4 Bromo 2 Iodobenzenamine
Iodobenzene

4-Bromo-2-Iodobenzenamine

Fengxi Chemical

    Specifications

    HS Code

    132417

    Chemical Formula C6H5BrIN
    Molecular Weight 284.92 g/mol
    Appearance Solid (usually white to off - white)
    Melting Point Data may vary, around [specific value if known] °C
    Boiling Point Data may vary, around [specific value if known] °C
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
    Density Data may vary, around [specific value if known] g/cm³
    Pka Data may vary, around [specific value if known]
    Hazard Class May be harmful if swallowed, inhaled or in contact with skin
    Chemical Formula C6H5BrIN
    Molecular Weight 300.92
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Low (organic compound)
    Solubility In Organic Solvents Soluble (e.g., dichloromethane, chloroform)
    Density Data needed
    Odor Typical of aromatic amines (odor data may vary)
    Stability Stable under normal conditions
    Hazard Class Harmful if swallowed, inhaled or in contact with skin (hazards may vary)
    Chemical Formula C6H5BrIN
    Molar Mass 300.92 g/mol
    Appearance Solid
    Solubility In Water Low (organic compound, non - polar nature)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Stability Sensitive to light and air, may oxidize over time
    Odor Typical of aromatic amines, pungent

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

    Packing & Storage
    Packing 500 g of 4 - bromo - 2 - iodobenzenamine packaged in a sealed, labeled chemical - grade bottle.
    Storage 4 - bromo - 2 - iodobenzenamine should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly - sealed container to prevent moisture absorption and potential reactions. Since it may be toxic, ensure proper labeling and storage in a location inaccessible to unauthorized personnel.
    Shipping 4 - bromo - 2 - iodobenzenamine is shipped in sealed, corrosion - resistant containers. It's transported under strict regulations due to its chemical nature, ensuring proper handling to prevent spills and maintain safety during transit.
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    4-Bromo-2-Iodobenzenamine
    General Information
    Historical Development
    Fu 4 - Bromo - 2 - Iodobenzenamine is also an organic compound. At the beginning of its development, chemists worked hard to explore the synthesis method with various skills. At the beginning, the reaction conditions were harsh, and the yield was quite low, only a small amount of crude products could be obtained. However, the ambition of scholars was not discouraged, and after years of research, the reaction path was improved. Or find new catalysts, or adjust the temperature and pressure subtly, gradually increasing the yield and purity.
    Over the years, this compound has emerged in the fields of medicine and materials. In medicine, it may be a lead compound to help create new drugs; in materials, it can be used as a building unit for special structures. Its development path, not overnight, is the painstaking work of countless chemists, after repeated trial and error, optimization, to have today's achievements, for scientific progress, benefit many industries.
    Product Overview
    4 - Bromo - 2 - Iodobenzenamine, this is a unique chemical substance. It has a unique structure, bromine (Bromo) and iodine (Iod) atoms are conjugated at a specific position in the benzene ring, and connected with an amino group (benzenamine).
    Looking at its physical properties, it may be in the state of powder, white or yellowish in color, and the texture is fine. In terms of chemical properties, it has diverse reactivity because it contains halogen atoms and amino groups. Bromine and iodine atoms can participate in reactions such as nucleophilic substitution, and amino groups can also play a key role in many reactions, such as salting with acids or participating in condensation reactions.
    In the process of synthesis, it can be prepared by various paths. This substance can be used in the field of organic synthesis, or as an important intermediary, which can be used as the cornerstone of more complex organic molecules, which can contribute to chemical research and production. It also has potential application value in the field of fine chemistry.
    Physical & Chemical Properties
    4 - Bromo - 2 - Iodobenzenamine is an important chemical substance. Its physical properties are yellowish in color, crystalline at room temperature, and have a certain melting point. At this temperature, it changes from solid state to liquid state. Its solubility is soluble in organic solvents such as ethanol and ether, but its solubility in water is very small.
    On its chemical properties, the presence of amino groups makes it alkaline and can react with acids to form salts. And the characteristics of bromine and iodine atoms make this substance active in reactions such as nucleophilic substitution. Its phenyl ring structure gives it aromaticity and participates in the typical reactions of many aromatic compounds. Due to these unique physical and chemical properties, 4-Bromo-2-Iodobenzenamine is widely used in the field of organic synthesis and can be used as an intermediate for the preparation of a variety of complex organic compounds.
    Technical Specifications & Labeling
    4 - Bromo - 2 - Iodobenzenamine is also a chemical product. The quality of the product is very important.
    If you want to use this product, you must follow the quality of the product. The extraction of raw materials must be carefully selected to ensure its quality. The quality of the product, such as the quality, quality, and quality, etc., must be carefully controlled. If there is a deviation in the quality, or the quality of the product is insufficient, the quality of the product is guaranteed.
    To the product, the product is not good. Its transformation formula, molecular weight, quality and other information are clear one by one. This is to provide convenience to users, so that they can be used according to their needs. And on the package, there are also clear warnings to inform safety attention. In this way, the production and use of this 4-Bromo-2-Iodobenzenamine can be safe and safe.
    Preparation Method
    Preparation of 4 - Bromo - 2 - Iodobenzenamine
    If you want to make 4 - Bromo - 2 - Iodobenzenamine, you should use good materials and exquisite technology.
    ** In terms of raw materials **: Select suitable benzene-based compounds as the base, followed by brominating agents, iodizing agents, etc. For brominating agents, bromine or its salts can be used, and the same is true for iodizing agents. High purity is required to ensure the purity of the reaction.
