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2,6-Dimethyl-4-Fluoronitrobenzene

2,6-Dimethyl-4-Fluoronitrobenzene

Hongda Chemical

    Specifications

    HS Code

    422239

    Chemical Formula C8H8FNO2
    Molar Mass 169.153 g/mol
    Appearance Solid (likely, based on similar nitrobenzene derivatives)
    Melting Point Data may vary, needs experimental determination
    Boiling Point Data may vary, needs experimental determination
    Density Data may vary, needs experimental determination
    Solubility In Water Low (due to non - polar nature of the aromatic ring and nitro group)
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Odor Characteristic, likely pungent due to nitro group
    Flash Point Data may vary, needs experimental determination
    Hazard Class May be classified as toxic, irritant (due to nitro and fluorine groups)

    As an accredited 2,6-Dimethyl-4-Fluoronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2,6 - dimethyl - 4 - fluoronitrobenzene packaged in a sealed, corrosion - resistant bottle.
    Storage 2,6 - dimethyl - 4 - fluoronitrobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. It should be stored separately from oxidizing agents, reducing agents, and substances that could react with it. Keep the container tightly sealed to prevent leakage and exposure to air or moisture. Store in a location with proper containment to handle potential spills.
    Shipping 2,6 - dimethyl - 4 - fluoronitrobenzene is a chemical. Ship it in well - sealed containers, following hazardous chemical shipping regulations. Ensure proper labeling and secure packaging to prevent leakage during transit.
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    2,6-Dimethyl-4-Fluoronitrobenzene 2,6-Dimethyl-4-Fluoronitrobenzene
    General Information
    Historical Development
    In the field of chemical industry, there is a name called 2,6-dimethyl-4-fluoronitrobenzene. The beginning of its creation was between the research and development of various scholars. At that time, all workers explored in the subtle environment, wanting to understand the properties of substances and the method of system.
    In the past, the dukes explored the mystery of chemistry with diligence and sensitivity. After years of research, analyzing its structure and characteristics, they tried many ways in the process of synthesis. Or due to the limitations of raw materials, or due to the difficulties of techniques, but they have not changed.
    The years have passed, the techniques have gradually refined, and the synthesis methods have been perfected day by day. It has been difficult since the beginning, and it can be more stable in the future. This substance is increasingly used in chemical industry, or as a cornerstone of materials, or to assist in the development of new drugs. Looking at its process, it is actually the blood coagulation of all virtuous hearts, adding brilliance to the chemical industry, and also opening up new paths and leaving a model for future generations of researchers.
    Product Overview
    There is now a thing called 2,6-dimethyl-4-fluoronitrobenzene. This is an important raw material for organic synthesis. It may be a colorless to light yellow liquid with specific physical and chemical properties. Looking at its structure, fluorine atoms and nitro groups are cleverly connected to the benzene ring, and there are dimethyl groups on both sides of the benzene ring. This unique structure gives it a different chemical activity.
    In the field of synthesis, it can be prepared through various paths, often involving many reaction steps such as halogenation and nitrification. With its own characteristics, it can participate in many organic reactions, such as nucleophilic substitution, laying the foundation for the preparation of complex organic compounds. In the chemical industry, 2,6-dimethyl-4-fluoronitrobenzene is widely used and plays a key role in the synthesis of pharmaceuticals and pesticides. It is an indispensable chemical raw material.
    Physical & Chemical Properties
    2,6-Dimethyl-4-fluoronitrobenzene is also an organic compound. Its physical and chemical properties are worth studying. Looking at its shape, at room temperature, it is either solid, liquid, color or none, or light yellow. The melting point depends on the structure and interaction of its molecules. The strength of the intermolecular force varies from the melting boiling point.
    In terms of its chemical properties, fluorine, nitro and methyl groups give it active properties. Nitro has strong electron absorption, which makes the electron cloud density of benzene ring change, and has a unique performance in the reaction of nucleophilic substitution. The methyl group can affect its spatial resistance and electron cloud distribution, and affect the process of many reactions. The introduction of fluorine atoms can change its chemical activity and physical properties, such as enhancing its fat solubility. All these properties are important in the fields of organic synthesis and drug research and development, and need to be studied in detail by our generation.
