Linshang Chemical
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2-((2,6-Dichlorophenyl)Amino)Benzeneacetic Acid
Linshang Chemical
|
HS Code |
707011 |
| Chemical Formula | C14H10Cl2NO2 |
| Molecular Weight | 294.14 |
| Appearance | Solid |
| Solubility In Water | Low solubility |
| Solubility In Organic Solvents | Soluble in some organic solvents |
As an accredited 2-((2,6-Dichlorophenyl)Amino)Benzeneacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2-((2,6 - dichlorophenyl)amino)benzeneacetic acid in a sealed plastic container. |
| Storage | 2-(2,6 - dichlorophenylamino)benzeneacetic acid should be stored in a cool, dry place away from direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and contact with air, which could potentially lead to degradation. Store it separately from incompatible substances, like strong oxidizers or bases, to avoid chemical reactions. |
| Shipping | 2-(2,6 - dichlorophenyl)amino benzeneacetic acid is shipped in well - sealed containers, following strict chemical transportation regulations. Packaged to prevent leakage, ensuring safe transit to destination. |
Competitive 2-((2,6-Dichlorophenyl)Amino)Benzeneacetic Acid 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-((2,6-Dichlorophenyl)Amino)Benzeneacetic Acid in China?
As a trusted 2-((2,6-Dichlorophenyl)Amino)Benzeneacetic Acid manufacturer, we deliver:
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As a leading 2-((2,6-Dichlorophenyl)Amino)Benzeneacetic Acid 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 chemical properties of 2- ((2,6-dichlorophenyl) amino) phenylacetic acid?
(2 - (2,6 - dihydroxyphenyl) amino) phenyl) thiophene-2-carboxylic acid, this substance is acidic, because it contains carboxyl groups, it can weakly ionize hydrogen ions in water. It has certain stability, the solid state is relatively stable at room temperature, but extreme conditions such as high temperature and strong acid and alkali will cause structural changes. Because of the conjugated system containing benzene ring, thiophene ring and other conjugated systems, it has certain light absorption characteristics, which can be detected and identified under specific wavelengths of light. It also has certain solubility, with a certain solubility in polar organic solvents such as ethanol and dimethyl sulfoxide, and relatively small solubility in water, which affects its dispersion and reaction in different systems. Because its structure contains multiple activity checking points, it can participate in a variety of chemical reactions, such as carboxyl groups can be esterified, amino groups can participate in nucleophilic substitution, etc. These reactive activities make it an important intermediate in the field of organic synthesis, which can be used to prepare organic compounds such as drugs and functional materials.
What are the uses of 2- ((2,6-dichlorophenyl) amino) phenylacetic acid?
(2 - ((2,6 - dihydroxyphenyl) amino) benzoic acid, this substance has a wide range of uses.
In the field of medicine, it is often the key raw material for the synthesis of many drugs. Due to its specific chemical structure, it can be combined with specific targets in organisms, thus exhibiting pharmacological activity. For example, some drugs with anti-inflammatory effects, in the development and synthesis process, 2 - ((2,6 - dihydroxyphenyl) amino) benzoic acid is an important starting material. After a series of chemical modifications and reactions, the final anti-inflammatory drug with definite efficacy is obtained, which brings good news to those who relieve inflammatory pain.
In the field of materials science, it also has extraordinary performance. It can be used as a component of functional materials for the preparation of polymer materials with special properties. Because its structure contains reactive groups, it can participate in polymer polymerization reactions, giving materials such as good thermal stability, mechanical properties or optical properties. For example, in some advanced composite materials, after adding this substance, the heat resistance of the material is significantly improved, making it suitable for special equipment in high temperature environments.
Furthermore, in the dye industry, it also occupies a place. With its own structural characteristics, it can be used as an intermediate for the synthesis of new dyes. After proper chemical transformation, dye molecules with bright colors and good stability can be constructed, which can be used in textile, printing and other industries to add brilliant colors to fabrics and printed matter, and the dyed fabrics have good color fastness and will not fade for a long time.
