4 Bromo 2 Iodophenol
Iodobenzene

4-Bromo-2-Iodophenol

Fengxi Chemical

    Specifications

    HS Code

    720200

    Name 4 - Bromo - 2 - Iodophenol
    Molecular Formula C6H4BrIO
    Molecular Weight 286.899 g/mol
    Appearance Solid (likely white to off - white)
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Density Data needed
    Pka Data needed
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Flash Point Data needed
    Chemical Formula C6H4BrIO
    Molar Mass 284.805 g/mol
    Appearance Solid (usually white to off - white)
    Physical State At Room Temperature Solid
    Melting Point 76 - 79 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, dichloromethane
    Odor Odorless or very faint odor
    Hazard Class Irritant (can cause skin, eye and respiratory tract irritation)

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

    Packing & Storage
    Packing 100g of 4 - bromo - 2 - iodophenol in a sealed, labeled chemical - resistant bottle.
    Storage 4 - bromo - 2 - iodophenol should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly - sealed container to prevent moisture absorption and evaporation. Store it separately from oxidizing agents, as it may react with them. Label the storage container clearly for easy identification and safety.
    Shipping 4 - bromo - 2 - iodophenol is shipped in sealed, corrosion - resistant containers. It's carefully packaged to prevent breakage and leakage. Shipment follows strict hazardous chemical regulations to ensure safe transport.
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    4-Bromo-2-Iodophenol
    General Information
    Historical Development
    Fu 4 - Bromo - 2 - Iodophenol, which began to appear in the transformation, has not been studied in detail. However, looking at the evolution of Fu chemistry, various sages worked hard to explore the physical properties and production methods, and gradually became clear.
    At the beginning, the method of research was still simple, and the amount obtained was also sparse. Later learning followed, the process was refined, and the technique was improved, so that the yield gradually increased and the quality became purer. In the past, it was subject to techniques, and it could only be micro-controlled to study its properties; now, due to the goodness of the law, it can be widely produced and meet all needs.
    As the years passed, the use of 4 - Bromo - 2 - Iodophenol in the fields of medicine and materials gradually became apparent. Either for the foundation of pharmaceuticals, or for the yuan of materials, to help all industries move forward. Its process in history, from hidden and obvious, from the micro to the author, for the rise of chemistry, the progress of all industries, contributed to the building blocks, and contributed.
    Product Overview
    4 - Bromo - 2 - Iodophenol is a particularly heavy compound involved in the process of chemical research. Its shape is [specific form, such as white crystalline powder, etc.], and its properties are [related properties, such as certain stability or specific reactivity].
    This compound occupies a significant place in the field of organic synthesis. It can be used as a key intermediate to assist in the construction of many complex organic molecules. Its unique structure, bromine and iodine atoms in the phenol-based ortho-position, endow with different reactivity.
    Preparation method, obtained by multi-step reaction. At first, based on [starting material], through [specific reaction steps and conditions, such as reaction with a reagent at a certain temperature], an intermediate product is obtained; then, after [subsequent reaction steps], 4-Bromo-2-Iodophenol is finally obtained.
    It has considerable potential for practical applications, pharmaceutical research and development or materials science. If it can provide a unique structural unit for the creation of new drugs, it is expected to play a key role in the treatment of specific diseases; in the field of materials, it may be able to give materials specific photoelectric properties, opening up new avenues for the research and development of new materials.
    Physical & Chemical Properties
    4 - Bromo - 2 - Iodophenol is an organic compound, and its physical and chemical properties are of great research value. From the perspective of physical properties, at room temperature, this substance may be in a solid state, with a specific melting point and boiling point. This property is of great significance in the separation and purification process. The determination of its melting point can help to distinguish the purity.
    In terms of chemical properties, the presence of bromine and iodine in the molecule gives it unique reactivity. The reactivity of phenolic hydroxyl groups makes it easy to participate in many chemical reactions. For example, it can neutralize with bases to form corresponding phenolates. At the same time, bromine and iodine atoms can participate in nucleophilic substitution reactions and can be replaced by other nucleophilic reagents, and then various derivatives can be derived. This compound may have potential applications in the field of organic synthesis, and can be used as an intermediate to prepare more complex organic molecules, contributing to the development of organic chemistry.
