Linshang Chemical
PRODUCTS
Benzene, 2-Chloro-4-Fluoro-1-(Trifluoromethyl)-
Linshang Chemical
|
HS Code |
198383 |
| Chemical Formula | C7H3ClF4 |
| Molar Mass | 198.545 g/mol |
| Solubility In Water | Expected to be low as it is an organic halide |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
| Chemical Formula | C7H3ClF4 |
| Molecular Weight | 196.54 |
| Appearance | Typically a colorless to light - colored liquid or solid |
| Boiling Point | Data may vary, likely in a certain range based on purity |
| Melting Point | Specific value depends on purity and measurement conditions |
| Density | Varies with temperature and purity |
| Solubility | Solubility in organic solvents may be significant, less so in water |
| Vapor Pressure | Depends on temperature |
| Flash Point | Determined by appropriate testing methods |
| Refractive Index | Characteristic value for the compound |
| Stability | Stable under normal conditions, but may react with certain reagents |
As an accredited Benzene, 2-Chloro-4-Fluoro-1-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2 - chloro - 4 - fluoro - 1 - (trifluoromethyl) benzene in sealed chemical - grade containers. |
| Storage | Store “Benzene, 2 - chloro - 4 - fluoro - 1 - (trifluoromethyl)-” in a cool, well - ventilated area, away from heat, sparks, and open flames. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Isolate it from oxidizing agents and reactive substances. Comply with local regulations for storing hazardous chemicals to prevent leakage and ensure safety. |
| Shipping | The chemical "Benzene, 2 - chloro - 4 - fluoro - 1 - (trifluoromethyl)-" should be shipped in accordance with strict hazardous materials regulations. Use appropriate, well - sealed containers and ensure proper labeling for safe transportation. |
Competitive Benzene, 2-Chloro-4-Fluoro-1-(Trifluoromethyl)- 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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy Benzene, 2-Chloro-4-Fluoro-1-(Trifluoromethyl)- in China?
As a trusted Benzene, 2-Chloro-4-Fluoro-1-(Trifluoromethyl)- manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading Benzene, 2-Chloro-4-Fluoro-1-(Trifluoromethyl)- 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 this product 2-chloro-4-fluoro-1- (trifluoromethyl) benzene
This is a rather complex chemical substance called "This product 2-alkane-4-ene-1- (trienomethyl) naphthalene". Its chemical properties contain many wonders, and let me tell them all.
In this substance, the "alkane" group part makes the molecular structure stable to a certain extent. Alkane groups are usually connected by a single carbon-carbon bond, and this structure gives the molecule relatively stable characteristics. Under generally mild conditions, it is not easy to react violently with other substances.
The existence of the "alkene" group adds activity to the molecule. Olefins contain carbon-carbon double bonds, and the electron cloud density at the double bond is high, which is easy to attack by electrophilic reagents, thus triggering various addition reactions. For example, when encountering hydrogen halide, addition can occur, and halogen atoms and hydrogen atoms are added to the carbon atoms at both ends of the double bond.
In addition, the structure of the "naphthalene" ring also has unique chemical properties. Naphthalene is a fused ring aromatic hydrocarbon and has certain aromaticity. The aromaticity makes the naphthalene ring tend to maintain the stability of its conjugated system during chemical reactions, so it is prone to electrophilic substitution reactions. Under appropriate conditions, nitrification and sulfuric acid can occur with reagents such as nitric acid and sulfuric acid, and nitro and sulfonic acid groups are introduced into the naphthalene ring
As for the substituent "triene methyl", it will affect the electron cloud distribution of the naphthalene ring and the whole molecule, thereby changing the reactivity and selectivity of the substance. It may change the electron cloud density at a specific location of the naphthalene ring, and guide the reaction to occur at a specific location in reactions such as electrophilic substitution.
In summary, the chemical properties of the substance combine stability and reactivity. The stability comes from the alkyl part, and the reactivity is endowed by the alkenyl group, naphthalene ring and special substituent. Under different reaction conditions, it can exhibit a variety of chemical reaction characteristics.
In this substance, the "alkane" group part makes the molecular structure stable to a certain extent. Alkane groups are usually connected by a single carbon-carbon bond, and this structure gives the molecule relatively stable characteristics. Under generally mild conditions, it is not easy to react violently with other substances.
The existence of the "alkene" group adds activity to the molecule. Olefins contain carbon-carbon double bonds, and the electron cloud density at the double bond is high, which is easy to attack by electrophilic reagents, thus triggering various addition reactions. For example, when encountering hydrogen halide, addition can occur, and halogen atoms and hydrogen atoms are added to the carbon atoms at both ends of the double bond.
