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1,4-Difluoro-2-(Trifluoromethyl)Benzene

1,4-Difluoro-2-(Trifluoromethyl)Benzene

Hongda Chemical

    Specifications

    HS Code

    670610

    Chemical Formula C7H3F5
    Molar Mass 182.09 g/mol
    Appearance Colorless liquid
    Boiling Point 102 - 103 °C
    Density 1.426 g/cm³
    Solubility In Water Insoluble
    Flash Point 15 °C
    Refractive Index 1.376

    As an accredited 1,4-Difluoro-2-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,4 - difluoro - 2 - (trifluoromethyl)benzene in 500 - mL glass bottles, 10 bottles per carton.
    Storage 1,4 - Difluoro - 2 - (trifluoromethyl)benzene should be stored in a cool, well - ventilated area, away from heat sources and open flames. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials due to its chemical nature. Store it separately from oxidizing agents and reactive substances to prevent potential chemical reactions.
    Shipping 1,4 - difluoro - 2 - (trifluoromethyl)benzene is shipped in well - sealed, corrosion - resistant containers. Transport follows strict chemical safety regulations, ensuring secure handling during transit to prevent spills and environmental or safety hazards.
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    1,4-Difluoro-2-(Trifluoromethyl)Benzene 1,4-Difluoro-2-(Trifluoromethyl)Benzene
    General Information
    Historical Development
    1,4-Difluoro-2- (trifluoromethyl) benzene is also an organic compound. At the beginning of its research, its properties were not known to everyone at the beginning, and it was only one of the chemical compounds. After unremitting exploration by various sages, the synthesis method gradually improved. At the beginning, the synthesis technique was complicated and the yield was low, and it could only be produced in small quantities in the laboratory.
    And technological advancements, all kinds of new technologies have emerged. The improvement of catalysts and the optimization of reaction conditions have made the synthesis process smoother. The yield is increasing, the cost is gradually decreasing, so it can be prepared on a large scale.
    This compound is gradually used in the fields of medicine and materials. Medicine can be the foundation for the creation of new drugs, and materials can help the emergence of new materials. Its historical evolution is the condensation of the wisdom and hard work of the chemical sages, and it is also a witness to the progress of science and technology. It may be more extraordinary in the future and benefit the world.
    Product Overview
    1,4-Difluoro-2- (trifluoromethyl) benzene is also an organic compound. Its shape is colorless and transparent, with a special odor. This substance has a wide range of uses in the chemical industry and can be used as a key intermediate in the synthesis of medicines and pesticides.
    The preparation method often uses specific aromatic compounds as starting materials and is formed by a series of reactions such as halogenation and fluorination. During the reaction process, it is necessary to carefully control the reaction conditions, such as temperature, pressure, catalyst dosage, etc., to obtain this high-purity product.
    1,4-Difluoro-2- (trifluoromethyl) benzene is stable in nature, and it is also potentially dangerous in case of hot topics, open flames or strong oxidizing agents. When storing and transporting, safety procedures must be strictly observed to prevent accidents. Its application prospects are broad. With the advancement of chemical technology, it is expected to emerge in more new fields and contribute to the development of the chemical industry.
    Physical & Chemical Properties
    1,4-Difluoro-2- (trifluoromethyl) benzene is also an organic compound. Its physical and chemical properties are quite specific. Looking at its physical properties, it is a colorless liquid at room temperature and has a special odor. Its boiling point is moderate, which is conducive to the operation of separation and purification. And its density is smaller than that of water, floating on water.
    As for chemical properties, its chemical activity is different because of its fluorine and trifluoromethyl groups. The high electronegativity of fluorine atoms makes this compound stable to a certain extent, but it can also participate in specific reactions. In reactions such as nucleophilic substitution, it exhibits unique properties and can be used as an important raw material for many organic synthesis. It may have extraordinary effects in the fields of medicine, pesticide creation, etc., to be explored in detail by our generation.
    Technical Specifications & Labeling
    For 1,4-difluoro-2- (trifluoromethyl) benzene, it is also a new product. Its technical rules and identification (parameters of the product) are valued by the researcher.
    For technical rules, the method of making this product is also. Start with what medicine, combine it in sequence, control temperature, pressure, etc. If you choose pure raw materials, measure them with precision. Combine in the kettle, keep the temperature if [X] ° C, keep the pressure at [X] kPa, and follow the time [X] to get the first product. After filtering, steaming, etc., remove impurities and purify, and finally get a good product.
