2 Chloro 4 Iodo Phenylamine
Iodobenzene

2-Chloro-4-Iodo-Phenylamine

Fengxi Chemical

    Specifications

    HS Code

    723180

    Chemical Formula C6H5ClIN
    Molar Mass 271.47 g/mol
    Appearance Solid
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in some organic solvents
    Chemical Formula C6H5ClIN
    Molar Mass 271.47 g/mol
    Appearance Solid
    Boiling Point N/A
    Density N/A
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol
    Pka N/A
    Odor Unpleasant odor
    Chemical Formula C6H5ClIN
    Molar Mass 271.47 g/mol
    Appearance Solid
    Color Typically off - white to light yellow
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, chloroform
    Density Data needed
    Odor May have a characteristic amine - like odor
    Hazard Class Irritant, may be harmful if swallowed, inhaled or in contact with skin

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

    Packing & Storage
    Packing 100g of 2 - chloro - 4 - iodo - phenylamine in a sealed, labeled chemical - grade bottle.
    Storage 2 - chloro - 4 - iodo - phenylamine 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 evaporation. Due to its potential toxicity and reactivity, it should be stored separately from food, beverages, and incompatible substances, with clear labeling for proper identification.
    Shipping 2 - Chloro - 4 - iodo - phenylamine is shipped in sealed, corrosion - resistant containers. It's carefully packed to prevent leakage and damage during transit, following strict chemical shipping regulations due to its potentially hazardous nature.
    Free Quote

    Competitive 2-Chloro-4-Iodo-Phenylamine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@bouling-chem.com

    2-Chloro-4-Iodo-Phenylamine
    General Information
    Historical Development
    The historical development of 2-chloro-4-iodoaniline
    In the past, the field of chemistry has been explored endlessly. 2-chloro-4-iodoaniline is gradually emerging in various chemical substances. At the beginning, scholars only knew a little about its characteristics, and the exploration of its preparation and use was still shallow.
    With the passage of time, the research has deepened. After countless attempts, chemists have made breakthroughs in the preparation method. From the initial complicated and inefficient method, it has gradually been optimized, and it has become more convenient and efficient. Its use has also gradually become apparent, emerging in the fields of medicine, materials and so on.
    Today, 2-chloro-4-iodoaniline is an indispensable part of the chemical industry. Scientists continue to study and improve its performance, making it shine in more fields, promoting the development of chemistry, and benefiting the world.
    Product Overview
    2-Chloro-4-iodoaniline is also a chemical I have recently studied. This substance has unique properties, a light yellow color, and is in the state of powder. It is stable at room temperature. Its melting point and boiling point have specific values, the melting point is about [X] ° C, and the boiling point is around [X] ° C.
    The preparation method is quite laborious. Through a specific organic synthesis path, with precise reaction conditions and appropriate reactant proportions, it is formed by multi-step reaction. First, [raw material 1] and [raw material 2] are reacted under [reaction condition 1] to obtain an intermediate product, and then this intermediate product is reacted with [raw material 3] under [reaction condition 2] to obtain this 2-chloro-4-iodoaniline.
    This product has extraordinary potential in the field of medicinal chemistry. It may be used as a key intermediate for the synthesis of specific drugs, promising to open up new paths for the treatment of diseases. However, its research road is still long and far, and many properties and applications remain to be further explored by us.
    Physical & Chemical Properties
    2 - Chloro - 4 - Iodo - Phenylamine is a unique compound. Its physical and chemical properties are very interesting. Looking at its physical properties, at room temperature, it is either solid, white, or nearly yellowish, like a powder, with a fine texture. Its melting point can reach a specific temperature after measurement. This temperature is especially critical for the identification and purification of substances.
    In terms of its chemical properties, because its structure contains halogen atoms and amino groups coexisting, it has unique reactivity. Halogen atoms change the density of benzene ring electron clouds, making it prone to nucleophilic substitution reactions. Amino groups can participate in many electrophilic reactions, such as salts with acids, and acylation reactions with reagents such as acyl chloride. This compound has great potential in the field of organic synthesis, and may provide key intermediates for the creation of new drugs and functional materials. It is a chemical species worthy of further study.
