Linshang Chemical
PRODUCTS
4-Benzenediol,2-Chloro-1
Linshang Chemical
|
HS Code |
431251 |
| Chemical Formula | C6H5ClO2 |
| Molar Mass | 144.56 g/mol |
| Appearance | Solid (likely white or off - white) |
| Solubility In Water | Low solubility, as it has a non - polar benzene ring and a relatively small polar group |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether, due to its organic nature |
| Density | Estimated density based on similar aromatic compounds, around 1.3 - 1.4 g/cm³ |
| Pka | Estimated pKa based on phenolic group, around 9 - 10 |
As an accredited 4-Benzenediol,2-Chloro-1 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2 - chloro - 1,4 - benzenediol packaged in 1 - kg containers. |
| Storage | 4 - benzenediol, 2 - chloro - 1 (2 - chloro - 1,4 - benzenediol) should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly - sealed container to prevent moisture absorption and contamination. It may be best stored in a dedicated chemical storage cabinet, clearly labeled for easy identification and to ensure proper handling. |
| Shipping | 4 - benzenediol, 2 - chloro - 1 is shipped in well - sealed, corrosion - resistant containers. Transport follows strict chemical safety regulations to prevent spills, ensuring safe delivery due to its potentially hazardous nature. |
Competitive 4-Benzenediol,2-Chloro-1 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
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4-Catechol, what is the chemical structure of 2-chloro-1?
The chemical structure of 4-azodiamyl ring, 2-chloro-1-is a field of study in the field of organic chemistry. It is explained in the style of ancient proverbs in "Tiangong Kaiwu".
In this compound, the "4-azodiamyl ring" is a ring structure formed by five atoms, and the amyl ring is occupied by nitrogen atoms at its fourth position. Nitrogen, one of the chemical elements, often has specific chemical properties and bonding methods in compounds. This nitrogen atom is connected to other atoms on the amyl ring by chemical bonds, maintaining the structural stability of the amyl ring.
And "2-chlorine" refers to the second position of the amyl ring, with chlorine atoms connected to it. Chlorine is also a chemical element, with a relatively large atomic radius and a unique electron cloud structure. The combination of chlorine atoms and the amyl ring gives the compound a different chemical activity. Because of its high electronegativity, it can make the compound exhibit different reaction tendencies in many chemical reactions.
As for "1 -", although the subsequent group is not clear here, it must also be a key part of the description of the structure of the compound. Or a specific functional group, or an identification of other atomic connection check points. This part interacts with nitrogen diamyl ring and chlorine atom to construct a complete chemical structure.
Overall view, the chemical structure of this compound is made of an amyl ring as the basic skeleton, and atoms such as nitrogen and chlorine are connected to it at specific positions. Each part interacts to determine its physical and chemical properties. Such a structure has important application value in many fields such as organic synthesis and drug development, or because of its unique properties.
In this compound, the "4-azodiamyl ring" is a ring structure formed by five atoms, and the amyl ring is occupied by nitrogen atoms at its fourth position. Nitrogen, one of the chemical elements, often has specific chemical properties and bonding methods in compounds. This nitrogen atom is connected to other atoms on the amyl ring by chemical bonds, maintaining the structural stability of the amyl ring.
And "2-chlorine" refers to the second position of the amyl ring, with chlorine atoms connected to it. Chlorine is also a chemical element, with a relatively large atomic radius and a unique electron cloud structure. The combination of chlorine atoms and the amyl ring gives the compound a different chemical activity. Because of its high electronegativity, it can make the compound exhibit different reaction tendencies in many chemical reactions.
As for "1 -", although the subsequent group is not clear here, it must also be a key part of the description of the structure of the compound. Or a specific functional group, or an identification of other atomic connection check points. This part interacts with nitrogen diamyl ring and chlorine atom to construct a complete chemical structure.