    ** Production process **: First make the benzene-based substrate and brominating agent react at a suitable temperature and pressure according to a specific ratio. The temperature is controlled at XX degrees Celsius, and the pressure is maintained at XX kPa. After several hours of reaction, the brominated intermediate is obtained. Then, the intermediate is co-located with the iodizing agent, the reaction conditions are adjusted, the temperature is raised to XX degrees Celsius, and the pressure is fine-tuned to XX kPa, and the reaction is reacted again. This two-step reaction needs to be protected by inert gas to prevent impurities from intervening.
    ** Reaction step **: The first step is bromination, and the stirring rate should be stable to fully blend the reactants. The second step is iodization, pay attention to the monitoring of the reaction process, and measure the degree of reaction by spectroscopy.
    ** Catalytic mechanism **: The selection of a high-efficiency catalyst can reduce the activation energy of the reaction and This catalyst can specifically adsorb the reactants, promote the breaking and recombination of chemical bonds, and improve the yield and purity of the products. In this way, 4-Bromo-2-Iodobenzenamine can be obtained through fine operation.
    Chemical Reactions & Modifications
    The recent study of 4 - Bromo - 2 - Iodobenzenamine has given much thought to the chemical reaction and modification.
    The way of its reaction used to be traditional methods and follow established rules, but the effect was not ideal. In this reaction, if the conditions are slightly different, the results are very different. The temperature and the amount of agent are all about success or failure.
    As for modification, it is not easy. To change its properties, you need to understand the beauty of its structure and the reason for its bonding. Try various means, or add other things to complement it, or change the reaction environment, hoping to obtain new quality.
    Although the road ahead is difficult, our generation of chemical researchers should be persistent and follow the example of ancient tenacity, not afraid of trial and error, and repeatedly explore. With time, we will be able to make breakthroughs in the reaction and modification of 4-Bromo-2-Iodobenzenamine, and obtain exquisite methods to add new colors to the field of chemistry.
    Synonyms & Product Names
    4-Bromo-2-iodoaniline, a synonym for this substance and a trade name, is quite important. Looking back at the past, the names of chemical substances have changed with the times.
    In today's world, 4-bromo-2-iodoaniline, whose synonyms may be named according to structural characteristics, is also named according to its chemical properties. The trade name is often a business marketing consideration, or it is concise and easy to remember, or it contains unique meanings.
    In the past, chemical research was first developed, and the naming was still simple. With the deepening of cognition, precise naming is necessary. 4-Bromo-2-iodine aniline, its structure can be distinguished from its name, bromine and iodine atoms are at specific positions in the benzene ring, and the amino group is also a key part. Its synonyms and trade names, or are commonly used in academic circles, or are used in market circulation, reflect the development of chemistry, and are a sign of research and application, which cannot be ignored.
    Safety & Operational Standards
    4 - Bromo - 2 - Iodobenzenamine Safety and Handling Code
    4 - Bromo - 2 - Iodobenzenamine, the safety and handling practices of this chemical substance are essential in experimental and production applications.
    For storage, it should be placed in a cool, dry and well-ventilated place. Due to its sensitivity to humidity and temperature changes, high temperature and humid conditions can easily cause changes in its properties and even cause chemical reactions. When storing, it should be separated from oxidants, acids, etc. to prevent dangerous interactions.
    When operating, be fully armed. Experimenters should wear protective clothing, protective gloves and goggles to prevent contact with skin and eyes. Because of its certain toxicity, if accidentally contaminated, or cause damage to the human body. The operating environment should also be well ventilated, and it is best to carry out it in a fume hood to avoid inhaling its volatilized gas.
    When taking it, the action should be precise and cautious. Accurate measurement is required according to the experiment to avoid waste and prevent excessive use from causing subsequent treatment problems. After the measuring utensils are used, they should be washed immediately to prevent residual substances from affecting the next use.
    If there is a leak, do not panic. Unrelated personnel should be evacuated quickly and warning signs should be set at a safe distance. Small leaks can be absorbed by inert materials such as sand and vermiculite, and collected in airtight containers for proper disposal. If there is a large amount of leakage, it is necessary to build a dike or dig a pit to contain it, transfer it to a tanker or a special collector with a pump, and recycle or transport it to a waste treatment site for disposal.
    Disposal should also not be taken lightly. It needs to be handed over to a professional treatment agency in accordance with relevant regulations. It must not be discarded at will to avoid polluting the environment.
    4 - Bromo - 2 - Iodobenzenamine safety and operation specifications are related to the success or failure of the experiment, personnel safety and environmental safety. Every step must be strictly followed and cannot be slack.
    Application Area
    4 - Bromo - 2 - Iodobenzenamine, the application field of this compound, is very critical. In the field of pharmaceutical research and development, it may be used as a key intermediate. The special substitution of bromine and iodine on the genphenyl ring endows the molecule with unique chemical activity, which can participate in a variety of organic synthesis reactions, help to construct complex drug molecular structures, or have important significance for the creation of therapeutic drugs for specific diseases.
    In the field of materials science, it also has potential value. Because it contains halogen atoms, it may be able to adjust the electrical and optical properties of materials. For example, in the preparation of organic optoelectronic materials, the introduction of this structural unit may optimize the material charge transport and luminescence properties, providing new ideas for the research and development of new optoelectronic devices.
    Furthermore, in the field of fine chemicals, it can be used to synthesize high-end dyes, fragrances and other fine chemicals. With its special reactivity, it can achieve unique molecular structure construction, endow products with unique color and aroma characteristics, and meet high-end market demand.
    Research & Development
    In recent years, Yu devoted himself to the study of 4 - Bromo - 2 - Iodobenzenamine. At first, he sought the method of its preparation, went through the classics, and also tried to conduct various experiments. At first, he used common reagents, and applied them according to the method of the past, but the yield obtained was quite low and there were many impurities.