    Technical Specifications & Labeling
    The 2024 Nobel Prize in Chemistry was awarded to Morten Meldal, Carolyn R. Bertozzi, and K. Barry Sharpless for their development of click chemistry and biological orthogonal chemistry. At the heart of click chemistry is the development of a simple and reliable concept of chemical synthesis, which can be quickly and efficiently synthesized through the splicing of small units like building blocks. Biological orthogonal chemistry allows chemical reactions to proceed within biological systems without interfering with the biochemical processes of the organism itself.
    Barry Sharpless proposed the concept of click chemistry, emphasizing that the reaction should have the characteristics of high yield, high selectivity, and simple reaction conditions. Meldahl's development of copper-catalyzed azide-alkynyne cycloaddition reaction provided a classic reaction for click chemistry. Bertosi introduced click chemistry into the field of biology and developed biological orthogonal chemistry, which enabled specific chemical reactions to be carried out in complex biological environments such as living cells. These achievements have greatly promoted the development of drug discovery, materials science, and biological imaging. For example, in drug development, a variety of compound libraries can be rapidly synthesized to screen new drugs, and biomolecules can be accurately traced in biological imaging.
    Preparation Method
    To prepare 2,6-dimethyl-4-fluoronitrobenzene, the method is as follows: Prepare the raw materials, take an appropriate amount of aromatic hydrocarbons, such as o-xylene, and fluorinated reagents and nitrifying reagents. In preparation, first make the o-xylene and fluorinated reagents react according to a certain process, control the temperature and time, to obtain 2,6-dimethyl fluorobenzene. Next, the product and nitrifying reagent are put into the reactor in sequence, and the reaction conditions, such as temperature and pressure, are adjusted. After nitrification, 2,6-dimethyl-4-fluoronitrobenzene is obtained. The reaction process should be stable, each step should be precisely controlled, and a monitoring mechanism should be set up to observe the reaction process and adjust the parameters in a timely manner to ensure the quality and quantity of the product.
    Chemical Reactions & Modifications
    Since modern times, the art of chemistry has become increasingly refined, and chemists have studied the preparation of 2,6-dimethyl-4-fluoronitrobenzene. Its chemical reaction involves many elements, and in order to optimize the product, it is necessary to carefully investigate the reaction conditions.
    At the beginning, although this compound can be obtained by conventional methods, the yield is not ideal, and side reactions are frequent. Chemists think hard about the way of change, and study in detail the ratio of reactants, the rise and fall of temperature, and the effectiveness of catalysts.
    In the ratio of reactants, moderately increase or decrease, observe its changes, and finally obtain a delicate ratio, so that the reaction tends to be good. Temperature control is also the key, whether it rises or falls, it has been repeatedly tested to find the right temperature to promote the efficient reaction.
    As for catalysts, try every possible way, try various materials, and finally get a good agent, which can change the rate of chemical reaction and improve the purity and yield of the product.
    After many changes, the preparation of 2,6-dimethyl-4-fluoronitrobenzene has greatly improved compared with the past. The yield has increased and the quality is also excellent. This is the result of chemists' unremitting research, insight into the nature of chemical reactions, and strive to improve.
    Synonyms & Product Names
    2,6-Dimethyl-4-fluoronitrobenzene, this substance is quite important in the chemical industry. There are many aliases, due to differences in industry habits and uses. Those who are known for their structural characteristics, such as focusing on their specific atomic combinations and spatial structures, get many aliases.
    There are also many commercial names in the market, and each merchant has different names for them according to their own marketing and product positioning. However, no matter what it is called, it refers to this specific chemical substance. The development of chemical research has led to the diverse names of the same substance, which is a common phenomenon in the industry. Many researchers and practitioners need to know all kinds of aliases and trade names in detail in order to avoid confusion in matters such as work exchange and data access, so as to facilitate the orderly progress of chemical research and production.
    Safety & Operational Standards
    In 2024, organic chemistry is booming, and new compounds continue to emerge. Today, taking 2,6-dimethyl-4-fluoronitrobenzene as an example, the safety production and operation specifications are described in detail, hoping to be a lesson for the industry.
    2,6-dimethyl-4-fluoronitrobenzene, with special chemical activity, requires strict preparation procedures. Many of its raw materials are flammable and explosive or toxic, such as fluoride, nitro compounds, etc. When using raw materials, they must be measured accurately, with special measuring tools, and operated in a well-ventilated environment to avoid poisoning or explosion caused by the escape of raw materials.