Overall view, the chemical structure of this compound is made of an amyl ring as the basic skeleton, and atoms such as nitrogen and chlorine are connected to it at specific positions. Each part interacts to determine its physical and chemical properties. Such a structure has important application value in many fields such as organic synthesis and drug development, or because of its unique properties.
What are the physical properties of 4-catechol and 2-chloro-1?
4-Silica-diglycerin, 2-alkane-1 This substance has a rather unique behavior. Silica-diglycerin is mild in nature, often in a stable state, and is not easy to react violently with ordinary substances. Its color is clear, clear like water, and has no peculiar smell. It is like a spirit hidden in all things. Under normal circumstances, it exists in a liquid state, just like a smart flow, smooth and not sticky.
2-alkane-1 also has its uniqueness. Its texture is light, as if a breeze can blow. The color is also transparent, but compared with silicon-diglycerin, the smell is slightly different, slightly fragrant, but not pungent, and it feels fresh. Under normal conditions, it is also liquid, but its fluidity is better than that of silicon Ergan, such as smart water, which flows when it encounters a gap. Its density is lighter, as if it can float on the water, just like a light boat on the water.
Both have good insulation, like an invisible barrier, which can block the passage of current. In terms of heat conduction, the performance is not outstanding, just like a wall of heat insulation, which can slow down the transfer of heat. And both are chemically stable, not afraid of the erosion of ordinary acids and alkalis, like a strong castle, protecting its own integrity. Although it is a chemical substance, it has a relatively small impact on the environment, as if it is in harmony with nature, and it does not disturb, silently showing its physical wonders in the world.
2-alkane-1 also has its uniqueness. Its texture is light, as if a breeze can blow. The color is also transparent, but compared with silicon-diglycerin, the smell is slightly different, slightly fragrant, but not pungent, and it feels fresh. Under normal conditions, it is also liquid, but its fluidity is better than that of silicon Ergan, such as smart water, which flows when it encounters a gap. Its density is lighter, as if it can float on the water, just like a light boat on the water.
Both have good insulation, like an invisible barrier, which can block the passage of current. In terms of heat conduction, the performance is not outstanding, just like a wall of heat insulation, which can slow down the transfer of heat. And both are chemically stable, not afraid of the erosion of ordinary acids and alkalis, like a strong castle, protecting its own integrity. Although it is a chemical substance, it has a relatively small impact on the environment, as if it is in harmony with nature, and it does not disturb, silently showing its physical wonders in the world.
4-Catechol, what are the chemical properties of 2-chloro-1?
The chemical properties of 4-benzodiketone and 2-chloro-1-are a key point of inquiry in the field of chemistry. This compound has multiple significant chemical properties.
The first to bear the brunt is that the structure of 4-benzodiketone contains two carbonyl groups, which gives it a certain electrophilicity. Carbonyl carbons are positively electrically charged and prone to attack by nucleophiles. For example, nucleophilic addition reactions can occur with reagents containing nucleophilic atoms such as nitrogen and oxygen. When catalyzed with alcohols under acidic or basic conditions, ketal derivatives can be formed. Such reactions are often used in organic synthesis to protect carbonyl groups or to construct new carbon-oxygen bond structures.
Furthermore, the chlorine atom in the 2-chlorine-1-structure makes this part exhibit unique properties. The chlorine atom has a certain electronegativity, which affects the electron cloud density of the carbon atom connected to it. This chlorine atom has considerable exoticism, and under suitable conditions, such as in nucleophilic substitution reactions, it can be replaced by other nucleophilic groups. For example, when reacting with nucleophiles such as sodium alcohol in an alkaline environment, the chlorine atom can be replaced by alkoxy groups to form ether compounds, which is an extremely important step in the design of organic synthesis routes.
