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1,2-Diamino-3,4-Difluorobenzene

1,2-Diamino-3,4-Difluorobenzene

Hongda Chemical

    Specifications

    HS Code

    530477

    Chemical Formula C6H6F2N2
    Molar Mass 144.12 g/mol
    Appearance Solid (predicted)
    Solubility In Water Insoluble (predicted)
    Solubility In Organic Solvents Soluble in some organic solvents (predicted)

    As an accredited 1,2-Diamino-3,4-Difluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,2 - diamino - 3,4 - difluorobenzene in 1 - kg sealed bags for chemical packaging.
    Storage 1,2 - Diamino - 3,4 - difluorobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly closed container, preferably made of corrosion - resistant material, to prevent moisture absorption and reaction with air components. Ensure proper labeling for easy identification and to comply with safety regulations.
    Shipping 1,2 - diamino - 3,4 - difluorobenzene is shipped in sealed, corrosion - resistant containers. It follows strict chemical shipping regulations to ensure safe transportation, safeguarding from environmental factors and potential hazards.
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    1,2-Diamino-3,4-Difluorobenzene 1,2-Diamino-3,4-Difluorobenzene
    General Information
    Historical Development
    1,2-Diamino-3,4-difluorobenzene is also an organic compound. Its origin can be traced back to the time of chemical research in the past. At that time, various sages were deeply cultivating in the field of chemistry and wanted to explore new compounds, so they paid attention to such compounds.
    At the beginning, the road of exploration was difficult, the synthesis method was not good, and the yield was quite low. However, the determination of scholars did not give up because of difficulties. After years of study, the skills have gradually refined, and the synthesis method has also been improved.
    In later generations, science and technology have advanced, and the understanding of this compound has deepened. Its use in medicine, materials and other fields has gradually shown. The exploration of the past has paved the way for today's applications. This is a good example of the development of chemistry, and it is also evident in the unremitting efforts of scholars.
    Product Overview
    1,2-diamino-3,4-difluorobenzene is a unique chemical substance. Its color is pure and clear, and it is like a crystalline powder, which often exists in the field of fine chemistry. This substance has a delicate structure, and diamino and difluoro groups are attached to the benzene ring, forming a unique chemical structure.
    In the process of synthesis, precise steps and conditions are required. First take a suitable benzene-based substrate, and use a specific reagent and catalytic method to lead the amino group and fluorine to the appropriate position of the benzene ring. In the meantime, temperature, pressure and reaction time are all key factors. If there is a slight difference, it is difficult to form a pure product.
    It has a wide range of uses. In the development of medicine, it is an important intermediate for the synthesis of special drugs, and helps to create new antibacterial and antiviral drugs. In material science, it can participate in the preparation of materials with special photoelectric properties, endowing materials with excellent characteristics. It is an indispensable substance in the chemical industry. It needs to be further explored by our generation to develop its more potential.
    Physical & Chemical Properties
    In the case of 1,2-diamino-3,4-difluorobenzene, its material has specific physical and chemical properties. Looking at its shape, it is solid at room temperature, pure in color and uniform in quality. Its melting and boiling point has a fixed number, and the melting point is moderate, causing gradual melting when heated. This change is a sign of physics.
    In terms of its chemical properties, both amino and fluorine groups in the molecule are active. Amino groups are basic and can be combined with acids to form a salt genus. Fluorine groups have strong electronegativity, and often cause the transition of electron clouds in the reaction, resulting in different reaction activities of molecules. Its ability to involve various reactions such as nucleophilic substitution is also clear due to its special structure.
    The physical and chemical properties of this substance are useful in many fields. It is either a raw material for the synthesis of fine chemicals, or a key intermediate in drug development. With its unique properties, it contributes to the advancement of science and technology.
    Technical Specifications & Labeling
    1,2-Diamino-3,4-difluorobenzene is an important substance for chemical research. Its technical specifications and labels (product parameters) are related to many research applications.
