Linshang Chemical
PRODUCTS
1-Amino-2,3,4,5,6-Pentachloro-Benzene
Linshang Chemical
|
HS Code |
373634 |
| Name | 1-Amino-2,3,4,5,6-Pentachloro-Benzene |
| Molecular Formula | C6H2Cl5N |
| Molecular Weight | 276.35 |
| Appearance | Solid (likely white to off - white) |
| Melting Point | Data needed |
| Boiling Point | Data needed |
| Solubility In Water | Low solubility |
| Solubility In Organic Solvents | Soluble in some organic solvents like chloroform, benzene |
| Density | Data needed |
| Odor | May have a characteristic chemical odor |
| Stability | Stable under normal conditions, but can react under certain chemical or physical stimuli |
As an accredited 1-Amino-2,3,4,5,6-Pentachloro-Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - amino - 2,3,4,5,6 - pentachloro - benzene: Packed in 1 - kg containers. |
| Storage | 1 - amino - 2,3,4,5,6 - pentachloro - benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, ignition sources, and oxidizing agents. Store it in a tightly - sealed container, preferably made of corrosion - resistant materials. This helps prevent decomposition, potential leakage, and dangerous reactions, ensuring safety during storage. |
| Shipping | 1 - amino - 2,3,4,5,6 - pentachloro - benzene is a hazardous chemical. Shipping must comply with strict regulations. It should be properly packaged, labeled, and transported by carriers approved for hazardous substances. |
Competitive 1-Amino-2,3,4,5,6-Pentachloro-Benzene 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 1-Amino-2,3,4,5,6-Pentachloro-Benzene in China?
As a trusted 1-Amino-2,3,4,5,6-Pentachloro-Benzene 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 1-Amino-2,3,4,5,6-Pentachloro-Benzene 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 main use of 1 - amino - 2, 3, 4, 5, 6 - pentachloro - benzene
1-Amino-2,3,4,5,6-pentachlorobenzene is one of the organic compounds. Its main uses, in the past, involved chemical research and specific industrial processes.
In the field of chemical research, this compound is often the key object to explore the mechanism of organic reactions. By observing the various reactions it participates in, chemists gain insight into the chemical interaction between chlorine atoms and amino groups on the benzene ring structure, as well as the distribution of electron clouds involved, the mystery of chemical bond breaking and formation, in order to understand the subtle laws of organic reactions, and provide a theoretical foundation for the optimization of the creation and synthesis path of new compounds.
In industrial use, it may have been used in the preparation of specific pesticides. Due to its structure containing multiple chlorine atoms, it has certain biological activity and may have repellent and poisoning effects on some pests. Using it as a raw material and through specific chemical transformation, pesticide products with unique insecticidal properties can be prepared to protect crops from pest infestation and protect agricultural yields.
Of course, this compound may have environmental persistence and bioaccumulation due to its polychlorine structure. Over time, it may remain and accumulate in the ecological environment, endangering ecological balance and biological health. Today, in view of the promotion of environmental awareness and the promotion of green chemistry, the use and production of such compounds are strictly regulated and restricted to protect the harmony and sustainability of the earth's ecology.
In the field of chemical research, this compound is often the key object to explore the mechanism of organic reactions. By observing the various reactions it participates in, chemists gain insight into the chemical interaction between chlorine atoms and amino groups on the benzene ring structure, as well as the distribution of electron clouds involved, the mystery of chemical bond breaking and formation, in order to understand the subtle laws of organic reactions, and provide a theoretical foundation for the optimization of the creation and synthesis path of new compounds.
In industrial use, it may have been used in the preparation of specific pesticides. Due to its structure containing multiple chlorine atoms, it has certain biological activity and may have repellent and poisoning effects on some pests. Using it as a raw material and through specific chemical transformation, pesticide products with unique insecticidal properties can be prepared to protect crops from pest infestation and protect agricultural yields.
Of course, this compound may have environmental persistence and bioaccumulation due to its polychlorine structure. Over time, it may remain and accumulate in the ecological environment, endangering ecological balance and biological health. Today, in view of the promotion of environmental awareness and the promotion of green chemistry, the use and production of such compounds are strictly regulated and restricted to protect the harmony and sustainability of the earth's ecology.