Furthermore, different functional groups in the molecule of the compound will interact with each other. The presence of carbonyl groups may affect the reactivity of chlorine atoms, and vice versa. For example, the electron-withdrawing effect of carbonyl groups may enhance the ability of chlorine atoms to leave, thus promoting nucleophilic substitution reactions to occur more easily. At the same time, the selectivity of functional groups in different positions in chemical reactions is also worthy of attention. By reasonably regulating the reaction conditions, selective reactions to specific functional groups can be achieved, and the precise synthesis of target products can be achieved. In the field of organic synthesis, in-depth insight into the chemical properties of 4-benzodione and 2-chlorine-1 is of great significance for designing efficient and precise synthesis routes and preparing organic compounds with specific functions.
The first to bear the brunt is that the structure of 4-benzodiketone contains two carbonyl groups, which gives it a certain electrophilicity. Carbonyl carbons are positively electrically charged and prone to attack by nucleophiles. For example, nucleophilic addition reactions can occur with reagents containing nucleophilic atoms such as nitrogen and oxygen. When catalyzed with alcohols under acidic or basic conditions, ketal derivatives can be formed. Such reactions are often used in organic synthesis to protect carbonyl groups or to construct new carbon-oxygen bond structures.
Furthermore, the chlorine atom in the 2-chlorine-1-structure makes this part exhibit unique properties. The chlorine atom has a certain electronegativity, which affects the electron cloud density of the carbon atom connected to it. This chlorine atom has considerable exoticism, and under suitable conditions, such as in nucleophilic substitution reactions, it can be replaced by other nucleophilic groups. For example, when reacting with nucleophiles such as sodium alcohol in an alkaline environment, the chlorine atom can be replaced by alkoxy groups to form ether compounds, which is an extremely important step in the design of organic synthesis routes.
Furthermore, different functional groups in the molecule of the compound will interact with each other. The presence of carbonyl groups may affect the reactivity of chlorine atoms, and vice versa. For example, the electron-withdrawing effect of carbonyl groups may enhance the ability of chlorine atoms to leave, thus promoting nucleophilic substitution reactions to occur more easily. At the same time, the selectivity of functional groups in different positions in chemical reactions is also worthy of attention. By reasonably regulating the reaction conditions, selective reactions to specific functional groups can be achieved, and the precise synthesis of target products can be achieved. In the field of organic synthesis, in-depth insight into the chemical properties of 4-benzodione and 2-chlorine-1 is of great significance for designing efficient and precise synthesis routes and preparing organic compounds with specific functions.
What is the main use of 4-catechol, 2-chloro-1?
The main uses of 4-diacetamide and 2-chloro-1 are in the "Tiangong", which is mostly used in the field of chemical production.
In the preparation of one, 4-diacetamide can be used as a key ingredient in the synthesis of chemical compounds due to its special chemical properties. It can be used in many ways to help the construction of chemical molecules. For example, in the synthesis process of some chemical compounds, 4-diacetamide can be specific and introduced into the molecular skeleton of the chemical compound, so as to give the required biological activity and chemical properties of the chemical compound, so as to reduce the effect of pain.
And 2-chloro-1 is also important in chemical engineering. First, in the synthesis of chemical compounds, it is often used as alkylation. It can introduce chloroalkyl groups into other chemical compound molecules. This process can change the chemical properties and physical properties of the chemical compounds, and expand its application in different fields. For example, in the synthesis of polymer materials with special properties, 2-chloro-1 can be used as a starting material for polymerization and reaction. It is a step to synthesize polymers with specific properties, such as corrosion resistance and high resistance. Second, 2-chloro-1 is an important raw material in the production of some refined chemical products. For example, some high-performance raw materials, additives, etc., 2-chloro-1 can be synthesized into a series of raw materials to improve the performance of the raw materials, so that the raw materials have better adhesion, wear resistance, or the addition of raw materials to improve the stability and efficiency. In addition, both of them play an indispensable role in the fields of engineering, production, and manufacturing, and promote the development of the same.
