Linshang Chemical
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1,3,5-Trichloro-2,4,6-Trifluorobenzene
Linshang Chemical
|
HS Code |
710071 |
| Chemical Formula | C6Cl3F3 |
| Molar Mass | 248.41 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 155 - 157 °C |
| Melting Point | -27 °C |
| Density | 1.63 g/cm³ |
| Solubility In Water | Insoluble |
| Vapor Pressure | At 20°C, relatively low |
| Flash Point | 63 °C |
| Refractive Index | n20/D 1.468 |
As an accredited 1,3,5-Trichloro-2,4,6-Trifluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle of 1,3,5 - trichloro - 2,4,6 - trifluorobenzene with secure chemical - grade packaging. |
| Storage | 1,3,5 - Trichloro - 2,4,6 - trifluorobenzene 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 closed container, preferably made of corrosion - resistant materials. Ensure the storage location is separate from incompatible substances to prevent potential chemical reactions. |
| Shipping | 1,3,5 - trichloro - 2,4,6 - trifluorobenzene is shipped in well - sealed, corrosion - resistant containers. It follows strict hazardous chemical shipping regulations, ensuring secure transport to prevent leakage and environmental or safety risks. |
Competitive 1,3,5-Trichloro-2,4,6-Trifluorobenzene 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-Trifluorobenzene 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 physical properties of 1,3,5-trichloro-2,4,6-trifluorobenzene?
1, 3, and 5 are the three yang, and 2, 4, and 6 are the three yin. According to "Tiangong Kaiwu", everything in the world contains the principle of yin and yang, and this six-number is no exception.
Three yang things are more vigorous, active, and active in nature. From the perspective of natural things, if the sun is the extreme of the sun, it is radiant, endows all things with light and heat, dominates the light of the day, and has a strong driving force and creativity. Like 1, it is the foundation for the germination of all things and is full of pioneering power; 3. In many cultures and affairs, it often expresses a complete and stable state, such as the tripod of three legs, which stands firmly in the world, symbolizing the stability and sustainability of the sun; 5 is in the middle, with the ability to reconcile yin and yang, and contains the meaning of dignity. In the five elements, the earth lives in the center, which is the root of the growth of all things, and the thickness and neutralization of the sun.
The three yin things are more supple, negative, and passive in nature. The moon can be the representative of yin, soft and clear, reflecting the night, and the masculinity of the sun, such as 2, often expressing opposition and balance, like the two poles of yin and yang, mutual restriction and interdependence; 4 in traditional concepts, often related to the four sides, the four sides are established, seem to have convergence and calmness, and express the tranquility and preservation of yin; 6 has the meaning of smooth and perfect, but this perfection is not the perfection of the positive expansion of yang, but the success of yin, the completion of tolerance and acceptance, and the width and tolerance of yin.
The characteristics of yin and yang represented by these six numbers are reflected in everything in the world. Whether it is a natural phenomenon or a change in personnel, they can be observed and analyzed according to this principle of yin and yang. Yang moves and yin is quiet, yang advances and yin retreats, and the intersection of yin and yang produces the wonders of all things changing.
Three yang things are more vigorous, active, and active in nature. From the perspective of natural things, if the sun is the extreme of the sun, it is radiant, endows all things with light and heat, dominates the light of the day, and has a strong driving force and creativity. Like 1, it is the foundation for the germination of all things and is full of pioneering power; 3. In many cultures and affairs, it often expresses a complete and stable state, such as the tripod of three legs, which stands firmly in the world, symbolizing the stability and sustainability of the sun; 5 is in the middle, with the ability to reconcile yin and yang, and contains the meaning of dignity. In the five elements, the earth lives in the center, which is the root of the growth of all things, and the thickness and neutralization of the sun.
The three yin things are more supple, negative, and passive in nature. The moon can be the representative of yin, soft and clear, reflecting the night, and the masculinity of the sun, such as 2, often expressing opposition and balance, like the two poles of yin and yang, mutual restriction and interdependence; 4 in traditional concepts, often related to the four sides, the four sides are established, seem to have convergence and calmness, and express the tranquility and preservation of yin; 6 has the meaning of smooth and perfect, but this perfection is not the perfection of the positive expansion of yang, but the success of yin, the completion of tolerance and acceptance, and the width and tolerance of yin.