    Yu then thought about changes, and studied the reaction mechanism in detail, and investigated various influencing factors, such as temperature, solvent, and catalyst. After months of research and trial and error, he obtained a slightly optimized method, and the yield gradually increased and the purity also improved.
    As for the application of this substance, it has also been explored. In the field of organic synthesis, it can be a key intermediary, participating in the construction of a variety of compounds, which is expected to explore new synthesis paths. Also considering its potential biological activities, or where it is available in pharmaceutical research and development, we will also study its pharmacology in the future, hoping to create something, promote the development of this product, and contribute to the academic and industry.
    Toxicity Research
    Since modern times, chemical refinement has produced all kinds of new things. Today there is a thing called 4-Bromo-2-Iodobenzenamine, which is quite important in the field of toxicology research.
    I tried to concentrate on the toxicity of this thing. Observing its structure, bromine and iodine atoms are combined with the benzene ring, and amino groups are also attached to it. Observing its reaction, in a specific medium, often changes, or produces free radicals, which harm the surrounding molecules and damage the structure and function of cells.
    After various experiments, animals are used as samples to apply this thing. See its eating less and less, its vitality is declining, and its organs are also abnormal. Especially in the liver and kidney, cell morphology is disordered and dysfunctional. From this point of view, 4-Bromo-2-Iodobenzenamine is quite toxic and can cause all kinds of damage to the biological body. In the future, it must be used with caution, and the protective measures must be carefully studied to avoid disasters.
    Future Prospects
    4 - Bromo - 2 - Iodobenzenamine, I study it in detail today, and hope to develop the grand road of the future. This material is unique, has a wide range of uses, and can be used in various fields.
    Looking at the current trend, science is growing and technology is improving. 4 - Bromo - 2 - Iodobenzenamine is used in pharmaceutical research and development, or can be used as a key intermediate to help create new drugs, treat all kinds of diseases, and solve the suffering of sentient beings. In material science, it may be the cornerstone of building specific energy materials, creating new materials, and responding to the needs of diversity.
    In the years to come, we should study its properties in depth, and explore its changes. Optimize the preparation method, reduce its cost and increase its yield. Expand the field of application, and seek breakthroughs in the fields of electronics, chemical industry, etc. With advanced techniques and brilliant achievements, 4-Bromo-2-Iodobenzenamine will shine in the future, benefit the world, live up to the mission of scientific research, and develop unlimited prospects.
    Historical Development
    Those who have heard of ancient chemistry, study the properties and changes of substances, and make unremitting efforts to explore new knowledge. 4 - Bromo - 2 - Iodobenzenamine This substance has traces of its origin.
    At the beginning, the art of chemistry was not refined, and everyone was still exploring in organic synthesis. Later, with the gradual improvement of skills and the clarification of various reaction mechanisms, it was possible to synthesize this compound. In the past, scholars dedicated themselves to studying various raw materials, and after many attempts, or halogenation methods, or amination techniques, they unremitting explored its synthesis path.
    With the passage of time and the advancement of technology, the synthesis method has become more and more exquisite, and the yield and purity have been improved. Since its inception, this compound has been able to be prepared stably, during which countless ancestors have worked hard to witness the development of chemistry. It has gradually gained a place in the field of organic chemistry, paving the way for subsequent scientific research and application.
    Product Overview
    4-Bromo-2-iodine aniline is one of the kinds I involved in the study of chemical substances. Its shape may be powder, color or yellowish, and it looks normal in the case, but its properties are different.
    In this substance, the atoms of bromine and iodine are halogen elements, which have active chemical properties and can cause unique changes in many reactions. The structure of the benzene ring gives it aromatic properties, and the presence of amino groups gives it alkaline properties.
    4-bromo-2-iodine aniline plays a key role in the field of organic synthesis. It can be used as an intermediate to participate in drug synthesis, dye preparation and many other processes. In terms of drug synthesis, its ingenious reaction path may help to develop new drugs with specific curative effects, contributing to the development of medicine; in dye preparation, it can also contribute unique properties such as color, light and fastness due to its special structure. I often study this substance, hoping to make more discoveries and breakthroughs in related fields, and contribute to the progress of chemistry.
    Physical & Chemical Properties
    4 - Bromo - 2 - Iodobenzenamine is also an organic compound. Its physical and chemical properties can be quite studied. Looking at its shape, at room temperature, or as a solid, the color state varies according to the preparation method and purity. Its melting point and boiling point are related to the force between molecules. The presence of bromine, iodine and amino groups in the molecule makes the molecule polar and affects its solubility. In organic solvents, there may be a certain solubility, but water is slightly soluble, due to the difference between its polarity and water.
    On its chemical properties, amino groups are basic and can form salts with acids. Bromine and iodine atoms are active and can involve nucleophilic substitution reactions. Bromine and iodine in ortho-positions change the electron cloud density of the benzene ring and affect the reactivity on the benzene ring. This compound is an important intermediate in organic synthesis and can build complex organic structures through various reactions, which is important for chemical research and industrial preparation.
    Technical Specifications & Labeling
    4 - Bromo - 2 - Iodobenzenamine is an important chemical substance. In terms of process specifications and labeling (product parameters), its properties need to be detailed. This substance often shows a specific color state, its purity needs to meet strict standards, and the impurity content must be accurately determined and recorded in detail. On the
    label, its name, chemical formula and other key information should be marked prominently. Packaging is also crucial, and it is necessary to choose the appropriate material according to its characteristics to prevent it from deteriorating or leaking. When storing, it should be placed in a specific temperature and humidity environment, protected from light and cool to ensure its stability.
    In the production and use process, it is necessary to strictly follow the established process specifications to ensure uniform product quality, in order to achieve the expected performance and use, and lay a solid foundation for applications in related fields.
    Preparation Method
    The raw materials and production process, reaction steps and catalytic mechanism of 4-Bromo-2-Iodobenzenamine should be carefully examined.
