Linshang Chemical
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2,6-Dinitro-1,4-Dichlorobenzene
Linshang Chemical
|
HS Code |
219482 |
| Chemical Formula | C6H2Cl2N2O4 |
| Molecular Weight | 249.00 |
| Appearance | Yellow solid |
| Melting Point | 167 - 169 °C |
| Boiling Point | Decomposes |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like benzene, toluene |
| Density | 1.70 g/cm³ |
| Vapor Pressure | Low |
| Flash Point | Non - flammable |
| Stability | Stable under normal conditions, but may react with strong oxidizing agents |
As an accredited 2,6-Dinitro-1,4-Dichlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2,6 - dinitro - 1,4 - dichlorobenzene packaged in a sealed chemical - grade bottle. |
| Storage | 2,6 - dinitro - 1,4 - dichlorobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly closed container to prevent vapor leakage. Store it separately from oxidizing agents, reducing agents, and combustibles to avoid potential reactions. Adhere to safety regulations during storage. |
| Shipping | 2,6 - dinitro - 1,4 - dichlorobenzene is a hazardous chemical. It should be shipped in accordance with strict regulations, using properly labeled, sealed containers to prevent leakage and ensure safe transportation during transit. |
Competitive 2,6-Dinitro-1,4-Dichlorobenzene 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 2,6-Dinitro-1,4-Dichlorobenzene in China?
As a trusted 2,6-Dinitro-1,4-Dichlorobenzene 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 2,6-Dinitro-1,4-Dichlorobenzene 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 use of 2,6-dinitro-1,4-dichlorobenzene?
2% 2C6-diamino-1% 2C4-dihydroxynaphthalene is one of the organic compounds. It has a wide range of uses and is often a key raw material for the preparation of a variety of brightly colored dyes in the dye industry. Due to its unique chemical structure, it can undergo a series of chemical reactions to derive many dye products with specific colors and properties, which can impart lasting and brilliant colors to fabrics, leather and other materials.
In the field of medicinal chemistry, it is also of great significance. Due to its chemical properties, it may participate in the construction of some drug molecules, providing a potential chemical framework for the development of new drugs. Scientists hope to develop compounds with specific pharmacological activities for the treatment and prevention of diseases by modifying and modifying their structures.
In addition, in the field of materials science, 2% 2C6-diamino-1% 2C4-dihydroxynaphthalene can be used as a basic unit for constructing high-performance materials. After rational design and synthesis, materials with special electrical, optical or mechanical properties can be prepared, such as used in electronic devices, optical sensors and other fields, to help improve the performance and function of related devices.
With its unique chemical structure, this compound has shown important application value in dyes, medicine, materials and many other fields, providing indispensable chemical support for the development of various fields.
In the field of medicinal chemistry, it is also of great significance. Due to its chemical properties, it may participate in the construction of some drug molecules, providing a potential chemical framework for the development of new drugs. Scientists hope to develop compounds with specific pharmacological activities for the treatment and prevention of diseases by modifying and modifying their structures.
In addition, in the field of materials science, 2% 2C6-diamino-1% 2C4-dihydroxynaphthalene can be used as a basic unit for constructing high-performance materials. After rational design and synthesis, materials with special electrical, optical or mechanical properties can be prepared, such as used in electronic devices, optical sensors and other fields, to help improve the performance and function of related devices.
With its unique chemical structure, this compound has shown important application value in dyes, medicine, materials and many other fields, providing indispensable chemical support for the development of various fields.
What are the physical and chemical properties of 2,6-dinitro-1,4-dichlorobenzene?
The physicochemical properties of 2% 2C6-diamino-1% 2C4-dihydronaphthalene are worth in-depth investigation. The color state of this substance, at room temperature, is often white to light yellow crystalline powder, just like the accumulation of fine snow, which is quite delicate.
When it comes to solubility, it is slightly soluble in organic solvents, such as ethanol, acetone, etc., but it is very little soluble in water. It is like being in the world of water, but it is unique and difficult to blend with water.
The melting point is about a specific range, which is its inherent characteristic, just like the human nature, and it is not easy to change. The number of its melting point is one of the important markers for the identification of this substance, just like a human fingerprint, which is unique.