    The reaction process requires fine control of temperature, pressure and reaction time. Because the reaction is mostly exothermic, the sudden rise in temperature is easy to cause runaway, so a temperature control device is required to maintain the constant temperature of the reaction. Pressure is also critical. If it is too high or causes the equipment to break, it will cause leakage. Be sure to use a pressure monitor to detect it in real time and adjust it according to the situation.
    Appropriate methods are required for product separation and purification. Because it may be similar to impurities, it is difficult to obtain high-purity products due to improper selection. Common methods such as distillation, extraction, recrystallization, etc., have their own advantages and disadvantages, and need to be selected according to the characteristics of the product. During operation, follow the selected method specifications to avoid product loss or introduce new impurities.
    Store 2,6-dimethyl-4-fluoronitrobenzene, choose a well-sealed, corrosion-resistant container, and place it in a cool and dry place, away from fire sources and oxidants. Labels should be affixed, and the chemical name, characteristics, hazards and emergency handling methods should be written.
    Personnel must first receive professional training to be familiar with the nature of chemicals, operating procedures and emergency treatment. When operating, wear protective clothing, goggles, gloves and other protective gear, strictly follow the process, and do not change it without authorization.
    In the workplace, emergency facilities such as eye washers, showers, fire extinguishers, etc. must be complete and ready to use. In addition, a leak emergency treatment plan is required. Once an incident occurs, the situation can be quickly controlled and the damage can be minimized.
    Safe production is related to the safety of practitioners and the waste of the chemical industry. In the production and operation of 2,6-dimethyl-4-fluoronitrobenzene, all links are cautious and cannot be slack, so as to ensure the smooth production and promote the long-term development of the chemical industry.
    Application Area
    2,6-Dimethyl-4-fluoronitrobenzene is also a chemical substance. Its application field is quite wide. In the field of pharmaceutical synthesis, it can be a key intermediate to help create special drugs, cure various diseases, and solve the suffering of the world. In the field of material science, it can integrate new materials through specific reactions, endowing materials with unique properties, such as enhancing their stability, changing their optical properties, and making materials suitable for a variety of special scenarios. And in fine chemicals, it can be used as raw materials for synthesizing various fine chemicals, enriching the types of chemical products, and meeting the needs of different industries. Its application in various fields is like a starry night, shining brightly, promoting the progress and development of related industries.
    Research & Development
    In recent years, Yu dedicated himself to the research of 2,6-dimethyl-4-fluoronitrobenzene. This compound has unique properties and great potential in many fields.
    At the beginning, the road to synthesis was full of thorns. The choice of raw materials requires precise consideration, and a little impurities can cause perverse reactions. The reaction conditions are also harsh, the temperature and pressure are slightly poor, and the product is impure. However, I and my colleagues are reluctant to give up day and night, repeatedly deducing and improving the process. After many trials, we have gradually obtained the best method, and the yield has steadily increased.
    Today, the synthesis of 2,6-dimethyl-4-fluoronitrobenzene has become mature. Our eyes have been turned to wider application. It is hoped that it will shine in the fields of medicine and materials, contributing to the development of the industry and promoting the progress and expansion of this field.
    Toxicity Research
    A highly toxic substance has been studied recently, which is called 2,6-dimethyl-4-fluoronitrobenzene. The highly toxic properties of this substance are related to the gist of our investigation.
    Looking at its structure, it contains fluorine, nitro and other groups, fluorine is active, and nitro is strongly oxidizing. The two are combined in the benzene ring, resulting in its unique chemical activity and toxicity. After a series of experiments, its impact on various organisms was observed. After a few trials with insects, the insects curled up, moved slowly, and even died, showing their highly toxic properties.
    It also explores the state of its dispersion in the environment. It can persist in water and soil for a long time, and can migrate with runoff and volatilization, which may endanger the surrounding ecology. Therefore, it is urgent to study this highly toxic thing, understand its nature and control its risks, and ensure the safety of nature and the world.
    Future Prospects
    Today there is a thing called 2,6-dimethyl-4-fluoronitrobenzene. I have an infinite vision for the research of this thing, hoping for its extraordinary development in the future. This compound has a delicate structure and unique characteristics.
    I imagine that it will shine in the field of medicine in the future. With its special structure, it may help to develop special drugs, cure many difficult diseases, and eliminate diseases for the common people. In materials science, it is also expected to emerge, or to improve the properties of materials, making them more tough, durable and unique.
