Linshang Chemical
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2,6-Dihydroxychlorobenzene
Linshang Chemical
|
HS Code |
639251 |
| Chemical Formula | C6H4Cl(OH)2 |
| Molar Mass | 158.55 g/mol |
| Appearance | White to off - white solid |
| Odor | May have a characteristic phenolic odor |
| Melting Point | Around 108 - 112 °C |
| Boiling Point | Approximately 258 - 260 °C |
| Solubility In Water | Slightly soluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
| Pka | Data for acidic phenolic hydroxyl groups relevant |
| Flash Point | Caution, flammable properties, specific value data needed |
As an accredited 2,6-Dihydroxychlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 - gram bottle packaging for 2,6 - dihydroxychlorobenzene chemical. |
| Storage | 2,6 - Dihydroxychlorobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store it in tightly - sealed containers to prevent moisture absorption and exposure to air, which could potentially lead to degradation or chemical reactions. |
| Shipping | 2,6 - Dihydroxychlorobenzene should be shipped in tightly - sealed containers, safeguarded from moisture and heat. It must comply with relevant chemical transportation regulations to ensure safe transit. |
Competitive 2,6-Dihydroxychlorobenzene 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 2,6-Dihydroxychlorobenzene in China?
As a trusted 2,6-Dihydroxychlorobenzene 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-Dihydroxychlorobenzene 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 2,6-dihydroxychlorobenzene?
Dimercaptopropanol is also a good antidote. Its main use is to treat all kinds of metal and metalloid poisoning.
In the past, in industrial production or accidents, people often came into contact with poisons such as mercury, arsenic, antimony, etc., so this medicine showed great power. Taking mercury poisoning as an example, mercury poison enters the body, messes up the internal organs, harms the nervous system, and causes all kinds of evils, such as increased mouth and saliva, swollen gums and pain, tremors in the limbs, and trance. Dimercaptopropanol has a dimercapto group in its molecule, which can be tightly bound to mercury ions to form a stable complex. This complex is easily soluble and can be excreted in urine to relieve mercury toxicity.
And if arsenic poisoning, arsenic damage cell metabolism, damage organ function, causing vomiting, abdominal pain, diarrhea, and even life-threatening. Dimercaptopropanol can also combine with arsenic to make arsenic toxic, excreted from the body, and save people in danger.
When antimony poisoning occurs, antimony disrupts the cardiovascular and nervous systems. With its special structure, dimercaptopropanol combines with antimony to save people from danger and gradually restore human body function.
Therefore, dimercaptopropanol has great effect in the field of detoxification. It is an essential medicine for solving metal and metal-like poisoning, saving countless poisoned people from water and fire, and protecting the health of life and spirits.
In the past, in industrial production or accidents, people often came into contact with poisons such as mercury, arsenic, antimony, etc., so this medicine showed great power. Taking mercury poisoning as an example, mercury poison enters the body, messes up the internal organs, harms the nervous system, and causes all kinds of evils, such as increased mouth and saliva, swollen gums and pain, tremors in the limbs, and trance. Dimercaptopropanol has a dimercapto group in its molecule, which can be tightly bound to mercury ions to form a stable complex. This complex is easily soluble and can be excreted in urine to relieve mercury toxicity.
And if arsenic poisoning, arsenic damage cell metabolism, damage organ function, causing vomiting, abdominal pain, diarrhea, and even life-threatening. Dimercaptopropanol can also combine with arsenic to make arsenic toxic, excreted from the body, and save people in danger.
When antimony poisoning occurs, antimony disrupts the cardiovascular and nervous systems. With its special structure, dimercaptopropanol combines with antimony to save people from danger and gradually restore human body function.
Therefore, dimercaptopropanol has great effect in the field of detoxification. It is an essential medicine for solving metal and metal-like poisoning, saving countless poisoned people from water and fire, and protecting the health of life and spirits.
What are the production methods of 2,6-dihydroxychlorobenzene?
The preparation method of diphenyl ethane has been used in ancient times, and it is mostly passed down according to ancient methods, supplemented by today's skills, and strives for excellence.