    Technical Specifications & Labeling
    4 - Bromo - 2 - Iodophenol is an important chemical product. Its preparation process requires strict technical specifications. The first step is to select suitable raw materials to ensure its purity and quality. During the reaction process, parameters such as temperature and pressure must be precisely controlled. If the ratio of raw materials, established standards must be followed to make the reaction sufficient and efficient.
    The identification of the product (commodity parameters) is also crucial. Key information such as its chemical composition and purity grade should be clearly marked. This can help users accurately understand the characteristics of the product and ensure the safety and effect of use. In the quality inspection process, accurate testing methods should be used according to established technical specifications and standards to detect the content of bromine, iodine and other components and impurities in the product in detail to ensure that the product quality meets the requirements.
    Preparation Method
    To prepare 4-Bromo-2-Iodophenol, the raw materials, production process, reaction steps and catalytic mechanism are as follows.
    First take phenol as the initial raw material, use potassium bromide and potassium iodate as reaction aids, in acidic medium, use sulfuric acid as the catalyst, sulfuric acid can promote the protonation of the reaction system and speed up the reaction process. In the first step, phenol is substituted with bromine ion and iodate ion. Bromine ion and iodate ion react under acidic conditions to form an active bromine and iodine intermediate. This intermediate is electrophilically substituted with the phenyl ring of phenol, and the hydroxyl group is an ortho-para-locator. Due to spatial hindrance and electronic effect, it is mainly substituted at the ortho and para-sites of the hydroxyl group to form 4-bromo-2-iodophenol crude product. After the
    reaction is completed, it is extracted with an organic solvent and separated by using the difference in solubility of the product in different solvents. After recrystallization and purification, a suitable solvent is selected. According to the change of solubility of the product and impurities in the solvent at different temperatures, the impurities are removed to obtain a pure 4-Bromo-2-Iodophenol product. In the whole process, sulfuric acid catalysis enhances the activity of the reactants, prompts the reaction to proceed efficiently, and realizes product purification through extraction and recrystallization.
    Chemical Reactions & Modifications
    I have a lot of experience in the chemical reaction and modification of 4 - Bromo - 2 - Iodophenol. The beauty of its reaction lies in the change of conditions, which can lead to different results. If an appropriate agent is used, the temperature and pressure can be adjusted, and the reaction can be expected.
    At the beginning, the reaction is often difficult to control and the product is impure. I think it is necessary to explore the reaction mechanism in depth. After many tests, it is crucial to know the proportion of reactants and the properties of solvents. When modifying, if you want to increase its stability or change its activity, you need to design it delicately.
    Seek it from ancient methods, refer to the theories of various sages, and combine your own experience. Fine-tuning the reaction conditions, or adding more solvents, or adding additives, will eventually improve. The hardships here are not enough for humanity. However, seeing that the performance of the product is gradually improving, the joy in my heart is indescribable. Looking forward to the later researchers, many breakthroughs have been made here, making this chemical substance available to the world and benefiting people.
    Synonyms & Product Names
    4 - Bromo - 2 - Iodophenol is also the same as 4 - Bromo - 2 - Iodophenol. In the field of our research and development, its trade name is the same as the main information.
    If the husband is the same, it is the same name and refers to this thing. For example, in ancient books, or where there is "2 - iodine - 4 - bromophenol", this is also the same as 4 - Bromo - 2 - Iodophenol. The name of the chemical is different, or there is a different order, but it refers to one.
    When it comes to the trade name, it is involved in the circulation of the merchant. Merchants or merchants, or seeking easy access, use the name. If it is sold in the market, or has the name of special, it is expected to be used in a variety of products. However, it is not named, but it is 4 - Bromo - 2 - Iodophenol. Our researchers, please explain the same product name in order to explore, use, and use it.
    Safety & Operational Standards
    4 - Bromo - 2 - Iodophenol is an important chemical product, which is crucial for its safety and operating practices.
    In the experimental operation site, it is essential to ensure good ventilation. This substance has a certain degree of volatility. If the air circulation is not smooth, its volatile components accumulate, or cause damage to the respiratory organs of the experimenter, it may also cause other potential health risks. Therefore, the ventilation facility should be kept in normal operation at all times to maintain the fresh air in the experimental environment.
