Linshang Chemical
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1,3,5-Trichloro-2,4,6-Triiodobenzene
Linshang Chemical
|
HS Code |
672147 |
| Chemical Formula | C6Cl3I3 |
| Molar Mass | 531.14 g/mol |
| Appearance | Solid (usually white or off - white) |
| Boiling Point | N/A (decomposes before boiling) |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in some non - polar organic solvents like chloroform, benzene |
| Odor | Odorless or very faint odor |
| Stability | Unstable under certain conditions, especially in the presence of reducing agents or high temperatures |
As an accredited 1,3,5-Trichloro-2,4,6-Triiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1,3,5 - trichloro - 2,4,6 - triiodobenzene packaged in a sealed glass bottle. |
| Storage | 1,3,5 - Trichloro - 2,4,6 - triiodobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly - sealed container to prevent moisture absorption and potential reactions. Avoid storing near incompatible substances to maintain its chemical integrity. |
| Shipping | 1,3,5 - trichloro - 2,4,6 - triiodobenzene is a chemical. Ship it in well - sealed containers, following all hazardous materials regulations. Ensure proper labeling and use appropriate shipping methods to prevent leakage and ensure safety during transit. |
Competitive 1,3,5-Trichloro-2,4,6-Triiodobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 1,3,5-Trichloro-2,4,6-Triiodobenzene 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 1, 3, 5 - trichloro - 2, 4, 6 - triiodobenzene?
1% 2C3% 2C5 - trichloro - 2% 2C4% 2C6 - triiodobenzene, Chinese name 1,3,5 - trichloro - 2,4,6 - triiodobenzene. This is an organohalogenated aromatic hydrocarbon with unique chemical properties. Let me explain in detail for you.
Its chemical properties are the first to recommend stability. The aromatic ring structure gives it relatively stable properties. Under normal conditions, it is not easy to spontaneously produce significant chemical reactions. Just like a calm old man, who is not surprised by changes.
Furthermore, the presence of halogen atoms adds a different color to its chemical properties. Chlorine and iodine atoms have different electronegativity and atomic radii. The electronegativity of chlorine atom is relatively high, and the electron cloud density is biased towards itself, which makes the electron cloud density of benzene ring decrease, and the electrophilic substitution activity of benzene ring decreases. Although the electronegativity of iodine atom is not as good as that of chlorine, the atomic radius is large, and the steric hindrance effect is obvious. These two effects are intertwined and affect the reactivity and selectivity of the compound.
In the electrophilic substitution reaction, the electron cloud density of the benzene ring decreases due to the electron-absorbing induction effect of the halogen atom, and the reaction conditions are more severe than that of benzene. And the halogen atom is an ortho-para-site, and the new substituent tends to enter the ortho-site or para-site of the halogen atom. < b In case of nucleophilic reagents, the halogen atom can be replaced by a nucleophilic group to form a new organic compound.
In terms of redox reaction, the valence state of the halogen atom in this compound is relatively stable and generally not prone to redox reaction. However, under the action of strong oxidizing agents or reducing agents, the valence state of the halogen atom may be changed, resulting in changes in molecular structure and properties.
1,3,5-trichloro-2,4,6-triiodobenzene ring interacts with the halogen atom, presenting unique chemical properties and potential application value in organic synthesis, materials science and other fields.
Its chemical properties are the first to recommend stability. The aromatic ring structure gives it relatively stable properties. Under normal conditions, it is not easy to spontaneously produce significant chemical reactions. Just like a calm old man, who is not surprised by changes.
Furthermore, the presence of halogen atoms adds a different color to its chemical properties. Chlorine and iodine atoms have different electronegativity and atomic radii. The electronegativity of chlorine atom is relatively high, and the electron cloud density is biased towards itself, which makes the electron cloud density of benzene ring decrease, and the electrophilic substitution activity of benzene ring decreases. Although the electronegativity of iodine atom is not as good as that of chlorine, the atomic radius is large, and the steric hindrance effect is obvious. These two effects are intertwined and affect the reactivity and selectivity of the compound.