From this perspective, 2- ((2,6-dihydroxyphenyl) amino) benzoic acid has important uses in medicine, materials, dyes and other fields, and is an indispensable organic compound.
In the field of medicine, it is often the key raw material for the synthesis of many drugs. Due to its specific chemical structure, it can be combined with specific targets in organisms, thus exhibiting pharmacological activity. For example, some drugs with anti-inflammatory effects, in the development and synthesis process, 2 - ((2,6 - dihydroxyphenyl) amino) benzoic acid is an important starting material. After a series of chemical modifications and reactions, the final anti-inflammatory drug with definite efficacy is obtained, which brings good news to those who relieve inflammatory pain.
In the field of materials science, it also has extraordinary performance. It can be used as a component of functional materials for the preparation of polymer materials with special properties. Because its structure contains reactive groups, it can participate in polymer polymerization reactions, giving materials such as good thermal stability, mechanical properties or optical properties. For example, in some advanced composite materials, after adding this substance, the heat resistance of the material is significantly improved, making it suitable for special equipment in high temperature environments.
Furthermore, in the dye industry, it also occupies a place. With its own structural characteristics, it can be used as an intermediate for the synthesis of new dyes. After proper chemical transformation, dye molecules with bright colors and good stability can be constructed, which can be used in textile, printing and other industries to add brilliant colors to fabrics and printed matter, and the dyed fabrics have good color fastness and will not fade for a long time.
From this perspective, 2- ((2,6-dihydroxyphenyl) amino) benzoic acid has important uses in medicine, materials, dyes and other fields, and is an indispensable organic compound.
What is the preparation method of 2- ((2,6-dichlorophenyl) amino) phenylacetic acid?
To prepare ((2,6-dioxybenzyl) amino) benzyloxy acetic acid, the following method can be used:
Take 2,6-dioxybenzaldehyde first, and react it with an appropriate halobenzaldehyde in an alkaline environment. This alkaline environment can be created by alkaline agents such as sodium hydroxide or potassium carbonate. During the reaction, the halogen atom of the halobenzyl is nucleophilically substituted with the hydroxyl group of the 2,6-dioxybenzaldehyde to obtain (2,6-dioxybenzyl) benzyl ether intermediates. This step requires fine regulation of the reaction temperature and time. The temperature may be maintained between 50 and 80 degrees Celsius for about 3 to 6 hours (corresponding to 6 to 12 hours) to ensure that the reaction is sufficient and there are few side reactions.
After obtaining this intermediate, react it with an appropriate amination reagent. The amination reagent can be selected from ammonia or organic amines. This reaction also requires specific conditions. In an appropriate solvent, such as an alcohol solvent, control the temperature at 30 to 60 degrees Celsius, and after 4 to 8 hours (corresponding to 8 to 16 hours), the amino group is successfully introduced to obtain (2,6-dioxybenzyl) aminobenzyl ether.
In the final step, (2,6-dioxybenzyl) aminobenzyl ether is reacted with chloroacetic acid under alkaline conditions. This alkaline condition is provided by sodium carbonate or sodium bicarbonate. During the reaction, the temperature should be maintained at 40-70 degrees Celsius, about 5-9 hours (corresponding to 10-18 hours). The carboxyl group of chloroacetic acid undergoes a substitution reaction with (2,6-dioxybenzyl) aminobenzyl ether to obtain ((2,6-dioxybenzyl) amino) benzyloxy acetic acid.
After each step of the reaction, purification methods such as extraction, recrystallization or column chromatography are required to ensure the purity of the product before the next step of the reaction can be carried out, so that the target product can be efficiently and high-quality.
Take 2,6-dioxybenzaldehyde first, and react it with an appropriate halobenzaldehyde in an alkaline environment. This alkaline environment can be created by alkaline agents such as sodium hydroxide or potassium carbonate. During the reaction, the halogen atom of the halobenzyl is nucleophilically substituted with the hydroxyl group of the 2,6-dioxybenzaldehyde to obtain (2,6-dioxybenzyl) benzyl ether intermediates. This step requires fine regulation of the reaction temperature and time. The temperature may be maintained between 50 and 80 degrees Celsius for about 3 to 6 hours (corresponding to 6 to 12 hours) to ensure that the reaction is sufficient and there are few side reactions.
