Linshang Chemical
PRODUCTS
4-Amino-6-(Trichlorovinyl)-M-Benzenedisulfonamide
Linshang Chemical
|
HS Code |
174904 |
| Chemical Formula | C8H6Cl3N3O4S2 |
| Appearance | Unknown |
| Melting Point | Unknown |
| Boiling Point | Unknown |
| Solubility In Water | Unknown |
| Solubility In Organic Solvents | Unknown |
| Pka Value | Unknown |
| Logp Value | Unknown |
| Vapor Pressure | Unknown |
As an accredited 4-Amino-6-(Trichlorovinyl)-M-Benzenedisulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide in sealed chemical - grade bags. |
| Storage | 4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly - sealed container to prevent moisture absorption and potential reactions. Ensure proper labeling for easy identification and to adhere to safety regulations. |
| Shipping | 4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide, a chemical, should be shipped in properly sealed, corrosion - resistant containers. Follow all relevant chemical shipping regulations to ensure safe transportation. |
Competitive 4-Amino-6-(Trichlorovinyl)-M-Benzenedisulfonamide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 4-Amino-6-(Trichlorovinyl)-M-Benzenedisulfonamide in China?
As a trusted 4-Amino-6-(Trichlorovinyl)-M-Benzenedisulfonamide manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 4-Amino-6-(Trichlorovinyl)-M-Benzenedisulfonamide supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the chemical structure of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide?
4 - amino - 6- (trichlorovinyl) - m - benzenedisulfonamide, the reaction of the compound has a subtle effect. Its name can be described in its outline.
"4 - amino" refers to the 4-position of benzene, which has an amino group (- NH2O). The amino group is a nitrogen-containing group. The nitrogen atom has an orphan, and the property is active. It can be multiplexed and reversed, and the activity of the compound is large.
"6 - (trichlorovinyl) " indicates that there is trichlorovinyl (- CCl = CCl ²) in the 6-position of benzene. In this group, the carbon-carbon group is incompatible with the compound, and it is easy to form an anti-addition, and the existence of three chlorine atoms, due to the large property of chlorine atoms, makes the group have a absorptive effect, which affects the sub-cloud density distribution of benzene.
"m-benzenedisulfonamide", meaning benzene disulfonamide group. Benzene is used as the backbone of the compound, and the second sulfonamide group (-SO2O NH ²). The sulfur atom in the sulfonamide group is related to the oxygen atom and the amino phase. This makes the compound have certain properties, and can form equal molecular interactions. The physical properties of the compound, such as melting and solubility, are all useful.
In addition, 4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide is composed of a benzene core with an amino group, trichlorovinyl group, and a benzene disulfonamide group. Each group interacts to give this compound its unique chemical properties and reaction activity.
"4 - amino" refers to the 4-position of benzene, which has an amino group (- NH2O). The amino group is a nitrogen-containing group. The nitrogen atom has an orphan, and the property is active. It can be multiplexed and reversed, and the activity of the compound is large.
"6 - (trichlorovinyl) " indicates that there is trichlorovinyl (- CCl = CCl ²) in the 6-position of benzene. In this group, the carbon-carbon group is incompatible with the compound, and it is easy to form an anti-addition, and the existence of three chlorine atoms, due to the large property of chlorine atoms, makes the group have a absorptive effect, which affects the sub-cloud density distribution of benzene.
"m-benzenedisulfonamide", meaning benzene disulfonamide group. Benzene is used as the backbone of the compound, and the second sulfonamide group (-SO2O NH ²). The sulfur atom in the sulfonamide group is related to the oxygen atom and the amino phase. This makes the compound have certain properties, and can form equal molecular interactions. The physical properties of the compound, such as melting and solubility, are all useful.
In addition, 4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide is composed of a benzene core with an amino group, trichlorovinyl group, and a benzene disulfonamide group. Each group interacts to give this compound its unique chemical properties and reaction activity.
What are the main uses of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide
4-Amino-6- (trichlorovinyl) -m-benzenedisulfonamide, Chinese name is often 4-amino-6- (trichlorovinyl) isophenyldisulfonamide. This substance is mainly used in agriculture and industry.
In agriculture, it can be used as a plant growth regulator. By regulating the balance of hormones in plants, it affects the growth process of plants. It can promote the development of crop roots, make the root system more developed, strengthen its ability to absorb water and nutrients, and thereby improve crop stress resistance, such as drought resistance and lodging resistance. During the flowering period of crops, appropriate application of this substance can adjust the flowering period, improve the pollination success rate, increase the fruit setting rate, and ultimately promote crop production and income.
In the industrial field, it plays an important role in the synthesis of some special materials. When synthesizing special plastics or fiber materials, adding this compound can improve the properties of the material. For example, improve the stability and corrosion resistance of the material, broaden the application range of the material, and make it more suitable for extreme environments or special working conditions. In the coating industry, it may be used as an additive to improve the adhesion, wear resistance and chemical corrosion resistance of the coating, prolong the service life of the coating, and improve the protective effect of the coating.