    Looking at this substance, the first purity of the technical specifications must be extremely high, and impurities must not be too many before it can be used in high-end experiments. On the label, its chemical name "1,2-Diamino-3,4-Difluorobenzene" must be stated to prevent confusion. In the product parameters, the physical and chemical properties should also be detailed, such as melting point, boiling point, solubility, etc., which are all key. In this way, researchers can properly use it in various experiments according to their characteristics to ensure that the research is accurate and promote the progress of the chemical field.
    Preparation Method
    The preparation method of 1,2-diamino-3,4-difluorobenzene is related to the raw material and production process, reaction steps and catalytic mechanism.
    To prepare this product, first take an appropriate amount of fluorobenzene as the starting material, and add a precise ratio of aminating reagents, such as liquid ammonia, to a specific reactor. Adjust the temperature to a suitable range, about 150-200 ° C, and apply the appropriate pressure, about 3-5 MPa. This reaction requires the help of specific metal catalysts, such as copper-based catalysts, to accelerate the reaction process.
    At the beginning of the reaction, fluorobenzene interacts with aminating reagents, and fluorine atoms are gradually replaced by amino groups. After several hours of reaction, the reaction liquid was cooled to room temperature after being monitored by gas chromatography. Subsequently, the product was extracted with an organic solvent, and then refined through reduced pressure distillation, recrystallization and other steps to remove impurities, and finally obtained pure 1,2-diamino-3,4-difluorobenzene. This process has been repeatedly optimized to improve the yield and purity to meet the needs of industry.
    Chemical Reactions & Modifications
    Recent advances in chemistry have deepened the study of 1, 2 - Diamino - 3, 4 - Difluorobenzene. Its chemical reaction and modification are of great importance to chemical research.
    Looking at the reaction, adding a catalytic agent to a specific medium can lead to subtle changes. In the molecular structure, amino groups interact with fluorine groups, making the reaction unique. Or nucleophilic substitution, or electron cloud rearrangement, are all ways of reaction.
    As for modification, it is designed to optimize performance. It can be chemically modified to adjust its activity and stability. For example, adding specific groups to change its solubility or increase its reactivity. This is what chemists are trying their best to do. They hope to use new ideas and new methods to make 1,2-Diamino-3,4-Difluorobenzene more effective in chemical, pharmaceutical and other fields. It can be used by the world, promoting the progress of science and technology, and benefiting all people.
    Synonyms & Product Names
    1,2-diamino-3,4-difluorobenzene is also a chemical substance. Its synonymous name may have another name in the industry. This substance has a wide range of uses and is crucial in the fields of chemical and pharmaceutical research and development.
    In the past, the names of many chemical substances gradually changed with the deepening of research and the expansion of cognition. Synonymous names may vary from region to region and research groups. Today's 1,2-diamino-3,4-difluorobenzene, or other names elsewhere, but its essence has not changed.
    As for the product name, it also varies depending on the marketing strategy and product characteristics of the manufacturer. However, regardless of its name, it is a specific chemical substance that is identified to help researchers and users clarify its meaning and facilitate research and production.
    Safety & Operational Standards
    1,2-diamino-3,4-difluorobenzene, this is a chemical substance. Safety and operating practices are of paramount importance during its preparation and use.
    All operations involving this substance should be done in a well-ventilated place. Because of its irritation and toxicity, it can be harmful to human health if inhaled, ingested or in contact with the skin. When operating, be sure to wear appropriate protective equipment, such as protective gloves, goggles and gas masks, to avoid direct contact and inhalation.
    Furthermore, during operation, the established operating procedures should be strictly followed. Weighing, mixing and other steps should be done carefully to ensure accurate dosage and orderly operation. The instruments used should also be calibrated and cleaned in advance to ensure the accuracy and reliability of the experimental results.
    When storing this substance, also pay attention to proper methods. It should be placed in a cool, dry and ventilated place, away from fire sources and oxidants. At the same time, the storage area should be clearly marked to prevent accidental use.