The characteristics of yin and yang represented by these six numbers are reflected in everything in the world. Whether it is a natural phenomenon or a change in personnel, they can be observed and analyzed according to this principle of yin and yang. Yang moves and yin is quiet, yang advances and yin retreats, and the intersection of yin and yang produces the wonders of all things changing.
What are the chemical properties of 1,3,5-trichloro-2,4,6-trifluorobenzene?
1% 2C3% 2C5 is trihalogen; 2% 2C4% 2C6 is tribromobenzene. The chemical properties of the two are different, and let me tell you one by one.
First of all, trihalides have high activity of halogen atoms. From the perspective of nucleophilic substitution reaction, halogen atoms are easily attacked by nucleophilic reagents, causing halogen atoms to leave and form new compounds. The capping halogen atom has strong electronegativity, which makes the carbon atoms connected to it positively charged, and is easy to attract nucleophilic reagents to approach. In an alkaline environment, trihalides can react with nucleophilic reagents such as water or alcohols, and halogen atoms are replaced by hydroxyl or alkoxy groups.
Furthermore, halogen atoms of trihalides can participate in the elimination reaction. When confronted with a strong base, the beta-hydrogen atom and the halogen atom can co-eliminate a molecule of hydrogen halide to form unsaturated bonds, such as alkenes or alkynes. This reaction requires specific reaction conditions, such as suitable bases, temperatures, etc.
As for tribromobenzene, its chemical properties are mainly related to the characteristics of the benzene ring. The benzene ring has a conjugated system and its properties are relatively stable. However, because the bromine atom has a certain electron-withdrawing effect, it will affect the distribution of the benzene ring electron cloud.
In the electrophilic substitution reaction, tribromobenzene is more difficult to react than benzene. The electron-withdrawing action of the capped bromine atom reduces the density of the benzene ring electron cloud and increases the difficulty However, under certain conditions, electrophilic substitution reactions such as halogenation, nitrification, and sulfonation can still occur, and the reaction check point is controlled by the localization effect of bromine atoms. Bromine atoms are ortho and para-localizers, so electrophilic substitution reactions mostly occur in the adjacent and para-localizations of bromine atoms.
In addition, the bromine atoms of tribromobenzene can also participate in some special reactions, such as reacting with metal reagents, which can form organometallic compounds, which can be used in organic synthesis steps such as building carbon-carbon bonds.
In summary, the chemical properties of trihalides and tribromobenzene are significantly different, and each plays a unique role in the field of organic synthesis and chemical research. It needs to be used rationally according to specific needs and reaction conditions
First of all, trihalides have high activity of halogen atoms. From the perspective of nucleophilic substitution reaction, halogen atoms are easily attacked by nucleophilic reagents, causing halogen atoms to leave and form new compounds. The capping halogen atom has strong electronegativity, which makes the carbon atoms connected to it positively charged, and is easy to attract nucleophilic reagents to approach. In an alkaline environment, trihalides can react with nucleophilic reagents such as water or alcohols, and halogen atoms are replaced by hydroxyl or alkoxy groups.
Furthermore, halogen atoms of trihalides can participate in the elimination reaction. When confronted with a strong base, the beta-hydrogen atom and the halogen atom can co-eliminate a molecule of hydrogen halide to form unsaturated bonds, such as alkenes or alkynes. This reaction requires specific reaction conditions, such as suitable bases, temperatures, etc.
As for tribromobenzene, its chemical properties are mainly related to the characteristics of the benzene ring. The benzene ring has a conjugated system and its properties are relatively stable. However, because the bromine atom has a certain electron-withdrawing effect, it will affect the distribution of the benzene ring electron cloud.
In the electrophilic substitution reaction, tribromobenzene is more difficult to react than benzene. The electron-withdrawing action of the capped bromine atom reduces the density of the benzene ring electron cloud and increases the difficulty However, under certain conditions, electrophilic substitution reactions such as halogenation, nitrification, and sulfonation can still occur, and the reaction check point is controlled by the localization effect of bromine atoms. Bromine atoms are ortho and para-localizers, so electrophilic substitution reactions mostly occur in the adjacent and para-localizations of bromine atoms.
In addition, the bromine atoms of tribromobenzene can also participate in some special reactions, such as reacting with metal reagents, which can form organometallic compounds, which can be used in organic synthesis steps such as building carbon-carbon bonds.
In summary, the chemical properties of trihalides and tribromobenzene are significantly different, and each plays a unique role in the field of organic synthesis and chemical research. It needs to be used rationally according to specific needs and reaction conditions
What are the main uses of 1,3,5-trichloro-2,4,6-trifluorobenzene?