In the electrophilic substitution reaction, the electron cloud density of the benzene ring decreases due to the electron-absorbing induction effect of the halogen atom, and the reaction conditions are more severe than that of benzene. And the halogen atom is an ortho-para-site, and the new substituent tends to enter the ortho-site or para-site of the halogen atom. < b In case of nucleophilic reagents, the halogen atom can be replaced by a nucleophilic group to form a new organic compound.
In terms of redox reaction, the valence state of the halogen atom in this compound is relatively stable and generally not prone to redox reaction. However, under the action of strong oxidizing agents or reducing agents, the valence state of the halogen atom may be changed, resulting in changes in molecular structure and properties.
1,3,5-trichloro-2,4,6-triiodobenzene ring interacts with the halogen atom, presenting unique chemical properties and potential application value in organic synthesis, materials science and other fields.
What are the physical properties of 1, 3, 5 - trichloro - 2, 4, 6 - triiodobenzene?
1% 2C3% 2C5 - trichloro - 2% 2C4% 2C6 - triiodobenzene is an organic compound. Its physical properties are worthy of detailed investigation.
First of all, its appearance is often solid under normal temperature and pressure. This is due to the forces between molecules, such as van der Waals forces and hydrogen bonds, which make the molecules closely arranged, so that they form a solid state. Its color, or white to light yellow powder, is determined by the light absorption and reflection characteristics of its molecular structure.
On the melting point, the presence of chlorine atoms and iodine atoms in the molecular structure enhances the intermolecular forces, resulting in a higher melting point. However, the exact value depends on the precise experimental determination.
As for the boiling point, it is also quite high. Due to its large molecular weight and relatively large chemical bond energy between atoms, a large amount of energy needs to be supplied to overcome the intermolecular forces in order to vaporize it.
In terms of solubility, this compound is non-polar or weakly polar, so it has good solubility in non-polar organic solvents, such as benzene and carbon tetrachloride; in polar solvents such as water, it has poor solubility. This is based on the principle of similarity and miscibility, that is, polar molecules are easily soluble in polar solvents, and non-polar molecules are easily soluble in non-polar solvents.
The density is larger than that of water. Because the relative atomic mass of chlorine and iodine atoms in the molecule is large, the mass per unit volume increases.
The physical properties of this compound are due to its unique molecular structure, the number and location distribution of chlorine and iodine atoms, which deeply affect the intermolecular forces and overall properties.
First of all, its appearance is often solid under normal temperature and pressure. This is due to the forces between molecules, such as van der Waals forces and hydrogen bonds, which make the molecules closely arranged, so that they form a solid state. Its color, or white to light yellow powder, is determined by the light absorption and reflection characteristics of its molecular structure.
On the melting point, the presence of chlorine atoms and iodine atoms in the molecular structure enhances the intermolecular forces, resulting in a higher melting point. However, the exact value depends on the precise experimental determination.
As for the boiling point, it is also quite high. Due to its large molecular weight and relatively large chemical bond energy between atoms, a large amount of energy needs to be supplied to overcome the intermolecular forces in order to vaporize it.
In terms of solubility, this compound is non-polar or weakly polar, so it has good solubility in non-polar organic solvents, such as benzene and carbon tetrachloride; in polar solvents such as water, it has poor solubility. This is based on the principle of similarity and miscibility, that is, polar molecules are easily soluble in polar solvents, and non-polar molecules are easily soluble in non-polar solvents.
The density is larger than that of water. Because the relative atomic mass of chlorine and iodine atoms in the molecule is large, the mass per unit volume increases.
The physical properties of this compound are due to its unique molecular structure, the number and location distribution of chlorine and iodine atoms, which deeply affect the intermolecular forces and overall properties.
What are the main uses of 1, 3, 5 - trichloro - 2, 4, 6 - triiodobenzene?
1% 2C3% 2C5 - trichloro - 2% 2C4% 2C6 - triiodobenzene is 1,3,5 - trichloro - 2,4,6 - triiodobenzene, which is widely used in scientific research and industry.
In the context of scientific research, it is an important intermediate in organic synthesis. The art of organic synthesis aims to create various organic compounds to meet the needs of medicine, materials, etc. 1,3,5 - trichloro - 2,4,6 - triiodobenzene Due to its unique molecular structure, it can be introduced by chemical means through various reactions such as substitution and addition to introduce other functional groups, and then construct complex organic molecules. For example, when synthesizing new drug molecules, using this as the starting material and carefully designed reaction routes can prepare compounds with specific biological activities, paving the way for the development of new drugs.