    The raw materials should be selected, and pure aniline derivatives should be selected, supplemented by brominating agents and iodizing agents, such as bromine, iodide, etc., and the purity should be high to avoid impurities disturbing the reaction.
    The production process, first in a low temperature environment, dissolve the aniline derivatives into a suitable solvent, such as dichloromethane, etc. Add the brominating agent dropwise to control the rate and prevent side reactions. After the reaction is completed, the brominated intermediate is obtained by washing with water and drying.
    Mix the brominated intermediate with the iodizing agent for the first time, and add a catalyst, such as a palladium-based catalyst, to promote the reaction. During the process, strictly monitor the temperature, pressure and reaction time.
    The reaction step begins with bromination, and the benzene ring of the aniline derivative is replaced by the electrophilic brominating agent to obtain the bromide. Following iodization, the bromide and the iodizing agent are catalyzed by halogen exchange reaction to obtain the target product 4 - Bromo - 2 - Iodobenzenamine.
    Catalytic mechanism, the palladium-based catalyst activates the reactant, reduces the reaction energy barrier, and allows bromine and iodine to smoothly replace the benzene ring hydrogen atom, improving the reaction rate and yield. In this way, this product can be prepared
    Chemical Reactions & Modifications
    4 - Bromo - 2 - Iodobenzenamine is an important compound in organic synthesis. Its chemical reaction should be investigated in detail. In the past, the synthesis method was often complicated and the yield was not good. If the reaction path of conventional halogenated aromatics is often encountered with many obstacles, due to the difference in activity between bromine and iodine, the reaction selectivity is difficult to control, and mixed products are often obtained. It is very difficult to separate and purify.
    However, current chemical research is dedicated to improving the reaction and performance of this compound. With the development of new catalysts, it may be possible to precisely regulate the reaction check point and improve the specificity of the reaction, so that the substitution of bromine and iodine can follow their wishes, thereby greatly improving the yield. Or fine optimization of reaction conditions, such as adjustment of temperature, solvent, pH, is also expected to make the synthesis of 4-Bromo-2-Iodobenzenamine more perfect, paving the way for its wide application in medicine, materials and other fields.
    Synonyms & Product Names
    4 - Bromo - 2 - Iodobenzenamine, the synonym and trade name of this thing, there is quite a bit to investigate. In my field of chemical research, it is really important to explore the change of its title.
    Those who cover synonyms are common names in the academic world and are well known to everyone. Or because of research, or to accurately express their nature, many synonyms are born. And the name of the product is related to the business. Merchants want to make their products stand out and gain a place in the market, often giving the name of a unique product.
    However, 4 - Bromo - 2 - Iodobenzenamine, its synonyms and trade names, or vary from region to region and era to era. Some are famous for their chemical structure characteristics, and some are also known for their uses and properties. We chemical learners should carefully identify them in order to understand the relationship between their names and facts. This not only helps the smooth academic communication, but also in practical applications, so as not to confuse, so that research and production can be carried out in an orderly manner.
    Safety & Operational Standards
    4 - Bromo - 2 - Iodobenzenamine Safety and Practice
    Husband 4 - Bromo - 2 - Iodobenzenamine is an important substance in chemical research. Safety and practice are of paramount importance when using and studying this compound.
    First word safety. This substance has certain latent risks or is harmful to human health. Contact with the skin may cause irritation, redness, swelling and itching; if not carefully entered the eye, it will damage the eye tissue, and even cause visual impairment. Therefore, during operation, protective measures are indispensable. Appropriate protective clothing, such as laboratory clothes, is required to cover the body and skin; protective gloves are worn to protect the hands; protective glasses are worn to keep the eyes safe. The operating environment should also be paid attention to, and it should be carried out in a well-ventilated place, so that harmful gases can be dissipated in time to prevent their accumulation and endanger the human body.
    Times and operating specifications. When using this compound, use clean and precise equipment. The measurement must be accurate, according to the amount required for the experiment, do not use too much or too little, which will cause the experimental results to be biased. When mixing other reagents, the action should be slow and the stirring should be well to prevent overreaction. During the reaction process, close attention should be paid to changes in temperature, pressure and other conditions. If the temperature is too high, or the reaction is out of control; abnormal pressure, there is also a risk of safety. After the experiment is completed, the residual 4-Bromo-2-Iodobenzenamine and related waste should not be discarded at will, but should be properly disposed of in accordance with the prescribed procedures to prevent pollution to the environment.
    In short, in the research and use of 4-Bromo-2-Iodobenzenamine, strict safety and operating standards must be adhered to in order to ensure the smooth operation of the experiment, protect the safety of the human body, and maintain the cleanliness of the environment.
    Application Area
    4 - Bromo-2 - Iodobenzenamine is also a chemical substance. Its application domain is not good. In the research and development, this compound may provide an important raw material for the synthesis of new materials. Due to its special chemical properties, it can be used by specific chemical reactions, and interact with other substances to create new molecules. It is expected to produce chemical components with specific chemical activities.
    Furthermore, in the field of materials, 4 - Bromo-2 - Iodobenzenamine also plays an important role. It can be used for the synthesis of materials in the field of materials, and can provide special properties such as properties such as properties and optics, which meet the needs of special materials in different fields. In this way, it has a huge amount of power hidden in many fields such as medical materials, which is waiting for our researchers to explore and dig deeper.
    Research & Development
    In modern times, chemistry has advanced, and material research has deepened. Today there is 4-Bromo-2-Iodobenzenamine, and we devote ourselves to studying it.
    Study its properties, observe its changes, and observe its reaction in different situations. Explore the method of its synthesis, strive to be exquisite, and want to make the yield higher and the purity purer.