    Furthermore, when the experimenter is exposed to this chemical, protective measures are essential. Wear professional laboratory clothes, protective gloves and goggles. 4 - Bromo-2 - Iodophenol may cause irritation or even corrosion to the skin and eyes. Protective gloves can avoid direct contact with the skin, and goggles can effectively protect the eyes from possible splash damage.
    In terms of operating standards, the use of this chemical must be accurate. Use a suitable measuring tool and measure according to the exact dose required for the experiment. Excessive use is not only a waste of resources, but may also lead to deviations in experimental results and even cause dangerous chemical reactions.
    When storing, 4 - Bromo-2 - Iodophenol should be kept in a cool, dry place away from sources of ignition and other flammable materials. The nature of this chemical may change due to factors such as temperature, humidity and fire source, which in turn affects its quality. In serious cases, it may cause safety accidents such as fires.
    If you accidentally come into contact with this chemical during the experiment, you should take corresponding emergency measures immediately. If it comes into contact with the skin, rinse quickly with a large amount of water, and then seek medical attention according to the specific situation; if it enters the eyes, you need to rinse the eyes with a large amount of water immediately and seek professional medical assistance as soon as possible.
    Strictly abide by the safety and operation standards of 4-Bromo-2-Iodophenol to ensure the smooth progress of the experiment and protect the safety and health of the experimenters.
    Application Area
    4-Bromo-2-iodophenol is a wonder of chemistry. Its application field is quite wide. In the field of pharmaceutical creation, it can be used as a key intermediate to help synthesize special drugs to treat various diseases and seek well-being for health. In the context of material research and development, it can endow materials with unique properties, such as improving their optical or electrical characteristics, making materials emerge in many high-tech fields. And in the field of fine chemicals, it can be ingeniously reacted to derive a variety of high-value-added products, enrich chemical categories, and meet various industrial and life needs. In fact, it cannot be ignored in chemical research and application, contributing to the development of many fields and promoting the progress of science and technology and life.
    Research & Development
    Today there is a thing called 4 - Bromo - 2 - Iodophenol, which is very important in the field of our chemical research. We do our best to study this thing.
    Investigate its properties, observe its reactions in detail, and hope to explore its mysteries. In the laboratory, we have repeated experiments and observed its changes in different ways. Observe its function with various things, record it in detail, and dare not slack off in the slightest.
    We are well aware that the road of research is long, so we must persevere. We hope to make breakthroughs, so that this substance can be used in industry, medicine and other fields to promote the progress and development of human society. Every experiment is the cornerstone of success. Only by making unremitting explorations can we hope to reach the bright realm and realize its grand vision of research and development.
    Toxicity Research
    The recent toxicity study of 4-Bromo-2-Iodophenol is quite important. Let's take a look at the molecular structure of its molecule, with bromine and iodine atoms on the side of the phenol group. Halogen atoms often have special chemical properties, or can cause changes in their toxicity.
    According to common sense, halogenated phenols often have certain biological activities and toxicity. In this 4-Bromo-2-Iodophenol, bromine and iodine dihalogen atoms coexist, and they may have specific effects with proteins, nucleic acids and other macromolecules in organisms. It may disturb its normal physiological functions, causing cell lesions and metabolic disorders.
    However, in order to clarify its exact toxicity, detailed experiments are needed. To observe its impact on various types of cells, measure its lethal dose and other key indicators to determine the strength of its toxicity and the target of its effect. Only in this way can we have a definite understanding of its toxicity and provide a solid foundation for future application and prevention.
    Future Prospects
    Although the current knowledge of Guanfu 4 - Bromo - 2 - Iodophenol is limited, our generation is eagerly looking forward to its future in the process of chemical research.
    The chemist explores the mystery of material changes and reveals the secrets of natural laws. The unique structure of this compound gives it different chemical properties.
    In the future, it may emerge in the field of organic synthesis. Its bromine and iodine activity check points can lead to various reactions, paving the way for the creation of novel and complex organic molecules. For example, it can be used to build special functional materials, improve the electrical and optical properties of materials with their unique electronic effects, or apply it to new optoelectronic components, opening a chapter in the innovation of optoelectronic devices.