In the industry, it also has outstanding performance in the field of materials science. In the preparation of special polymer materials, 1,3,5-trichloro-2,4,6-triiodobenzene can participate in the polymerization reaction, giving the polymer material special properties. For example, it has excellent flame retardancy, heat resistance or electrical properties. In the manufacture of electronic materials, polymer materials containing this structure can be used to manufacture the insulating layer of printed circuit boards, which guarantees the stable operation of the circuit board with its excellent thermal stability and electrical insulation. Due to its chlorine, iodine, and other halogen elements, it can be used as a catalyst or co-catalyst in some catalytic reactions, leveraging its halogen atom characteristics to adjust the reaction rate and selectivity, improve the reaction efficiency and product purity, and play an important role in the optimization of chemical production processes.
In the context of scientific research, it is an important intermediate in organic synthesis. The art of organic synthesis aims to create various organic compounds to meet the needs of medicine, materials, etc. 1,3,5 - trichloro - 2,4,6 - triiodobenzene Due to its unique molecular structure, it can be introduced by chemical means through various reactions such as substitution and addition to introduce other functional groups, and then construct complex organic molecules. For example, when synthesizing new drug molecules, using this as the starting material and carefully designed reaction routes can prepare compounds with specific biological activities, paving the way for the development of new drugs.
In the industry, it also has outstanding performance in the field of materials science. In the preparation of special polymer materials, 1,3,5-trichloro-2,4,6-triiodobenzene can participate in the polymerization reaction, giving the polymer material special properties. For example, it has excellent flame retardancy, heat resistance or electrical properties. In the manufacture of electronic materials, polymer materials containing this structure can be used to manufacture the insulating layer of printed circuit boards, which guarantees the stable operation of the circuit board with its excellent thermal stability and electrical insulation. Due to its chlorine, iodine, and other halogen elements, it can be used as a catalyst or co-catalyst in some catalytic reactions, leveraging its halogen atom characteristics to adjust the reaction rate and selectivity, improve the reaction efficiency and product purity, and play an important role in the optimization of chemical production processes.
What are the synthesis methods of 1, 3, 5 - trichloro - 2, 4, 6 - triiodobenzene?
1% 2C3% 2C5 - trichloro - 2% 2C4% 2C6 - triiodobenzene, that is, 1,3,5 - trichloro - 2,4,6 - triiodobenzene, is synthesized as follows:
To prepare 1,3,5 - trichloro - 2,4,6 - triiodobenzene, benzene can be taken as the starting material. Benzene first reacts with chlorine, and benzene can react with chlorine gas under the action of catalysts such as iron chloride. This reaction can introduce chlorine atoms. Due to the same activity of hydrogen atoms on the benzene ring, various isomers of chlorobenzene will be formed, and the reaction conditions need to be carefully regulated so that the reaction mainly generates m-dichlorobenzene.
The substitution reaction of m-dichlorobenzene with iodine is a key step. Generally, it needs to be carried out in a special catalyst and suitable reaction environment. For example, some metal salts are used as catalysts, and in a specific organic solvent, temperature, pressure and other conditions are controlled to gradually replace the remaining hydrogen atoms on the benzene ring with iodine atoms, and mainly replace them at specific positions of m-dichlorobenzene, and finally generate 1,3,5-trichloro-2,4,6-triiodobenzene. In this process, it is extremely important to control the reaction conditions. If the temperature is too high or too low, and the amount of catalyst is not used properly, the product may be impure or the yield may be low. In addition, attention should be paid to the separation and purification steps during the reaction to obtain high-purity 1,3,5-trichloro-2,4,6-triiodobenzene.
To prepare 1,3,5 - trichloro - 2,4,6 - triiodobenzene, benzene can be taken as the starting material. Benzene first reacts with chlorine, and benzene can react with chlorine gas under the action of catalysts such as iron chloride. This reaction can introduce chlorine atoms. Due to the same activity of hydrogen atoms on the benzene ring, various isomers of chlorobenzene will be formed, and the reaction conditions need to be carefully regulated so that the reaction mainly generates m-dichlorobenzene.