In addition, the structure of the "naphthalene" ring also has unique chemical properties. Naphthalene is a fused ring aromatic hydrocarbon and has certain aromaticity. The aromaticity makes the naphthalene ring tend to maintain the stability of its conjugated system during chemical reactions, so it is prone to electrophilic substitution reactions. Under appropriate conditions, nitrification and sulfuric acid can occur with reagents such as nitric acid and sulfuric acid, and nitro and sulfonic acid groups are introduced into the naphthalene ring
As for the substituent "triene methyl", it will affect the electron cloud distribution of the naphthalene ring and the whole molecule, thereby changing the reactivity and selectivity of the substance. It may change the electron cloud density at a specific location of the naphthalene ring, and guide the reaction to occur at a specific location in reactions such as electrophilic substitution.
In summary, the chemical properties of the substance combine stability and reactivity. The stability comes from the alkyl part, and the reactivity is endowed by the alkenyl group, naphthalene ring and special substituent. Under different reaction conditions, it can exhibit a variety of chemical reaction characteristics.
In which industries is 2-chloro-4-fluoro-1- (trifluoromethyl) benzene used?
2 + -Alkane-4-ene-1- (triethylmethyl) naphthalene, this substance has a wide range of uses and is used in many industries.
In the pharmaceutical industry, it may be used for drug research and development. Because the compound has a specific chemical structure and properties, it may become a key intermediate in the synthesis of new drugs. Medical experts say: "The formation of a drug begins with the properties of a substance, and it is combined with the magic of the law." The unique structure of this compound may endow the drug with unique pharmacological activity, or help to overcome difficult diseases and add new weapons to the medical profession.
In the field of materials science, it can also be used. The quality of materials is related to the structure and composition. This compound may be incorporated into polymer materials through a specific process to improve material properties. Such as making it have better thermal stability, mechanical properties, etc. Or providing new materials with excellent performance for construction, electronics and other industries, just as "skilled craftsmen use materials, carefully selected to be sturdy and durable."
Furthermore, in the field of fine chemicals, it can be used as synthetic raw materials such as fragrances and dyes. The fragrance of fragrances lies in the delicate combination of ingredients; the color of dyes originates from the unique reaction of substances. This compound may be converted into fragrant and rich fragrances or colorful dyes through clever synthesis paths, adding colorful colors to life, just like "The beauty of chemical industry, turning the ordinary into magic, giving life a splendor."
In the field of organic synthetic chemistry, it is often used as an important starting material or intermediate. Organic synthesis, such as building an exquisite pavilion, requires precision in every step. This compound is rich in reaction check points, can open up a variety of synthesis routes, synthesize complex and special functional organic compounds, and help organic synthetic chemistry continue to move forward. It can be said that "the road of organic synthesis, based on this, expands infinite possibilities."
In the pharmaceutical industry, it may be used for drug research and development. Because the compound has a specific chemical structure and properties, it may become a key intermediate in the synthesis of new drugs. Medical experts say: "The formation of a drug begins with the properties of a substance, and it is combined with the magic of the law." The unique structure of this compound may endow the drug with unique pharmacological activity, or help to overcome difficult diseases and add new weapons to the medical profession.
In the field of materials science, it can also be used. The quality of materials is related to the structure and composition. This compound may be incorporated into polymer materials through a specific process to improve material properties. Such as making it have better thermal stability, mechanical properties, etc. Or providing new materials with excellent performance for construction, electronics and other industries, just as "skilled craftsmen use materials, carefully selected to be sturdy and durable."
Furthermore, in the field of fine chemicals, it can be used as synthetic raw materials such as fragrances and dyes. The fragrance of fragrances lies in the delicate combination of ingredients; the color of dyes originates from the unique reaction of substances. This compound may be converted into fragrant and rich fragrances or colorful dyes through clever synthesis paths, adding colorful colors to life, just like "The beauty of chemical industry, turning the ordinary into magic, giving life a splendor."
In the field of organic synthetic chemistry, it is often used as an important starting material or intermediate. Organic synthesis, such as building an exquisite pavilion, requires precision in every step. This compound is rich in reaction check points, can open up a variety of synthesis routes, synthesize complex and special functional organic compounds, and help organic synthetic chemistry continue to move forward. It can be said that "the road of organic synthesis, based on this, expands infinite possibilities."
What are the preparation methods of 2-chloro-4-fluoro-1- (trifluoromethyl) benzene?
The method of preparing 3-hydroxy-4-ene-1- (triethylmethyl) naphthalene follows the path of organic synthesis. The main ones are the following numbers:
First, the naphthalene is used as a group, and an appropriate substituent is introduced into the naphthalene ring by means of an electrophilic substitution reaction. If the halogenated naphthalene is used as the starting point, nucleophilic substitution is performed with a reagent with triethylmethyl group under suitable catalyst and reaction conditions. Among them, the choice of catalysts is very important, such as certain metal salts or organometallic compounds, which can promote the progress of the reaction and increase the yield of the product. The temperature, time and solvent of the reaction also need to be carefully checked and adjusted.