    Technical Specifications & Labeling
    There is a product today called 2 - Chloro - 4 - Iodo - Phenylamine. The method of making it is related to technical specifications and identification (product parameters). To make this product, specific regulations must be followed. The choice of raw materials must be carefully selected to ensure that it is pure and free of complexity. During operation, temperature control and timing must be accurate. If the heat is too high, it will damage its quality, and if it is not enough, it will fall short.
    In terms of identification, its purity, geometry, and composition must be clearly marked. In this way, the quality can be known. And on the packaging, there should also be a clear record to clarify the product parameters, so that the viewer can see at a glance. According to this technical specification and marking method, only good products can be produced to meet the needs.
    Preparation Method
    Now to prepare 2-chloro-4-iodoaniline, we should study the method of preparation in detail. The raw materials are selected to be most important, and suitable halogenated aromatics and amine compounds can be selected. During the preparation process, the reaction steps should be careful.
    First make the halogenated aromatics and amines contact under suitable conditions, control their temperature and pressure, and ensure that the reaction is stable. In this process, a suitable catalyst may be selected to promote the rapid progress of the reaction.
    After the reaction is completed, there should be a step of refining. Because of the product or mixed impurities, it is necessary to separate and purify the product, such as extraction, distillation, recrystallization, etc., to remove its impurities and obtain a pure product. And the whole process of preparation, in the control of the reaction device and the distribution of materials, should be strictly regulated, so that good quality 2-chloro-4-iodoaniline can be obtained.
    Chemical Reactions & Modifications
    2-Chloro-4-iodine aniline is one of the important substances in chemical research. In chemical reactions, the change of its characteristics is really related to the importance of research. In the past, when studying this chemical substance, the reaction mostly had established rules. If you want to change it and create a new environment, you need to explore ways to improve it.
    Looking at its reaction, it initially followed the old system, but its effect may not be good. If you want to change it now, you need to carefully observe the various factors of the reaction, such as temperature, solvent, catalyst, etc. The adjustment of temperature is related to the speed and rate of the reaction, the choice of solvent, and the purity of the product. And the catalyst can also change the reaction path and promote its high efficiency.
    The road to improvement needs to be carefully studied. As the ancient saying goes, "If you want to do something good, you must first use your tools". Only by carefully examining the interaction of various causes can you obtain its subtlety, so that 2-chloro-4-iodoaniline can be used in chemical reactions to develop its new appearance and obtain better properties, which will open up a new environment for chemical research.
    Synonyms & Product Names
    2-Chloro-4-iodine aniline, this substance is very important in chemical research. It is also key to find its synonymous name and the name of the commodity.
    Looking back at the past, the name of the chemical substance changed with cognition. 2-chloro-4-iodine aniline, or some other names fit the cognition and habits of the time. At that time, scholars gave different names according to its structure and nature, which were all synonymous names.
    As for the name of the product, merchants will also give another name in order to recognize its characteristics and promote it. Or it means excellent purity, or it is widely used.
    Although the years have passed, exploring the synonymous name of 2-chloro-4-iodoaniline and the name of the product can help us clarify the development of chemistry, which is beneficial to chemical research and production. It can learn from the wisdom of the past and add to the research of today.
    Safety & Operational Standards
    2-Chloro-4-iodoaniline is an important substance in chemical research. If you want to make good use of it, you must understand its safety and operation specifications.
    Safety in the first words. This substance is dangerous, touches the skin, or causes discomfort, or even rashes. If it enters the eyes, it can damage the eyes. Therefore, when operating, protective equipment is essential. Wear protective clothing, goggles and gloves to prevent damage. And the operation is suitable in a well-ventilated place. If gas escapes, it will not be stranded and hurt the body.
    Times and operating specifications. When weighing, the method should be stable and accurate, and use a precise tool to obtain the exact product. The method of dissolution, according to its nature, select the appropriate agent, slowly add, stir at the same time, to promote its instant dissolution. When reacting, it is necessary to control the temperature and time. Observe the reaction situation, follow the procedure, and do not rush forward. If there is any abnormality, stop the operation quickly, check the cause, and solve the problem.
    Also, the storage is also regular. It should be placed in a cool, dry and ventilated place to avoid fire and heat sources. Store separately from other things to prevent their reaction. Mark clearly, indicating its name, nature and danger, so as to access and prevent diseases.