What are the environmental effects of 1 - amino - 2, 3, 4, 5, 6 - pentachloro - benzene
1 + -Amino-2,3,4,5,6-pentachlorobenzene, this substance has a significant impact on the environment. It is an organic halide with high stability and fat solubility, which is difficult to degrade in the environment and easy to accumulate.
Viewed in the atmosphere, it can spread with air, causing a wider range of pollution. When it rains, or falls on the ground and water bodies with rain, causing soil and water to be polluted. In the soil, it will inhibit the activity of soil microorganisms, hinder nutrient circulation and decomposition of organic matter, and then damage soil fertility, hinder plant growth and development, and cause crop yield and quality deterioration.
As for the water body, it can be ingested by aquatic organisms and enriched through the food chain, which poses a great threat to the survival and reproduction of aquatic organisms, or causes biodiversity impairment. And if people drink water containing this pollutant, or eat contaminated aquatic organisms, it will endanger their health, such as causing liver and kidney damage, interfering with endocrine, and even teratogenic, carcinogenic, and mutagenic.
Furthermore, it persists in the environment for a long time, or interacts with other pollutants to generate more toxic substances, making environmental problems more complicated and difficult. Therefore, such pollutants should be given high attention, and effective prevention and control and governance methods should be actively explored to ensure the safety of the environment and human health.
Viewed in the atmosphere, it can spread with air, causing a wider range of pollution. When it rains, or falls on the ground and water bodies with rain, causing soil and water to be polluted. In the soil, it will inhibit the activity of soil microorganisms, hinder nutrient circulation and decomposition of organic matter, and then damage soil fertility, hinder plant growth and development, and cause crop yield and quality deterioration.
As for the water body, it can be ingested by aquatic organisms and enriched through the food chain, which poses a great threat to the survival and reproduction of aquatic organisms, or causes biodiversity impairment. And if people drink water containing this pollutant, or eat contaminated aquatic organisms, it will endanger their health, such as causing liver and kidney damage, interfering with endocrine, and even teratogenic, carcinogenic, and mutagenic.
Furthermore, it persists in the environment for a long time, or interacts with other pollutants to generate more toxic substances, making environmental problems more complicated and difficult. Therefore, such pollutants should be given high attention, and effective prevention and control and governance methods should be actively explored to ensure the safety of the environment and human health.
What are the preparation methods of 1 - amino - 2, 3, 4, 5, 6 - pentachloro - benzene
1 + -Amino-2,3,4,5,6-pentachlorobenzene, which is an organic compound. The preparation method can be obtained by the corresponding benzene ring derivative through multi-step reaction.
One method is to take benzene as the starting material and chlorinate it to introduce chlorine atoms into the benzene ring to obtain polychlorobenzene. Under specific reaction conditions, a suitable chlorinating agent is selected, such as chlorine gas. Under the catalysis of catalysts such as ferric chloride, benzene and chlorine gas undergo electrophilic substitution reaction to gradually generate chlorobenzene derivatives containing different chlorine atoms. After separation and purification, 2,3,4,5,6-pentachlorobenzene is obtained. Subsequently, 2,3,4,5,6-pentachlorobenzene is reacted with amino-containing reagents, such as ammonia or its derivatives. Under suitable solvents and reaction conditions, a nucleophilic substitution reaction occurs, and the chlorine atom at a specific position on the benzene ring is replaced by an amino group to obtain 1 + -amino-2,3,4,5,6-pentachlorobenzene.
Another method is to use an amino-containing benzene derivative as the starting material, and then carry out the chlorination reaction. However, it is necessary to pay attention to the control of the reaction conditions and the amount of chlorination agent, so that the chlorine atom is selectively introduced into the specific position of the benzene ring, and the final product is obtained. During the chlorination process, attention should be paid to the reaction temperature, time, and the type and amount of catalyst, because these factors will affect the structure and yield of the product.
Preparation of 1 + -amino-2,3,4,5,6-pentachlorobenzene requires careful selection of appropriate preparation methods according to the availability of raw materials, the feasibility of reaction conditions, and the purity requirements of the target product. After each step of the reaction, proper separation and purification operations should be carried out to improve the purity and yield of the product.