In the preparation of one, 4-diacetamide can be used as a key ingredient in the synthesis of chemical compounds due to its special chemical properties. It can be used in many ways to help the construction of chemical molecules. For example, in the synthesis process of some chemical compounds, 4-diacetamide can be specific and introduced into the molecular skeleton of the chemical compound, so as to give the required biological activity and chemical properties of the chemical compound, so as to reduce the effect of pain.
And 2-chloro-1 is also important in chemical engineering. First, in the synthesis of chemical compounds, it is often used as alkylation. It can introduce chloroalkyl groups into other chemical compound molecules. This process can change the chemical properties and physical properties of the chemical compounds, and expand its application in different fields. For example, in the synthesis of polymer materials with special properties, 2-chloro-1 can be used as a starting material for polymerization and reaction. It is a step to synthesize polymers with specific properties, such as corrosion resistance and high resistance. Second, 2-chloro-1 is an important raw material in the production of some refined chemical products. For example, some high-performance raw materials, additives, etc., 2-chloro-1 can be synthesized into a series of raw materials to improve the performance of the raw materials, so that the raw materials have better adhesion, wear resistance, or the addition of raw materials to improve the stability and efficiency. In addition, both of them play an indispensable role in the fields of engineering, production, and manufacturing, and promote the development of the same.
What is the preparation method of 4-catechol, 2-chloro-1?
To prepare 4-benzodimethylketone and 2-chloro-1-one, the following ancient method can be used.
First take an appropriate amount of benzyl compound and dissolve it in a specific organic solvent. The organic solvent must have good solubility and stable properties, and no side reactions with the reactants occur. Move the benzyl compound solution to a clean reactor. The material of the reactor must be chemically resistant.
Gradually add a suitable alkaline catalyst. The amount of this catalyst needs to be precisely controlled. If it is too small, the reaction will be slow, and if it is too much, it will easily lead to side reactions. Under specific temperature and pressure conditions, turn on the stirring device to fully mix the reactants and accelerate the reaction process. The temperature needs to be strictly controlled according to the reaction characteristics, the fluctuation range should not be too large, and the pressure needs to be maintained stable. During the
reaction, the reaction process should be closely monitored, and various analytical methods, such as thin-layer chromatography, can be used to clarify the degree of reaction. After the benzyl compound is partially converted into the corresponding intermediate, a chlorine-containing reagent is introduced. This reagent also needs to be diluted with an appropriate solvent and slowly added to the reaction system to avoid too violent reaction.
Continue stirring and maintain suitable reaction conditions, so that the intermediate can fully react with the chlorine-containing reagent to generate 2-chloro-1-one. Then, the reaction product is separated and purified. The organic solvent is first removed by distillation, and then the product is further purified by means of column chromatography or recrystallization to obtain high-purity 2-chloro-1-ketone.
As for the preparation of 4-benzodimethyl ketone, in another reaction system, benzyl compound and another specific ketone compound can be used as raw materials. Similarly, a suitable organic solvent is dissolved, and a specific acidic catalyst or basic condensing agent is added to induce the condensation reaction of the two according to specific reaction conditions.
After the reaction is completed, 4-benzyldimethyl ketone is also separated and purified from the reaction mixture through a series of separation and purification steps such as distillation, extraction, and column chromatography to obtain a pure 4-benzyldimethyl ketone product. The whole preparation process requires fine operation and strict control of various reaction conditions and parameters to obtain satisfactory product yield and purity.
First take an appropriate amount of benzyl compound and dissolve it in a specific organic solvent. The organic solvent must have good solubility and stable properties, and no side reactions with the reactants occur. Move the benzyl compound solution to a clean reactor. The material of the reactor must be chemically resistant.