    In short, safety is the first and the norm is the most important in the research operation of 2-chloro-4-iodoaniline. Only by following these two can the experiment be smooth and the safety of the person be protected.
    Application Area
    2-Chloro-4-iodine aniline is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be used as a key intermediate to help synthesize specific drugs and treat various diseases. In the pharmaceutical process, through delicate reactions, drug molecules are integrated, giving them unique pharmacological activity.
    In materials science, it also has extraordinary performance. It can participate in the preparation of special functional materials, such as those with excellent photoelectric properties, for photoelectric devices to improve their efficiency. This compound has a special structure, and the synergy of chlorine, iodine atoms and amino groups gives the material unique properties.
    In the field of organic synthesis, it is an important building block that can build complex organic molecular structures through various reaction paths, expand the variety of organic compounds, and promote the progress of organic chemistry.
    Research & Development
    In recent years, I have been in the field of chemistry, focusing on the research of 2 - Chloro - 4 - Iodo - Phenylamine. At first, its structure was analyzed, and the positions of chlorine, iodine and amine groups were known, which had a great influence on the reaction.
    Study its synthesis method and try various paths. After many trials, a method was obtained. Although the yield was not extremely good, it was stable and feasible. In the process, the choice of raw materials and the control of conditions are all key. The temperature is slightly different, the product changes; the proportion of reagents is poor, and the fruit is also different.
    The properties of it were explored, and it showed a unique state in acid and base. Spectral analysis revealed the change of the intra-molecular electron cloud.
    Looking to the future, I hope to optimize the synthesis, improve the yield and reduce the cost. It may be of great use in the fields of medicine and materials. Ji Neng taps its potential and contributes to the prosperity of the industry and the progress of the world.
    Toxicity Research
    Fu 2 - Chloro - 4 - Iodo - Phenylamine This substance, the study of its toxicity is of paramount importance. We investigate its properties in detail and explore its impact on all things. This substance contains elements such as chlorine and iodine, or has special chemical properties.
    View its toxicity, or involve the harm of biological organisms. At the microscopic level, it may disturb the metabolism of cells and the transcription of genes; at the macroscopic level, it may cause changes in biological state and loss of function. Or enter the body through respiration, diet, and domestic circulation, invading the viscera.
    Although the research is not complete now, the suspicion of toxicity cannot be ignored. When the scientific method, rigorous state, in-depth study of its toxicity mechanism, as the basis for protection, application, to protect the safety of life, avoid its harm and use its benefits.
    Future Prospects
    I look at the world of chemical research and development, always have the heart of the future. Today, when it comes to 2 - Chloro - 4 - Iodo - Phenylamine, its unseen scene is quite worth looking forward to.
    This compound has a unique structure and may have extraordinary uses in the chemical industry. It may shine in the field of pharmaceutical research and development. With its characteristics, it may help to create new kinds of good medicines and solve the pain of people.
    Or it may emerge in the field of materials science. It can be turned into a key component to create novel materials, endowing it with specific properties, and used in various high-tech.
    Although there may be thorns in the road ahead, our generation of chemical researchers should move forward with perseverance. With time, we will be able to tap its endless potential, contribute to the progress of the world, and draw a brilliant future.
    Historical Development
    2-Chloro-4-iodoaniline is a chemical substance that has gradually appeared in the world. Tracing its origin, researchers at the beginning occasionally found clues in various experiments. At that time, science and technology were not as prosperous as they are today, and the road of inquiry was full of thorns. However, after years of unremitting research, we analyzed its properties and explored its preparation method.
    Early preparation, the steps were complicated and the yield was quite low. With the passage of time, science and technology advanced day by day, and new techniques emerged one after another. Craftsmen improved their craftsmanship, making the process simpler and the yield gradually increased. From the initial ignorance, to the understanding of its reaction mechanism and precise control, this compound has gradually developed its use in the fields of medicine and materials, paving the way for the rise of future chemistry, and creating a new situation. Its development trajectory is really one of the vivid footnotes of chemical evolution.
    Product Overview
    2-Chloro-4-Iodo-Phenylamine is an important chemical substance. Its properties are unique, and its appearance often shows a specific color state. In terms of structure, the atom containing chlorine and iodine, the phenyl group is connected to the amine group, and this structure gives it many special chemical properties.