    In addition, in medicinal chemistry, its biological activity may be excavated. After reasonable modification, it is expected to become a targeted drug lead compound, which is a cure for difficult diseases and a cure for people.
    Although there is a long way to go, we chemical researchers should have tenacity and perseverance. We hope to unleash the future potential of this compound and contribute to scientific progress and human well-being.
    Historical Development
    4 - Bromo - 2 - Iodophenol is a chemical substance. Tracing its historical development, chemists in the past have been exploring the synthesis of organic compounds and working tirelessly. At that time, the exploration of halogenated phenols became more and more popular, and many scholars participated in it.
    At first, it was difficult to synthesize such substances, the reaction conditions were harsh, and the yield was low. However, chemists maintained perseverance and tried different methods and reagents repeatedly. After long-term exploration, breakthroughs were made in the selection of reaction raw materials and the use of catalysts.
    With the passage of time, new synthesis technologies emerged, making the preparation of 4 - Bromo - 2 - Iodophenol more efficient and stable. The potential applications of this substance in the fields of medicine and materials have also gained increasing attention, laying the foundation for further research and wide application.
    Product Overview
    4 - Bromo - 2 - Iodophenol is an important chemical substance. Its properties are unique and its appearance often takes on a specific form. This compound is of great significance in many fields of chemical research. In its structure, bromine (Bromo) and iodine (Iodine) atoms are cleverly connected to the phenol (Phenol) base, giving it special chemical properties.
    In terms of reactivity, due to the presence of bromine and iodine atoms, the substance can participate in a variety of organic reactions under specific conditions, exhibiting unique reaction paths and products. In the field of synthesis, chemists can precisely prepare it through exquisitely designed reaction steps according to its characteristics, laying the foundation for the construction of more complex compounds in the future. The study of this substance plays an important role in understanding the chemical behavior of halophenolic compounds and promoting the development of organic chemistry.
    Physical & Chemical Properties
    4 - Bromo - 2 - Iodophenol is an important chemical substance that has attracted much attention in the field of chemical research. Its physical properties, in terms of its appearance, are often white to pale yellow crystalline powder, which is easy to observe and process. Its melting point is in a specific range, about XX ° C to XX ° C. This property is quite valuable in the separation and purification of substances. Its purity can be judged by the determination of melting point.
    When it comes to chemical properties, the atoms of bromine and iodine in this substance give it unique reactivity. The presence of phenolic hydroxyl groups allows it to participate in many chemical reactions, such as neutralization with bases, to generate corresponding phenolates. In organic synthesis, 4-Bromo-2-Iodophenol can be used as a key intermediate. With its activity of bromine and iodine atoms, it can be substituted with a variety of reagents to construct complex organic molecular structures and contribute to the development of organic synthetic chemistry.
    Technical Specifications & Labeling
    4 - Bromo - 2 - Iodophenol is an important chemical product. Its technical specifications and identification (product parameters) are crucial. When it comes to technical specifications, it is necessary to precisely control the steps and conditions of synthesis. From the selection of raw materials, high-purity starting materials need to be selected to ensure the smooth progress of the reaction. During the synthesis process, the temperature, reaction time and the proportion of reactants need to be strictly controlled. For example, in a specific reaction vessel, the corresponding reagents are added in a precise proportion to maintain a moderate temperature, and the product can be prepared after several hours of reaction.
    As for the identification (product parameters), its chemical purity should be clearly marked, which is related to the applicability of the product in various application scenarios. At the same time, it is necessary to indicate its physical properties, such as color, shape, etc. In addition, the storage conditions should also be clearly marked to ensure the stability and quality of the product. In this way, this product can be properly used and circulated in the chemical industry.
    Preparation Method
    4 - Bromo - 2 - Iodophenol is an important organic compound, and its preparation method is crucial. The preparation raw materials can be o-iodophenol and brominating reagents.
    Synthetic process: In an appropriate reaction vessel, dissolve o-iodophenol in a suitable organic solvent, such as dichloromethane. In a low temperature environment, slowly add a brominating reagent, such as liquid bromine or N-bromosuccinimide (NBS). The reaction temperature and reaction process need to be closely monitored to prevent side reactions.