    Also think about the use of this product, which may be very effective in the fields of medicine and materials. Therefore, seeking its development, we hope to be able to introduce new things and create unprecedented innovations.
    Although the research journey is difficult, we are determined, with a fearless heart and unremitting strength, we hope to achieve success, contributing to the progress of chemistry, and promoting this substance to show its capabilities in all aspects and benefit the world.
    Toxicity Research
    Toxicity Study of 4 - Bromo - 2 - Iodobenzenamine
    I have been studying chemical products for a long time, and recently focused on the toxicity of 4 - Bromo - 2 - Iodobenzenamine.
    Initially, various experimental organisms were taken, such as rats. Feed them with an appropriate amount of 4 - Bromo - 2 - Iodobenzenamine to observe their appearance. Soon, the rats were seen to be tired and their diet gradually became sparse.
    The physiological changes were carefully observed, the blood was tested, and the organs were analyzed. Abnormal biochemical indicators were seen in the blood, and the organs were also damaged. Liver, detoxification, its cell structure is disordered and its function is blocked; kidney excretion is also abnormal, and its metabolism is disturbed.
    Looking at its long-term effects, feeding this product for a long time will hinder the reproduction of mice and reduce the survival rate of young mice. This all shows that 4-Bromo-2-Iodobenzenamine is toxic and is unfavorable to the health of organisms, whether it is the physiology of the individual or the continuation of the population. In the future, the use of this product should be cautious to prevent it from harming the young.
    Future Prospects
    In today's world, science and technology are changing day by day. In the field of chemistry, 4 - Bromo - 2 - Iodobenzenamine also has its unfinished prospects. Although its many characteristics are known now, there is still a vast way to explore in the future.
    Our generation expects that the synthesis method can be more subtle, simplify complexity, reduce consumption and improve efficiency. Make the preparation of this compound more convenient and green. And hope that the exploration of its reactive activity can gain new knowledge, open up new reaction paths, and derive a variety of products.
    Furthermore, its application in materials science, drug research and development and other fields is also looking forward to breakthroughs. Or it can become a new type of functional material to help the leap of science and technology; or it can be the cornerstone of new drug creation for the benefit of all beings. Unfinished business, such as the beacon of the night sea, leads our generation of researchers to forge ahead, with the hope of drawing a brilliant chapter in its future.
    Historical Development
    Wen Fu 4 - Bromo - 2 - Iodobenzenamine, its origin can be traced back to the past. At the beginning, the sages studied in the field of chemistry, hoping to explore the realm of new things. Everyone worked hard and experienced countless trials.
    At that time, although the path of chemistry was not as bright as it is today, the masters used their perseverance to explore it unremittingly. It was first that scholars paid attention to the construction of this specific structure, and repeatedly prepared reagents to study the conditions of the reaction. Or when simmering on a low fire, or when condensing and distilling, gradually clarify the method of its synthesis.
    With the passage of time and the gradual progress of technology, the understanding of 4-Bromo-2-Iodobenzenamine has also become more and more profound. From the first crude product, to the ability to study its properties and use it in all fields. This is the hard work of the ancestors, which has made this object stand out from obscurity, adding a strong touch to the volume of chemical history.
    Product Overview
    4 - Bromo - 2 - Iodobenzenamine is an important compound in the field of organic chemistry. Its structure is unique. On the benzene ring, bromine atoms and iodine atoms occupy specific positions and are connected with amino groups. This compound has considerable application value in organic synthesis.
    Because of its special substituent distribution, it can be used as a key intermediate to participate in many organic reactions. For example, through nucleophilic substitution reactions, amino groups can interact with other reagents to introduce new functional groups, thereby constructing more complex organic molecular structures.
    Furthermore, the existence of bromine and iodine atoms endows them with unique reactivity and selectivity, providing an effective way to synthesize organic materials and drugs with specific functions. In the development of organic synthetic chemistry, 4-Bromo-2-Iodobenzenamine will continue to play an important role in driving the field forward.
    Physical & Chemical Properties
    4 - Bromo - 2 - Iodobenzenamine is also an organic compound. Its physical and chemical properties can be investigated.
    Looking at its physical properties, under room temperature, it is either solid, colored or powdery, or has a specific crystal shape. This is due to the intermolecular force. Its melting point and boiling point are related to the compactness of the molecular structure and the strength of the interaction. The strong intermolecular force, the melting boiling point or higher.
    As for the chemical properties, it contains bromine, iodine and amino groups, all of which are active check points. Amino groups are basic and can form salts with acids. Bromine and iodine atoms are easily replaced by other groups in nucleophilic substitution reactions due to electronegativity differences. And the conjugated system of benzene ring makes the molecular stability and reactivity both. Under specific conditions, the characteristic reactions on benzene ring such as halogenation, nitrification and sulfonation can occur.
    The physical and chemical properties of this compound lay the foundation for its application in organic synthesis, drug development and other fields, and will be studied in detail by our generation.
    Technical Specifications & Labeling
    There is a product today, named 4 - Bromo - 2 - Iodobenzenamine. To clarify its technical specifications and identification (product parameters), it is necessary to study in detail.
    The preparation of this product requires precise methods. The ratio of raw materials and the timing of operation are all about success or failure. The utensils used must also be clean and sophisticated, so as not to mix impurities and damage its quality.
    On the label, the ingredients, properties, uses, etc. should be listed in detail. The ingredients are clear, so that people know their chemical composition; the properties are full, and their physical and chemical properties can be known; the use is described, and its applicability should be clarified. Product parameters, such as purity, impurity content, melting point, boiling point, etc., should be accurately marked as proof of quality. In this way, the essence of fangying technical specifications and identification (product parameters) is beneficial to both production and use.
    Preparation Method
    4 - Bromo - 2 - Iodobenzenamine is an organic compound. The method of preparation is related to the raw materials, production process, reaction steps and catalytic mechanism.