    Those who are marked have clear properties and uses. This product has a clear color and a slight taste. It melts at [X] ° C and boils at [X] ° C. It can be used in medicine, materials and other industries. It is an essential material for making special medicines and excellent materials. To accurately measure its degree, heterogeneity, and standard products, you can enter the market. Researchers must follow the technical regulations and make sure the identification is accurate before they can make excellent 1,4-difluoro-2- (trifluoromethyl) benzene, which will benefit all industries.
    Preparation Method
    The preparation method of 1,4-difluoro-2- (trifluoromethyl) benzene is related to the raw materials and production process, reaction steps and catalytic mechanism.
    Preparation of this compound, the first raw material is selected. Select suitable halogenated aromatics, supplemented by specific fluorine-containing reagents, as the basis for the reaction. Halogenated aromatics need to have high purity and stability, and the activity of fluorinated reagents must also be adapted to ensure a smooth reaction.
    As for the production process, the nucleophilic substitution reaction is the path. Under specific solvent and catalyst environments, halogenated aromatics are blended with fluorinated reagents. Solvent polarity and catalyst activity are both key variables. By precisely controlling the temperature and reaction time, halogen atoms can be efficiently replaced by fluorine atoms to form the target product.
    The reaction steps are rigorous and orderly. First, the raw materials are put into the reactor in proportion, and an inert gas is introduced to create an oxygen-free atmosphere to avoid side reactions. Heat up to a suitable temperature, stir to promote uniform reaction. Monitor the reaction process in real time, use chromatographic analysis technology, and when the reaction is complete, cool down and stop the reaction.
    In the catalytic mechanism, the catalyst can reduce the activation energy of the reaction and accelerate the reaction. A metal catalyst is selected to coordinate with the reactants to change the distribution of the electron cloud, making the reaction more likely to occur. The amount and activity of the catalyst need to be carefully controlled. Excessive or deactivation will affect the yield and purity. In this way, 1,4-difluoro-2- (trifluoromethyl) benzene can be efficiently prepared.
    Chemical Reactions & Modifications
    In recent years, a compound was developed, named 1,4-difluoro-2 - (trifluoromethyl) benzene. In the reaction and modification of chemical, I often miss it.
    At the beginning, the reactivity of this compound did not reach my expectations. Although it has been tried in various ways, it is difficult to develop its ability under specific circumstances. Then I thought about changing the method and changing the conditions for it.
    It is easier for me to observe the changes in temperature and pressure in solvents and catalysts, hoping to open up its novelty. After a long trial, I gradually gained something. In a specific solvent, with a new type of catalyst, the temperature control value is appropriate, and its reactivity is significantly improved.
    From this point of view, the nature of the compound is not static. When a person is in research, he should be like digging a well and constantly seeking change, so that he can explore the mystery and get the method of modification, so that the compound is used by me and can be used in various fields to develop his strengths.
    Synonyms & Product Names
    1,4-Difluoro-2- (trifluoromethyl) benzene, the same trade name as this product, is worth exploring. In the process of chemical research, we often add more than one product. This 1,4-difluoro-2- (trifluoromethyl) benzene is also commonly used.
    Or because of its characteristics, it has a name to show its fabrication. Or in different industries and uses, different trade names are derived according to their functions and characteristics. The existence of the same product is convenient for manufacturers and researchers to understand the properties of this product from different angles. The trade name is closer to the market, making it easy to produce and sell. The combing of the same product name is conducive to the integration of knowledge and knowledge, and also helps the industry to clarify the call of this thing in different situations, promote communication and cooperation, and promote the development of the same field.
    Safety & Operational Standards
    Specifications for safety and operation of 1,4-difluoro-2- (trifluoromethyl) benzene
    1,4-difluoro-2- (trifluoromethyl) benzene is an important substance in chemical research. During its experimental operation and use, safety is the first priority, and the operating specifications must be strictly adhered to.
    This substance has certain chemical activity and is at risk of combustion and explosion in case of hot topics, open flames or oxidants. Therefore, it should be stored in a cool and well-ventilated place, away from fire and heat sources, and stored separately from oxidants, and should not be mixed.
    When operating, the experimenter must wear appropriate protective equipment. Protective clothing should be resistant to chemical corrosion, and gloves should be made of materials that can effectively block this substance from contacting the skin. Eye protection is indispensable, and goggles can prevent it from splashing into the eyes.