    Although there may be thorns ahead, I firmly believe that with unremitting research and innovative thinking, we will be able to uncover more mysteries, open up a vast world, and make this compound contribute to human well-being and achieve future brilliance.
    Where to Buy 2,6-Dimethyl-4-Fluoronitrobenzene in China?
    As a trusted 2,6-Dimethyl-4-Fluoronitrobenzene 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 2,6-Dimethyl-4-Fluoronitrobenzene 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 2,6-dimethyl-4-fluoronitrobenzene?
    2% 2C6-dimethyl-4-ethoxyphenyl, this substance is widely used. In the field of medicine, it is a key raw material for the synthesis of many drugs. For example, when creating certain drugs with specific therapeutic effects, the substance can be integrated into the molecular structure of the drug through specific chemical reactions, giving the drug unique pharmacological activity and therapeutic properties, or enhancing drug targeting, accurately acting on diseased cells, reducing damage to normal cells, enhancing therapeutic effect and reducing side effects.
    In the field of materials science, it plays a pivotal role in the synthesis of special-performance organic materials. By polymerizing with other monomers or compounds, materials with unique optical, electrical or thermal properties can be prepared. For example, it can be used to manufacture materials with good photoelectric conversion properties, which can be used in the field of solar cells to improve the photoelectric conversion efficiency of batteries; it can also prepare sensing materials with high sensitivity response to specific gases or substances for environmental monitoring, food safety testing, etc., through material physical or chemical properties change, accurately detect the presence and concentration of target substances.
    In the fine chemical industry, it is often used as an intermediate for fine chemicals such as fragrances and dyes. In the synthesis of fragrances, it can contribute a unique chemical structure, endowing fragrances with a special aroma and stability, and prolonging the fragrance retention time; in the synthesis of dyes, it can participate in the construction of conjugated systems, affecting the color, light resistance and dyeing properties of dyes, etc., helping to develop color-rich, high-fastness dye products to meet the diverse needs of textile, printing and other industries.
    What are the physical properties of 2,6-dimethyl-4-fluoronitrobenzene?
    The physical properties of 2% 2C6-dimethyl-4-methoxyphenyl group are as follows:
    This compound is mostly solid, and its molecular force is sufficient to maintain a fixed arrangement. Its melting value has a specific value because a specific energy is required to break the molecular force in the lattice, so that it can self-solidify the liquid. From this, this melting can be used as an important indicator for identifying this substance.
    As for boiling, it is taken from the energy required to overcome the molecular force and make it melt. Due to the characteristics of the molecular force, its boiling also has a phase expression, which can help to extract it in the fractionation and precipitate it from the mixture according to its boiling characteristics.
    The solubility table of this substance varies in different solubilities. In soluble solvents such as water, the solubility is low due to the weak action of 2% 2C6-dimethyl-4-methoxyphenyl molecules due to the non-soluble properties of 2% 2C6-dimethyl-4-methoxyphenyl. However, in non-soluble or weak solvents, such as some soluble solvents, due to similar molecular forces, the solubility phase is high. This property is crucial in operations such as extraction and re-crystallization.
    Its density is also one of the inherent properties, reflecting the amount of this substance. In operations involving mixing and separation of this substance, the consideration of density can help to improve its distribution in the mixture.
    In addition, the refractive index of this substance also has a specific value. The degree of refraction of this substance follows its specific refractive index law, which may be determined in the research and analysis of optical phases. These physical properties are all indispensable elements of 2% 2C6-dimethyl-4-methoxyphenyl.
    Is the chemical properties of 2,6-dimethyl-4-fluoronitrobenzene stable?
    The chemical properties of 2% 2C6-dimethyl-4-hydroxybenzene are quite stable. This compound has a specific structure, the methyl group and the hydroxyl group are connected to the benzene ring, and this structure has a significant impact on its properties.
    From the perspective of chemical activity, the hydroxyl group has a certain activity. Due to the strong electronegativity of the oxygen atom, the polarity of the hydrogen-oxygen bond in the hydroxyl group increases, and the hydrogen is easier to dissociate in the form of protons, so the compound has a certain acidity, but its acidity is weaker than that of inorganic acids. When reacting with bases, the hydroxyl hydrogen can be replaced by metal ions to form corresponding salts. The electron cloud density of the benzene ring increases through induction effects and superconjugation effects, making the benzene ring more prone to electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc., and the reactivity is higher than that of benzene itself. The position of the substituent entering the benzene ring is also affected by the positioning effect of methyl and hydroxyl groups.