Gradually add a suitable alkaline catalyst. The amount of this catalyst needs to be precisely controlled. If it is too small, the reaction will be slow, and if it is too much, it will easily lead to side reactions. Under specific temperature and pressure conditions, turn on the stirring device to fully mix the reactants and accelerate the reaction process. The temperature needs to be strictly controlled according to the reaction characteristics, the fluctuation range should not be too large, and the pressure needs to be maintained stable. During the
reaction, the reaction process should be closely monitored, and various analytical methods, such as thin-layer chromatography, can be used to clarify the degree of reaction. After the benzyl compound is partially converted into the corresponding intermediate, a chlorine-containing reagent is introduced. This reagent also needs to be diluted with an appropriate solvent and slowly added to the reaction system to avoid too violent reaction.
Continue stirring and maintain suitable reaction conditions, so that the intermediate can fully react with the chlorine-containing reagent to generate 2-chloro-1-one. Then, the reaction product is separated and purified. The organic solvent is first removed by distillation, and then the product is further purified by means of column chromatography or recrystallization to obtain high-purity 2-chloro-1-ketone.
As for the preparation of 4-benzodimethyl ketone, in another reaction system, benzyl compound and another specific ketone compound can be used as raw materials. Similarly, a suitable organic solvent is dissolved, and a specific acidic catalyst or basic condensing agent is added to induce the condensation reaction of the two according to specific reaction conditions.
After the reaction is completed, 4-benzyldimethyl ketone is also separated and purified from the reaction mixture through a series of separation and purification steps such as distillation, extraction, and column chromatography to obtain a pure 4-benzyldimethyl ketone product. The whole preparation process requires fine operation and strict control of various reaction conditions and parameters to obtain satisfactory product yield and purity.
What is the chemical structure of this product "4-benzenediol, 2-chloro-1"?
"The chemical structure of this '4-benzenediol, 2-chloro-1 'is above the benzene ring, with one hydroxyl group (-OH) at the first and fourth positions, and one chlorine atom (-Cl) at the second position. The benzene ring is a six-membered carbon ring with a stable structure of conjugated double bonds. The hydroxyl group is bonded by hydrogen and oxygen atoms, and its oxygen atom is single-bonded to the benzene ring carbon. The chlorine atom is also single-bonded to the specific carbon position of the benzene ring.
In this structure, the electron cloud of the benzene ring changes due to the connection of the hydroxyl group and the chlorine atom. The hydroxyl group is the electron cloud density of the benzene ring, which can increase the density of the benzene ring electron cloud. In the electrophilic substitution reaction, the reaction is more likely to occur in the ortho and para-position of the hydroxyl group. Although the chlorine atom is a halogen atom, it has an electron-absorbing induction effect, but it also affects the electron cloud distribution of the benzene ring due to the conjugation of the lone pair electron with the benzene ring. This structure makes the compound have unique physical and chemical properties and may be important in organic synthesis, pharmaceutical chemistry and other fields. "
In this structure, the electron cloud of the benzene ring changes due to the connection of the hydroxyl group and the chlorine atom. The hydroxyl group is the electron cloud density of the benzene ring, which can increase the density of the benzene ring electron cloud. In the electrophilic substitution reaction, the reaction is more likely to occur in the ortho and para-position of the hydroxyl group. Although the chlorine atom is a halogen atom, it has an electron-absorbing induction effect, but it also affects the electron cloud distribution of the benzene ring due to the conjugation of the lone pair electron with the benzene ring. This structure makes the compound have unique physical and chemical properties and may be important in organic synthesis, pharmaceutical chemistry and other fields. "
What are the main uses of "4-benzenediol, 2-chloro-1" products?
"4-Phenylenediol, 2-Chloro-1" This product has a wide range of uses. In the field of medicine, it can be used as a key intermediate to synthesize drugs with special curative effects. Due to its unique structure, it can participate in the construction of drug molecules, help drugs act precisely on targets, improve curative effect and reduce side effects.
In the chemical industry, it can be used to manufacture high-performance materials. By virtue of its own chemical properties, it reacts with other compounds to generate materials with excellent physical and chemical properties, such as high-temperature, high-strength engineering plastics, which are used in aerospace, automobile manufacturing and other industries that require strict materials.
