Linshang Chemical
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2,5-Dihydroxy-1-Chlorobenzene
Linshang Chemical
|
HS Code |
699593 |
| Chemical Formula | C6H4Cl(OH)2 |
| Molar Mass | 146.55 g/mol |
| Appearance | Solid |
| Odor | Unknown |
| Melting Point | Unknown |
| Boiling Point | Unknown |
| Solubility In Water | Unknown |
| Solubility In Organic Solvents | Unknown |
| Density | Unknown |
| Acidity Pka | Unknown |
As an accredited 2,5-Dihydroxy-1-Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,5 - dihydroxy - 1 - chlorobenzene packaged in a sealed plastic container. |
| Storage | 2,5 - Dihydroxy - 1 - chlorobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from sources of heat, ignition, and oxidizing agents. Store in a tightly closed container, preferably made of corrosion - resistant material. Label the container clearly. This helps prevent decomposition, potential reactions, and ensures safe storage over time. |
| Shipping | 2,5 - dihydroxy - 1 - chlorobenzene should be shipped in well - sealed, corrosion - resistant containers. Ensure proper labeling indicating its chemical nature. Ship via methods compliant with hazardous chemical transport regulations to prevent spills and ensure safety. |
Competitive 2,5-Dihydroxy-1-Chlorobenzene 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.
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Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 2,5-Dihydroxy-1-Chlorobenzene in China?
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As a leading 2,5-Dihydroxy-1-Chlorobenzene 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 2,5-dihydroxy-1-chlorobenzene?
The main use of dithio-1 -cyanonaphthalene is particularly important. Although this substance is not directly described in "Tiangong Kaiwu", its use can be explained in terms of chemical reasons.
Dithio-1 -cyanonaphthalene, in the field of organic synthesis, is often a key intermediate. In organic synthesis, such as Jianguangsha, the intermediate is the cornerstone beam. With its unique structure, it contains dithio and cyano groups, both of which have active chemical properties and can lead to various chemical reactions.
Dithio, which is nucleophilic, can combine with many electrophilic reagents to form new carbon-sulfur bonds. This bond plays a crucial role in the construction of organic molecules, which can increase the complexity and diversity of molecules. Cyanyl groups are not idle. They can be converted into carboxyl groups, amino groups and other important functional groups through hydrolysis, reduction and other reactions, paving the way for the synthesis of polymers.
In the field of medicinal chemistry, dithio-1 -cyanonaphthalene may be used as the parent nucleus of lead compounds. Lead compounds, such as the journey of pharmaceutical research and development, guide the direction of new drug creation. Because of their special structure, or biological activity, they can interact with targets in organisms. After modification and optimization, they may become new drugs with outstanding efficacy and contribute to the treatment of diseases and diseases.
It can also be used in the field of materials science. After rational design and reaction, it may be introduced into polymer materials to give new properties to the materials. Such as enhancing the stability of the materials and improving their electrical or optical properties. Because of its sulfur and cyanyl content, it may affect the electron cloud distribution of the materials, which in turn affects their macroscopic properties, making the materials suitable for special needs, such as photoelectric materials, high-performance polymers, etc.
Dithio-1 -cyanonaphthalene, in the field of organic synthesis, is often a key intermediate. In organic synthesis, such as Jianguangsha, the intermediate is the cornerstone beam. With its unique structure, it contains dithio and cyano groups, both of which have active chemical properties and can lead to various chemical reactions.
Dithio, which is nucleophilic, can combine with many electrophilic reagents to form new carbon-sulfur bonds. This bond plays a crucial role in the construction of organic molecules, which can increase the complexity and diversity of molecules. Cyanyl groups are not idle. They can be converted into carboxyl groups, amino groups and other important functional groups through hydrolysis, reduction and other reactions, paving the way for the synthesis of polymers.
In the field of medicinal chemistry, dithio-1 -cyanonaphthalene may be used as the parent nucleus of lead compounds. Lead compounds, such as the journey of pharmaceutical research and development, guide the direction of new drug creation. Because of their special structure, or biological activity, they can interact with targets in organisms. After modification and optimization, they may become new drugs with outstanding efficacy and contribute to the treatment of diseases and diseases.