The substitution reaction of m-dichlorobenzene with iodine is a key step. Generally, it needs to be carried out in a special catalyst and suitable reaction environment. For example, some metal salts are used as catalysts, and in a specific organic solvent, temperature, pressure and other conditions are controlled to gradually replace the remaining hydrogen atoms on the benzene ring with iodine atoms, and mainly replace them at specific positions of m-dichlorobenzene, and finally generate 1,3,5-trichloro-2,4,6-triiodobenzene. In this process, it is extremely important to control the reaction conditions. If the temperature is too high or too low, and the amount of catalyst is not used properly, the product may be impure or the yield may be low. In addition, attention should be paid to the separation and purification steps during the reaction to obtain high-purity 1,3,5-trichloro-2,4,6-triiodobenzene.
What are the precautions for using 1, 3, 5 - trichloro - 2, 4, 6 - triiodobenzene?
1% 2C3% 2C5 - trichloro - 2% 2C4% 2C6 - triiodobenzene is an organic compound. When using it, many things need to be paid attention to.
First safety protection. This compound contains chlorine and iodine atoms, and may be toxic and irritating. When taking it, be sure to wear suitable protective equipment, such as gloves, goggles and protective clothing, to prevent it from contacting the skin, eyes and respiratory tract. The operation should be carried out in a well-ventilated area, preferably in a fume hood to avoid inhalation of volatile gaseous substances.
This is the storage condition. Store it in a cool, dry and ventilated place, away from fire and oxidants. Due to its chemical properties or more active, improper storage or deterioration, affecting the use effect, or even causing safety accidents.
Furthermore, the use process needs to be precisely controlled. According to specific experimental or production needs, accurate measurement is required to avoid waste, and to prevent subsequent treatment problems or safety hazards caused by excessive dosage. The residue after use must not be discarded at will, and must be properly disposed of in accordance with relevant regulations to prevent environmental pollution.
Also, before conducting relevant operations, it is necessary to fully understand its chemical properties and reaction characteristics. Knowing its stability, possible chemical reactions, etc., can effectively avoid unexpected reactions during operation and ensure the safety of personnel and facilities.
In addition, if you accidentally come into contact with this compound during the experiment or production process, appropriate emergency measures should be taken immediately. If it comes into contact with the skin, rinse with plenty of water immediately; if it enters the eyes, rinse with running water immediately and seek medical attention; if inhaled, quickly move to a fresh air place and seek medical treatment if necessary.
In short, use 1% 2C3% 2C5 - trichloro - 2% 2C4% 2C6 - triiodobenzene must be careful and strictly follow safety regulations and operating procedures to ensure the safety and smooth use of the process.
First safety protection. This compound contains chlorine and iodine atoms, and may be toxic and irritating. When taking it, be sure to wear suitable protective equipment, such as gloves, goggles and protective clothing, to prevent it from contacting the skin, eyes and respiratory tract. The operation should be carried out in a well-ventilated area, preferably in a fume hood to avoid inhalation of volatile gaseous substances.
This is the storage condition. Store it in a cool, dry and ventilated place, away from fire and oxidants. Due to its chemical properties or more active, improper storage or deterioration, affecting the use effect, or even causing safety accidents.
Furthermore, the use process needs to be precisely controlled. According to specific experimental or production needs, accurate measurement is required to avoid waste, and to prevent subsequent treatment problems or safety hazards caused by excessive dosage. The residue after use must not be discarded at will, and must be properly disposed of in accordance with relevant regulations to prevent environmental pollution.
Also, before conducting relevant operations, it is necessary to fully understand its chemical properties and reaction characteristics. Knowing its stability, possible chemical reactions, etc., can effectively avoid unexpected reactions during operation and ensure the safety of personnel and facilities.
In addition, if you accidentally come into contact with this compound during the experiment or production process, appropriate emergency measures should be taken immediately. If it comes into contact with the skin, rinse with plenty of water immediately; if it enters the eyes, rinse with running water immediately and seek medical attention; if inhaled, quickly move to a fresh air place and seek medical treatment if necessary.
In short, use 1% 2C3% 2C5 - trichloro - 2% 2C4% 2C6 - triiodobenzene must be careful and strictly follow safety regulations and operating procedures to ensure the safety and smooth use of the process.
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