    Reaction steps: The brominating reagent undergoes an electrophilic substitution reaction with o-iodophenol, and the bromine atom replaces the hydrogen atom at a specific position on the benzene ring to generate 4-Bromo-2-Iodophenol. After the reaction is completed, the product is separated and purified through post-processing steps such as extraction, washing, and drying.
    Catalytic mechanism: This reaction can choose Lewis acid such as ferric chloride or aluminum tribromide as a catalyst, which can enhance the activity of the brominating reagent, promote the smooth progress of the electrophilic substitution reaction, and improve the yield and purity of the product. In this way, 4-Bromo-2-Iodophenol can be obtained.
    Chemical Reactions & Modifications
    4 - Bromo - 2 - Iodophenol is an organic compound, and its preparation involves specific chemical reactions, which are related to chemical reactions and modifications. In today's synthesis, phenols are often used as starting materials, and bromine and iodine atoms are introduced by halogenation.
    In the past, such compounds were synthesized under harsh reaction conditions and the yield was not ideal. However, through chemists' unremitting research, many improvements have been made. On the one hand, the catalyst used in the reaction is optimized to greatly improve its activity and selectivity, thereby improving the purity and yield of the product. For example, the application of new metal catalysts can precisely adjust the reaction check point and reduce side reactions.
    On the other hand, the control of the reaction solvent and temperature is more precise. A suitable solvent can enhance the solubility and reactivity of the reactants, and a suitable temperature ensures that the reaction proceeds efficiently in the expected direction. This improvement makes the synthesis of 4-Bromo-2-Iodophenol more efficient and stable, meeting the needs of various fields for this compound.
    Synonyms & Product Names
    4 - Bromo - 2 - Iodophenol has a unique position in the field of my chemical research. Its synonyms and trade names are an indispensable part of scientific research and communication.
    Looking at past research, many scholars refer to this thing under different names. Or give it another name according to the characteristics of its chemical structure; or give it another name due to the special preparation method. As for the trade name, merchants will also give different names according to market demand and product positioning.
    In academic discussions, the precise use of synonyms can make communication smoother. The clarity of the trade name helps the order of market transactions. The synonyms and trade names of 4 - Bromo - 2 - Iodophenol reflect the evolution of cognition in the field of chemistry and the diversity of business practices, providing many clues and convenience for our researchers to explore in depth.
    Safety & Operational Standards
    4 - Bromo-2 - Iodophenol Safety and Operation Specifications
    Fu 4 - Bromo-2 - Iodophenol is an important substance in chemical research. In all aspects of its experimental operation and storage, it is necessary to strictly abide by safety and operation specifications to ensure the smooth operation of the experiment and the safety of personnel.
    #1. Storage Regulations
    This substance should be placed in a cool, dry and well-ventilated place. Avoid being close to fire and heat sources. Because it may have certain chemical activity, it is dangerous when exposed to heat or open flames. And it needs to be stored separately from oxidants, acids and other substances to prevent chemical reactions. The storage place should be equipped with suitable materials to contain the leakage, so as to prevent the timely treatment of accidental leakage.
    #2. The essentials of operation
    When operating, the experimenter must wear appropriate protective equipment. Protective clothing is required to avoid the substance coming into contact with the skin, because it may be irritating or even corrosive to the skin. Protective gloves should also be worn, and the material should be able to effectively block the substance. Face protection is also indispensable. A protective mask can be worn to prevent the substance from splashing into the eyes.
    Operate in the fume hood to ensure the air circulation in the experimental environment and avoid the accumulation of volatile gas from the substance in the room, which endangers the health of the experimenter. During the operation, the action should be steady and light to prevent the container from rupturing due to violent vibration and causing leakage. If the substance is used for reaction, the reaction conditions, such as temperature, pressure, reaction time, etc., need to be strictly controlled, and the operation should be precise according to the established experimental plan. It cannot be changed at will.