It can also be used in the field of materials science. After rational design and reaction, it may be introduced into polymer materials to give new properties to the materials. Such as enhancing the stability of the materials and improving their electrical or optical properties. Because of its sulfur and cyanyl content, it may affect the electron cloud distribution of the materials, which in turn affects their macroscopic properties, making the materials suitable for special needs, such as photoelectric materials, high-performance polymers, etc.
What are the physical properties of 2,5-dihydroxy-1-chlorobenzene
The physical properties of difluoromethane, also known as chlorodifluoromethane and Freon-22, are as follows:
At room temperature and pressure, difluoromethane is a colorless, almost odorless gas. The boiling point is\ (-40.8 ^ {\ circ} C\) and the freezing point is\ (-160 ^ {\ circ} C\). It is easily vaporized at room temperature and absorbs a lot of heat when vaporized. This property makes it often used as a refrigerant.
Difluoromethane has a higher density than air, about\ (3.09g/L\) (under standard conditions). It is slightly soluble in water, and at\ (25 ^ {\ circ} C\), it can dissolve about\ (0.15\) grams of dichloromethane per\ (100\) grams of water. But it can be miscible with organic solvents such as ethanol and ether in any ratio.
From the perspective of critical parameters, its critical temperature is\ (96.2 ^ {\ circ} C\), and the critical pressure is\ (4.99MPa\). When the temperature and pressure reach the critical state, dichloromethane will exhibit a special state that is neither gaseous nor liquid, and the difference between gas and liquid phases disappears.
The chemical properties of dichloromethane are relatively stable, and it is not easy to react under normal conditions. However, at high temperatures or in the presence of catalysts, it will decompose. Moreover, because it contains chlorine atoms, under ultraviolet radiation, chlorine radicals will be generated, which has a certain destructive effect on the ozone layer. With the emphasis on environmental protection, its use is gradually restricted and replaced by some more environmentally friendly refrigerants.
At room temperature and pressure, difluoromethane is a colorless, almost odorless gas. The boiling point is\ (-40.8 ^ {\ circ} C\) and the freezing point is\ (-160 ^ {\ circ} C\). It is easily vaporized at room temperature and absorbs a lot of heat when vaporized. This property makes it often used as a refrigerant.
Difluoromethane has a higher density than air, about\ (3.09g/L\) (under standard conditions). It is slightly soluble in water, and at\ (25 ^ {\ circ} C\), it can dissolve about\ (0.15\) grams of dichloromethane per\ (100\) grams of water. But it can be miscible with organic solvents such as ethanol and ether in any ratio.
From the perspective of critical parameters, its critical temperature is\ (96.2 ^ {\ circ} C\), and the critical pressure is\ (4.99MPa\). When the temperature and pressure reach the critical state, dichloromethane will exhibit a special state that is neither gaseous nor liquid, and the difference between gas and liquid phases disappears.
The chemical properties of dichloromethane are relatively stable, and it is not easy to react under normal conditions. However, at high temperatures or in the presence of catalysts, it will decompose. Moreover, because it contains chlorine atoms, under ultraviolet radiation, chlorine radicals will be generated, which has a certain destructive effect on the ozone layer. With the emphasis on environmental protection, its use is gradually restricted and replaced by some more environmentally friendly refrigerants.
What are the chemical properties of 2,5-dihydroxy-1-chlorobenzene?
The chemical properties of difluoryl-1 -chloronaphthalene are quite unique. In this compound, the introduction of difluoryl gives it a specific electronic effect. Fluorine atoms have strong electronegativity, which can change the distribution of molecular electron clouds, resulting in different chemical activities and reaction check points.
In the nucleophilic substitution reaction, the electron absorption of fluorine atoms can reduce the density of the carbon atom electron cloud connected to it, making it more vulnerable to attack by nucleophilic reagents. However, the carbon-fluorine bond connected to the fluorine atom has a higher bond energy, and under some reaction conditions, it will also hinder the cracking and substitution of the bond by the nucleophilic tester.