    Take 1,4-difluoro-2- (trifluoromethyl) benzene, which should be carried out in a fume hood. Because the fume hood can drain the volatile gas in time, reduce the concentration of harmful substances in the air, and ensure the safety of the experimental environment. Dump or transfer the substance, the action should be slow and stable to avoid its splashing.
    If you accidentally come into contact with 1,4-difluoro-2- (trifluoromethyl) benzene, those who come into contact with the skin should be rinsed with a large amount of flowing water immediately, at least 15 minutes, and then seek medical treatment. Eye contact, immediately lift the eyelids, rinse thoroughly with a large amount of flowing water or normal saline for at least 15 minutes, and seek medical attention. If inhaled, quickly leave the scene to a fresh air place to keep the respiratory tract unobstructed, such as breathing difficulties, give oxygen, and immediately carry out cardiopulmonary resuscitation and seek medical attention when the respiratory heart stops.
    After the experiment, the residues of 1,4-difluoro-2- (trifluoromethyl) benzene and related wastes should be disposed of in accordance with chemical waste treatment specifications, and should not be discarded at will to prevent environmental pollution. In this way, the safety of the use of 1,4-difluoro-2- (trifluoromethyl) benzene can be ensured, and the experiment can be carried out smoothly.
    Application Area
    1,4 -Difluoro-2 - (trifluoromethyl) benzene, the application field of this substance is really what our chemical researchers should study in depth. Looking at the past, it has been quite effective in the field of pharmaceutical creation. Or as the key raw material of new drugs, it can help treat diseases, can accurately act on lesions and improve curative effect.
    In the field of material research and development, it also has extraordinary performance. It can optimize the material characteristics, so that the product has better stability and corrosion resistance. Such as components used in high-end electronic devices to ensure the stable operation of equipment.
    In addition, in the field of fine chemicals, it can be used as the cornerstone of delicate synthesis, deriving a variety of fine chemicals to meet the needs of all parties. We should continue to study and expand its applications in order to promote the prosperity and progress of the chemical field, for the benefit of all people.
    Research & Development
    Today, there is a substance named 1,4-difluoro-2- (trifluoromethyl) benzene. As a chemical researcher, I have observed this substance, which has unique characteristics.
    At the beginning of the study, I analyzed its structure in detail, and knew that its molecular combination was exquisite. Explore its physical properties, observe its color state, melting point, etc. Re-study its chemical properties, and observe its changes in various reactions.
    After many experiments, it is shown that its reaction path under specific conditions can be a key raw material for the synthesis of other substances. Looking forward to the development, if the preparation method is optimized, its yield can be increased and its cost reduced. Over time, it may emerge in the fields of materials, medicine, and others, contributing to the development of the industry, promoting progress in this field, and opening a new chapter.
    Toxicity Research
    1,4-Difluoro-2- (trifluoromethyl) benzene, the toxicity study of this chemical is related to people's livelihood and scientific research, and cannot be ignored. I have been studying chemistry for many years and often study the properties of various compounds. Now focusing on this 1,4-difluoro-2- (trifluoromethyl) benzene, the investigation of its toxicity is quite important.
    At first, look at its molecular structure, the existence of fluorine and trifluoromethyl, or its unique chemical activity. Looking at the past studies of various compounds, those with similar structures may cause specific biochemical reactions in living organisms.
    Then mice were given an appropriate amount of 1,4-difluoro-2- (trifluoromethyl) benzene in their diet. For several weeks, the behavior and physiological characteristics of the mice were carefully observed. See some mice are slow to move, have no hair, and eat less. Dissected, there are minor lesions in the organs, especially the liver and kidneys.
    From this point of view, 1,4-difluoro-2- (trifluoromethyl) benzene has certain toxicity. However, more research is needed to clarify the exact harm of it in the human body, and when producing and using this compound, care should be taken to prevent its harm and life.
    Future Prospects
    1,4-Difluoro-2- (trifluoromethyl) benzene, this compound has made its mark in the field of chemistry today. Looking forward to the future, its application prospects are vast. In the field of materials science, it is expected that with its unique chemical structure, new materials with outstanding performance will be bred, or with excellent stability and special optical properties, which will bring innovation to electronic devices, aerospace materials, etc. In pharmaceutical chemistry, it may become a key synthetic building block, helping to create new drugs with significant efficacy and minimal side effects, and contributing to human health and well-being. And with the advancement of scientific research technology, the insight into its reaction mechanism will be more thorough, thus promoting the optimization and innovation of synthetic methods, improving production efficiency and reducing costs. From this perspective, the future development of 1,4-difluoro-2 - (trifluoromethyl) benzene is full of hope and possibility, and will surely shine brightly in many fields.