1,3,5-Trinitrogen-2,4,6-triazobenzene, although this compound has no name in the era mentioned in "Tiangong Kaiwu", it can be analyzed as follows in ancient Chinese.
In this substance, the part of trinitrogen, nitrogen, was known in ancient times, although it was not explicitly stated, its properties may be analogous to the subtlety of qi. Qi, in the ancient concept, is the foundation of all things. Although nitrogen is invisible, it is also a genus of qi. Trinitrogen gathers together, or has special properties, such as changes in stability and activity.
2,4,6-Triazobenzene structure, benzene ring, its shape is like a ring, the structure of the ring in ancient times or can be analogous to the shape of the jade ring, although the material is different, but its ring state can be imagined. Triazobenzene is attached to the benzene ring, like a star in the sky, its position is different, so that the properties of the compound are very different.
As for its main use, it is deduced from the ancient situation, or it can be used as an auxiliary for some special processes. In the dyeing process, it can help the dye to be fixed in the fabric, so that the color lasts for a long time, just like the ancient dyer, mixed with various natural materials, and if this compound exists at that time, it may be a help, so that the color of the dye will not fade over time. In the art of metallurgy, or can participate in the refining of ores, assist in the separation of impurities, such as the use of medicinal stones to refine hardware, this trinitrogen compound can be used as a similar effect to medicinal stones to make metals more pure. Although this material is not contained in "Tiangong Kaiwu", its chemical properties, auxiliary effects in industry and technology, or similar to other things recorded in the book, are all potential for the ancients to improve technology and improve product quality.
In this substance, the part of trinitrogen, nitrogen, was known in ancient times, although it was not explicitly stated, its properties may be analogous to the subtlety of qi. Qi, in the ancient concept, is the foundation of all things. Although nitrogen is invisible, it is also a genus of qi. Trinitrogen gathers together, or has special properties, such as changes in stability and activity.
2,4,6-Triazobenzene structure, benzene ring, its shape is like a ring, the structure of the ring in ancient times or can be analogous to the shape of the jade ring, although the material is different, but its ring state can be imagined. Triazobenzene is attached to the benzene ring, like a star in the sky, its position is different, so that the properties of the compound are very different.
As for its main use, it is deduced from the ancient situation, or it can be used as an auxiliary for some special processes. In the dyeing process, it can help the dye to be fixed in the fabric, so that the color lasts for a long time, just like the ancient dyer, mixed with various natural materials, and if this compound exists at that time, it may be a help, so that the color of the dye will not fade over time. In the art of metallurgy, or can participate in the refining of ores, assist in the separation of impurities, such as the use of medicinal stones to refine hardware, this trinitrogen compound can be used as a similar effect to medicinal stones to make metals more pure. Although this material is not contained in "Tiangong Kaiwu", its chemical properties, auxiliary effects in industry and technology, or similar to other things recorded in the book, are all potential for the ancients to improve technology and improve product quality.
What are the preparation methods of 1,3,5-trichloro-2,4,6-trifluorobenzene?
There are many ways to make trichloro and tribromomethane, so let me go through them one by one.
First, methane is reacted with chlorine and bromine gas by light. Put methane in a place with sufficient light and slowly pass chlorine or bromine gas. The hydrogen atoms in methane can be gradually replaced by chlorine or bromine. After multiple steps, trichloromethane or tribromomethane can be obtained. However, the by-products of this reaction are complicated, and the separation and purification are quite difficult.
Second, methanol is used as the starting material. Methanol and hydrogen chloride or hydrogen bromide can form chloromethane or bromomethane under the action of a specific catalyst, and then chloromethane or bromomethane can be further reacted with chlorine or bromine gas to produce trichloromethane or tribromomethane. This path is relatively controllable, and the yield may be improved.
Third, use carbon tetrachloride or carbon tetrabromide as raw material. If carbon tetrachloride is taken as an example, in the presence of a suitable reducing agent, carbon tetrachloride can be partially reduced to produce trichloromethane. Similarly, carbon tetrabromide can be produced by a similar reaction to tribromomethane. This method requires finding a suitable reducing agent and reaction conditions to ensure the smooth progress of the reaction.
Fourth, use ethanol as the starting material. Ethanol is first oxidized to acetaldehyde, which is then haloformed with chlorine or bromine. Under alkaline conditions, acetaldehyde reacts with excess chlorine or bromine to eventually produce trichloromethane or tribromomethane. This reaction condition is milder and relatively convenient to operate.