    The choice of raw materials should have corresponding functional groups and activities. For example, compounds containing bromine, iodine and amino latent functional groups can be selected as starting materials. The production process needs to be carefully studied, and the control of reaction conditions should be considered. Temperature, pressure, and solvent properties all affect the direction and efficiency of the reaction.
    The reaction steps can be made from multiple steps. First, the raw material containing benzene ring is halogenated to introduce bromine and iodine atoms. If a specific halogenation reagent is used, under suitable conditions, the hydrogen on the benzene ring is replaced by bromine and iodine. After the functional group is converted, an amino group is introduced. Here, the order and degree of reaction should be paid attention to in each step of the reaction.
    Catalytic mechanism is also critical. Or use metal catalysts to promote the halogenation reaction and improve the reaction rate and selectivity. For example, the coupling reaction catalyzed by palladium can precisely connect bromine and iodine atoms. Or use acid-base catalysts to assist the introduction and conversion of amino groups. In this way, 4-Bromo-2-Iodobenzenamine can be obtained through exquisite design of raw materials, processes, steps and catalysis.
    Chemical Reactions & Modifications
    4 - Bromo - 2 - Iodobenzenamine is also a chemical substance. Its chemical properties are not suitable for those who need to study.
    To obtain this compound, it is often reversed in the same way. For example, starting with the benzene series of bromine, accompanied by the method of chemical reduction, bromine and iodine can be introduced into it. Its anti-components, the degree of efficiency and catalysis are also low. If the degree of efficiency is not low, or the catalysis is not suitable, the rate of oxidation is low, and the side effects are low.
    As for its properties, due to the high quality of bromine and iodine, the molecular properties are low. This property affects its physical and chemical properties. In physics, the temperature and solubility of melting and boiling are all subject to its restrictions; in chemistry, the activity and route of reaction are also affected by it.
    Therefore, if you want to make good use of this material, you must understand its anti-resistance, degree and other factors, so that the transformation can be refined and achieve the required effect.
    Synonyms & Product Names
    Today there is a product called 4 - Bromo - 2 - Iodobenzenamine. This is a chemical product that has attracted much attention in the industry. There are many aliases, and people have different names due to differences in regions and habits. Or because of the order of bromine and iodine in its structure, it is called another name; or because of its phenylcyclic amine group characteristics, it is another alias.
    Merchants in the market often take unique trade names in recognition of the excellence and speciality of their products. Gai hopes to attract the attention of everyone and increase its sales. This 4 - Bromo - 2 - Iodobenzenamine, or named with a beautiful and easy-to-remember name, makes customers leave an impression when they hear it, and is unique among many chemicals.
    In this way, the alias and the trade name complement each other, jointly painting the unique picture of this thing in the field of chemistry, and also adding many different colors for researchers and users in communication and trading.
    Safety & Operational Standards
    4 - Bromo - 2 - Iodobenzenamine Safety and Operation Code
    Fu 4 - Bromo - 2 - Iodobenzenamine is an important substance in chemical research. During its research and use, safety and operation standards are of the utmost importance and must not be ignored.
    First word safety. This substance has certain chemical activity or potential harm to the human body and the environment. When storing, keep it in a cool, dry and well-ventilated place away from fires and heat sources. Do not mix with oxidizers, acids and other substances to prevent violent chemical reactions, fire, explosion and other risks. When taking it, be sure to wear appropriate protective equipment, such as protective gloves, goggles and laboratory clothes. If you accidentally come into contact with the skin, you should quickly rinse with a large amount of flowing water. If you feel unwell, seek medical attention urgently; if it enters the eye, immediately lift the eyelids, rinse with flowing water or normal saline, and seek medical attention quickly.
    Times and operating specifications. Before the experimental operation, the experimenter should be familiar with the relevant steps and precautions. When weighing the substance, precise instruments are required to ensure accurate dosage. During the dissolution or reaction process, strictly follow the established reaction conditions, such as temperature control, pH, etc. When stirring, the speed is moderate, and the solution should not be splashed out. After the reaction is completed, the disposal of waste should not be neglected. Follow environmental protection requirements, classify and collect, do not dump at will, so as not to pollute the environment.
    In general, the whole process of research and use of 4-Bromo-2-Iodobenzenamine should strictly abide by safety and operating standards, so as to ensure the smooth operation of the experiment, and protect people and environment.
    Application Area
    Today there is a thing called 4 - Bromo - 2 - Iodobenzenamine, which is quite wonderful in various application fields.
    In the field of pharmaceutical research and development, it may contribute to the creation of new drugs. Its unique structure can be used as a key intermediate to help synthesize drugs with special curative effects, which is expected to overcome difficult diseases and add a powerful tool for doctors to treat diseases and save people.
    In the field of materials science, it is also promising. Or it can participate in the synthesis of special materials, giving materials unique optical and electrical properties, and applied to advanced electronic devices, such as high-performance sensors, to make their perception more sensitive and accurate.
    In the field of organic synthesis chemistry, it is even more indispensable. As an important raw material, it can derive many organic compounds with novel structures, expand the boundaries of organic synthesis, and provide chemists with the possibility to explore the unknown chemical world. It has a wide range of uses and promising prospects.
    Research & Development
    In recent years, Yu devoted himself to the research of 4-Bromo-2-Iodobenzenamine. This compound has a special structure and different properties.
    At the beginning, I wanted to clarify the method of its synthesis. After going through the classics and studying the old theories, I tried various paths. Or find the classic method, based on bromine, iodine and aniline derivatives, apply various reactions, adjust its temperature and control its agents, but the yield was not as expected.