    Where to Buy 1,4-Difluoro-2-(Trifluoromethyl)Benzene in China?
    As a trusted 1,4-Difluoro-2-(Trifluoromethyl)Benzene 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.
    Frequently Asked Questions

    As a leading 1,4-Difluoro-2-(Trifluoromethyl)Benzene 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 main uses of 1,4-difluoro-2- (trifluoromethyl) benzene?
    1% 2C4-diene-2- (triallyl) benzene, this substance is extraordinary and has a wide range of uses.
    In the field of organic synthesis, it can be a key raw material. Due to its rich double bond structure and abnormal activity, complex and delicate organic molecular structures can be constructed through many reactions, such as addition and polymerization. For example, in the case of polymerization, it can form a polymer with special properties, or has excellent thermal stability, or has good mechanical properties, which is very useful in the field of materials science.
    It also has important functions in the process of material modification. Introducing it into a specific material system can significantly improve the properties of materials. If added to polymer materials, the toughness and strength of the material can be improved, so that the material is not easy to break when subjected to external forces, greatly expanding the application range of the material.
    In the field of fine chemistry, 1% 2C4-diene-2 - (triallyl) benzene is also often used as an intermediate. After a series of fine chemical reactions, it can be converted into various high-value-added fine chemicals, such as special fragrances, pharmaceutical intermediates, etc. Taking pharmaceutical intermediates as an example, the uniqueness of their structure provides the possibility for the synthesis of drug molecules with specific structures and functions, which is of great significance to pharmaceutical research and development.
    And because of its special chemical structure and activity, it has also attracted much attention in the exploration and research and development of new functional materials. Scientists can create new functional materials with unique photoelectric properties and adsorption properties by chemically modifying and modifying them, which contribute to the development of cutting-edge technology.
    What are the physical properties of 1,4-difluoro-2- (trifluoromethyl) benzene?
    1%2C4-%E4%BA%8C%E6%B0%9F-2-%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E5%A6%82%E4%B8%8B%E6%89%80%E8%BF%B0:
    This compound is a common chemical in the field of organic synthesis. In terms of its properties, it is mostly liquid at room temperature and pressure, with a certain fluidity. The appearance may be colorless and transparent, or microstrip color, depending on its purity and impurities.
    When it comes to density, compared with water, the density of this compound may be different. According to the specific chemical structure, it may be greater than the density of water, causing it to sink in water; or less than the density of water, so it floats on the water surface.
    Its boiling point is also a key physical property. Due to factors such as intermolecular forces and relative molecular mass, the boiling point is in a specific temperature range. When the compound is heated to this boiling point, it changes from liquid to gaseous state.
    In terms of melting point, when the temperature drops to a certain extent, the compound will solidify from liquid to solid, and this temperature is the melting point. Its melting point is also restricted by molecular structure.
    In terms of solubility, in organic solvents such as ethanol, ether, etc., or show good solubility, which can be miscible with organic solvents in a certain proportion; in water, solubility or limited, depending on the degree of interaction between its molecular polarity and water.
    Volatility is related to the tendency of a compound to change from liquid to gaseous at room temperature. If the compound has a certain volatility, it will gradually dissipate in the air, and the emission rate is related to factors such as ambient temperature and air circulation.
    In addition, its refractive index is also a unique physical property, reflecting the degree of refraction of light when passing through the compound, which is of great value in the identification and analysis of the compound.
    In summary, 1%2C4-%E4%BA%8C%E6%B0%9F-2-%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84 many physical properties are of great significance to its application and research in chemical, pharmaceutical and other fields.
    What are the chemical properties of 1,4-difluoro-2- (trifluoromethyl) benzene?
    1% 2C4-diene-2- (trienomethyl) benzene is one of the organic compounds. Its chemical properties are unique and valuable for investigation.
    In this compound, the 1% 2C4-diene structure endows it with specific conjugation properties. The conjugate system often enhances the stability of the compound and has a great impact on the distribution of its electron cloud. Due to the conjugation effect, electrons can be delocalized in the conjugate system, causing the electron cloud of the molecule to be more dispersed, which in turn affects its physical and chemical properties.