    #3. Emergency measures
    If a leak occurs accidentally, the first thing to do is to quickly evacuate the personnel in the leaked contaminated area to a safe area, isolate them, and strictly restrict access. Emergency personnel need to wear self-contained positive pressure breathing apparatus and anti-toxic clothing. Do not let the leakage come into contact with combustible substances. In the event of a small amount of leakage, it can be absorbed by sand, vermiculite or other inert materials. A large number of leaks need to be built embankment or dig a pit to contain, and transferred to a tanker or special collector by pump, recycled or transported to a waste treatment site for disposal.
    If a person accidentally comes into contact with the substance, those who have skin contact should immediately remove the contaminated clothing, rinse with a large amount of flowing water for at least 15 minutes, and then seek medical attention. Those who have eye contact should 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 in time. Inhalers should quickly leave the scene to a fresh air place to keep the respiratory tract unobstructed. If breathing difficulties, give oxygen. If breathing stops, immediately perform artificial respiration and seek medical attention.
    All these safety and operating standards are important guidelines related to 4-Bromo-2-Iodophenol in chemical research. Experimenters must observe and strictly follow them to achieve the purpose of safety experiments and scientific research.
    Application Area
    4 - Bromo - 2 - Iodophenol is a unique chemical substance. In the field of pharmaceutical research and development, it shows unique application value. Due to its special molecular structure, it may be used as a key intermediate for the synthesis of compounds with specific pharmacological activities. For example, when developing targeted drugs for specific diseases, 4 - Bromo - 2 - Iodophenol can combine with other functional groups through a series of chemical reactions to construct drug molecules that precisely act on disease targets.
    In the field of materials science, this substance also has potential applications. It may participate in the preparation of materials with special optical or electrical properties. After ingenious design and synthesis, optical materials that respond uniquely to specific wavelengths of light may be produced and applied to optoelectronic devices, such as sensors and photodetectors, providing opportunities for the improvement of material properties and the development of new functions.
    Research & Development
    Recently, I have been researching chemistry in my country, focusing on 4 - Bromo - 2 - Iodophenol. Its properties are unique, and it has extraordinary ability in organic synthesis.
    At the beginning, I explored its structure, and analyzed the wonder of its atomic connection, revealing the source of its chemical activity. After various experiments, I found out how it and other substances change over time, and investigated the properties of temperature and solvent in detail. Knowing that it is in a certain situation, the reaction is fast and pure, and the yield is quite good.
    Thinking about the development of this product, if the process is optimized and the cost is reduced, it will be widely used in the fields of medicine and materials. With time, good research, or can open up new ways, for the chemical progress, add bricks and mortar, so that 4 - Bromo - 2 - Iodophenol to develop its talents, benefit to everyone.
    Toxicity Research
    4 - Bromo - 2 - Iodophenol Toxicity Study
    In recent times, the technology of chemistry has advanced day by day, and new substances have emerged. 4 - Bromo - 2 - Iodophenol is also one of the substances in chemical research. However, its toxicity must be investigated carefully.
    The toxicity of this substance is related to the life of living beings and the ecology of the world, which cannot be ignored. Looking at past studies, either immersed in water or exposed to gas, the organism touches it, and every change occurs. In microinsects, it may cause reproduction disorder; in plants and trees, it may cause loss of vitality. And it enters the water body, tosses and circulates, and harms the aquarium of fish and shrimp, and the ecological balance is broken because of it.
    It is also tested on the way into the body, either through the mouth and nose, or through the skin. After entering the body, it may disturb the functions of the organs, disrupt the transportation of qi and blood, and damage the ability of nerves. Therefore, due to the toxicity study of 4-Bromo-2-Iodophenol, care should be taken to ensure the safety of all things and the peace of life.
    Future Prospects
    Husband 4 - Bromo - 2 - Iodophenol is also a new substance of transformation. Its unique characteristics, the unique nature, in the field of transformation, the undeveloped, can be seen.
    Its manufacture, bromine-iodine phase, phenol-based nucleus, is so delicate, it must be amazing. In the synthesis, or in need of, it can lead the opposite direction and help to make exquisite. The field of catalysis, or, with its characteristics, promotes the speed of transformation and increases the speed of substances.
    The road of transformation, there is also hope. It may be able to make special effects, cure the disease, and save the suffering of life. And it can be used in the field of materials, or it can be used to make new materials, with extraordinary properties, and it can be used in general utensils to increase its function.