4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide has important application value in agriculture and industry, and provides assistance for the development of related fields through different action mechanisms.
In agriculture, it can be used as a plant growth regulator. By regulating the balance of hormones in plants, it affects the growth process of plants. It can promote the development of crop roots, make the root system more developed, strengthen its ability to absorb water and nutrients, and thereby improve crop stress resistance, such as drought resistance and lodging resistance. During the flowering period of crops, appropriate application of this substance can adjust the flowering period, improve the pollination success rate, increase the fruit setting rate, and ultimately promote crop production and income.
In the industrial field, it plays an important role in the synthesis of some special materials. When synthesizing special plastics or fiber materials, adding this compound can improve the properties of the material. For example, improve the stability and corrosion resistance of the material, broaden the application range of the material, and make it more suitable for extreme environments or special working conditions. In the coating industry, it may be used as an additive to improve the adhesion, wear resistance and chemical corrosion resistance of the coating, prolong the service life of the coating, and improve the protective effect of the coating.
4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide has important application value in agriculture and industry, and provides assistance for the development of related fields through different action mechanisms.
What is the safety of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide?
4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide, this is a chemical substance, the name of which is rarely used by ordinary people, but its safety is of paramount importance. Today, it is said in ancient and elegant words.
This chemical substance may be involved in general diseases. Its toxicity cannot be ignored. If it enters the human body, it may cause diseases such as vomiting, abdominal pain, and diarrhea. If it is inhaled by the respiratory tract, it may cause respiratory problems such as vomiting, abdominal pain, and diarrhea.
Furthermore, the influence of its environment cannot be ignored. In nature, or degradation, it is damaged by water and soil, and it is harmful to insects. In water, such groups of insects, or suffer from it, cause the group to wither. In the soil, the growth of plants, or by it, is hindered.
However, it is not entirely harmful. In the field of labor, or in the production of certain materials. However, the use of this material must be used with caution. Those who handle this material should be protected against secrecy, such as clothing for use, wearing eyes, and equipped with anti-poison equipment. Use it, properly placed, do not dye the four.
Therefore, the safety of 4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide should be treated with the heart of the world. Use it properly and prevent it comprehensively, so as to avoid its harm and use it to ensure the safety of people's environment.
This chemical substance may be involved in general diseases. Its toxicity cannot be ignored. If it enters the human body, it may cause diseases such as vomiting, abdominal pain, and diarrhea. If it is inhaled by the respiratory tract, it may cause respiratory problems such as vomiting, abdominal pain, and diarrhea.
Furthermore, the influence of its environment cannot be ignored. In nature, or degradation, it is damaged by water and soil, and it is harmful to insects. In water, such groups of insects, or suffer from it, cause the group to wither. In the soil, the growth of plants, or by it, is hindered.
However, it is not entirely harmful. In the field of labor, or in the production of certain materials. However, the use of this material must be used with caution. Those who handle this material should be protected against secrecy, such as clothing for use, wearing eyes, and equipped with anti-poison equipment. Use it, properly placed, do not dye the four.
Therefore, the safety of 4 - amino - 6 - (trichlorovinyl) - m - benzenedisulfonamide should be treated with the heart of the world. Use it properly and prevent it comprehensively, so as to avoid its harm and use it to ensure the safety of people's environment.
What are the synthesis methods of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide
The synthesis method of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide (4-amino-6- (trichlorovinyl) isophenyldisulfonamide) is an important matter in chemical preparation. There are many paths to follow for its synthesis.
First, it can be started from the starting material containing the benzene ring. Introduce the sulfonyl chloride group at a specific position of the benzene ring first. This step often requires a suitable sulfonation reagent, such as fuming sulfuric acid, to precisely sulfonate the corresponding position on the benzene ring at a specific temperature and reaction conditions to generate a sulfonyl chloride-containing intermediate. Then, the intermediate is reacted with an appropriate amine compound, and the amino group will replace the chlorine atom in the sulfonyl chloride to form a sulfonamide structure. This reaction requires controlling the pH, temperature and reaction time of the reaction system to ensure that the reaction proceeds in the desired direction.
Second, for the introduction of trichlorovinyl, the strategy of reacting halogenated olefins with intermediates can be adopted. In the presence of suitable catalysts, such as some metal catalysts, the halogenated olefin and the intermediate that has formed the sulfonamide structure undergo nucleophilic substitution or addition reaction, so that the trichlorovinyl is smoothly connected to a specific position on the benzene ring to complete the synthesis of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide.
