Linshang Chemical
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3,6-Dichlorobenzene-1,2,4-Tricarboxylic Acid
Linshang Chemical
|
HS Code |
118006 |
| Chemical Formula | C9H3Cl2O6 |
| Molar Mass | 279.02 g/mol |
| Appearance | Solid |
| Color | Typically white or off - white |
| Odor | May have a characteristic chemical odor |
| Solubility In Water | Low solubility in water |
| Solubility In Organic Solvents | Soluble in some organic solvents like ethanol, acetone |
| Acidity | A carboxylic acid, acidic in nature |
As an accredited 3,6-Dichlorobenzene-1,2,4-Tricarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of 3,6 - dichlorobenzene - 1,2,4 - tricarboxylic Acid in sealed plastic bags. |
| Storage | 3,6 - dichlorobenzene - 1,2,4 - tricarboxylic acid 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 a tightly closed container to prevent moisture absorption and potential contamination, ensuring its stability and safety during storage. |
| Shipping | 3,6 - dichlorobenzene - 1,2,4 - tricarboxylic acid should be shipped in sealed, corrosion - resistant containers. Ensure compliance with chemical transportation regulations to prevent spills and exposure during transit. |
Competitive 3,6-Dichlorobenzene-1,2,4-Tricarboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.
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What is the main use of 3,6-dichlorobenzene-1,2,4-tricarboxylic acid?
What is the main purpose of 3% 2C6 - carbon dioxide - 1% 2C2% 2C4 - tricarboxylic acid? This is a key question related to biological metabolism. The following is described in ancient Yaxian.
Carbon dioxide is used in biological metabolism, and its use is quite important. When plants perform photosynthesis, carbon dioxide is one of the raw materials. Under light, chloroplasts ingest carbon dioxide and water, and through a series of complex biochemical reactions, synthesize carbohydrates and other organic substances, and release oxygen at the same time. This process maintains the carbon and oxygen balance of the earth, which is of great significance for the stability of the ecosystem.
The tricarboxylic acid cycle, also known as the citric acid cycle, is a key link in cellular respiration. Under aerobic conditions, sugar, fat, protein and other energy substances are preliminarily decomposed to form acetyl-coenzyme A, which enters the tricarboxylic acid cycle. During the cycle, acetyl-coenzyme A is gradually oxidized and decomposed, releasing a large amount of energy, which is stored in the form of ATP (adenosine triphosphate) for various life activities of cells. At the same time, the tricarboxylic acid cycle also produces many intermediate products, such as α-ketoglutaric acid, oxaloacetic acid, etc. These intermediate products can be used as raw materials for biosynthesis and participate in the synthesis of amino acids, fatty acids and other substances. Therefore, carbon dioxide is the cornerstone of photosynthesis, which is related to the synthesis of organic matter and the release of oxygen; the tricarboxylic acid cycle is the hub of cell productivity and material synthesis, and is indispensable in the growth, development, reproduction and other life activities of organisms. The two play their respective roles in the biological metabolic system and complement each other to jointly maintain the delicate operation of life.
Carbon dioxide is used in biological metabolism, and its use is quite important. When plants perform photosynthesis, carbon dioxide is one of the raw materials. Under light, chloroplasts ingest carbon dioxide and water, and through a series of complex biochemical reactions, synthesize carbohydrates and other organic substances, and release oxygen at the same time. This process maintains the carbon and oxygen balance of the earth, which is of great significance for the stability of the ecosystem.
The tricarboxylic acid cycle, also known as the citric acid cycle, is a key link in cellular respiration. Under aerobic conditions, sugar, fat, protein and other energy substances are preliminarily decomposed to form acetyl-coenzyme A, which enters the tricarboxylic acid cycle. During the cycle, acetyl-coenzyme A is gradually oxidized and decomposed, releasing a large amount of energy, which is stored in the form of ATP (adenosine triphosphate) for various life activities of cells. At the same time, the tricarboxylic acid cycle also produces many intermediate products, such as α-ketoglutaric acid, oxaloacetic acid, etc. These intermediate products can be used as raw materials for biosynthesis and participate in the synthesis of amino acids, fatty acids and other substances. Therefore, carbon dioxide is the cornerstone of photosynthesis, which is related to the synthesis of organic matter and the release of oxygen; the tricarboxylic acid cycle is the hub of cell productivity and material synthesis, and is indispensable in the growth, development, reproduction and other life activities of organisms. The two play their respective roles in the biological metabolic system and complement each other to jointly maintain the delicate operation of life.
What are the physical properties of 3,6-dichlorobenzene-1,2,4-tricarboxylic acid
Fudioxy fluoride is active and highly oxidizing. It is a colorless gas at room temperature and pressure, and has a special odor. Its chemical properties are active and can react with many substances. It is often used as a strong oxidizing agent and plays a key role in many chemical reactions.
As for tricarboxylic acids, they are organic acids, many of which are acidic and can partially ionize hydrogen ions in water. Its physical properties are different, and most of them are solid or liquid, with certain solubility. Such as citric acid, which is colorless crystal and has a sour taste. It is easily soluble in solvents such as water and ethanol. It is often used as a sour agent in the food industry to increase the flavor of food. There is also malic acid, which is also a common tricarboxylic acid. It is white crystalline and has a special sour taste. It is used in food, medicine and other fields.