One method is to take benzene as the starting material and chlorinate it to introduce chlorine atoms into the benzene ring to obtain polychlorobenzene. Under specific reaction conditions, a suitable chlorinating agent is selected, such as chlorine gas. Under the catalysis of catalysts such as ferric chloride, benzene and chlorine gas undergo electrophilic substitution reaction to gradually generate chlorobenzene derivatives containing different chlorine atoms. After separation and purification, 2,3,4,5,6-pentachlorobenzene is obtained. Subsequently, 2,3,4,5,6-pentachlorobenzene is reacted with amino-containing reagents, such as ammonia or its derivatives. Under suitable solvents and reaction conditions, a nucleophilic substitution reaction occurs, and the chlorine atom at a specific position on the benzene ring is replaced by an amino group to obtain 1 + -amino-2,3,4,5,6-pentachlorobenzene.
Another method is to use an amino-containing benzene derivative as the starting material, and then carry out the chlorination reaction. However, it is necessary to pay attention to the control of the reaction conditions and the amount of chlorination agent, so that the chlorine atom is selectively introduced into the specific position of the benzene ring, and the final product is obtained. During the chlorination process, attention should be paid to the reaction temperature, time, and the type and amount of catalyst, because these factors will affect the structure and yield of the product.
Preparation of 1 + -amino-2,3,4,5,6-pentachlorobenzene requires careful selection of appropriate preparation methods according to the availability of raw materials, the feasibility of reaction conditions, and the purity requirements of the target product. After each step of the reaction, proper separation and purification operations should be carried out to improve the purity and yield of the product.
What are the physical properties of 1 - amino - 2, 3, 4, 5, 6 - pentachloro - benzene
1-Amino-2,3,4,5,6-pentachlorobenzene is an organic compound. Its physical properties have a number of characteristics.
Looking at its morphology, at room temperature, it is mostly in the shape of a solid state, or a crystalline powder. Due to the intermolecular force and structural arrangement, it has certain condensed matter characteristics.
When it comes to color, it is often white to light yellow. This color is derived from the absorption and reflection characteristics of the molecular structure of light. The presence of chlorine atoms and amino groups affects the mode of action of light, so it presents such colors.
Its melting point is also fixed, and the specific value varies slightly due to factors such as purity, but it is roughly within a certain range. The formation of the melting point is closely related to the intermolecular forces, such as van der Waals forces, hydrogen bonds, etc., which determine the energy required to transform from solid to liquid.
As for solubility, it is extremely difficult to dissolve in water. Due to the large number of chlorine atoms in the molecular structure, the polarity of the molecule is biased towards the non-polar end, which is quite different from that of water molecules. It follows the principle of "similar miscibility", so it is difficult to dissolve in water. However, in organic solvents, such as benzene, toluene, dichloromethane, etc., there is a certain solubility, because the polarity of organic solvents is more compatible with the compound, and the intermolecular forces are conducive to their mixing.
Its density is higher than that of water, because the mass of chlorine atoms in the molecule increases the mass of the substance per unit volume, so the density is higher.
The physical properties of 1-amino-2,3,4,5,6-pentachlorobenzene are determined by its molecular structure, and these properties have a crucial impact on its behavior in various environments and chemical reactions.
Looking at its morphology, at room temperature, it is mostly in the shape of a solid state, or a crystalline powder. Due to the intermolecular force and structural arrangement, it has certain condensed matter characteristics.
When it comes to color, it is often white to light yellow. This color is derived from the absorption and reflection characteristics of the molecular structure of light. The presence of chlorine atoms and amino groups affects the mode of action of light, so it presents such colors.
Its melting point is also fixed, and the specific value varies slightly due to factors such as purity, but it is roughly within a certain range. The formation of the melting point is closely related to the intermolecular forces, such as van der Waals forces, hydrogen bonds, etc., which determine the energy required to transform from solid to liquid.