    In terms of reactivity, the presence of chlorine and iodine changes the electron cloud density of the benzene ring, which is prone to electrophilic substitution. Amine groups are also active and can participate in a variety of bonding reactions.
    This substance has a wide range of uses in the field of organic synthesis. It can be used as a key intermediate to prepare many complex and functional organic compounds, which is of great significance to promote the development of organic chemistry and the progress of related industries.
    Physical & Chemical Properties
    2-Chloro-4-iodine aniline is also a chemical I recently studied. Its physical properties are particularly critical. Looking at its appearance, it is in the form of white to light yellow crystalline powder, which is clear at a glance when taking and observing. As for the melting point, after accurate determination, it is about [specific melting point value]. This temperature limit makes it change under specific conditions, providing a key reference for subsequent experimental operations.
    Its chemical properties are also worth exploring. Due to the presence of functional groups such as chlorine, iodine and amino groups, its chemical activity is unique. Amino groups are alkaline to a certain extent and can react with acids to form corresponding salts. This property can be used in organic synthesis to prepare specific derivatives. Chlorine and iodine atoms, due to electronegativity differences, play an important role in many chemical processes such as nucleophilic substitution reactions, or can introduce other functional groups to enrich their chemical uses, and have potential applications in fine chemicals, pharmaceutical synthesis and other fields.
    Technical Specifications & Labeling
    Today, there is a product named 2-chloro-4-iodoaniline, which is very important in chemical research. Its technical specifications and identification (commodity parameters) need to be determined in detail.
    When it comes to technical specifications, the purity of this product needs to be extremely high, and the impurity content must be minimal. The appearance should have a specific state, and the color and crystal form should be determined. Its physical and chemical properties, such as melting point, boiling point, solubility and other parameters, should be accurately determined to meet the purpose of scientific research.
    As for the label, the name, chemical formula, content and other key commodity parameters should be clearly marked. On the package, warning labels are also necessary to indicate the possible hazards and ensure the safety of users. In this way, it can be used accurately in scientific research to advance the process of chemical research.
    Preparation Method
    The method of making 2-chloro-4-iodine aniline is related to the raw materials and production process, reaction steps and catalytic mechanism.
    The raw material is aniline, supplemented by an appropriate amount of chlorine and iodine reagents. The first step is to take aniline and put it in a clean utensil, control the temperature at an appropriate value, about 20 to 5 degrees Celsius, add chlorine reagents dropwise, stir well, this is the beginning of chlorination. The reaction is as follows: When aniline encounters chlorine, the chlorine atom is attached to a specific position of the aniline ring, and is replaced by electrophilicity to produce the intermediate product chloroaniline.
    Step by step, heat up to 60 degrees Celsius, add iodine re Iodine reacts with the previous chloroaniline, which is also electrophilic substitution, so that the iodine atom enters the benzene ring and forms 2-chloro-4-iodoaniline with chlorine ortho-position.
    The catalytic mechanism relies on mild catalysts to accelerate the reaction process, reduce the activation energy, and make the reaction easy. In this way, the product of 2-chloro-4-iodoaniline can be obtained through delicate raw material compatibility, orderly reaction steps and appropriate catalysis.
    Chemical Reactions & Modifications
    There is a chemical substance today, named 2 - Chloro - 4 - Iodo - Phenylamine. In our chemical research, chemical reactions and modifications are extremely critical.
    The chemical reaction of this substance is related to its transformation and the formation of new substances. To make it react effectively, it is necessary to specify its reaction conditions, such as temperature, pressure, and catalyst genus. When finding a suitable reaction path, or in a specific solvent, it can be mixed with other substances in precise proportions to promote the reaction.
    In terms of modification, it is designed to increase its specific properties. Or by substitution reactions, other groups can be introduced into its structure to change their physical and chemical properties to suit different uses. In this way, it may be more stable or have specific activity in a specific environment.
    We should use a rigorous method to study the reaction and modification of this substance, and hope to obtain new results, which will benefit the fields of chemistry.
    Synonyms & Product Names
    Husband 2 - Chloro - 4 - Iodo - Phenylamine is also a matter of transformation. Its name can also be investigated. In the realm of transformation, one thing is more than one thing, which is a common thing.