In addition, there are also compounds with similar structures as starting materials, and the synthesis goal is achieved by transforming and modifying specific functional groups. First, some functional groups of the starting compound are protected to prevent unnecessary changes in subsequent reactions. Then, various organic reactions, such as oxidation, reduction, substitution, etc., are used to gradually construct the desired structure of the target molecule, and finally remove the protecting group to obtain a pure 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide product. Each step requires careful regulation of reaction conditions to improve the purity and yield of the product.
First, it can be started from the starting material containing the benzene ring. Introduce the sulfonyl chloride group at a specific position of the benzene ring first. This step often requires a suitable sulfonation reagent, such as fuming sulfuric acid, to precisely sulfonate the corresponding position on the benzene ring at a specific temperature and reaction conditions to generate a sulfonyl chloride-containing intermediate. Then, the intermediate is reacted with an appropriate amine compound, and the amino group will replace the chlorine atom in the sulfonyl chloride to form a sulfonamide structure. This reaction requires controlling the pH, temperature and reaction time of the reaction system to ensure that the reaction proceeds in the desired direction.
Second, for the introduction of trichlorovinyl, the strategy of reacting halogenated olefins with intermediates can be adopted. In the presence of suitable catalysts, such as some metal catalysts, the halogenated olefin and the intermediate that has formed the sulfonamide structure undergo nucleophilic substitution or addition reaction, so that the trichlorovinyl is smoothly connected to a specific position on the benzene ring to complete the synthesis of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide.
In addition, there are also compounds with similar structures as starting materials, and the synthesis goal is achieved by transforming and modifying specific functional groups. First, some functional groups of the starting compound are protected to prevent unnecessary changes in subsequent reactions. Then, various organic reactions, such as oxidation, reduction, substitution, etc., are used to gradually construct the desired structure of the target molecule, and finally remove the protecting group to obtain a pure 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide product. Each step requires careful regulation of reaction conditions to improve the purity and yield of the product.
What are the physical and chemical properties of 4-amino-6- (trichlorovinyl) -m-benzenedisulfonamide
4-Amino-6- (trichlorovinyl) -isophenyldisulfonamide is an organic compound. Its physical and chemical properties are worth exploring.
Looking at its physical properties, under room temperature, this compound may be in a solid state. In its molecular structure, it contains polar groups such as sulfonamide and amino groups, and the interaction can enhance the attractive force between molecules, so it usually exists in a solid state. Its color may be white to off-white powder, which is a common appearance of many compounds containing such functional groups. The melting point of this compound is related to its purity and structural stability. If the structure is regular and the intermolecular force is uniform, the melting point is relatively fixed, which can be an important indicator for the identification of this compound.
As for its solubility, due to its polar functional groups, it may have a certain solubility in polar solvents. Water is a typical polar solvent, but its molecules are large and contain hydrophobic trichlorovinyl, so its solubility in water may be limited. Organic solvents such as alcohols and ketones can form intermolecular forces with them to increase their solubility. Alcohol solvents can form hydrogen bonds with amino groups and sulfonamide groups to promote dissolution.
On its chemical properties, amino groups are basic and can react with acids to form salts. This property can be used to regulate the solubility and reactivity of compounds in organic synthesis. Sulfonamide groups also have unique reactivity and can participate in reactions such as nucleophilic substitution. Trichlorovinyl groups, which contain unsaturated bonds, can undergo addition reactions, such as addition to hydrogen halides, enriching their chemical conversion pathways. This compound may exhibit various chemical behaviors under different reaction conditions, providing many possibilities for organic synthesis and materials science.
Looking at its physical properties, under room temperature, this compound may be in a solid state. In its molecular structure, it contains polar groups such as sulfonamide and amino groups, and the interaction can enhance the attractive force between molecules, so it usually exists in a solid state. Its color may be white to off-white powder, which is a common appearance of many compounds containing such functional groups. The melting point of this compound is related to its purity and structural stability. If the structure is regular and the intermolecular force is uniform, the melting point is relatively fixed, which can be an important indicator for the identification of this compound.
As for its solubility, due to its polar functional groups, it may have a certain solubility in polar solvents. Water is a typical polar solvent, but its molecules are large and contain hydrophobic trichlorovinyl, so its solubility in water may be limited. Organic solvents such as alcohols and ketones can form intermolecular forces with them to increase their solubility. Alcohol solvents can form hydrogen bonds with amino groups and sulfonamide groups to promote dissolution.
On its chemical properties, amino groups are basic and can react with acids to form salts. This property can be used to regulate the solubility and reactivity of compounds in organic synthesis. Sulfonamide groups also have unique reactivity and can participate in reactions such as nucleophilic substitution. Trichlorovinyl groups, which contain unsaturated bonds, can undergo addition reactions, such as addition to hydrogen halides, enriching their chemical conversion pathways. This compound may exhibit various chemical behaviors under different reaction conditions, providing many possibilities for organic synthesis and materials science.
Scan to WhatsApp