After obtaining this intermediate, react it with an appropriate amination reagent. The amination reagent can be selected from ammonia or organic amines. This reaction also requires specific conditions. In an appropriate solvent, such as an alcohol solvent, control the temperature at 30 to 60 degrees Celsius, and after 4 to 8 hours (corresponding to 8 to 16 hours), the amino group is successfully introduced to obtain (2,6-dioxybenzyl) aminobenzyl ether.
In the final step, (2,6-dioxybenzyl) aminobenzyl ether is reacted with chloroacetic acid under alkaline conditions. This alkaline condition is provided by sodium carbonate or sodium bicarbonate. During the reaction, the temperature should be maintained at 40-70 degrees Celsius, about 5-9 hours (corresponding to 10-18 hours). The carboxyl group of chloroacetic acid undergoes a substitution reaction with (2,6-dioxybenzyl) aminobenzyl ether to obtain ((2,6-dioxybenzyl) amino) benzyloxy acetic acid.
After each step of the reaction, purification methods such as extraction, recrystallization or column chromatography are required to ensure the purity of the product before the next step of the reaction can be carried out, so that the target product can be efficiently and high-quality.
What is the market price of 2- ((2,6-dichlorophenyl) amino) phenylacetic acid?
The price of (2 - (2,6 - dioxybenzyl) amino) benzyl) malic acid in the market is difficult to judge. The price of the cover often changes for many reasons, just like the time, the geographical location, and the plan are intertwined, which affects the whole body.
Looking at the price of this drug, the first to bear the brunt is the supply of raw materials. If the origin of raw materials is good weather and abundant, it will be easy to obtain, the cost will drop, and the price may stabilize and low. On the contrary, in case of natural disasters, raw materials are scarce, and high prices are required to buy, the price of this medicine will be high. Furthermore, the skill of making is also critical. If the craftsman's skills are exquisite and can be refined efficiently, it will save time and effort, and the price will be appropriate; if the skills are crude, time-consuming and material-intensive, the price will be high.
And the supply and demand of the city also affect its price. If there are many people who ask for it, but there are few who supply it, the price will rise in pursuit of profit; if the supply exceeds the demand, the merchant will sell it quickly, or reduce the price. There are also merchants who plan to price it according to their own calculations, taking into account the amount of profit and market share, and also make the price different.
is based on the fact that in order to determine the market price of (2 - ((2,6 - dioxybenzyl) amino) benzyl) malic acid, it is necessary to carefully investigate the source of raw materials, the method of production, the supply and demand of the market, and the business strategy. In summary, the general idea can be obtained, but the price is difficult to determine in the end, and it is often subject to change.
Looking at the price of this drug, the first to bear the brunt is the supply of raw materials. If the origin of raw materials is good weather and abundant, it will be easy to obtain, the cost will drop, and the price may stabilize and low. On the contrary, in case of natural disasters, raw materials are scarce, and high prices are required to buy, the price of this medicine will be high. Furthermore, the skill of making is also critical. If the craftsman's skills are exquisite and can be refined efficiently, it will save time and effort, and the price will be appropriate; if the skills are crude, time-consuming and material-intensive, the price will be high.
And the supply and demand of the city also affect its price. If there are many people who ask for it, but there are few who supply it, the price will rise in pursuit of profit; if the supply exceeds the demand, the merchant will sell it quickly, or reduce the price. There are also merchants who plan to price it according to their own calculations, taking into account the amount of profit and market share, and also make the price different.
is based on the fact that in order to determine the market price of (2 - ((2,6 - dioxybenzyl) amino) benzyl) malic acid, it is necessary to carefully investigate the source of raw materials, the method of production, the supply and demand of the market, and the business strategy. In summary, the general idea can be obtained, but the price is difficult to determine in the end, and it is often subject to change.