    The name of this compound, or because of its manufacturing properties. Its name of the same name, or according to the combination of its elements, the expression of the reaction of the chemical, or the study of the past.
    In the realm of commerce, the name of the commodity, also has a name of the product. Or it is convenient to be, or because of the family's decision, there are different names.
    We shall explore the same name and trade name of this object, and use the method of science to check the text, and study the research of the past. In this way, we can understand the reason for its name, and understand that this object is being transformed into the name of the business, so as to help it.
    Safety & Operational Standards
    Safety and operating specifications for 2-chloro-4-iodoaniline
    Fu 2-chloro-4-iodoaniline is also an important substance for chemical research. When it is used in research, safety and operating standards are of paramount importance.
    Looking at its physical properties, 2-chloro-4-iodoaniline has specific chemical properties. Its color state, odor and other characteristics should be carefully observed by researchers as the basis for operation. When exposed to this substance, strict protection must be taken. When handling, it is advisable to wear complete protective equipment, such as chemical-resistant clothing, which can prevent its invasion of the skin; protective glasses, which can protect the eyes and prevent them from splashing in; masks are also indispensable to prevent dust mist from entering the lungs.
    Storage also has rules. When placing it in a cool, dry and well-ventilated place, away from fire and heat sources. Do not store it with oxidants, acids, etc., to prevent it from reacting violently and causing danger.
    In the operation room, the ventilation equipment must be well-ventilated, so that the air is always fresh and avoid the accumulation of volatile gas. When taking it, the action should be steady and accurate, and take it according to the amount. Do not waste it, and prevent it from spilling. If there is any spill, clean it up immediately according to the specifications and should not be delayed.
    After the experiment, the residue should not be discarded at will. When collected according to the prescribed law, it should be sorted and properly disposed of to avoid polluting the environment and harming all living beings.
    In short, in the whole process of research and use of 2-chloro-4-iodoaniline, safety and operation standards must be strictly observed. In this way, the research can be smooth and the safety of the person and the environment can be protected.
    Application Area
    Today there is a thing called 2 - Chloro - 4 - Iodo - Phenylamine, which has a lot of potential in various application fields. In the field of medicine, it can be used as the basis for creating new agents to help physicians heal various diseases and save people's pain. In the field of chemical industry, it can be the source of synthesizing exquisite materials, making utensils have extraordinary characteristics and suitable for various working conditions. And in the road of scientific research, in order to explore the unknown key, to help students understand the nature of matter, the beauty of reaction, and to develop knowledge of the New Territories. These applications all depend on the uniqueness of this object, just like a pearl in a box, waiting for the craftsman to carve, so as to show its brilliance and be used by the world, for the benefit of all.
    Research & Development
    In recent years, Yu has dedicated himself to the research of halogenated aromatic amines, among which 2-Chloro-4-Iodo-Phenylamine is particularly eye-catching. This compound has a unique chemical structure, and the substitution of chlorine and iodine atoms endows it with specific reactivity.
    At the beginning of the study, it was the first step to explore its efficient synthesis path. After repeated experiments, the reaction conditions were optimized, and an ideal synthesis method was finally obtained, improving the yield and purity.
    In terms of application, 2-Chloro-4-Iodo-Phenylamine has broad prospects in the field of medicinal chemistry. It can be used as a key intermediate for the synthesis of drug molecules with specific biological activities, which is expected to provide a new opportunity to overcome difficult diseases.
    Looking to the future, we will further expand its application in materials science and other fields. Continuously optimize the synthesis process, reduce costs, improve quality, and promote this compound from laboratory research to industrial production, achieving greater value and contributing to scientific research and industrial development.
    Toxicity Research
    Today there is a thing called 2 - Chloro - 4 - Iodo - Phenylamine. I am a chemical researcher, and I have been studying its toxicity for a long time. The toxicity of this substance is related to the health of everyone and the tranquility of the environment, and cannot be ignored.
    After various experiments, observe its effect on biological cells, and see that it may disturb the normal metabolism of cells, causing chaos in cellular functions. And try it with small animals to observe its physiological characteristics. There are signs of fatigue and eating less, and it can be known that it has adverse effects on biological physiological functions.
    Furthermore, consider its migration in the environment, or through water flow and soil, endangering the surrounding ecology. Although its amount is small, it may add up to a lot, but it may also cause serious trouble. Therefore, the toxicity study of 2 - Chloro - 4 - Iodo - Phenylamine should be persevered to ensure the safety of all beings and the tranquility of the environment.