In terms of stability, in the conventional temperature and humidity environment, it can still maintain relative stability, just like a calm person, not moved by the waves of the outside world. However, if placed in a place of high temperature, high humidity or strong light, it is like a fragile flower, prone to decomposition or deterioration, and its chemical structure is also changed.
As for its chemical activity, it contains two amino groups and dihydronaphthalene structures, giving it unique reactivity. Amino groups are nucleophilic, just like brave warriors, easy to react with electrophilic reagents, such as acylation, alkylation, etc., resulting in many derivatives with different characteristics. The structure of dihydronaphthalene also allows it to participate in a variety of organic reactions, adding a strong touch to the field of organic synthesis. These physical and chemical properties are of crucial significance in many fields such as chemical industry and medicine, just as the cornerstone is indispensable in a tall building.
When it comes to solubility, it is slightly soluble in organic solvents, such as ethanol, acetone, etc., but it is very little soluble in water. It is like being in the world of water, but it is unique and difficult to blend with water.
The melting point is about a specific range, which is its inherent characteristic, just like the human nature, and it is not easy to change. The number of its melting point is one of the important markers for the identification of this substance, just like a human fingerprint, which is unique.
In terms of stability, in the conventional temperature and humidity environment, it can still maintain relative stability, just like a calm person, not moved by the waves of the outside world. However, if placed in a place of high temperature, high humidity or strong light, it is like a fragile flower, prone to decomposition or deterioration, and its chemical structure is also changed.
As for its chemical activity, it contains two amino groups and dihydronaphthalene structures, giving it unique reactivity. Amino groups are nucleophilic, just like brave warriors, easy to react with electrophilic reagents, such as acylation, alkylation, etc., resulting in many derivatives with different characteristics. The structure of dihydronaphthalene also allows it to participate in a variety of organic reactions, adding a strong touch to the field of organic synthesis. These physical and chemical properties are of crucial significance in many fields such as chemical industry and medicine, just as the cornerstone is indispensable in a tall building.
What is the production method of 2,6-dinitro-1,4-dichlorobenzene?
The preparation of 2% 2C6-dinitro-1% 2C4-dihydroxybenzene is a delicate chemical technique. If Gu Zhifang's family talks about this, or goes:
To make this thing, first take appropriate raw materials. With benzene as the base, its properties are stable, but through ingenious methods, it can be transformed into new substances. Before the benzene ring, nitro groups are introduced. For the entry of nitro groups, suitable reagents and conditions need to be selected. Often a mixed acid of concentrated nitric acid and concentrated sulfuric acid is used as a nitrate inducer. This mixed acid has strong oxidizing and nitrifying properties. At a specific temperature and duration, it is co-placed with benzene, and the temperature control is accurate. Do not overplay. Due to high temperature, the reaction is easy to get out of control, resulting in impure or unexpected changes in the product. After this operation, nitro groups are gradually added to the benzene ring to obtain benzene derivatives containing nitro groups.
Then, the hydroxyl group is introduced at the predetermined position. This step requires other methods, or hydrolysis and substitution techniques. Appropriate reagents should be used to respond to the benzene derivatives containing nitro groups. During hydrolysis, mild conditions are selected to gradually change the groups next to the nitro group to hydroxyl groups. This process also needs to be carefully controlled. The choice of solvent, the temperature and duration of the reaction are all related to the quality and quantity of the product. After many debugging, the nitro group is at 2,6 and the hydroxyl group is at 1,4, and the final result is 2,6-dinitro-1,4-dihydroxybenzene.
The delicacy of this lies in the grasp of the elements of the reaction, which is completely different, or leads to completely different results. Ancient alchemy and pharmaceuticals also emphasized the matching of heat and materials, and the same is true. Although the chemical method has advanced with the world, it is rigorous and delicate, and it is the same in ancient and modern times.
To make this thing, first take appropriate raw materials. With benzene as the base, its properties are stable, but through ingenious methods, it can be transformed into new substances. Before the benzene ring, nitro groups are introduced. For the entry of nitro groups, suitable reagents and conditions need to be selected. Often a mixed acid of concentrated nitric acid and concentrated sulfuric acid is used as a nitrate inducer. This mixed acid has strong oxidizing and nitrifying properties. At a specific temperature and duration, it is co-placed with benzene, and the temperature control is accurate. Do not overplay. Due to high temperature, the reaction is easy to get out of control, resulting in impure or unexpected changes in the product. After this operation, nitro groups are gradually added to the benzene ring to obtain benzene derivatives containing nitro groups.