    In terms of waste disposal, it must not be discarded at will. The waste generated by the experiment should be sorted, collected and treated in accordance with relevant regulations to prevent pollution to the environment.
    Only by strictly adhering to safety and operating standards can we ensure that the research and use of 1,2-diamino-3,4-difluorobenzene can achieve the purpose of personnel safety and environmental friendliness, and can also promote the smooth development of related scientific research.
    Application Area
    1,2-diamino-3,4-difluorobenzene is a special compound in the field of chemistry. Its application field is quite wide. In the way of pharmaceutical research and development, it can be a key intermediate to help create new antibacterial and anti-cancer drugs. With its unique chemical structure, it may be able to precisely fit with specific targets in the body and exert therapeutic effects. In the field of materials science, it can also emerge. Using this as raw material, through exquisite synthesis process, advanced materials with specific electrical and optical properties can be prepared, such as functional materials for high-end display technology, to help it present more brilliant colors and better display effects. From this perspective, 1,2-diamino-3,4-difluorobenzene has great potential in many practical fields, which is waiting for us to explore and make good use of it.
    Research & Development
    In recent years, I have learned a lot about the research of 1,2-diamino-3,4-difluorobenzene. This compound has unique properties and has great potential in various fields.
    At the beginning, I explored the method of its synthesis, but encountered many difficulties. The choice of raw materials, the degree of matching, and the reaction environment all need to be carefully considered. After countless attempts, a feasible method can be obtained. The process of synthesis is like carving beautiful jade, and every step needs to be careful.
    And the initial synthesis, study its properties in detail. Observe its physical properties and measure its chemical activity. This substance has good stability, but under specific conditions, it can show a lively state, which is really wonderful.
    As for the application path, after repeated exploration, it has been found in the fields of medicine and materials, which may be of great use. In medicine, it is expected to become a key ingredient of new drugs; in materials, it may improve performance.
    Although it has been achieved today, there is still a long way to go. In the future, we must continue to study and expand its application, hoping to contribute to the academic and industry, promote its development, and benefit everyone.
    Toxicity Research
    The study of taste and smell of physical properties is crucial to people's livelihood. Today there is 1, 2 - Diamino - 3, 4 - Difluorobenzene, and the study of its toxicity should not be ignored.
    Watching the things of the past, the development of toxicity, or the disease in the body, or the legacy in the environment. 1, 2 - Diamino - 3, 4 - Difluorobenzene Although it is new in research, its toxicology should also be investigated in detail.
    The first exploration of its chemical properties, in the structure, the amino group and fluorine atoms are combined, or there is a unique response, and it touches with various molecules in the organism. It is unknown how it changes.
    The second time it enters the body, it either enters the lungs through breathing, or penetrates through the skin. After entering the body, it flows through the meridians, and wherever it passes, the cells and organs may be disturbed by it.
    Furthermore, in the environment, if this thing escapes, water and soil organisms are in danger. Flowers, plants and trees may be harmed by it; insects, fish, birds and beasts may also be at risk.
    Therefore, the study of toxicity must be rigorous and scientific, and the harm must be investigated in detail, in order to prevent the foundation of disease, protect the health of all living beings, and protect the peace of heaven and earth.
    Future Prospects
    1, 2 - Diamino - 3, 4 - Difluorobenzene is also a thing of transformation. In today's world, science and technology are increasing, and the research of this thing is also deepening. Its future prospects can be improved.
    This object can be used in many fields. In the field of cultivation, it may be the cornerstone of new research, helping those who solve the problem of disease. In the field of materials, it may be an element that can become a new type of material, and the material is special.
    Those who study and research are exhausted and explore its secrets. In a few days, 1, 2 - Diamino - 3, 4 - Difluorobenzene will be able to bring great benefits to the future world, causing things to flourish, and creating a new situation.
    Where to Buy 1,2-Diamino-3,4-Difluorobenzene in China?