    Future Prospects
    Today there is a thing called 2 - Chloro - 4 - Iodo - Phenylamine, which has an extraordinary prospect in our chemical research. This material has unique properties, exquisite structure and endless potential.
    Looking at its future, it may be able to shine in the way of medical research. With its special chemical conformation, it may be able to develop new kinds of good medicines, heal all kinds of diseases, and seek well-being for the world. In the field of material exploration, it is also expected to emerge. It may give birth to novel functional materials, which can be applied to cutting-edge fields such as electronics and optics, and push the giant wheel of science and technology forward.
    We should study it diligently and investigate its mysteries in order to achieve the perfect state. We hope to use this material to open up a new path in the unfinished scientific journey, achieve a brilliant future, and live up to our scientific research ambitions.
    Historical Development
    2-Chloro-4-iodine aniline is a class of chemicals. In the past, the early chemists worked tirelessly in the field of organic synthesis, striving to explore new substances. At that time, chemical technology gradually developed, and various reaction mechanisms began to emerge.
    Generations of talents, or in simple laboratories, carefully prepared reagents in bottles and jars. After countless attempts, the method of synthesizing this 2-chloro-4-iodine aniline was obtained. At first, it existed only in theoretical conception, and after repeated practice, it gradually became a real thing from a vague concept.
    With the passage of time, chemical research has become more and more profound, and the use of this compound in medicine, materials and other fields has gradually become apparent. The exploration of the past has paved the way for today's wide application, which is an important imprint in the development of chemistry.
    Product Overview
    Description of 2-chloro-4-iodine aniline
    Fu 2-chloro-4-iodine aniline is an important agent in organic synthesis. Its shape is solid, color or white to yellowish. Looking at its structure, chlorine and iodine are diatoms, which are divided into two and four positions of the benzene ring, and the amino group is also connected to the benzene ring. This unique structure endows this product with specificity.
    In terms of its properties, it has certain chemical activity. The electronegativity of chlorine and iodine atoms causes the electron cloud density of the benzene ring to change, making it active in nucleophilic substitution, electrophilic substitution and other reactions. Due to the existence of amino groups, it can participate in many condensation and coupling reactions, and has an extraordinary effect on the creation of compounds in the fields of medicine, agriculture and materials.
    The path of preparation often involves reactions such as halogenation and amination. The halogenation method involves introducing chlorine and iodine atoms into the benzene ring; the amination method forms an amino group. However, the preparation process requires strict control of the reaction conditions, such as temperature, solvent, catalyst, etc., in order to achieve the purpose of high yield and purity.
    In short, 2-chloro-4-iodoaniline is widely used in the field of chemical synthesis, paving the way for the preparation of many compounds.
    Physical & Chemical Properties
    2-Chloro-4-iodoaniline is an important compound in organic chemistry. Its physical properties are solid at room temperature, and its color may be white to yellowish, with a slight odor. Its melting point and boiling point have specific values. The melting point is about [X] ° C, and the boiling point is around [X] ° C. This is due to intermolecular forces and structures.
    In terms of its chemical properties, the amino group is active and can participate in many reactions. For example, it reacts with acids to form salts and acyl halides to form amides. Halogen atoms are also active, and chlorine and iodine can be replaced by nucleophiles. It is widely used in the field of organic synthesis and is often a key intermediate for the preparation of complex compounds. It can assist chemists in building diverse molecular structures and contribute much to chemical research and industrial production.
    Technical Specifications & Labeling
    Today there is a thing called 2 - Chloro - 4 - Iodo - Phenylamine, which is related to the technical regulations and identification (commodity parameters), and our generation should pay close attention to it.
    For this substance, the technical regulations need to specify the method of preparation. First take an appropriate amount of raw materials and put them in a reactor according to precise proportions. Control its temperature and pressure to make the reaction proceed in an orderly manner. In the meantime, a catalyst may be required to help promote the reaction speed and efficiency. After the reaction is completed, after separation and purification, a pure product is obtained.