What are the relevant safety precautions for 2- ((2,6-dichlorophenyl) amino) phenylacetic acid?
2-%28%282%2C6-%E4%BA%8C%E6%B0%AF%E8%8B%AF%E5%9F%BA%29%E6%B0%A8%E5%9F%BA%29%E8%8B%AF%E4%B9%99%E9%85%B3%E4%BA%8E%E5%AE%89%E5%85%A8%E7%9B%B8%E5%85%B3%E4%B9%8B%E4%BA%8B, many matters need to be paid attention to.
This compound has specific chemical properties. When using and storing, it should be kept away from fire and heat sources. Because of its flammability, it is easy to cause combustion and explosion in case of open flames and hot topics. Therefore, it should be placed in a well-ventilated place to ensure air circulation and reduce danger.
When operating, safety procedures must be strictly followed. Operators should be specially trained and proficient in the operation essentials. Wear appropriate protective equipment, such as protective glasses, gloves, etc. throughout the operation to avoid contact with skin and eyes. If inadvertent contact, rinse with plenty of water immediately and seek medical attention in time according to the severity of the injury.
For storage, it should be placed in a cool, dry and well-ventilated warehouse. Keep away from oxidants, acids, etc., because they are mixed with these substances or react violently, causing safety hazards. The warehouse should be equipped with emergency treatment equipment and suitable containment materials for timely response in case of unexpected emergencies.
During transportation, ensure that the container does not leak, collapse, fall or damage. Follow the prescribed route and do not stop in densely populated areas and traffic arteries.
Also pay attention to its potential impact on the environment, avoid random discharge, and prevent pollution to soil, water bodies, etc. In the event of a leak, personnel from the leaked contaminated area should be quickly evacuated to a safe area, and quarantined, and access should be strictly restricted. Emergency responders wear self-contained positive pressure respirators and anti-virus clothing to cut off the leakage source as much as possible, ventilate reasonably, and accelerate the spread. Small leaks are absorbed with sand, vermiculite or other inert materials, and large leaks are built into embankments or dug for containment, covered with foam to reduce vapor disasters. Transfer to a tanker or special collector with an explosion-proof pump for recycling or transportation to a waste treatment site for disposal.
This compound has specific chemical properties. When using and storing, it should be kept away from fire and heat sources. Because of its flammability, it is easy to cause combustion and explosion in case of open flames and hot topics. Therefore, it should be placed in a well-ventilated place to ensure air circulation and reduce danger.
When operating, safety procedures must be strictly followed. Operators should be specially trained and proficient in the operation essentials. Wear appropriate protective equipment, such as protective glasses, gloves, etc. throughout the operation to avoid contact with skin and eyes. If inadvertent contact, rinse with plenty of water immediately and seek medical attention in time according to the severity of the injury.
For storage, it should be placed in a cool, dry and well-ventilated warehouse. Keep away from oxidants, acids, etc., because they are mixed with these substances or react violently, causing safety hazards. The warehouse should be equipped with emergency treatment equipment and suitable containment materials for timely response in case of unexpected emergencies.
During transportation, ensure that the container does not leak, collapse, fall or damage. Follow the prescribed route and do not stop in densely populated areas and traffic arteries.
Also pay attention to its potential impact on the environment, avoid random discharge, and prevent pollution to soil, water bodies, etc. In the event of a leak, personnel from the leaked contaminated area should be quickly evacuated to a safe area, and quarantined, and access should be strictly restricted. Emergency responders wear self-contained positive pressure respirators and anti-virus clothing to cut off the leakage source as much as possible, ventilate reasonably, and accelerate the spread. Small leaks are absorbed with sand, vermiculite or other inert materials, and large leaks are built into embankments or dug for containment, covered with foam to reduce vapor disasters. Transfer to a tanker or special collector with an explosion-proof pump for recycling or transportation to a waste treatment site for disposal.
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