First, it is prepared by condensation reaction with phenol and acetone as raw materials. In the kettle, put phenol and acetone in an appropriate proportion, and use sulfuric acid, ion exchange resin, etc. as catalysts, and control the temperature moderately to make it fully react. In this process, temperature, catalyst dosage and reaction time are all key. If the temperature is too high, side reactions will increase, and the product will be impure; if the temperature is too low, the reaction rate will be slow and time-consuming. The amount of catalyst also needs to be precisely controlled, too much will increase the cost, and the subsequent separation will be complicated; too little will result in low reaction efficiency. After the reaction is completed, the product can be purified by distillation, extraction, crystallization and other steps to obtain diphenylethane.
Second, the phase transfer catalysis method is used. In this method, the addition of a phase transfer catalyst can make the reaction proceed smoothly at the two-phase interface, improving the reaction rate and selectivity. In the reaction system, except for phenol and acetone, the phase transfer catalyst can promote easier contact with the reactants and break the mass transfer limit. For example, the use of quaternary ammonium phase transfer catalysts can efficiently synthesize diphenylethane under suitable reaction conditions. After the reaction, a series of separation and purification operations are required to obtain a pure product.
Third, there is a method of using solid acid as a catalyst. Solid acid catalysts have many advantages such as easy separation, reusability, and low corrosion to equipment. A specific solid acid catalyst is placed in the reaction system to react with phenol and acetone. This process optimizes the reaction conditions, such as adjusting temperature, pressure, material ratio, etc., which can improve the yield and quality of diphenyl ethane. And due to the characteristics of solid acid catalysts, subsequent processing is simple, which can reduce environmental pollution and is in line with today's concept of green chemistry.
First, it is prepared by condensation reaction with phenol and acetone as raw materials. In the kettle, put phenol and acetone in an appropriate proportion, and use sulfuric acid, ion exchange resin, etc. as catalysts, and control the temperature moderately to make it fully react. In this process, temperature, catalyst dosage and reaction time are all key. If the temperature is too high, side reactions will increase, and the product will be impure; if the temperature is too low, the reaction rate will be slow and time-consuming. The amount of catalyst also needs to be precisely controlled, too much will increase the cost, and the subsequent separation will be complicated; too little will result in low reaction efficiency. After the reaction is completed, the product can be purified by distillation, extraction, crystallization and other steps to obtain diphenylethane.
Second, the phase transfer catalysis method is used. In this method, the addition of a phase transfer catalyst can make the reaction proceed smoothly at the two-phase interface, improving the reaction rate and selectivity. In the reaction system, except for phenol and acetone, the phase transfer catalyst can promote easier contact with the reactants and break the mass transfer limit. For example, the use of quaternary ammonium phase transfer catalysts can efficiently synthesize diphenylethane under suitable reaction conditions. After the reaction, a series of separation and purification operations are required to obtain a pure product.
Third, there is a method of using solid acid as a catalyst. Solid acid catalysts have many advantages such as easy separation, reusability, and low corrosion to equipment. A specific solid acid catalyst is placed in the reaction system to react with phenol and acetone. This process optimizes the reaction conditions, such as adjusting temperature, pressure, material ratio, etc., which can improve the yield and quality of diphenyl ethane. And due to the characteristics of solid acid catalysts, subsequent processing is simple, which can reduce environmental pollution and is in line with today's concept of green chemistry.
What is the market outlook for 2,6-dihydroxychlorobenzene?
In today's world, the market prospect of dimethylhydroxiridium is quite promising. Dimethylhydroxiridium is very useful in the field of organic synthesis and catalysis.
In the field of organic synthesis, it can provide efficient catalysis for reactions, enabling many reactions that were difficult to achieve in the past to be carried out smoothly. Taking the construction of carbon-carbon bonds as an example, with the catalysis of dimethylhydroxiridium, the yield and selectivity of the reaction can be improved under mild conditions. This property has made it favored by organic synthesis chemists, and it has been widely explored and applied in drug research and development, material preparation, etc.