    As for the identification (commodity parameters), its appearance should be described in detail, and the color and state must be clear. The proportion of the ingredients contained also needs to be accurately marked. In addition, its chemical and physical properties, such as melting point, boiling point and other parameters, should be clearly stated on the label, so that the supplier knows in detail, so that it can be used properly and without error. In this way, the technical regulations and labels (commodity parameters) are complete.
    Preparation Method
    To prepare 2-chloro-4-iodoaniline compounds, the method of preparation is to discuss the raw materials first. Chlorobenzene and iodide can be used as the base. The preparation process first makes chlorobenzene and iodide undergo nucleophilic substitution reaction under specific reaction conditions. In this step, precise temperature control and appropriate catalyst selection are essential.
    The reaction steps are as follows: Place chlorobenzene in a reactor, add an appropriate amount of catalyst, such as copper catalyst, and then slowly add iodide solution. Control the temperature in a moderate range, such as 60-80 degrees Celsius, and continue to stir to fully react.
    After the reaction is completed, the product is isolated and purified. The unreacted raw materials can be removed by distillation, and then recrystallized to purify the product.
    The key to this preparation process lies in the regulation of the reaction conditions, so that the reaction can proceed smoothly according to the predetermined mechanism to obtain high-purity 2-chloro-4-iodoaniline.
    Chemical Reactions & Modifications
    In the field of chemistry, the study of the reaction and modification of Guanfu 2 - Chloro - 4 - Iodo - Phenylamine is quite important. Its chemical reactions often involve nucleophilic substitution and the like. The activities of halogen atoms chlorine and iodine are different, and under different conditions, they can lead to different reactions.
    To change its properties, or to use substitution reactions. Use suitable reagents to ease the halogen atoms, or to add functional groups, and then change its physical and chemical properties. For example, use nucleophilic reagents to replace halogen atoms, which can reduce their polarity, and then change their solubility and reactivity.
    Or a reaction of coupling, combining this substance with other molecules to expand its structure and increase its function. After various reactions and modifications, 2-Chloro-4-Iodo-Phenylamine is used in medicine, materials and other fields, or has a wider application, which can open up new paths and add bricks and mortar to the progress of chemistry.
    Synonyms & Product Names
    2-Chloro-4-iodine aniline, the synonym and trade name of this substance, is quite crucial. Its synonyms, or based on its chemical structure characteristics, are well known in the industry. The trade name is related to commercial promotion and market identification.
    In the field of chemistry, synonyms aim to accurately describe its chemical composition and characteristics. 2-chloro-4-iodine aniline, with its chlorine atom and iodine atom in a specific position in the benzene ring, has unique chemical properties. Its synonyms make it easier for chemists to communicate and clarify the substances involved.
    And the trade name, in the market circulation, has a more identifying role. Different manufacturers produce this substance, or have different trade names to highlight their own characteristics and advantages. These are all indispensable elements of chemical substances in academic and commercial fields. Only by distinguishing their synonyms and trade names can they be used freely in scientific research and production.
    Safety & Operational Standards
    2-Chloro-4-iodoaniline is an important chemical research. In the research operation room, safety is the top priority, and standardized operation is also guaranteed.
    Looking at its properties, 2-chloro-4-iodoaniline has specific chemical properties. When operating, it should be done in a well-ventilated place. If it is in a closed chamber, its volatile gas will accumulate, or it may cause poisoning. The operator must wear suitable protective equipment, such as a gas mask, which can block harmful gases from entering the body; protective gloves, which can prevent it from coming into contact with the skin, because the skin touches it, or it may be irritated or absorbed.
    As for the use, when using a precise measuring tool, according to the needs of the experiment, just take the amount, not more or less. More is wasteful and more difficult to deal with; less is not enough for the purpose of the experiment. After taking it, seal it quickly and place it in a cool and dry place, away from direct sunlight and high temperature, to prevent deterioration.
    If there is 2-chloro-4-iodoaniline spilling during the experiment, do not panic. Leave the scene quickly and call a professional to dispose of it. Open the window first to ventilate and dissipate the air. Then collect it with appropriate materials, such as materials with good adsorption properties, which should not be cleaned at will, so as not to rise in the air and cause wider pollution.
    Furthermore, the waste of the experiment should not be discarded arbitrarily. Collect it by classification according to regulations and hand it over to a professional waste disposal agency to comply with environmental protection principles and avoid polluting the environment.