    We don't know much about it today, but we have not yet seen the scene, such as the rise of the dynasty, the light is in sight. We who study and study the theory, study its application, hope to develop the ability of this compound, and use it for the benefit of the world.
    Where to Buy 4-Bromo-2-Iodophenol in China?
    As a trusted 4-Bromo-2-Iodophenol 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 4-Bromo-2-Iodophenol 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 4-bromo-2-iodophenol?
    4-Bromo-2-iodophenol, an organic compound, is widely used in chemical and scientific research fields.
    First, it is often used as a key intermediate in organic synthesis. Due to its high atomic activity of bromine and iodine in its structure, it is easy to participate in many chemical reactions, such as nucleophilic substitution reactions. With this reaction, it can be combined with many nucleophilic reagents to construct complex organic molecules, which is of great significance in the field of drug synthesis and materials science. For example, nucleophilic substitution reactions can be used to react with reagents containing specific functional groups to synthesize novel drug molecules with unique pharmacological activities, or to prepare polymer materials with special properties.
    Second, in the field of pharmaceutical research and development, 4-bromo-2-iodophenol plays an important role. Due to its special chemical structure, it may have certain biological activity. Researchers can explore and develop new antibacterial, anti-inflammatory and even anti-cancer drugs by modifying and modifying its structure. By systematically studying its interaction with targets in vivo, it may be possible to reveal new drug action mechanisms, which will contribute to human health.
    Third, in the field of materials science, 4-bromo-2-iodophenol is also useful. It can be used as a raw material for synthesizing functional materials, such as optoelectronic materials, liquid crystal materials, etc. Its special structure may endow materials with unique optical and electrical properties, injecting new impetus into the development of materials science and promoting technological innovation and progress in related fields.
    What are the physical properties of 4-bromo-2-iodophenol?
    4-Bromo-2-iodophenol is a kind of organic compound. Its physical properties are quite unique and are described as follows:
    Looking at its properties, under room temperature and pressure, 4-bromo-2-iodophenol often takes the form of a white to light yellow crystalline powder. The appearance of this morphology is closely related to its molecular structure and intermolecular interactions. The van der Waals forces and hydrogen bonds between molecules promote the formation of this specific aggregate state, making it appear powder-like and have a certain color.
    When it comes to melting point, the melting point of 4-bromo-2-iodophenol is between 98 ° C and 102 ° C. As an important physical property of a substance, the melting point depends on the strength of the intermolecular forces. In this compound, the bromine, iodine atoms and hydroxyl groups in the molecule affect the intermolecular forces through induction effects and conjugation effects, etc., and then determine the melting point range. When the temperature rises to this range, the molecule obtains enough energy to overcome the intermolecular forces, thus transforming from a solid state to a liquid state.
    Its solubility cannot be ignored. 4-Bromo-2-iodophenol is slightly soluble in water. Although its molecules contain hydroxyl groups, they can form hydrogen bonds with water, but the presence of bromine and iodine atoms enhances the hydrophobicity of the molecule. In general, the interaction with water molecules is weak, so it can only be slightly soluble. In organic solvents such as ethanol, ether, dichloromethane, etc., its solubility is better. This is because these organic solvents and 4-bromo-2-iodophenol molecules can interact with each other through similar phase dissolution principles, forming van der Waals forces and other interactions to promote their dissolution.
    In addition, 4-bromo-2-iodophenol has a certain degree of volatility. Although its volatility is not strong, under certain conditions, such as temperature increase and surface area increase, some molecules can obtain enough energy to break free from the binding of the condensation phase and enter the gas phase. This volatility is also related to its intermolecular force and vapor pressure. In confined spaces or specific environments, the impact of its volatilization needs to be considered.
    What are the chemical properties of 4-bromo-2-iodophenol?
    4-Bromo-2-iodophenol, this is an organic compound. It has the characteristics of phenols and halogenated aromatics.
    Phenolic properties: acidic, because its phenolic hydroxyl group can release protons. In case of alkali, it can form a salt and react with sodium hydroxide solution. The hydrogen of the phenolic hydroxyl group combines with hydroxide ions to form water to form sodium phenol. And it is prone to oxidation reaction, and it is gradually oxidized in the air, and the color becomes darker. In the presence of oxidizing agents, phenolic hydroxyl groups can be oxidized to quinones and other products.
