Linshang Chemical
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3,5-Dichloronitrobenzene
Linshang Chemical
|
HS Code |
399519 |
| Chemical Formula | C6H3Cl2NO2 |
| Molar Mass | 192.00 g/mol |
| Appearance | Yellow - green solid |
| Odor | Pungent odor |
| Melting Point | 57 - 59 °C |
| Boiling Point | 276 - 278 °C |
| Density | 1.625 g/cm³ (at 20 °C) |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in benzene, toluene, xylene, etc. |
| Vapor Pressure | Low vapor pressure |
As an accredited 3,5-Dichloronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle of 3,5 - dichloronitrobenzene with tight - sealed chemical - resistant packaging. |
| Storage | 3,5 - dichloronitrobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from sources of heat, ignition, and incompatible substances like strong oxidizing agents. Store in tightly - sealed containers to prevent leakage. Label storage areas clearly to ensure proper handling and to avoid potential safety hazards. |
| Shipping | 3,5 - Dichloronitrobenzene should be shipped in tightly - sealed containers, compliant with hazardous chemical regulations. Ensure proper labeling. Transport by approved carriers, taking precautions against spills and environmental exposure. |
Competitive 3,5-Dichloronitrobenzene 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 3,5-Dichloronitrobenzene in China?
As a trusted 3,5-Dichloronitrobenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
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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 3,5-Dichloronitrobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the main uses of 3,5-dichloronitrobenzene?
3,5-Dihydroxybenzyl is an important organic synthesis intermediate, which is widely used in the fields of medicine, pesticides, materials and so on. The following describes its main uses in classical Chinese:
In the field of medicine, this group is very important. Many drug molecules contain 3,5-dihydroxybenzyl structures, which can participate in the regulation of human physiological processes and show the effect of treating diseases due to their unique chemical properties and biological activities. For example, some anti-tumor drugs, by binding 3,5-dihydroxybenzyl to specific targets of tumor cells, block the signal pathway of tumor cell growth and proliferation, and inhibit tumor development. In the treatment of cardiovascular diseases, it can regulate blood lipids, improve vascular endothelial function, and achieve the prevention and treatment of cardiovascular diseases.
In the field of pesticides, 3,5-dihydroxybenzyl also has important applications. Pesticides synthesized from it are highly efficient, low toxic and environmentally friendly. Insecticides can be prepared, which can specifically bind to the target of action in insects by their special structure, interfere with the normal physiological activities of insects, and achieve the purpose of insecticide. It has a good control effect on crop pests such as aphids and borers, and has little impact on the environment and non-target organisms, which is beneficial to the sustainable development of agriculture.
In the field of materials, 3,5-dihydroxybenzyl can be used to prepare special polymer materials. Because it contains active hydroxyl groups, it can participate in the polymerization reaction and endow the material with special properties. For example, the preparation of high-performance engineering plastics can improve the mechanical properties, thermal stability and chemical stability of materials, and is widely used in high-end fields such as aerospace and automobile manufacturing. It can also be used to prepare functional coatings to enhance coating adhesion, corrosion resistance and oxidation resistance, and prolong material service life.
In the field of medicine, this group is very important. Many drug molecules contain 3,5-dihydroxybenzyl structures, which can participate in the regulation of human physiological processes and show the effect of treating diseases due to their unique chemical properties and biological activities. For example, some anti-tumor drugs, by binding 3,5-dihydroxybenzyl to specific targets of tumor cells, block the signal pathway of tumor cell growth and proliferation, and inhibit tumor development. In the treatment of cardiovascular diseases, it can regulate blood lipids, improve vascular endothelial function, and achieve the prevention and treatment of cardiovascular diseases.
In the field of pesticides, 3,5-dihydroxybenzyl also has important applications. Pesticides synthesized from it are highly efficient, low toxic and environmentally friendly. Insecticides can be prepared, which can specifically bind to the target of action in insects by their special structure, interfere with the normal physiological activities of insects, and achieve the purpose of insecticide. It has a good control effect on crop pests such as aphids and borers, and has little impact on the environment and non-target organisms, which is beneficial to the sustainable development of agriculture.