Second, a compound with alkenes and hydroxyls is used as a raw material, and a naphthalene ring is formed through a multi-step reaction. For example, by a condensation reaction, the molecules are connected, and then through the process of cyclization. In this condensation reaction, or by the method of aldol-ketone condensation, the molecules are polymerized under basic or acidic conditions. When cyclization, the chain molecules can be cycled by heat, light or catalyst, and they can be precisely controlled into the structure of 3-hydroxy- 4-ene-1- (triethylmethyl) naphthalene.
Third, the method of functional group conversion is used to start with compounds with similar structures. Such as naphthalene derivatives with similar substituents, by oxidation, reduction, halogenation, hydrolysis and other reactions, the functional group is transformed and gradually becomes the target product. In this way, it is necessary to be familiar with the reaction characteristics of each functional group, and to ensure that the order and conditions of the reaction are correct, in order to obtain pure and appropriate amounts of 3-hydroxy- 4-ene-1- (triethylmethyl) naphthalene.
The whole process of synthesis requires careful testing of the reaction situation, and the process of the reaction and the purity of the product are monitored by spectroscopy and chromatography. And the separation and purification of the product is also an important section, which can be obtained by distillation, recrystallization, column chromatography, etc. Pure 3-hydroxyl-4-ene-1 - (triethylmethyl) naphthalene.
First, the naphthalene is used as a group, and an appropriate substituent is introduced into the naphthalene ring by means of an electrophilic substitution reaction. If the halogenated naphthalene is used as the starting point, nucleophilic substitution is performed with a reagent with triethylmethyl group under suitable catalyst and reaction conditions. Among them, the choice of catalysts is very important, such as certain metal salts or organometallic compounds, which can promote the progress of the reaction and increase the yield of the product. The temperature, time and solvent of the reaction also need to be carefully checked and adjusted.
Second, a compound with alkenes and hydroxyls is used as a raw material, and a naphthalene ring is formed through a multi-step reaction. For example, by a condensation reaction, the molecules are connected, and then through the process of cyclization. In this condensation reaction, or by the method of aldol-ketone condensation, the molecules are polymerized under basic or acidic conditions. When cyclization, the chain molecules can be cycled by heat, light or catalyst, and they can be precisely controlled into the structure of 3-hydroxy- 4-ene-1- (triethylmethyl) naphthalene.
Third, the method of functional group conversion is used to start with compounds with similar structures. Such as naphthalene derivatives with similar substituents, by oxidation, reduction, halogenation, hydrolysis and other reactions, the functional group is transformed and gradually becomes the target product. In this way, it is necessary to be familiar with the reaction characteristics of each functional group, and to ensure that the order and conditions of the reaction are correct, in order to obtain pure and appropriate amounts of 3-hydroxy- 4-ene-1- (triethylmethyl) naphthalene.
The whole process of synthesis requires careful testing of the reaction situation, and the process of the reaction and the purity of the product are monitored by spectroscopy and chromatography. And the separation and purification of the product is also an important section, which can be obtained by distillation, recrystallization, column chromatography, etc. Pure 3-hydroxyl-4-ene-1 - (triethylmethyl) naphthalene.
What is the market outlook for 2-chloro-4-fluoro-1- (trifluoromethyl) benzene?
The market prospect of Jinfu trimethylolpropane is also related to many parties and cannot be ignored.
From the perspective of its usage, it has a wide range of uses. In the paint industry, it is an indispensable material. Given its good chemical stability and film-forming properties, the paint made is wear-resistant and resistant to chemical attack, so it is in constant demand in construction, machinery, vehicles and other fields. And in the production of polyester resin, it is a key raw material. The polyester resin made from this is widely used in fiber, plastics and other industries, because it can increase its strength and toughness, so that the quality of products is better.
Since the market supply and demand theory, with the gradual development of the economy, various related industries have flourished, and the demand for trimethylolpropane has also been increasing. On the supply side, although there are many workshops, the increase in output cannot be achieved overnight due to the complexity of the process and the constraints of raw materials. Therefore, there is tension between supply and demand, causing its price to fluctuate.
Since the advent of technology, new manufacturing methods and improved processes have been emerging. If new technologies can be widely promoted, they may increase their yield, reduce their cost, and then change their market structure. However, the implementation of new technologies also requires time and capital, and must be tested by the market.
Furthermore, policies and environmental protection regulations also have an impact on their market conditions. Stringent environmental protection, or the suspension or rectification of some workshops with outdated processes, has the effect of reducing supply. And if the policy encourages new technologies and green manufacturing, it will open up a new path for the development of the industry.
To sum up, the market prospect of trimethylolpropane, opportunities and challenges coexist. Although the rising demand is the benefit of its development, supply constraints, technological changes, policy regulations, etc. are all variables. Only when the industry assesses the situation, observes the changes in the market, and emphasizes the innovation of technology can it seize the opportunity in the city and seek long-term development.