    As a trusted 1,2-Diamino-3,4-Difluorobenzene 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 1,2-Diamino-3,4-Difluorobenzene 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 1,2-diamino-3,4-difluorobenzene?
    1,2-Dihydroxy-3,4-diethoxybenzene, although this substance is not directly recorded in Tiangong Kaiwu, its approximate cost can also be deduced from the perspective of ancient pharmacology and technology.
    In terms of pharmacology, compounds containing hydroxyl groups and ethoxy groups often have certain activities. Hydroxyl groups easily form hydrogen bonds with biomolecules in the body, or participate in chemical reactions, affecting cell metabolism. Ancient doctors often used substances with such structures as medicine to regulate human yin and yang. If it can enter the liver meridian, it can help to relieve liver qi and relieve liver depression; if it enters the heart meridian, it can calm the mind and relieve heart palpitations and upset diseases. Although there is no exact ancient text stating the medicinal properties of 1,2-dihydroxy-3,4-diethoxybenzene, the efficacy of similar structural herbs can be speculated.
    On the process, ethoxy can enhance the fat solubility of compounds. In ancient dyeing and fragrance making processes, substances often required have good solubility and adhesion. If this substance is used as a mordant or fragrance additive, it may make the color stronger and the aroma longer lasting. For example, the method of dyeing is recorded in "Tiangong Kaiwu", and many additives can improve the dyeing effect by virtue of their special structure. The characteristics of 1,2-dihydroxy-3,4-diethoxybenzene can be used in similar processes to help pigments better adhere to fabrics, or make fragrances last longer in the carrier.
    Furthermore, its structural stability may affect the reaction process. In ancient chemical processes such as alchemy and paste making, the stable structure can be used as a reaction medium or catalyst to control the reaction rate and direction. 1,2-Dihydroxy-3,4-diethoxybenzene or its own structure plays a key role in specific processes. Although it is not detailed in "Tiangong Kaiwu", it can be inferred according to the principles of ancient chemical processes.
    What are the physical properties of 1,2-diamino-3,4-difluorobenzene?
    1% 2C2-dihydroxy-3% 2C4-diethylnaphthalene is a class of organic compounds. Its physical properties are quite characteristic, let me tell you in detail.
    The color state of this substance is mostly a solid state at room temperature, but the specific color may vary depending on the purity and crystalline form. The common one is a white to light yellow solid.
    On its melting point, due to the specific arrangement and interaction of molecular structure, there is a relatively fixed value. This value is one of the important indicators for the identification of this substance, which can help Fang family to accurately distinguish in experiments.
    Boiling point is also one of its important physical properties. When given specific temperature and pressure conditions, this substance will change from liquid to gaseous state, and this boiling point value is of critical significance for its separation, purification, and application in chemical processes.
    Furthermore, its solubility also needs attention. In common organic solvents, such as ethanol and ether, there may be a certain solubility, but in water, its solubility may be quite limited due to the difference between molecular polarity and water molecules.
    As for density, it also has a corresponding value due to the mass and space occupied by molecules. This value is indispensable in chemical production, product design, and other fields, related to the measurement and mixing ratio of materials.
    Its crystal structure, microscopic view, the molecules are arranged in a specific way, this structure not only affects the above physical properties, but also closely related to chemical properties such as chemical reaction activity and stability.
    All these physical properties are important factors to consider in many fields such as scientific research, industrial production, material research and development, and in-depth investigation can make good use of this material and benefit various causes.
    Is the chemical properties of 1,2-diamino-3,4-difluorobenzene stable?
    The properties of 1% 2C2-dihydroxy-3% 2C4-diethoxy benzene are relatively stable. Its stability comes from the characteristics of its own chemical structure.
    Looking at its molecular structure, the presence of dihydroxy and diethoxy groups has an impact on the distribution of electron clouds in the benzene ring. Hydroxy and ethoxy groups are both donor groups, which will increase the density of the electron cloud in the benzene ring. This structure can enhance the conjugation effect of the electron cloud in the molecule. This conjugate system is like a stable "framework", which makes the molecular configuration not easy to change, thus improving the stability.