In the field of materials, 3,5-dihydroxybenzyl can be used to prepare special polymer materials. Because it contains active hydroxyl groups, it can participate in the polymerization reaction and endow the material with special properties. For example, the preparation of high-performance engineering plastics can improve the mechanical properties, thermal stability and chemical stability of materials, and is widely used in high-end fields such as aerospace and automobile manufacturing. It can also be used to prepare functional coatings to enhance coating adhesion, corrosion resistance and oxidation resistance, and prolong material service life.
What are the physical properties of 3,5-dichloronitrobenzene?
3,5-Dihydroxyphenylacetone, this substance is an organic compound. Its physical properties are quite unique, and it has important research and application value.
Looking at its properties, it is mostly white to light yellow crystalline powder under normal conditions, with fine texture. Its melting point is about 140-143 ° C. Near this temperature, the substance will gradually melt from solid to liquid state. This property can be used as an important basis in the identification and purification process.
In terms of solubility, it is slightly soluble in water, but can be better dissolved in organic solvents such as ethanol and ether. It has limited solubility in water, and although it contains hydroxyl groups in its molecular structure, it has a certain hydrophilicity, but the hydrophobicity of the overall structure is still dominant; while it has good solubility in ethanol and ether, because these organic solvents can form suitable interactions with the molecules of the substance, such as van der Waals force, hydrogen bond, etc., to promote its dissolution.
In addition, the substance also has certain stability. Under normal conditions, it is properly stored in a dry and cool place, and it is not easy to undergo obvious chemical changes. When encountering strong acids, strong bases or strong oxidants, its molecular structure may be affected, triggering chemical reactions and causing changes in properties. This requires that during storage and use, care should be taken to avoid contact with such substances. Overall, the physical properties of 3,5-dihydroxyphenylacetone lay the foundation for its application in many fields, such as organic synthesis, drug development, etc., which have attracted much attention and utilization due to their unique properties.
Looking at its properties, it is mostly white to light yellow crystalline powder under normal conditions, with fine texture. Its melting point is about 140-143 ° C. Near this temperature, the substance will gradually melt from solid to liquid state. This property can be used as an important basis in the identification and purification process.
In terms of solubility, it is slightly soluble in water, but can be better dissolved in organic solvents such as ethanol and ether. It has limited solubility in water, and although it contains hydroxyl groups in its molecular structure, it has a certain hydrophilicity, but the hydrophobicity of the overall structure is still dominant; while it has good solubility in ethanol and ether, because these organic solvents can form suitable interactions with the molecules of the substance, such as van der Waals force, hydrogen bond, etc., to promote its dissolution.
In addition, the substance also has certain stability. Under normal conditions, it is properly stored in a dry and cool place, and it is not easy to undergo obvious chemical changes. When encountering strong acids, strong bases or strong oxidants, its molecular structure may be affected, triggering chemical reactions and causing changes in properties. This requires that during storage and use, care should be taken to avoid contact with such substances. Overall, the physical properties of 3,5-dihydroxyphenylacetone lay the foundation for its application in many fields, such as organic synthesis, drug development, etc., which have attracted much attention and utilization due to their unique properties.
What are the chemical properties of 3,5-dichloronitrobenzene?
3% 2C5 -dihydroxybenzaldehyde, this is an organic compound. It has unique chemical properties, let me tell you in detail.
Looking at its structure, there are dihydroxy and monoaldehyde groups attached to the benzene ring, and this special structure gives it diversity. In terms of physical properties, it is usually a crystalline solid with a certain melting point and is soluble in specific organic solvents.
Chemical properties, aldehyde groups are active functional groups, with reducing properties, and can react with many oxidants, such as Torun reagent and Feilin reagent, to generate corresponding carboxylic acids. This reaction is quite important and is often used for qualitative detection of aldehyde groups.
Furthermore, the hydroxyl group is also an important activity checking point. First, esterification can occur, and ester compounds can be formed with carboxylic acids or anhydrides under the action of catalysts. Second, due to the presence of hydroxyl groups, the electron cloud density of the benzene ring increases, making the benzene ring more prone to electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. And the localization effect of hydroxyl groups makes the substituents mainly enter the adjacent and para-position of the hydroxyl group.