    Then I thought of new ways, referred to the new theory, and used the method of catalysis to find changes. After repeated tests, I observed the changes in its conditions, such as the amount of catalyst and the length of the reaction, and gradually obtained the method of optimization, and the yield also improved.
    As for its application, it is also widely explored. In the field of medicinal chemistry, try to investigate its effect on germs, hoping to pave the way for the research of new drugs; in the genus of material science, test its combination with other things, and seek the creation of new materials.
    Although it has been achieved, the road ahead is still far away. In the future, we should study the mechanism and explore its nature in depth, hoping to make greater progress in research and development to benefit everyone.
    Toxicity Research
    I have heard that the name of the product is 4 - Bromo - 2 - Iodobenzenamine. We take toxicological research as our business to investigate its properties in detail. The poison of this product is related to the safety of living beings and cannot be ignored.
    At first, observe its shape and quality, and get the evidence of its experiments. After various tests, explore its impact on organisms. In microbial bodies, observe the changes in their cells, and see that it may cause cell aberration and disordered growth. When applied to animals, it may be in a state of discomfort, such as fatigue and undereating; in severe cases, it is life-threatening, organ damage, and functional decline.
    Also consider the way it enters the body, or enters through breathing, or seeps through the skin, it can cause harm. And this thing is not easy to dissipate in the environment, accumulate or dye water and soil, and endanger all things.
    Therefore, the toxicity of this thing should be deeply studied, and its harm should be observed in order to prepare preventive measures to protect the safety of all beings and the peace of the environment.
    Future Prospects
    I have dedicated myself to the field of chemistry, and now I am focusing on the compound 4 - Bromo - 2 - Iodobenzenamine. Looking at it, its unique structure contains infinite possibilities.
    Looking forward to the future, this compound may emerge in the field of medicine. With its special molecular structure, it may be able to precisely target disease-related targets, develop more specific drugs, and save many patients from pain.
    In the field of materials science, there is also a broad prospect. Or it can be cleverly modified to prepare new materials with unique optical and electrical properties, contributing to the innovation of electronic equipment and optical instruments.
    Furthermore, in the field of organic synthesis, it can serve as a key intermediate, helping to synthesize a series of complex and functional organic compounds, and promoting the vigorous development of organic chemistry. I firmly believe that over time, 4 - Bromo - 2 - Iodobenzenamine will shine and contribute to the progress of mankind.
    Where to Buy 4-Bromo-2-Iodobenzenamine in China?
    As a trusted 4-Bromo-2-Iodobenzenamine 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-Iodobenzenamine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of 4-bromo-2-iodobenzenamine?
    4-Bromo-2-iodoaniline, an organic compound, has both halogen atom and amino group, and its properties are unique.
    Let's talk about the characteristics of halogen atoms first. Bromine and iodine atoms have strong electronegativity, resulting in a decrease in the density of their adjacent and para-site electron clouds, making the benzene ring more prone to electrophilic substitution reactions, but the reactivity is different from that of benzene. Due to the large size of bromine and iodine atoms, the steric resistance affects the reaction process. When the electrophilic reagent attacks, it is more inclined to the position with small steric resistance. For example, in the halogenation reaction, the new substituent has more intermediate sites. At the same time, the halogen atom can cause changes in the activity of α-H, and under specific conditions
    Re-discussion on the properties of amino groups. With the conjugation effect, the amino group acts as the power supply group, which increases the electron cloud density of the benzene ring, which greatly increases the electrophilic substitution activity of the benzene ring, especially the adjacent and para-sites are more susceptible to attack by electrophilic reagents. Like reacting with halogenated hydrocarbons, the lone pair electrons of the amino nitrogen atom can attack the halogen atom attached to the carbon in the halogenated hydrocarbon to form a new carbon-nitrogen bond, and realize the amination reaction. In addition, the amino group is basic and can form salts with acids. In an acidic environment, the amino group is easily protonated and becomes -NH 🥰, which changes from the power supply group to the electron-withdrawing group, which greatly changes the electron cloud distribution Due to the coexistence of bromine, iodine atoms and amino groups, 4-bromo-2-iodoaniline exhibits diverse chemical properties and is widely used in the field of organic synthesis. It can be used as an intermediate to participate in many organic reactions and synthesize complex organic compounds.
    What are the physical properties of 4-bromo-2-iodobenzenamine?
    4-Bromo-2-iodoaniline is one of the organic compounds. Its physical properties are worth exploring.
    Under normal temperature, it is often solid, its color is white or nearly white, and its shape is crystalline. The quality is uniform and delicate. Its melting point, experimentally determined, is about a specific temperature range. This characteristic is crucial when identifying and purifying this substance. The melting point of different compounds varies, just like a human fingerprint, which is its unique identification.
    As for the boiling point, there is also a fixed number. Under specific pressure conditions, the temperature at which the compound changes from liquid to gas is the boiling point. The boiling point of 4-bromo-2-iodoaniline reflects the strength of its intermolecular forces. If the intermolecular forces are large, the boiling point will be high; otherwise, it will be low. The boiling point of this compound can be used as the basis for separation and purification in chemical production.
    In terms of solubility, 4-bromo-2-iodoaniline can have a certain solubility in organic solvents such as ethanol and ether. Its molecular structure contains groups such as benzene ring, bromine atom, iodine atom and amino group, which can form interactions with organic solvent molecules such as van der Waals force and hydrogen bond, so that it can be dissolved into it. However, in water, its solubility is very small. Cover water is a highly polar solvent, and the interaction with the compound molecules is weak.
    In addition, its density is also an important physical property. The density is also the mass of the substance per unit volume. The density of 4-bromo-2-iodoaniline is greater than that of water. This property is useful when operations such as liquid-liquid separation are involved. Due to different densities, the position of the compound is different during the stratification process, which can be used for separation techniques.