    Furthermore, the benzene ring itself has special aromaticity, and its π electrons form a stable delocalized system. This aromatic structure endows the benzene ring with high stability, making it less susceptible to general chemical reactions. The benzene ring in 1% 2C2-dihydroxy-3% 2C4-diethoxybenzene has further enhanced aromaticity under the synergistic action of hydroxyl and ethoxy groups.
    In common chemical environments, this substance exhibits a certain degree of inertness to many common reagents. For example, under mild acid-base conditions, it is difficult to undergo reactions such as ring opening or bond breaking, and the stability formed by its structure can resist such relatively weak chemical reactions. Even in a moderately heated environment, without specific catalysts or strong reaction conditions, it can maintain its own structural integrity, demonstrating good thermal stability.
    In summary, 1% 2C2-dihydroxy-3% 2C4-diethoxy benzene exhibits relatively stable chemical properties due to its unique molecular structure-induced conjugation effect, enhanced aromaticity, and resistance to common chemical reactions.
    What are the synthesis methods of 1,2-diamino-3,4-difluorobenzene?
    The synthesis method of 1% 2C2-dihydroxy-3% 2C4-diethoxybenzene can be based on the ancient books and various ingenious methods.
    First, it can be obtained from common starting materials through several delicate reaction steps. First, take a suitable substrate, add a specific reagent to a special reactor, and simmer slowly over a slow fire to maintain a moderate temperature and duration. This process requires careful regulation of the temperature and reaction conditions. If there is a slight difference, it will fall short.
    Then, the obtained intermediate product is moved into another clean container, and then another reagent is added to stimulate the reaction. This step requires close attention to the process of the reaction, and timely adjustment of the ratio of heat and reactants to ensure that the reaction proceeds in the expected direction. Finally, 1% 2C2-dihydroxy-3% 2C4-diethoxybenzene can be obtained.
    Another method is based on the special path mentioned in ancient books. Select different starting materials, and add various additives in turn at a specific time and environment to make the materials blend and react with each other. At first, a breeze is used to make the reaction start smoothly; then, as the reaction deepens, the wind is increased to accelerate the reaction. In this process, the grasp of the time and the temperature and humidity of the environment are all crucial, and it is difficult to obtain pure products if you are not careful.
    Furthermore, there are also ancient extraction techniques. From natural products, this compound can also be obtained by repeated extraction with unique solvents, according to specific proportions and processes, and then through fine separation and purification processes. However, this approach requires extremely high requirements for the selection of raw materials and the extraction of solvents, and the operation is complicated, requiring exquisite skills and rich experience.
    What is the price range of 1,2-diamino-3,4-difluorobenzene in the market?
    1% 2C2-dihydroxy-3% 2C4-diethoxybenzene, this is a rare and special organic compound with potential application value in many fields such as medicine and chemical industry. However, its price fluctuates greatly in the market, often due to multiple factors such as quality, source, supply and demand situation, and preparation process.
    In terms of quality, high purity is difficult to prepare, the cost is high, and the price is naturally high; while the price of less pure is relatively close to the people. Its source is also a key factor. Natural extractors are expensive due to scarce resources and complicated extraction processes. Although the chemical synthesis method can increase the yield, the complexity of the synthesis process also affects the cost and price.
    At the supply and demand level, if the market demand is strong and the supply is limited, the price will rise; on the contrary, when the supply exceeds the demand, the price will fall. In terms of preparation technology, advanced and efficient processes can reduce costs and stabilize prices; traditional complex processes push up costs and prices.
    Generally speaking, the price per gram of ordinary purity may be in the range of tens of yuan to hundreds of yuan; if it is high purity and special quality, the price per gram can reach hundreds of yuan or even higher. However, the market conditions are changing rapidly, and the exact price needs to refer to the actual market situation and supplier quotations.