These two, one is a gas with strong oxidizing properties; the other is an organic acid, which is mostly acidic and has specific solubility, and can be used in different fields, which is of great significance to the development of chemical, food, pharmaceutical and other industries.
As for tricarboxylic acids, they are organic acids, many of which are acidic and can partially ionize hydrogen ions in water. Its physical properties are different, and most of them are solid or liquid, with certain solubility. Such as citric acid, which is colorless crystal and has a sour taste. It is easily soluble in solvents such as water and ethanol. It is often used as a sour agent in the food industry to increase the flavor of food. There is also malic acid, which is also a common tricarboxylic acid. It is white crystalline and has a special sour taste. It is used in food, medicine and other fields.
These two, one is a gas with strong oxidizing properties; the other is an organic acid, which is mostly acidic and has specific solubility, and can be used in different fields, which is of great significance to the development of chemical, food, pharmaceutical and other industries.
What are the chemical properties of 3,6-dichlorobenzene-1,2,4-tricarboxylic acid
The chemical properties of tetrachloroacetic acid, carbon dioxide and dichloroethane are different.
Carbon dioxide is a colorless and odorless gas at room temperature and pressure. It is stable, generally does not support combustion, nor is it flammable, and exists in the atmosphere. Soluble water forms carbonic acid, which is a weak acid that can neutralize with bases to form carbonates and water. And in photosynthesis, it is ingested by plants and turned into organic matter and oxygen.
Dichloroethane has two isomers, namely 1,2-dichloroethane and 1,1-dichloroethane. Usually referred to as dichloroethane refers to 1,2-dichloroethane, which is a colorless and slightly fragrant liquid. Flammable, its vapor and air can form explosive mixtures. The chemical properties are relatively active, and reactions such as substitution and elimination can occur. When it encounters alkali, it can be hydrolyzed into ethylene glycol; under specific conditions, it can eliminate hydrogen chloride to form vinyl chloride.
Trichloroacetic acid, a colorless crystal, has a pungent odor. Very acidic, can be completely ionized in water, and is much more acidic than ordinary carboxylic acids. It can react with bases, alcohols, etc., and can form esters with alcohols. Due to the electron-absorbing effect of chlorine atoms in its molecules, its carboxyl group activity is greatly increased. And it has strong corrosive properties, can coagulate proteins, and is widely used in organic synthesis and medicine.
The chemical properties of the three vary depending on the structure and composition, and they can each perform their own functions in different chemical processes and industrial uses.
Carbon dioxide is a colorless and odorless gas at room temperature and pressure. It is stable, generally does not support combustion, nor is it flammable, and exists in the atmosphere. Soluble water forms carbonic acid, which is a weak acid that can neutralize with bases to form carbonates and water. And in photosynthesis, it is ingested by plants and turned into organic matter and oxygen.
Dichloroethane has two isomers, namely 1,2-dichloroethane and 1,1-dichloroethane. Usually referred to as dichloroethane refers to 1,2-dichloroethane, which is a colorless and slightly fragrant liquid. Flammable, its vapor and air can form explosive mixtures. The chemical properties are relatively active, and reactions such as substitution and elimination can occur. When it encounters alkali, it can be hydrolyzed into ethylene glycol; under specific conditions, it can eliminate hydrogen chloride to form vinyl chloride.
Trichloroacetic acid, a colorless crystal, has a pungent odor. Very acidic, can be completely ionized in water, and is much more acidic than ordinary carboxylic acids. It can react with bases, alcohols, etc., and can form esters with alcohols. Due to the electron-absorbing effect of chlorine atoms in its molecules, its carboxyl group activity is greatly increased. And it has strong corrosive properties, can coagulate proteins, and is widely used in organic synthesis and medicine.
The chemical properties of the three vary depending on the structure and composition, and they can each perform their own functions in different chemical processes and industrial uses.
What is the preparation method of 3,6-dichlorobenzene-1,2,4-tricarboxylic acid?
The method of reducing carbon disulfide to arsenic trichloride is as follows:
To reduce carbon disulfide, you need to use sulfur and charcoal as raw materials. Take some sulfur first, put it in the crucible, and add it over fire. When the sulfur is melted into the liquid, add the charcoal powder that has been studied, and do not mix it. The heat should be uniform and determined, and the temperature should not be low. The two are biochemical reactions, and the generated condensation and collection are obtained to obtain carbon disulfide. The principle of its reaction is that sulfur and carbon are combined with each other at an appropriate temperature.
As for arsenic trichloride, the main material is arsenic and chlorine. Arsenic should be placed in a dense and dry container first, and the container should be resistant to corrosion. Then the chlorine is introduced, and the chlorine and arsenic are connected to the biochemical reaction. This process needs to pay attention to the control of the reaction rate, and the reaction should not be caused by the strong reaction. After the reaction is completed, the reaction process can be completed, and the arsenic trichloride can be obtained. This reaction is based on the chemical reaction of arsenic and chlorine, and the interaction between the two generates arsenic trichloride.