Then, the hydroxyl group is introduced at the predetermined position. This step requires other methods, or hydrolysis and substitution techniques. Appropriate reagents should be used to respond to the benzene derivatives containing nitro groups. During hydrolysis, mild conditions are selected to gradually change the groups next to the nitro group to hydroxyl groups. This process also needs to be carefully controlled. The choice of solvent, the temperature and duration of the reaction are all related to the quality and quantity of the product. After many debugging, the nitro group is at 2,6 and the hydroxyl group is at 1,4, and the final result is 2,6-dinitro-1,4-dihydroxybenzene.
The delicacy of this lies in the grasp of the elements of the reaction, which is completely different, or leads to completely different results. Ancient alchemy and pharmaceuticals also emphasized the matching of heat and materials, and the same is true. Although the chemical method has advanced with the world, it is rigorous and delicate, and it is the same in ancient and modern times.
What are the environmental effects of 2,6-dinitro-1,4-dichlorobenzene?
2% 2C6-diamino-1% 2C4-dihydroxyanthraquinone, this substance has a very important impact on the environment. Its color is dark and has specific chemical properties, and there are many variables in water and soil.
In water bodies, if this substance flows in, it may cause water quality discoloration. Because of its certain solubility, it may affect the survival of aquatic organisms. Aquatic plants may be blocked by light, photosynthesis is disturbed, and their growth situation is poor. Aquatic animals such as fish may accumulate in their bodies due to ingestion of this substance, affecting physiological functions, and even causing diseases in reproductive and immune systems.
As for soil, it may absorb this substance and change the chemical properties of soil. Soil microbial communities may be impacted, reducing the activity of some beneficial microorganisms, affecting soil nutrient cycling and transformation. Over time, soil fertility may decrease, affecting plant root absorption of nutrients, resulting in plant growth inhibition and crop yield reduction.
And 2% 2C6-diamino-1% 2C4-dihydroxyanthraquinone degrades slowly in the environment and can remain for a long time. Its potential harm will gradually accumulate over time. If there is a food chain in the surrounding environment, this substance may be transmitted and enriched along the food chain, eventually endangering higher trophic organisms, including humans. If people ingest food containing this substance, it may cause chronic damage to health, such as organ function damage, gene mutation and other risks. Therefore, its impact on the environment should be closely monitored to prevent problems before they occur.
In water bodies, if this substance flows in, it may cause water quality discoloration. Because of its certain solubility, it may affect the survival of aquatic organisms. Aquatic plants may be blocked by light, photosynthesis is disturbed, and their growth situation is poor. Aquatic animals such as fish may accumulate in their bodies due to ingestion of this substance, affecting physiological functions, and even causing diseases in reproductive and immune systems.
As for soil, it may absorb this substance and change the chemical properties of soil. Soil microbial communities may be impacted, reducing the activity of some beneficial microorganisms, affecting soil nutrient cycling and transformation. Over time, soil fertility may decrease, affecting plant root absorption of nutrients, resulting in plant growth inhibition and crop yield reduction.
And 2% 2C6-diamino-1% 2C4-dihydroxyanthraquinone degrades slowly in the environment and can remain for a long time. Its potential harm will gradually accumulate over time. If there is a food chain in the surrounding environment, this substance may be transmitted and enriched along the food chain, eventually endangering higher trophic organisms, including humans. If people ingest food containing this substance, it may cause chronic damage to health, such as organ function damage, gene mutation and other risks. Therefore, its impact on the environment should be closely monitored to prevent problems before they occur.
What are the safety protection measures for 2,6-dinitro-1,4-dichlorobenzene?
2% 2C6 - diamino - 1% 2C4 - dihydroxyanthraquinone. This material is dangerous. The safety protection measures are as follows:
1. Engineering control
It is suitable to operate in a well-ventilated place, and a local exhaust device needs to be installed. This is because the operation process may produce harmful gases. Good ventilation can disperse in time. The local exhaust device can be collected in a directional manner to reduce the concentration of harmful substances in the air and ensure the safety of operators.
2. Personal protective equipment
1. ** Respiratory system protection **: When the concentration in the air exceeds the standard, a self-priming filter gas mask (half mask) must be worn. When emergency rescue or evacuation, an air respirator should be worn. This is because the substance or irritate the respiratory tract, under specific conditions will be more life-threatening, suitable protective equipment can effectively block harmful substances.