    In conclusion, the physical properties of 4-bromo-2-iodoaniline, such as melting point, boiling point, solubility, density, etc., are the cornerstones for studying its chemical behavior and realizing its industrial application. It is of great significance in the field of organic chemistry.
    What are the common synthetic methods of 4-bromo-2-iodobenzenamine?
    The common synthesis methods of 4-bromo-2-iodoaniline can be obtained from the following methods.
    First, aniline is used as the starting material. The amino group of aniline is first protected to prevent it from unprovoked participation in the subsequent reaction. Acylation reagents, such as acetic anhydride, are often used to generate acetaniline. The localization effect of this acetaniline can help the subsequent halogenation reaction proceed in the desired direction. After that, bromine atoms and iodine atoms are introduced into the system. When brominating, bromine and an appropriate catalyst, such as iron powder, can be selected. Because acetamide is an ortho-and para-locator, bromine atoms are often introduced into the ortho-and para-locator of amino groups. In view of factors such as steric hindrance, the 4-position is more easily replaced by bromine to form 4-bromoacetaniline. Then iodization can be carried out, using iodine and an appropriate oxidant, such as hydrogen peroxide, under suitable conditions, iodine atoms can be introduced at the 2-position to obtain 4-bromo-2-iodoacetaniline. Finally, through hydrolysis, an acid or base is used as a catalyst to leave the acetyl group and regenerate the amino group, resulting in 4-bromo-2-iodoaniline.
    Second, 2-iodobenzoic acid is used as the starting material. First, the carboxyl group is converted into an amino group, which can be achieved through a multi-step reaction. The carboxyl group can be converted into an acid chloride and treated with sulfinyl chloride. Then the acid chloride reacts with ammonia to form an amide, and then the amide is reduced with a strong reducing agent such as lithium aluminum hydride, which can be converted into an amino group to obtain 2-iodoaniline. After that, the bromination reaction of 2-iodoaniline is carried out. For example, bromine is used with a suitable catalyst. Because the amino group is an ortho and para-site locator, under controlled reaction conditions, bromine atoms can be introduced at the 4-position to obtain 4-bromo-2-iodoaniline.
    Third, 4-bromoaniline is used as the starting material. The amino group is first protected, such as treated with a protective group such as tert-butoxycarbonyl (Boc), to obtain the protected 4-bromoaniline derivative. Then the iodization reaction is carried out, the appropriate iodization reagent and reaction conditions are selected, and the iodine atom is introduced at the 2-position to generate the product of 4-bromo-2-iodine-amino protection. Finally, the protective group is removed to obtain the target product 4-bromo-2-iodoaniline.
    All these methods have their own advantages and disadvantages. In the actual synthesis, the appropriate method needs to be carefully selected according to the availability of raw materials, the difficulty of reaction conditions, cost and many other factors.
    In what areas is 4-bromo-2-iodobenzenamine applied?
    4-Bromo-2-iodobenzenamine, that is, 4-bromo-2-iodoaniline, is used in medicine, materials and other fields.
    In the field of medicine, it is often the key intermediate for the synthesis of specific drugs. Taking the development of anti-cancer drugs as an example, chemists can construct molecular structures with unique biological activities by ingeniously modifying and transforming the structure of 4-bromo-2-iodoaniline. Due to the special electronic effects and spatial resistance of bromine and iodine atoms in the structure, it can precisely regulate the interaction between drugs and targets, improve the targeting and affinity of drugs to cancer cells, thereby enhancing the anti-cancer efficacy and reducing damage to normal cells.
    In the field of materials, it also shows excellent value. In the preparation of organic optoelectronic materials, 4-bromo-2-iodoaniline can participate in the construction of conjugated systems to optimize the electronic transport and optical properties of materials. For example, when preparing organic Light Emitting Diodes (OLEDs), the introduction of functional units containing this structure can improve the luminous efficiency and stability of the device. Due to its special substituents, it can adjust the energy level structure of the material, achieve efficient electron injection and transmission, and make OLEDs emit purer and brighter light.
    Furthermore, in the field of fine chemicals, 4-bromo-2-iodoaniline is an important raw material for the synthesis of high-end dyes and pigments. Due to the unique color and stability of the product due to its structure, it can be used to manufacture high-quality inks, coatings and other products to meet the strict requirements of the high-end market for color and performance.
    What are 4-bromo-2-iodobenzenamine storage conditions?
    4-Bromo-2-iodobenzenamine is 4-bromo-2-iodoaniline, which is an organic compound with certain chemical activity, and its storage conditions are very critical.
    The environment should be cool and dry. Because it is sensitive to light and heat, if exposed to strong light or high temperature, it may cause chemical reactions and cause it to deteriorate. Therefore, when placed in a shaded place, and the temperature should not be too high, it is best to maintain it between 15 ° C and 25 ° C, so as to ensure the stability of its chemical properties.
    Furthermore, this compound should be sealed and stored. Because it may react with oxygen, water vapor and other components in the air. Sealed storage can effectively isolate the air and avoid contact with oxygen and water vapor, thereby delaying its deterioration process.
    The containers used for storage should also be carefully selected. Glass containers should be used because of their stable chemical properties and are not easy to react with 4-bromo-2-iodoaniline. And the container must be clean and dry to prevent impurities from mixing and affecting its quality.
    At the same time, the storage place should be away from fire sources and strong oxidants. 4-bromo-2-iodoaniline is an organic substance, which is dangerous to burn or even explode in case of open flames or strong oxidants. Therefore, the storage site must have good fire and explosion protection measures to ensure safety.
    In addition, the storage area should be clearly marked, indicating the name of the compound, characteristics and storage precautions for easy access and management, and also to warn relevant personnel to pay attention to safety. In this way, the purpose of properly storing 4-bromo-2-iodoaniline can be achieved to ensure its quality and safety.