Therefore, carbon disulfide and arsenic trichloride need to follow a specific step and pay attention to the proportion of raw materials, the reaction rate and other factors, in order to successfully obtain it.
To reduce carbon disulfide, you need to use sulfur and charcoal as raw materials. Take some sulfur first, put it in the crucible, and add it over fire. When the sulfur is melted into the liquid, add the charcoal powder that has been studied, and do not mix it. The heat should be uniform and determined, and the temperature should not be low. The two are biochemical reactions, and the generated condensation and collection are obtained to obtain carbon disulfide. The principle of its reaction is that sulfur and carbon are combined with each other at an appropriate temperature.
As for arsenic trichloride, the main material is arsenic and chlorine. Arsenic should be placed in a dense and dry container first, and the container should be resistant to corrosion. Then the chlorine is introduced, and the chlorine and arsenic are connected to the biochemical reaction. This process needs to pay attention to the control of the reaction rate, and the reaction should not be caused by the strong reaction. After the reaction is completed, the reaction process can be completed, and the arsenic trichloride can be obtained. This reaction is based on the chemical reaction of arsenic and chlorine, and the interaction between the two generates arsenic trichloride.
Therefore, carbon disulfide and arsenic trichloride need to follow a specific step and pay attention to the proportion of raw materials, the reaction rate and other factors, in order to successfully obtain it.
What are the precautions for the use of 3,6-dichlorobenzene-1,2,4-tricarboxylic acid
Beryllium dioxide ($BeO_2 $), tricarboxylic acids (such as common citric acid and other organic acids containing three carboxyl groups) and 1,2,4-tricarboxylic acids need to pay attention to many key matters during use.
First, it is related to storage conditions. Both should be stored in a dry and cool place, away from heat sources and open flames. As a special compound, beryllium dioxide may react with water vapor if the storage environment humidity is too high, resulting in changes in its chemical properties. Tricarboxylic acids, especially those containing multiple carboxylic groups, may decompose in high temperature environments, thus affecting their effectiveness.
Second, safety protection cannot be ignored. When exposed to beryllium dioxide, you must wear appropriate protective equipment, such as gloves, goggles, etc. Because of its toxicity, if it accidentally touches the skin or enters the eyes, it will cause serious harm to the human body. Although tricarboxylic acids are usually relatively less toxic, some of them are highly corrosive and may also burn the skin, so protective measures are essential.
Third, the dosage should be precisely controlled. When beryllium dioxide is used as a catalyst and other purposes, the dosage should be strictly determined according to the scale and requirements of the specific reaction. If the dosage is too small, the desired reaction effect may not be achieved, and if the dosage is too large, it may cause side reactions. When tricarboxylic acids participate in various chemical reactions, such as as as complexing agents or adjusting the pH of the system, they also need to be precisely controlled to ensure that the reaction proceeds in the desired direction.
Fourth, pay attention to reaction compatibility. Before using beryllium dioxide and tricarboxylic acids in a specific reaction system, it is necessary to understand their compatibility with other substances in the system in detail. Beryllium dioxide may react with some metal ions to form precipitates or change the valence state of metal ions; tricarboxylic acids may neutralize with basic substances in the system due to the existence of multiple carboxylic groups, affecting the reaction process, so their interactions must be fully considered to ensure the smooth development of the reaction.
First, it is related to storage conditions. Both should be stored in a dry and cool place, away from heat sources and open flames. As a special compound, beryllium dioxide may react with water vapor if the storage environment humidity is too high, resulting in changes in its chemical properties. Tricarboxylic acids, especially those containing multiple carboxylic groups, may decompose in high temperature environments, thus affecting their effectiveness.
Second, safety protection cannot be ignored. When exposed to beryllium dioxide, you must wear appropriate protective equipment, such as gloves, goggles, etc. Because of its toxicity, if it accidentally touches the skin or enters the eyes, it will cause serious harm to the human body. Although tricarboxylic acids are usually relatively less toxic, some of them are highly corrosive and may also burn the skin, so protective measures are essential.
Third, the dosage should be precisely controlled. When beryllium dioxide is used as a catalyst and other purposes, the dosage should be strictly determined according to the scale and requirements of the specific reaction. If the dosage is too small, the desired reaction effect may not be achieved, and if the dosage is too large, it may cause side reactions. When tricarboxylic acids participate in various chemical reactions, such as as as complexing agents or adjusting the pH of the system, they also need to be precisely controlled to ensure that the reaction proceeds in the desired direction.
Fourth, pay attention to reaction compatibility. Before using beryllium dioxide and tricarboxylic acids in a specific reaction system, it is necessary to understand their compatibility with other substances in the system in detail. Beryllium dioxide may react with some metal ions to form precipitates or change the valence state of metal ions; tricarboxylic acids may neutralize with basic substances in the system due to the existence of multiple carboxylic groups, affecting the reaction process, so their interactions must be fully considered to ensure the smooth development of the reaction.
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