In addition, hydrogen bonds can be formed between molecules and molecules. The existence of intramolecular hydrogen bonds affects its physical properties, such as melting point and boiling point; intermolecular hydrogen bonds affect its solubility and aggregation state in solvents.
3% 2C5 -dihydroxybenzaldehyde is rich in chemical properties and has important uses in organic synthesis, medicinal chemistry and other fields. It can be used as a key intermediate in the preparation of many organic compounds.
Looking at its structure, there are dihydroxy and monoaldehyde groups attached to the benzene ring, and this special structure gives it diversity. In terms of physical properties, it is usually a crystalline solid with a certain melting point and is soluble in specific organic solvents.
Chemical properties, aldehyde groups are active functional groups, with reducing properties, and can react with many oxidants, such as Torun reagent and Feilin reagent, to generate corresponding carboxylic acids. This reaction is quite important and is often used for qualitative detection of aldehyde groups.
Furthermore, the hydroxyl group is also an important activity checking point. First, esterification can occur, and ester compounds can be formed with carboxylic acids or anhydrides under the action of catalysts. Second, due to the presence of hydroxyl groups, the electron cloud density of the benzene ring increases, making the benzene ring more prone to electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. And the localization effect of hydroxyl groups makes the substituents mainly enter the adjacent and para-position of the hydroxyl group.
In addition, hydrogen bonds can be formed between molecules and molecules. The existence of intramolecular hydrogen bonds affects its physical properties, such as melting point and boiling point; intermolecular hydrogen bonds affect its solubility and aggregation state in solvents.
3% 2C5 -dihydroxybenzaldehyde is rich in chemical properties and has important uses in organic synthesis, medicinal chemistry and other fields. It can be used as a key intermediate in the preparation of many organic compounds.
What is the production method of 3,5-dichloronitrobenzene?
The preparation method of 3,2,5-dihydroxybenzaldehyde is made by many delicate methods. One method is to use a specific phenolic compound as the starting material, and to obtain it through several reaction steps by means of chemical synthesis.
First take a suitable phenol and make it substitution with a specific reagent under the conditions of suitable temperature, pressure and suitable catalyst. This reaction aims to precisely introduce the corresponding group at a specific position of the phenol to lay the foundation for the subsequent generation of dihydroxybenzaldehyde. During the reaction, close attention must be paid to the temperature, pressure and catalyst dosage. A slight difference may cause deviation in the reaction, or reduce the yield, or obtain unexpected products.
After the substitution reaction is completed, the product needs to go through a fine separation and purification process to remove the unreacted raw materials and by-products. This step is often carried out by distillation, extraction, recrystallization, etc., taking advantage of the physical and chemical properties of different substances to purify the target product.
Then, the purified product is further oxidized, and in a cleverly regulated reaction environment, the specific group is converted into an aldehyde group, and the final product is 3,2,5-dihydroxybenzaldehyde. This oxidation reaction also requires strict control of the reaction conditions, such as the type and amount of oxidizing agent, reaction temperature and time, which all have a significant impact on the purity and yield of the product.
In addition, there are other production methods, either starting from different starting materials or using different reaction paths, but they all need to follow chemical principles, carefully design reaction steps, and operate rigorously in order to produce 3,2,5-dihydroxybenzaldehyde efficiently and with high quality.
First take a suitable phenol and make it substitution with a specific reagent under the conditions of suitable temperature, pressure and suitable catalyst. This reaction aims to precisely introduce the corresponding group at a specific position of the phenol to lay the foundation for the subsequent generation of dihydroxybenzaldehyde. During the reaction, close attention must be paid to the temperature, pressure and catalyst dosage. A slight difference may cause deviation in the reaction, or reduce the yield, or obtain unexpected products.
After the substitution reaction is completed, the product needs to go through a fine separation and purification process to remove the unreacted raw materials and by-products. This step is often carried out by distillation, extraction, recrystallization, etc., taking advantage of the physical and chemical properties of different substances to purify the target product.