As for the field of catalysis, dimethylhydroxyiridium exhibits excellent catalytic activity and stability in some important chemical reactions. For example, in some redox reactions, it can effectively reduce the activation energy of the reaction, accelerate the reaction process, and maintain good catalytic performance after the reaction, which can be recycled many times. This not only improves the efficiency of the reaction, but also fits the concept of green chemistry today, bringing potential huge benefits to industrial production.
Furthermore, with the progress of science and technology and the development of the industry, the demand for new catalytic materials is increasing day by day. As a class of compounds with great potential, dimethylhydroxyiridium is constantly emerging with new research results to expand its application range. With the increase in scientific research investment, it is expected to further explore its performance and emerge in more emerging fields. Therefore, Dimethyl Hydroxyiridium will definitely occupy an important position in the future market, and the future is promising.
In the field of organic synthesis, it can provide efficient catalysis for reactions, enabling many reactions that were difficult to achieve in the past to be carried out smoothly. Taking the construction of carbon-carbon bonds as an example, with the catalysis of dimethylhydroxiridium, the yield and selectivity of the reaction can be improved under mild conditions. This property has made it favored by organic synthesis chemists, and it has been widely explored and applied in drug research and development, material preparation, etc.
As for the field of catalysis, dimethylhydroxyiridium exhibits excellent catalytic activity and stability in some important chemical reactions. For example, in some redox reactions, it can effectively reduce the activation energy of the reaction, accelerate the reaction process, and maintain good catalytic performance after the reaction, which can be recycled many times. This not only improves the efficiency of the reaction, but also fits the concept of green chemistry today, bringing potential huge benefits to industrial production.
Furthermore, with the progress of science and technology and the development of the industry, the demand for new catalytic materials is increasing day by day. As a class of compounds with great potential, dimethylhydroxyiridium is constantly emerging with new research results to expand its application range. With the increase in scientific research investment, it is expected to further explore its performance and emerge in more emerging fields. Therefore, Dimethyl Hydroxyiridium will definitely occupy an important position in the future market, and the future is promising.
What are the physical and chemical properties of 2,6-dihydroxychlorobenzene?
Dimercaptoethylenediamine, also known as dithioethylenediamine, is a sulfur-containing organic compound. Its physical and chemical properties are unique, and it can be explained one by one.
Looking at its physical properties, it is mostly a colorless to light yellow liquid under normal conditions, with a strong special odor. Its boiling point is quite high, about 220 to 225 degrees Celsius. Due to the interaction between molecules such as hydrogen bonds, the molecules are tightly bound, and high energy is required to make them boil. The melting point is about -10 degrees Celsius, which indicates that it is in a liquid state at room temperature and exhibits good fluidity. In addition, dimercaptoethylenediamine can be miscible with water in a certain proportion. This is because the molecule contains polar groups such as amino and sulfhydryl groups, which can form hydrogen bonds with water molecules, so it has good water solubility.
In terms of its chemical properties, both the amino and sulfhydryl groups of dimercaptoethylenediamine have high reactivity. Amino groups can neutralize with acids to form corresponding salts. For example, when reacted with hydrochloric acid, dimercaptoethylenediamine hydrochloride will be formed. And sulfhydryl groups are also very active and easy to be oxidized. In air, they can be slowly oxidized to disulfide bonds, which makes them useful as reducing agents in some chemical reactions. At the same time, thiol groups can also complex with a variety of metal ions to form stable complexes. For example, with mercury ions, it can form extremely stable complexes, which are of great application value in the detection and removal of heavy metal ions.
Furthermore, the spatial location distribution of two mercapto groups and two amino groups of dimercaptoethylenediamine makes it possible to act as a polydentate ligand in organic synthesis, participating in many coordination chemical reactions, providing the possibility to construct complex complexes with complex structures and unique properties.
In summary, dimercaptoethylenediamine has shown important application potential in many fields such as chemical industry, medicine, analytical chemistry, etc. due to its special physical and chemical properties.