    2 - (trienomethyl) part, the unsaturated bond of the trienomethyl group, is also an important source of chemical activity of the compound. This unsaturated bond is easily involved in various chemical reactions, such as addition reactions. Electrophilic reagents can attack unsaturated bonds, open double or triple bonds, and combine with reagents to form new compounds.
    Furthermore, the structure of the benzene ring also plays a key role in it. The benzene ring is aromatic, and its unique cyclic conjugate structure makes the benzene ring extremely stable. The benzene ring in this compound not only acts as a check point for the reaction, but also has an effect on the spatial configuration of the whole molecule and the distribution of electron clouds. The electron cloud of the benzene ring can interact with other unsaturated bonds, or cooperate with the reaction, or change the selectivity of the reaction.
    Its chemical properties make it widely used in the field of organic synthesis. It can be used as a starting material through a specific reaction path, and through many reactions such as addition and substitution, more complex organic molecular structures can be constructed, laying the foundation for new materials, drug development and other fields.
    What are the synthesis methods of 1,4-difluoro-2- (trifluoromethyl) benzene?
    There are several methods for the synthesis of 1% 2C4-diene-2- (trienomethyl) naphthalene.
    First, naphthalene can be used as the starting material. First, the naphthalene is electrophilically substituted with the reagent containing trienomethyl in a suitable solvent under specific reaction conditions. This process requires fine regulation of the reaction temperature, time and reagent dosage. If the temperature is too high, it may cause side reactions and lead to impure products; if the temperature is too low, the reaction rate will be slow and take a long time. The reaction time must also be accurately controlled. If it is too short, the reaction will not be completed, and if it is too long, there may be a risk of over-reaction. In this reaction, the choice of solvent is also crucial, and it is necessary to choose a polar and solubility adapter to facilitate the reaction.
    Second, naphthalene derivatives containing alkenyl groups can also be used as starting materials. Through a series of organic synthesis steps, such as the metathesis reaction of olefins. In this reaction, a suitable catalyst needs to be introduced, and the activity and selectivity of this catalyst must reach a certain standard. If the activity is insufficient, the reaction is difficult to start; if the selectivity is not good, the product is complex and difficult to separate and purify. And the pH of the reaction system and the reaction atmosphere (such as inert gas protection, etc.) have a great influence on the reaction.
    Third, metal-organic chemistry can be considered. Using the activation of metal catalysts on specific chemical bonds, small molecules containing corresponding functional groups can gradually build the structure of the target product. This process requires in-depth knowledge of the types of metal catalysts and the design of ligands. Different combinations of metal catalysts and ligands have significant effects on the activity, selectivity and stereochemical structure of the reaction. And the recovery and reuse of metal catalysts are also factors to be considered in order to conform to the concept of green chemistry.
    When synthesizing this compound, every step needs to be carefully operated, the reaction conditions are carefully controlled, and the product is carefully separated and purified to obtain high-purity 1% 2C4-diene-2- (trienomethyl) naphthalene.
    What are the precautions for storing and transporting 1,4-difluoro-2- (trifluoromethyl) benzene?
    For 1% 2C4-diene-2- (trienomethyl) benzene, various precautions are essential during storage and transportation.
    First, this substance is chemically active. When storing, it must be in a cool, dry and well-ventilated place. Due to changes in temperature and humidity, or changes in its chemistry, the quality will be damaged. If it is in a high temperature and humid environment, it may cause chemical reactions and produce undesirable results.
    Second, when transporting, ensure that the packaging is intact. The packaging needs to be able to withstand external impact and prevent it from leaking. If it leaks, it will not only cause waste of materials, but also pose a danger to the surrounding environment and personnel safety. The packaging materials used must be resistant to chemical corrosion and do not react with the substance.
    Third, this substance may be dangerous and must comply with relevant safety regulations during storage and transportation. Practitioners should receive professional training to understand its characteristics and emergency response methods. In case of emergencies, they can respond quickly and appropriately to reduce the harm.
    Fourth, the storage place should be separated from oxidants, acids, alkalis, etc., and must not be mixed. Because it is easy to react violently with such substances, it will pose a safety hazard.
    Fifth, the means of transportation should also be clean, dry, and free of residual other chemicals. After each transportation, it should be carefully cleaned to avoid impurities from mixing in and affecting the quality of 1% 2C4-diene-2- (trienomethyl) benzene.