2. ** Eye Protection **: Wear chemical safety glasses to prevent the substance from contacting the eyes and avoid eye irritation or damage.
3. ** Body Protection **: Wear anti-poison infiltration work clothes to prevent the skin from contacting the substance and being absorbed or irritated.
4. ** Hand Protection **: Wear rubber gloves to protect the skin of the hands from damage.
III. Storage Precautions
Store in a cool and ventilated warehouse. Keep away from fire and heat sources. It should be stored separately from oxidants, acids, and edible chemicals, and should not be mixed. Equipped with corresponding varieties and quantities of fire-fighting equipment. The storage area should be equipped with suitable materials to contain leaks. This arrangement is designed to avoid hazards caused by temperature and humidity, fire sources, and interactions between substances.
IV. Emergency treatment measures
1. ** Emergency treatment for leaks **: Isolate the leaked contaminated area and restrict access. It is recommended that emergency personnel wear dust masks (full masks) and gas suits. Collect with a clean shovel in a dry, clean, covered container and transfer to a safe place. If there is a large amount of leakage, collect it for recycling or transport it to a waste treatment site for disposal.
2. ** First Aid Measures **:
- ** Skin Contact **: Immediately remove contaminated clothing, rinse with plenty of flowing water for at least 15 minutes, and seek medical attention.
- ** Eye Contact ** Immediately lift the eyelids, rinse thoroughly with plenty of flowing water or normal saline for at least 15 minutes, and seek medical attention.
- ** Inhalation **: Quickly leave the scene to a fresh place with fresh air to keep the respiratory tract unobstructed. If breathing difficulties, give oxygen. If breathing stops, immediately perform artificial respiration and seek medical attention.
- ** Ingestion **: Drink enough warm water, induce vomiting, and seek medical attention.
1. Engineering control
It is suitable to operate in a well-ventilated place, and a local exhaust device needs to be installed. This is because the operation process may produce harmful gases. Good ventilation can disperse in time. The local exhaust device can be collected in a directional manner to reduce the concentration of harmful substances in the air and ensure the safety of operators.
2. Personal protective equipment
1. ** Respiratory system protection **: When the concentration in the air exceeds the standard, a self-priming filter gas mask (half mask) must be worn. When emergency rescue or evacuation, an air respirator should be worn. This is because the substance or irritate the respiratory tract, under specific conditions will be more life-threatening, suitable protective equipment can effectively block harmful substances.
2. ** Eye Protection **: Wear chemical safety glasses to prevent the substance from contacting the eyes and avoid eye irritation or damage.
3. ** Body Protection **: Wear anti-poison infiltration work clothes to prevent the skin from contacting the substance and being absorbed or irritated.
4. ** Hand Protection **: Wear rubber gloves to protect the skin of the hands from damage.
III. Storage Precautions
Store in a cool and ventilated warehouse. Keep away from fire and heat sources. It should be stored separately from oxidants, acids, and edible chemicals, and should not be mixed. Equipped with corresponding varieties and quantities of fire-fighting equipment. The storage area should be equipped with suitable materials to contain leaks. This arrangement is designed to avoid hazards caused by temperature and humidity, fire sources, and interactions between substances.
IV. Emergency treatment measures
1. ** Emergency treatment for leaks **: Isolate the leaked contaminated area and restrict access. It is recommended that emergency personnel wear dust masks (full masks) and gas suits. Collect with a clean shovel in a dry, clean, covered container and transfer to a safe place. If there is a large amount of leakage, collect it for recycling or transport it to a waste treatment site for disposal.
2. ** First Aid Measures **:
- ** Skin Contact **: Immediately remove contaminated clothing, rinse with plenty of flowing water for at least 15 minutes, and seek medical attention.
- ** Eye Contact ** Immediately lift the eyelids, rinse thoroughly with plenty of flowing water or normal saline for at least 15 minutes, and seek medical attention.
- ** Inhalation **: Quickly leave the scene to a fresh place with fresh air to keep the respiratory tract unobstructed. If breathing difficulties, give oxygen. If breathing stops, immediately perform artificial respiration and seek medical attention.
- ** Ingestion **: Drink enough warm water, induce vomiting, and seek medical attention.
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