In the chlorine naphthalene part, the chlorine atom is also an electron-absorbing group, but the electron-absorbing ability is slightly weaker than that of the fluorine atom. In some chemical reactions, chlorine atoms can participate in the reaction as leaving groups, and new compounds can be formed by substitution reactions. At the same time, the conjugation system of naphthalene rings imparts certain stability and unique electron delocalization properties to the molecule, which affects the overall chemical properties.
In the redox reaction, difluoro-1-chloronaphthalene can exhibit different oxidation state changes according to the reaction conditions. Due to the electronegativity of fluorine and chlorine, the electron transfer path and difficulty in the molecule are different from those of ordinary aromatic compounds. In the field of organic synthesis, it can be used as an important intermediate. By rationally designing reaction paths and taking advantage of its special chemical properties, it can construct organic compounds with diverse structures, providing a key foundation for new material research and development, drug synthesis, and many other fields.
In the nucleophilic substitution reaction, the electron absorption of fluorine atoms can reduce the density of the carbon atom electron cloud connected to it, making it more vulnerable to attack by nucleophilic reagents. However, the carbon-fluorine bond connected to the fluorine atom has a higher bond energy, and under some reaction conditions, it will also hinder the cracking and substitution of the bond by the nucleophilic tester.
In the chlorine naphthalene part, the chlorine atom is also an electron-absorbing group, but the electron-absorbing ability is slightly weaker than that of the fluorine atom. In some chemical reactions, chlorine atoms can participate in the reaction as leaving groups, and new compounds can be formed by substitution reactions. At the same time, the conjugation system of naphthalene rings imparts certain stability and unique electron delocalization properties to the molecule, which affects the overall chemical properties.
In the redox reaction, difluoro-1-chloronaphthalene can exhibit different oxidation state changes according to the reaction conditions. Due to the electronegativity of fluorine and chlorine, the electron transfer path and difficulty in the molecule are different from those of ordinary aromatic compounds. In the field of organic synthesis, it can be used as an important intermediate. By rationally designing reaction paths and taking advantage of its special chemical properties, it can construct organic compounds with diverse structures, providing a key foundation for new material research and development, drug synthesis, and many other fields.
What is the production method of 2,5-dihydroxy-1-chlorobenzene?
The preparation method of 2% 2C5-difuranyl-1-bromobenzene, although the preparation method of this specific compound is not directly described in Tiangong Kaiwu, it can be deduced according to the relevant ideas of ancient chemical processes.
To make this product, the required raw materials can be prepared first. To obtain furan and bromobenzene related products, the two are key starting materials. In ancient chemical industry, the selection and purification of raw materials is extremely important, and purity is necessary to obtain good results.
For furan, it can be extracted from specific plants and refined through multiple processes. The extraction method of ancient times uses a suitable solvent and the characteristics of furan to skillfully separate it. Or between heating and condensation to make its purity gradually increase.
There is also a method for the preparation of bromobenzene. It can make benzene and bromine react under the action of suitable catalysts. Although there is no precise catalyst in ancient times, there may be something with similar functions. Use iron filings and the like to promote the reaction. During the reaction, it is necessary to control the temperature and time, observe the phenomenon, and adjust it in a timely manner.
When the raw materials of the two are ready, the reaction can be made. In a special container, mix furan and bromobenzene related reactants in an appropriate proportion. The material and size of the container are all exquisite, or they are made of ceramic or porcelain to meet the needs of the reaction. In the reaction, either heating or other conditions are applied to combine the two according to the desired chemical path to gradually form 2% 2C5-difuran-1-bromobenzene. After the reaction is completed, the pure target product is obtained by separation and purification, except for unreacted raw materials and by-products. The separation method, or filtration, distillation, etc., according to the nature of the product and impurities, selects an appropriate method to obtain 2% 2C5-difuran-1-bromobenzene.
To make this product, the required raw materials can be prepared first. To obtain furan and bromobenzene related products, the two are key starting materials. In ancient chemical industry, the selection and purification of raw materials is extremely important, and purity is necessary to obtain good results.
