviewed and well managed, in order to obtain its pure quality and use it for everything.
What are the chemical properties of 2,3,5,6-tetrachlorobenzene-1,4-dicarboxylate
The chemical properties of dicyandiamine, melamine, tetracyanoquinoline dimethane, tetracyanoethylene-tetrazene-1,4-dinitrophenylhydrazine are different.
dicyandiamine, also known as dicyandiamine, its properties are white crystalline powder. Melting point is quite high, about 209.5 ℃. Slightly soluble in water, ethanol, insoluble in ether and benzene. Weakly alkaline, can form salts with strong acids. Stable in air, decomposition reaction occurs when heated, and condensation reaction can occur with a variety of substances under certain conditions. It is often used as an important raw material for the synthesis of guanidine salts, melamine and other compounds.
Melamine, a white monoclinic crystal. Melting point 250 ℃, non-flammable. Slightly soluble in water and hot ethanol, very slightly soluble in hot ether. There are three amino groups in its molecule, which are weakly basic and can react with acids to form salts. Hydrolysis reaction can occur when heated or under acid or alkali conditions. The molecule contains three amino groups. Under certain conditions, polymerization reaction can occur to produce melamine formaldehyde resin. The resin is widely used in wood processing, plastics, coatings and other industries.
Tetracyanoquinoline dimethane (TCNQ), with dark green crystal appearance. It has strong electron acceptance ability and is a typical organic electron receptor. It is widely used in the field of organic semiconductor materials and can form charge transfer complexes with electron donors. These complexes often have unique electrical and optical properties. Its chemical stability depends to a certain extent on the environment, and chemical reactions may occur to change its structure and properties when encountering specific reagents.
tetracyanoethylene (TCNE) is a yellow crystal. It is chemically active and, as a strong electrophilic reagent, is prone to cycloaddition and other reactions with electron-rich systems. It is often used in organic synthesis to construct complex compounds containing cyanide groups. Due to the electron-withdrawing effect of cyanide groups, the molecules have a special electron cloud distribution, thus exhibiting unique reactivity.
tetrazene, generally refers to 1-hydrogen-tetrazene. It is prone to explosive decomposition when heated, impacted or rubbed, and is a more sensitive energetic material. It has poor stability in the dry state, and the molecular structure contains multiple nitrogen atoms, which have certain oxidizing and reducing properties. It can participate in the redox reaction under specific conditions.
1,4-dinitrophenylhydrazine, an orange-red crystalline powder. It is insoluble in water, slightly soluble in ethanol. It has oxidizing properties and can react specifically with carbonyl compounds such as alaldehyde and ketone to generate hydrazone derivatives. It is often used to identify carbonyl compounds such as alaldehyde and ketone. The resulting hydrazone products often have a specific melting point, and the type of carbonyl compound can be determined by measuring the melting point.
dicyandiamine, also known as dicyandiamine, its properties are white crystalline powder. Melting point is quite high, about 209.5 ℃. Slightly soluble in water, ethanol, insoluble in ether and benzene. Weakly alkaline, can form salts with strong acids. Stable in air, decomposition reaction occurs when heated, and condensation reaction can occur with a variety of substances under certain conditions. It is often used as an important raw material for the synthesis of guanidine salts, melamine and other compounds.
Melamine, a white monoclinic crystal. Melting point 250 ℃, non-flammable. Slightly soluble in water and hot ethanol, very slightly soluble in hot ether. There are three amino groups in its molecule, which are weakly basic and can react with acids to form salts. Hydrolysis reaction can occur when heated or under acid or alkali conditions. The molecule contains three amino groups. Under certain conditions, polymerization reaction can occur to produce melamine formaldehyde resin. The resin is widely used in wood processing, plastics, coatings and other industries.
Tetracyanoquinoline dimethane (TCNQ), with dark green crystal appearance. It has strong electron acceptance ability and is a typical organic electron receptor. It is widely used in the field of organic semiconductor materials and can form charge transfer complexes with electron donors. These complexes often have unique electrical and optical properties. Its chemical stability depends to a certain extent on the environment, and chemical reactions may occur to change its structure and properties when encountering specific reagents.
tetracyanoethylene (TCNE) is a yellow crystal. It is chemically active and, as a strong electrophilic reagent, is prone to cycloaddition and other reactions with electron-rich systems. It is often used in organic synthesis to construct complex compounds containing cyanide groups. Due to the electron-withdrawing effect of cyanide groups, the molecules have a special electron cloud distribution, thus exhibiting unique reactivity.
tetrazene, generally refers to 1-hydrogen-tetrazene. It is prone to explosive decomposition when heated, impacted or rubbed, and is a more sensitive energetic material. It has poor stability in the dry state, and the molecular structure contains multiple nitrogen atoms, which have certain oxidizing and reducing properties. It can participate in the redox reaction under specific conditions.
1,4-dinitrophenylhydrazine, an orange-red crystalline powder. It is insoluble in water, slightly soluble in ethanol. It has oxidizing properties and can react specifically with carbonyl compounds such as alaldehyde and ketone to generate hydrazone derivatives. It is often used to identify carbonyl compounds such as alaldehyde and ketone. The resulting hydrazone products often have a specific melting point, and the type of carbonyl compound can be determined by measuring the melting point.
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