As for solubility, it is extremely difficult to dissolve in water. Due to the large number of chlorine atoms in the molecular structure, the polarity of the molecule is biased towards the non-polar end, which is quite different from that of water molecules. It follows the principle of "similar miscibility", so it is difficult to dissolve in water. However, in organic solvents, such as benzene, toluene, dichloromethane, etc., there is a certain solubility, because the polarity of organic solvents is more compatible with the compound, and the intermolecular forces are conducive to their mixing.
Its density is higher than that of water, because the mass of chlorine atoms in the molecule increases the mass of the substance per unit volume, so the density is higher.
The physical properties of 1-amino-2,3,4,5,6-pentachlorobenzene are determined by its molecular structure, and these properties have a crucial impact on its behavior in various environments and chemical reactions.
What are the chemical properties of 1 - amino - 2, 3, 4, 5, 6 - pentachloro - benzene
1 + -Amino-2,3,4,5,6-pentachlorobenzene, this substance is one of the organic halides. Its chemical properties are unique and have the following numbers:
- ** High stability **: Because of its strong carbon-chlorine bond energy in the molecule, and the electronic effect of the chlorine atom stabilizes the molecular structure, the chemical stability is quite good. Under normal temperature and pressure, it is not easy to react with common water, oxygen, etc. However, in the presence of high temperature, strong light or specific catalysts, the stability may change.
- ** Lipophilicity is significant **: The chlorine atom is highly electronegative, causing the molecule to have a certain polarity. However, the symmetry of the overall structure makes its lipophilicity prominent. This property makes it easily soluble in organic solvents, such as benzene, toluene, etc., and easy to accumulate in adipose tissue in the environment, which is of great significance to bioaccumulation and ecotoxicity.
- * Reactive activity specificity **: The presence of amino groups gives it a certain reactivity. Amino groups can participate in a variety of reactions, such as salt-forming reactions with acids to generate corresponding salts. At the same time, under appropriate conditions, they can also participate in nucleophilic substitution reactions. Chlorine atoms can be replaced by other nucleophilic reagents to form new organic compounds.
- ** Weakly acidic or weakly basic **: Amino groups can embody certain alkalinity under specific conditions and can bind protons. Although its alkalinity is weaker than that of common inorganic bases, in organic reaction systems, this basic property can affect the reaction process and direction.
- ** Photochemical reactivity **: When irradiated by light, the electrons in the molecule can obtain energy to jump to the excited state, causing the carbon-chlorine bond to break, and photolysis occurs to generate chlorine-containing radicals and other decomposition products. This photochemical reaction plays a key role in the degradation and transformation of this substance in the environment.
- ** High stability **: Because of its strong carbon-chlorine bond energy in the molecule, and the electronic effect of the chlorine atom stabilizes the molecular structure, the chemical stability is quite good. Under normal temperature and pressure, it is not easy to react with common water, oxygen, etc. However, in the presence of high temperature, strong light or specific catalysts, the stability may change.
- ** Lipophilicity is significant **: The chlorine atom is highly electronegative, causing the molecule to have a certain polarity. However, the symmetry of the overall structure makes its lipophilicity prominent. This property makes it easily soluble in organic solvents, such as benzene, toluene, etc., and easy to accumulate in adipose tissue in the environment, which is of great significance to bioaccumulation and ecotoxicity.
- * Reactive activity specificity **: The presence of amino groups gives it a certain reactivity. Amino groups can participate in a variety of reactions, such as salt-forming reactions with acids to generate corresponding salts. At the same time, under appropriate conditions, they can also participate in nucleophilic substitution reactions. Chlorine atoms can be replaced by other nucleophilic reagents to form new organic compounds.
- ** Weakly acidic or weakly basic **: Amino groups can embody certain alkalinity under specific conditions and can bind protons. Although its alkalinity is weaker than that of common inorganic bases, in organic reaction systems, this basic property can affect the reaction process and direction.
- ** Photochemical reactivity **: When irradiated by light, the electrons in the molecule can obtain energy to jump to the excited state, causing the carbon-chlorine bond to break, and photolysis occurs to generate chlorine-containing radicals and other decomposition products. This photochemical reaction plays a key role in the degradation and transformation of this substance in the environment.
Scan to WhatsApp