For furan, it can be extracted from specific plants and refined through multiple processes. The extraction method of ancient times uses a suitable solvent and the characteristics of furan to skillfully separate it. Or between heating and condensation to make its purity gradually increase.
There is also a method for the preparation of bromobenzene. It can make benzene and bromine react under the action of suitable catalysts. Although there is no precise catalyst in ancient times, there may be something with similar functions. Use iron filings and the like to promote the reaction. During the reaction, it is necessary to control the temperature and time, observe the phenomenon, and adjust it in a timely manner.
When the raw materials of the two are ready, the reaction can be made. In a special container, mix furan and bromobenzene related reactants in an appropriate proportion. The material and size of the container are all exquisite, or they are made of ceramic or porcelain to meet the needs of the reaction. In the reaction, either heating or other conditions are applied to combine the two according to the desired chemical path to gradually form 2% 2C5-difuran-1-bromobenzene. After the reaction is completed, the pure target product is obtained by separation and purification, except for unreacted raw materials and by-products. The separation method, or filtration, distillation, etc., according to the nature of the product and impurities, selects an appropriate method to obtain 2% 2C5-difuran-1-bromobenzene.
What are the precautions for storing and transporting 2,5-dihydroxy-1-chlorobenzene?
Difluorodichloromethane, also known as Freon-12, does have many things to pay attention to during storage and transportation.
When storing, the first choice of environment. It must be placed in a cool and ventilated warehouse, away from fire and heat sources. This is because of its flammability, it can cause combustion and explosion in case of open flame and high heat. The temperature of the warehouse should not exceed 30 ° C, and the relative humidity should not exceed 80%. If the temperature is too high, it will cause its pressure to increase, and there is a risk of rupture and explosion of the container; if the humidity is too high, it may cause rust and corrosion of the container, which will damage the sealing.
Furthermore, storage needs to be classified, and it must not be mixed with oxidants, acids, alkalis, etc. Because of its active chemical properties, contact with these substances, or severe chemical reactions, resulting in danger.
In terms of transportation, vehicles must meet relevant safety standards. Before transportation, ensure that the container is well sealed and there is no risk of leakage. During transportation, it should be protected from exposure to the sun, rain, and high temperature. When driving, sharp brakes and sharp turns should be avoided to prevent the container from being damaged by collision.
When loading and unloading, the operation should also be cautious. It should be handled lightly, and it is strictly forbidden to drop or hit, so as not to damage the container. Operators need to wear appropriate protective equipment to prevent inadvertent contact and endanger health.
In short, when storing and transporting dichloromethane, there are strict requirements for the environment, operating standards, etc. A little carelessness can lead to safety accidents, which cannot be ignored.
When storing, the first choice of environment. It must be placed in a cool and ventilated warehouse, away from fire and heat sources. This is because of its flammability, it can cause combustion and explosion in case of open flame and high heat. The temperature of the warehouse should not exceed 30 ° C, and the relative humidity should not exceed 80%. If the temperature is too high, it will cause its pressure to increase, and there is a risk of rupture and explosion of the container; if the humidity is too high, it may cause rust and corrosion of the container, which will damage the sealing.
Furthermore, storage needs to be classified, and it must not be mixed with oxidants, acids, alkalis, etc. Because of its active chemical properties, contact with these substances, or severe chemical reactions, resulting in danger.
In terms of transportation, vehicles must meet relevant safety standards. Before transportation, ensure that the container is well sealed and there is no risk of leakage. During transportation, it should be protected from exposure to the sun, rain, and high temperature. When driving, sharp brakes and sharp turns should be avoided to prevent the container from being damaged by collision.
When loading and unloading, the operation should also be cautious. It should be handled lightly, and it is strictly forbidden to drop or hit, so as not to damage the container. Operators need to wear appropriate protective equipment to prevent inadvertent contact and endanger health.
In short, when storing and transporting dichloromethane, there are strict requirements for the environment, operating standards, etc. A little carelessness can lead to safety accidents, which cannot be ignored.
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