The methods for preparing trichloro and tribromomethane have their own advantages and disadvantages. In actual operation, it is necessary to carefully choose the appropriate method according to many factors such as raw material availability, cost, yield and product purity.
First, methane is reacted with chlorine and bromine gas by light. Put methane in a place with sufficient light and slowly pass chlorine or bromine gas. The hydrogen atoms in methane can be gradually replaced by chlorine or bromine. After multiple steps, trichloromethane or tribromomethane can be obtained. However, the by-products of this reaction are complicated, and the separation and purification are quite difficult.
Second, methanol is used as the starting material. Methanol and hydrogen chloride or hydrogen bromide can form chloromethane or bromomethane under the action of a specific catalyst, and then chloromethane or bromomethane can be further reacted with chlorine or bromine gas to produce trichloromethane or tribromomethane. This path is relatively controllable, and the yield may be improved.
Third, use carbon tetrachloride or carbon tetrabromide as raw material. If carbon tetrachloride is taken as an example, in the presence of a suitable reducing agent, carbon tetrachloride can be partially reduced to produce trichloromethane. Similarly, carbon tetrabromide can be produced by a similar reaction to tribromomethane. This method requires finding a suitable reducing agent and reaction conditions to ensure the smooth progress of the reaction.
Fourth, use ethanol as the starting material. Ethanol is first oxidized to acetaldehyde, which is then haloformed with chlorine or bromine. Under alkaline conditions, acetaldehyde reacts with excess chlorine or bromine to eventually produce trichloromethane or tribromomethane. This reaction condition is milder and relatively convenient to operate.
The methods for preparing trichloro and tribromomethane have their own advantages and disadvantages. In actual operation, it is necessary to carefully choose the appropriate method according to many factors such as raw material availability, cost, yield and product purity.
What are the precautions for the use of 1,3,5-trichloro-2,4,6-trifluorobenzene?
1% 2C3% 2C5 and 2% 2C4% 2C6 are chemical substances called trichlorine and trichloroethylene. When using these two, you need to pay attention to many matters.
Trichlorine is toxic and can harm human health. Its smell is pungent, if inhaled in excess, it can cause dizziness, nausea, vomiting, etc., and even life-threatening. Therefore, when using, be sure to ensure good ventilation, or wear a gas mask to prevent inhalation of toxic gases. In addition, trichlorine is flammable, and can cause combustion and explosion in case of open flames and hot topics. When storing and using, do not approach fire sources, heat sources, and keep away from oxidants.
As for trichloroethylene, it is also toxic and has an anesthetic effect on the central nervous system. Long-term exposure may cause many health problems, such as liver damage, skin allergies, etc. When using, it should also be carried out in a well-ventilated place. The operator should wear protective clothing, gloves and other protective equipment to avoid skin contact. Moreover, trichloroethylene can chemically react with certain metals, and the materials used should be carefully selected to prevent corrosion damage.
Both of these are dangerous chemicals, and the use and management must strictly follow relevant laws and operating procedures, and there must be no slack. Purchasing, storage, transportation and other links must be complete with procedures and qualifications, and the use records should also be detailed and accurate for inspection, so as to ensure safety and avoid accidents.
Trichlorine is toxic and can harm human health. Its smell is pungent, if inhaled in excess, it can cause dizziness, nausea, vomiting, etc., and even life-threatening. Therefore, when using, be sure to ensure good ventilation, or wear a gas mask to prevent inhalation of toxic gases. In addition, trichlorine is flammable, and can cause combustion and explosion in case of open flames and hot topics. When storing and using, do not approach fire sources, heat sources, and keep away from oxidants.
As for trichloroethylene, it is also toxic and has an anesthetic effect on the central nervous system. Long-term exposure may cause many health problems, such as liver damage, skin allergies, etc. When using, it should also be carried out in a well-ventilated place. The operator should wear protective clothing, gloves and other protective equipment to avoid skin contact. Moreover, trichloroethylene can chemically react with certain metals, and the materials used should be carefully selected to prevent corrosion damage.
Both of these are dangerous chemicals, and the use and management must strictly follow relevant laws and operating procedures, and there must be no slack. Purchasing, storage, transportation and other links must be complete with procedures and qualifications, and the use records should also be detailed and accurate for inspection, so as to ensure safety and avoid accidents.
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