From the perspective of its usage, it has a wide range of uses. In the paint industry, it is an indispensable material. Given its good chemical stability and film-forming properties, the paint made is wear-resistant and resistant to chemical attack, so it is in constant demand in construction, machinery, vehicles and other fields. And in the production of polyester resin, it is a key raw material. The polyester resin made from this is widely used in fiber, plastics and other industries, because it can increase its strength and toughness, so that the quality of products is better.
Since the market supply and demand theory, with the gradual development of the economy, various related industries have flourished, and the demand for trimethylolpropane has also been increasing. On the supply side, although there are many workshops, the increase in output cannot be achieved overnight due to the complexity of the process and the constraints of raw materials. Therefore, there is tension between supply and demand, causing its price to fluctuate.
Since the advent of technology, new manufacturing methods and improved processes have been emerging. If new technologies can be widely promoted, they may increase their yield, reduce their cost, and then change their market structure. However, the implementation of new technologies also requires time and capital, and must be tested by the market.
Furthermore, policies and environmental protection regulations also have an impact on their market conditions. Stringent environmental protection, or the suspension or rectification of some workshops with outdated processes, has the effect of reducing supply. And if the policy encourages new technologies and green manufacturing, it will open up a new path for the development of the industry.
To sum up, the market prospect of trimethylolpropane, opportunities and challenges coexist. Although the rising demand is the benefit of its development, supply constraints, technological changes, policy regulations, etc. are all variables. Only when the industry assesses the situation, observes the changes in the market, and emphasizes the innovation of technology can it seize the opportunity in the city and seek long-term development.
What to pay attention to when storing and transporting 2-chloro-4-fluoro-1- (trifluoromethyl) benzene
For 2 + -alkane-4-ene-1- (triene methyl) naphthalene, many matters need to be paid attention to in storage and transportation.
In terms of storage, the first environment should be selected. When placed in a cool and ventilated place, away from fire and heat sources. This is because of its certain volatility and flammability, it is easy to cause danger in case of open fire and hot topics. The warehouse temperature should not be too high to prevent it from accelerating its volatilization or causing abnormal chemical reactions. And it should be stored separately from oxidants, acids, bases, etc., and cannot be mixed. The cover is chemically active, contact with the above substances, or react violently, endangering safety. The storage area should also be equipped with suitable materials to contain leaks in case of leakage, which can be dealt with in time to avoid greater harm.
As for transportation, ensure that the packaging is complete and the loading is secure. During transportation, the speed should not be too fast to avoid sudden braking and bumps, and to prevent material leakage caused by package damage. Transportation vehicles should be equipped with corresponding varieties and quantities of fire equipment and leakage emergency treatment equipment. During transportation, it is necessary to prevent exposure to the sun, rain, and high temperature. During summer transportation, it is advisable to drive in the morning and evening to avoid the high temperature period at noon. If transported by road, drive according to the specified route and do not stop in densely populated areas and residential areas. And transport personnel must be professionally trained to be familiar with the characteristics of the substance and emergency treatment methods, and transport vehicles should also hang warning signs to alert surrounding vehicles and pedestrians. In this way, the storage and transportation of 2 + -alkane-4-ene-1- (trienyl methyl) naphthalene can be maximized to ensure safety.
In terms of storage, the first environment should be selected. When placed in a cool and ventilated place, away from fire and heat sources. This is because of its certain volatility and flammability, it is easy to cause danger in case of open fire and hot topics. The warehouse temperature should not be too high to prevent it from accelerating its volatilization or causing abnormal chemical reactions. And it should be stored separately from oxidants, acids, bases, etc., and cannot be mixed. The cover is chemically active, contact with the above substances, or react violently, endangering safety. The storage area should also be equipped with suitable materials to contain leaks in case of leakage, which can be dealt with in time to avoid greater harm.
As for transportation, ensure that the packaging is complete and the loading is secure. During transportation, the speed should not be too fast to avoid sudden braking and bumps, and to prevent material leakage caused by package damage. Transportation vehicles should be equipped with corresponding varieties and quantities of fire equipment and leakage emergency treatment equipment. During transportation, it is necessary to prevent exposure to the sun, rain, and high temperature. During summer transportation, it is advisable to drive in the morning and evening to avoid the high temperature period at noon. If transported by road, drive according to the specified route and do not stop in densely populated areas and residential areas. And transport personnel must be professionally trained to be familiar with the characteristics of the substance and emergency treatment methods, and transport vehicles should also hang warning signs to alert surrounding vehicles and pedestrians. In this way, the storage and transportation of 2 + -alkane-4-ene-1- (trienyl methyl) naphthalene can be maximized to ensure safety.
Scan to WhatsApp