In scientific research and exploration, it is an important experimental reagent. Researchers use it to conduct research on organic synthesis reactions, explore new reaction paths and methods, expand the boundaries of organic chemistry knowledge, and lay the foundation for the research and development of more innovative compounds.
In the field of electronics, its special electrical properties may be used to manufacture electronic components, such as participating in the synthesis of conductive polymers, providing the possibility of miniaturization and high performance of electronic devices.
This product is of great value in many fields and plays an indispensable role in promoting the development of various industries.
In the chemical industry, it can be used to manufacture high-performance materials. By virtue of its own chemical properties, it reacts with other compounds to generate materials with excellent physical and chemical properties, such as high-temperature, high-strength engineering plastics, which are used in aerospace, automobile manufacturing and other industries that require strict materials.
In scientific research and exploration, it is an important experimental reagent. Researchers use it to conduct research on organic synthesis reactions, explore new reaction paths and methods, expand the boundaries of organic chemistry knowledge, and lay the foundation for the research and development of more innovative compounds.
In the field of electronics, its special electrical properties may be used to manufacture electronic components, such as participating in the synthesis of conductive polymers, providing the possibility of miniaturization and high performance of electronic devices.
This product is of great value in many fields and plays an indispensable role in promoting the development of various industries.
What are the precautions for the production process of "4-benzenediol, 2-chloro-1"?
When preparing "4-phenylene glycol, 2-chlorine-1", many things need to be paid attention to. First, the preparation of materials, the raw materials used must be pure, if impurities exist, the reaction may be biased and the product impure. As "Tiangong Kaiwu" said "If you want to do a good job in your work, you must first sharpen your tools". The purity of raw materials is the basis for a smooth reaction and a good product.
Second, the reaction conditions are crucial. Temperature control needs to be precise, and high or low will affect the reaction process and product. If the temperature is too high, the reaction will be excessive, and side reactions will be plentiful; if the temperature is too low, the reaction will be slow, and the yield will not be high. Just like the heat is used in cooking, too much is too much. In the same way, the reaction time should also be moderate, the duration is not enough, the reaction is not complete; if the time is too long, resources will be wasted, and the product may have qualitative changes.
Furthermore, the reaction environment should not be underestimated. The solvent selection must be careful, and its solubility and stability are related to the success or failure of the reaction. And the reaction system should avoid impurities and interference. For example, "Tiangong Kaiwu" focuses on creating a suitable environment. This reaction also needs a clean and stable environment in order to make the reaction proceed in an orderly manner.
The operator must also be skilled. The weighing of materials needs to be accurate, and the difference between the amount and the amount should be thousands of miles. The operation steps must be carried out in accordance with regulations, and must not be done arbitrarily.
The post-processing steps should not be ignored. The product separation and purification must be proper to obtain a pure product. Impurities remain, affecting quality.
Preparation of "4-phenylene glycol, 2-chloro-1", materials, conditions, environment, operation and post-treatment are all key, one ring is careless, and everything is lost. It must be treated strictly in order to succeed.
Second, the reaction conditions are crucial. Temperature control needs to be precise, and high or low will affect the reaction process and product. If the temperature is too high, the reaction will be excessive, and side reactions will be plentiful; if the temperature is too low, the reaction will be slow, and the yield will not be high. Just like the heat is used in cooking, too much is too much. In the same way, the reaction time should also be moderate, the duration is not enough, the reaction is not complete; if the time is too long, resources will be wasted, and the product may have qualitative changes.
Furthermore, the reaction environment should not be underestimated. The solvent selection must be careful, and its solubility and stability are related to the success or failure of the reaction. And the reaction system should avoid impurities and interference. For example, "Tiangong Kaiwu" focuses on creating a suitable environment. This reaction also needs a clean and stable environment in order to make the reaction proceed in an orderly manner.