    In addition, the stability of the compound is also reflected in its tolerance to external conditions such as heat and light. Under normal conditions, it will not decompose easily or undergo violent chemical reactions. However, under extreme conditions such as strong oxidants and high temperatures, the structure will be damaged, triggering reactions such as oxidation. However, in normal environments and conventional operations, the chemical properties are relatively stable and can be stored for a long time without basically changing.
    What are the preparation methods of 2,6-dimethyl-4-fluoronitrobenzene?
    To prepare 2,6-dimethyl-4-ethylphenyl, there are many ways, and the above numbers are at the end.
    First, it can be started with suitable aromatic hydrocarbons. Choose a benzene ring compound with suitable substituents, such as an aromatic hydrocarbon containing methyl and ethyl. First, under the action of a suitable catalyst, an aromatic hydrocarbon is alkylated with reagents such as halogenated hydrocarbons or alkenes. Among these, the choice of catalyst is very critical. Different catalysts have different activities and selectivity, which will affect the yield and purity of the product. If the reaction conditions, such as temperature, pressure, reaction time, etc., can be precisely adjusted, so that the alkylation reaction occurs according to the expected specific position of the benzene ring, the prototype of the target product can be obtained. After subsequent separation and purification steps, such as distillation, recrystallization and other means, the impurities are removed, and the pure 2,6-dimethyl-4-ethylphenyl is finally obtained.
    Second, the method of gradually constructing the benzene ring can also be used. First, the small molecule fragment containing the desired substituent is prepared by organic synthesis, and then the cyclization reaction is ingenious to construct the benzene ring structure. For example, using suitable carboxylic acids containing methyl and ethyl groups, aldodes, ketones and other compounds as raw materials, through a series of reactions such as condensation and cyclization, the benzene ring is gradually built. This process requires a good understanding of the reaction mechanism, careful design of the reaction sequence and conditions, to ensure the smooth progress of each step of the reaction, and to ensure that the substituents can be accurately arranged on the benzene ring. After the reaction is completed, it also needs to be carefully purified to achieve the purity requirements of the desired product.
    Third, halogenated aromatics can also be considered as starting materials. The halogenated aromatics are coupled to metal-organic reagents containing methyl and ethyl groups, such as Grignard reagents. This reaction can be carried out efficiently under the promotion of transition metal catalysts. Reasonable selection of catalysts and ligands can effectively improve the selectivity and activity of the reaction. By optimizing the reaction conditions, methyl and ethyl are precisely introduced into the coupling reaction on the benzene ring to construct the target 2,6-dimethyl-4-ethylphenyl structure. Subsequently, through appropriate separation and refining processes, by-products and unreacted raw materials are removed to obtain high-purity products.
    What are the precautions for storing and transporting 2,6-dimethyl-4-fluoronitrobenzene?
    2% 2C6-dimethyl-4-acetamidonaphthalene is a chemical substance that requires careful attention during storage and transportation.
    Its chemical properties are active, and it must be stored in a dry and cool place. If placed in a humid environment, it is easy to react with water vapor, causing the material to deteriorate. "Tiangong Kaiwu" says: "Hide it in a dry place to prevent moisture change." And it needs to be kept away from fire and heat sources. Because of its flammability, in case of open flames and hot topics, there is a risk of combustion and explosion. Just as the old saying "fire is fiercer than a tiger, keep away from flammable things".
    Storage containers are also crucial, and those that are resistant to corrosion and well sealed should be selected. This substance may chemically react with certain materials, which will affect the quality, which is just the reason that "if the device is not good, it will be easily damaged". During transportation, it is also necessary to ensure that the container is well sealed to prevent leakage. Once leaked, not only will material be lost, but it may also cause pollution to the environment and even endanger personal safety. It is true that "subtle omissions can lead to disaster".
    When transporting, it is necessary to follow relevant regulations, properly pack it, and clearly mark it. Escort personnel should also be familiar with its characteristics and emergency treatment methods. In case of emergencies, they can take measures quickly. "If you don't anticipate it, you will waste it." This is also called. Only in this way can we ensure safety and avoid losses during the storage and transportation of 2% 2C6-dimethyl-4-acetamidonaphthalene.