    Halogenated aromatics: Due to the presence of bromine and iodine atoms, nucleophilic substitution reactions can occur. For example, under appropriate nucleophilic reagents and reaction conditions, bromine or iodine atoms can be replaced. Like with sodium alcohol in suitable solvents, bromine or iodine atoms can be replaced by alkoxy groups to form corresponding ether compounds. In addition, under metal catalysis, it can also participate in coupling reactions, such as with boron-containing reagents under palladium catalysis, Suzuki (Suzuki) coupling reactions can occur to form carbon-carbon bonds and generate new aryl compounds, which is very important in the field of organic synthesis.
    What is 4-bromo-2-iodophenol synthesis method?
    To prepare 4-bromo-2-iodophenol, the following method can be used.
    First, phenol is taken as the starting material. The phenyl ring of phenol has high reactivity due to the action of hydroxyl groups.
    The first step can cause the electrophilic substitution reaction of phenol and bromine. The phenol is placed in a suitable solvent, such as dichloromethane, at low temperature and under the action of a catalyst (such as iron powder), bromine is slowly dripped. Due to the adjacent and para-localization effects of hydroxyl groups, bromine preferentially replaces the adjacent and para-hydrogen atoms of hydroxyl groups to obtain a mixture of 2-bromophenol and 4-bromophenol. By means of separation, such as column chromatography, relatively pure 4-bromophenol can be obtained.
    In the next step, the obtained 4-bromophenol is obtained and reacted with iodine. Since bromine is an ortho-site and para-site locator on the phenyl ring, it can guide iodine atoms into the ortho-site of bromine. Under suitable conditions, a suitable oxidant, such as hydrogen peroxide or nitric acid, prompts 4-bromophenol to react with the iodine elemental substance. In this reaction, the oxidant can cause the iodine elemental substance to generate an electrophilic reagent, which can then attack the 4-bromophenol phenyl ring and realize the substitution of the iodine atom in the ortho-site of bromine, During the
    reaction, various reaction conditions, such as temperature, reagent dosage, reaction time, etc., need to be carefully adjusted to ensure that the reaction proceeds in the expected direction and improve the yield and purity of the product.
    4-bromo-2-iodophenol what are the precautions during use
    4-Bromo-2-iodophenol is a commonly used reagent in organic synthesis. When using it, many matters need to be paid attention to.
    First safety protection. This compound is toxic and irritating. When handling, be sure to wear suitable protective equipment, such as laboratory clothes, gloves and goggles, to prevent it from coming into direct contact with the skin and eyes. In case of inadvertent contact, rinse with plenty of water immediately and seek medical treatment according to the specific situation. At the same time, because it may be volatile, the operation should be carried out in a well-ventilated fume hood to avoid inhalation of its volatile gases and damage to the respiratory tract.
    Secondary storage conditions. 4-Bromo-2-iodophenol should be stored in a cool, dry and ventilated place, away from fire sources and oxidants. Because it is more sensitive to light and heat, it should be stored away from light. It can be stored in a brown bottle to prevent it from decomposing due to light and temperature changes, affecting quality and activity.
    Furthermore, when taking it, the dosage should be precisely controlled. Because of the amount used in the reaction, it often has a significant impact on the reaction result. Use clean and dry utensils during taking it to prevent impurities from mixing. Weighing must be accurate, and an analytical balance can be used to ensure the accuracy and repeatability of experimental data.
    Repeated, in chemical reactions, it is necessary to pay attention to its reaction characteristics. The activities of bromine and iodine atoms in 4-bromo-2-iodophenol are different, and under different reaction conditions, they will show different reactivity and selectivity. Before the reaction, the reaction mechanism and conditions should be studied in detail, such as temperature, solvent, catalyst and other factors on the reaction, in order to achieve the expected reaction effect.
    Finally, after the experiment is completed, the waste containing 4-bromo-2-iodophenol must be properly disposed of in accordance with relevant regulations. Do not dump at will to prevent pollution of the environment. According to its chemical properties, suitable methods should be used for harmless treatment to ensure environmental safety.