The operator must also be skilled. The weighing of materials needs to be accurate, and the difference between the amount and the amount should be thousands of miles. The operation steps must be carried out in accordance with regulations, and must not be done arbitrarily.
The post-processing steps should not be ignored. The product separation and purification must be proper to obtain a pure product. Impurities remain, affecting quality.
Preparation of "4-phenylene glycol, 2-chloro-1", materials, conditions, environment, operation and post-treatment are all key, one ring is careless, and everything is lost. It must be treated strictly in order to succeed.
What is the approximate market price of "4-benzenediol, 2-chloro-1"?
I don't know the price of "4-benzenediol, 2-chloro-1". This is a chemical substance, and its price often varies due to various factors such as the purity of the quality, the state of demand and supply, the difficulty of making it, and the place where it is sold.
If the quality is pure and there are many people who want it, and the supply is few, the price will be high; if the quality is complex and the demand is small and the supply is large, the price will be low. And in different places, the price varies, and in prosperous cities and remote villages, the price may be very different. If it is difficult to make, the cost will be high and the price will be high; if it is easy to make, the cost will be low and the price will be low.
If you want to know the exact price, you need to study the chemical market in detail, consult the merchants, and compare the price. I can't hide the price with a word, because there are many variables, it is difficult to judge.
If the quality is pure and there are many people who want it, and the supply is few, the price will be high; if the quality is complex and the demand is small and the supply is large, the price will be low. And in different places, the price varies, and in prosperous cities and remote villages, the price may be very different. If it is difficult to make, the cost will be high and the price will be high; if it is easy to make, the cost will be low and the price will be low.
If you want to know the exact price, you need to study the chemical market in detail, consult the merchants, and compare the price. I can't hide the price with a word, because there are many variables, it is difficult to judge.
What are the storage conditions for "4-benzenediol, 2-chloro-1"?
"4-Phenylenediol, 2-Chloro-1" This substance, the way to exist, is related to its properties. This is an organic compound with phenolic characteristics. Because it contains phenolic hydroxyl groups, it is easy to change in light, heat and oxygen, so it should be stored in cool, dark and dry places.
Cooler, low temperature can slow down the speed of its transformation. Heat causes molecular dynamics, which is easy to promote reactions and cause deterioration. Therefore, it is suitable for a temperature not exceeding 25 ° C. If conditions permit, 15-20 ° C is better.
Dark, protected from light. Light as energy can initiate many photochemical reactions, causing structural changes and sexual changes. Hidden in an opaque container, such as a brown bottle, it can reduce the influence of light.
If it is dry, it will be wet without water. Water is a common solvent and reactant, which can cause hydrolysis and isochange. Store in a sealed container, and the ambient humidity should be controlled at 40% -60% to prevent moisture.
And because of its certain poison and rot, the operator should be careful. When stored, it should also be separated from other objects, especially avoid mixing with strong oxygen agents, acids and alkalis to avoid danger. In this way, "4-phenylene glycol, 2-chlorine-1" should be kept for a long time and stable.
Cooler, low temperature can slow down the speed of its transformation. Heat causes molecular dynamics, which is easy to promote reactions and cause deterioration. Therefore, it is suitable for a temperature not exceeding 25 ° C. If conditions permit, 15-20 ° C is better.
Dark, protected from light. Light as energy can initiate many photochemical reactions, causing structural changes and sexual changes. Hidden in an opaque container, such as a brown bottle, it can reduce the influence of light.
If it is dry, it will be wet without water. Water is a common solvent and reactant, which can cause hydrolysis and isochange. Store in a sealed container, and the ambient humidity should be controlled at 40% -60% to prevent moisture.
And because of its certain poison and rot, the operator should be careful. When stored, it should also be separated from other objects, especially avoid mixing with strong oxygen agents, acids and alkalis to avoid danger. In this way, "4-phenylene glycol, 2-chlorine-1" should be kept for a long time and stable.
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