Then, the purified product is further oxidized, and in a cleverly regulated reaction environment, the specific group is converted into an aldehyde group, and the final product is 3,2,5-dihydroxybenzaldehyde. This oxidation reaction also requires strict control of the reaction conditions, such as the type and amount of oxidizing agent, reaction temperature and time, which all have a significant impact on the purity and yield of the product.
In addition, there are other production methods, either starting from different starting materials or using different reaction paths, but they all need to follow chemical principles, carefully design reaction steps, and operate rigorously in order to produce 3,2,5-dihydroxybenzaldehyde efficiently and with high quality.
What are the precautions for using 3,5-dichloronitrobenzene?
3,5-Dihydroxyphenyl should pay attention to the following things during use:
First, it is related to its stability. 3,5-Dihydroxyphenyl is active and easy to be oxidized in the air, causing its color to darken, affecting quality and performance. Therefore, when storing, it should be stored in a sealed container and placed in a cool, dry and dark place to prevent excessive contact with air and slow down the oxidation process.
Second, discuss solubility. This substance has different solubility in different solvents. It has poor solubility in water, but slightly better solubility in some organic solvents such as ethanol and acetone. When using, an appropriate solvent should be selected to dissolve according to specific needs to ensure that it can be evenly dispersed in the system and play its due role. If the solvent is not selected properly, or the dissolution is insufficient, it will affect the reaction or product quality.
Third, pay attention to its reactivity. 3,5-Dihydroxyphenyl has high hydroxyl activity and is easy to participate in many chemical reactions, such as esterification, etherification, etc. In actual use, it is necessary to precisely control the reaction conditions, such as temperature, pH, reaction time, etc. If the temperature is too high, or the reaction is too violent, it is difficult to control the reaction process, and unnecessary by-products are generated; pH discomfort will also affect the reaction rate and product purity.
Fourth, it is related to safety. Although there is no definitive evidence that it is highly toxic, there are many latent risks of chemicals. When operating, be sure to take necessary protective measures, such as laboratory clothes, gloves and goggles, to prevent it from contacting the skin and eyes. In case of accidental contact, rinse with plenty of water immediately, and seek medical treatment if necessary.
Fifth, consider the compatibility with other substances. When using 3,5-dihydroxyphenyl in a complex system, consider its compatibility with other components in the system. Or interact with certain substances, changing the physical and chemical properties of the system and affecting the overall performance. Before use, it is advisable to evaluate its compatibility through experiments to avoid adverse effects.
First, it is related to its stability. 3,5-Dihydroxyphenyl is active and easy to be oxidized in the air, causing its color to darken, affecting quality and performance. Therefore, when storing, it should be stored in a sealed container and placed in a cool, dry and dark place to prevent excessive contact with air and slow down the oxidation process.
Second, discuss solubility. This substance has different solubility in different solvents. It has poor solubility in water, but slightly better solubility in some organic solvents such as ethanol and acetone. When using, an appropriate solvent should be selected to dissolve according to specific needs to ensure that it can be evenly dispersed in the system and play its due role. If the solvent is not selected properly, or the dissolution is insufficient, it will affect the reaction or product quality.
Third, pay attention to its reactivity. 3,5-Dihydroxyphenyl has high hydroxyl activity and is easy to participate in many chemical reactions, such as esterification, etherification, etc. In actual use, it is necessary to precisely control the reaction conditions, such as temperature, pH, reaction time, etc. If the temperature is too high, or the reaction is too violent, it is difficult to control the reaction process, and unnecessary by-products are generated; pH discomfort will also affect the reaction rate and product purity.
Fourth, it is related to safety. Although there is no definitive evidence that it is highly toxic, there are many latent risks of chemicals. When operating, be sure to take necessary protective measures, such as laboratory clothes, gloves and goggles, to prevent it from contacting the skin and eyes. In case of accidental contact, rinse with plenty of water immediately, and seek medical treatment if necessary.
Fifth, consider the compatibility with other substances. When using 3,5-dihydroxyphenyl in a complex system, consider its compatibility with other components in the system. Or interact with certain substances, changing the physical and chemical properties of the system and affecting the overall performance. Before use, it is advisable to evaluate its compatibility through experiments to avoid adverse effects.
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