Looking at its physical properties, it is mostly a colorless to light yellow liquid under normal conditions, with a strong special odor. Its boiling point is quite high, about 220 to 225 degrees Celsius. Due to the interaction between molecules such as hydrogen bonds, the molecules are tightly bound, and high energy is required to make them boil. The melting point is about -10 degrees Celsius, which indicates that it is in a liquid state at room temperature and exhibits good fluidity. In addition, dimercaptoethylenediamine can be miscible with water in a certain proportion. This is because the molecule contains polar groups such as amino and sulfhydryl groups, which can form hydrogen bonds with water molecules, so it has good water solubility.
In terms of its chemical properties, both the amino and sulfhydryl groups of dimercaptoethylenediamine have high reactivity. Amino groups can neutralize with acids to form corresponding salts. For example, when reacted with hydrochloric acid, dimercaptoethylenediamine hydrochloride will be formed. And sulfhydryl groups are also very active and easy to be oxidized. In air, they can be slowly oxidized to disulfide bonds, which makes them useful as reducing agents in some chemical reactions. At the same time, thiol groups can also complex with a variety of metal ions to form stable complexes. For example, with mercury ions, it can form extremely stable complexes, which are of great application value in the detection and removal of heavy metal ions.
Furthermore, the spatial location distribution of two mercapto groups and two amino groups of dimercaptoethylenediamine makes it possible to act as a polydentate ligand in organic synthesis, participating in many coordination chemical reactions, providing the possibility to construct complex complexes with complex structures and unique properties.
In summary, dimercaptoethylenediamine has shown important application potential in many fields such as chemical industry, medicine, analytical chemistry, etc. due to its special physical and chemical properties.
What are the precautions for storing and transporting 2,6-dihydroxychlorobenzene?
For dimethyleneether, when storing and transporting, pay attention to many matters.
The first storage environment. This substance should be placed in a cool and ventilated place, away from fire and heat sources. Because dimethyleneether is volatile to a certain extent, if the ambient temperature is too high, or in case of open fire, it is easy to cause fire. Its storage place should be kept dry and protected from humid places to prevent quality damage due to moisture erosion. At the same time, it should be stored separately from oxidants and other substances. If the two come into contact with each other, or cause violent chemical reactions, it will cause danger.
Furthermore, regarding transportation. When transporting, it is necessary to ensure the integrity of the container and avoid leakage. The transport equipment used should be clean and dry, free of other impurities that may react with it. During transportation, severe bumps and collisions should be avoided to prevent the container from breaking and leaking Dimethyl ether. Escorts should be familiar with the characteristics of the substance and emergency response methods. In case of emergencies, they can be handled quickly and properly.
In addition, whether it is storage or transportation, it should be well marked. Clearly indicate the name of "Dimethyl Ether", as well as its dangerous properties, such as flammability, so that relevant personnel can see it at a glance. When operating, be careful to avoid accidents. And corresponding emergency rescue equipment and protective equipment should be provided. If there is a leak, rescue and cleaning can be carried out immediately to safeguard the safety of personnel and the environment.
The first storage environment. This substance should be placed in a cool and ventilated place, away from fire and heat sources. Because dimethyleneether is volatile to a certain extent, if the ambient temperature is too high, or in case of open fire, it is easy to cause fire. Its storage place should be kept dry and protected from humid places to prevent quality damage due to moisture erosion. At the same time, it should be stored separately from oxidants and other substances. If the two come into contact with each other, or cause violent chemical reactions, it will cause danger.
Furthermore, regarding transportation. When transporting, it is necessary to ensure the integrity of the container and avoid leakage. The transport equipment used should be clean and dry, free of other impurities that may react with it. During transportation, severe bumps and collisions should be avoided to prevent the container from breaking and leaking Dimethyl ether. Escorts should be familiar with the characteristics of the substance and emergency response methods. In case of emergencies, they can be handled quickly and properly.
In addition, whether it is storage or transportation, it should be well marked. Clearly indicate the name of "Dimethyl Ether", as well as its dangerous properties, such as flammability, so that relevant personnel can see it at a glance. When operating, be careful to avoid accidents. And corresponding emergency rescue equipment and protective equipment should be provided. If there is a leak, rescue and cleaning can be carried out immediately to safeguard the safety of personnel and the environment.
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