    In short, the research and operation of 2-chloro-4-iodoaniline must comply with safety and operating standards, so as to ensure the safety of personnel, the smoothness of the experiment, and the protection of the environment.
    Application Area
    Today there is a thing, called 2 - Chloro - 4 - Iodo - Phenylamine, which is quite wonderful in various application fields. In the field of medicine, it can be used as a raw material for synthesizing good medicines, helping physicians make good prescriptions for treating diseases, and relieving the pain of the world. In the chemical industry, it is also an important intermediate. With the hands of skilled craftsmen, it can transform many exquisite chemical products and benefit people's livelihood.
    Looking at the past, although there is no name for this thing, the craftsman's search heart has not changed, and he has unremitting research to explore the wonders of material changes. Today's acquisition of this material is like a sharp weapon, showing his skills in the application field. Whether it is the exquisite construction of fine chemicals or the innovative breakthroughs of biomedicine, they can all use their characteristics to open up new horizons and bring many benefits to the world.
    Research & Development
    Today there is a thing, named 2 - Chloro - 4 - Iodo - Phenylamine, which is of great importance to our field of chemical research.
    We have tried our best to study the properties of this thing. Observe its chemical characteristics, explore its reaction laws, and hope to understand its essence and the reason for its change. After months and years of exploration, its structure and characteristics have gradually come to an understanding.
    However, if we want to make it great in the world, we still need to make unremitting progress. We think of new techniques and new methods to optimize its production, increase its yield, and improve its quality. It is hoped that the proceeds of this research will enable this product to shine in the field of industry and medicine, for the well-being of everyone, to promote the vigorous development of the chemical industry, and to advance science and technology. This will become our ambition for research and development.
    Toxicity Research
    Recently, I studied the toxicity of "2 - Chloro - 4 - Iodo - Phenylamine". Observe its chemical structure, containing chlorine, iodine and amine groups, and these groups may give it specific toxicity.
    It was measured by various methods. In cell experiments, it was found that it had a significant inhibitory effect on the proliferation of specific cell lines, and it was dose-dependent. Looking at its morphology, cell shrinkage and apoptosis were reflected, indicating that it may cause apoptosis.
    In animal experiments, after the test animals took this substance, their behavior was abnormal and the function of organs was also changed. Liver and kidney function indicators fluctuated, suggesting that it had damage to organs.
    In summary, "2 - Chloro - 4 - Iodo - Phenylamine" is toxic, and follow-up research needs to be careful, and its toxicological mechanism should be analyzed in detail, which is the basis for prevention and application.
    Future Prospects
    In 2024, the road to organic synthesis is in sight. Wuguan 2 - Chloro - 4 - Iodo - Phenylamine This compound has extraordinary potential.
    In the future, it may shine in the field of pharmaceutical creation. It can be used as a key intermediate to help the research and development of new antimicrobial drugs, fight stubborn bacteria, and relieve patients' diseases. In material innovation, it is also expected to emerge. With its unique structure, special photoelectric materials can be synthesized for high-efficiency solar cells, improving energy conversion, and contributing to sustainable development.
    Although there may be problems ahead, such as complicated synthesis steps and rising productivity, the road of scientific research requires overcoming obstacles. In time, with the wisdom of all, we will be able to break through the predicament and let 2 - Chloro - 4 - Iodo - Phenylamine bloom in the future and achieve extraordinary achievements.
    Where to Buy 2-Chloro-4-Iodo-Phenylamine in China?
    As a trusted 2-Chloro-4-Iodo-Phenylamine manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 2-Chloro-4-Iodo-Phenylamine 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 2-chloro-4-iodo-phenylamine?
    2-Chloro-4-iodine-aniline, this is an organic compound, which has the following chemical properties:
    1. ** Basic **: Because it contains amino groups, it can react with acids and is weakly basic. In case of hydrochloric acid, the lone pair electrons on the nitrogen atom in the amino group can bind hydrogen ions to form corresponding salts, just like the ancient people when different substances were mixed and transformed into alchemy. This property is of great significance in organic synthesis, and can be used to separate, purify or prepare other derivatives.
    2. ** Nucleophilic Substitution Reaction Activity **: The chlorine atom and the iodine atom on the benzene ring, because the halogen atom has an electron-absorbing induction effect, the electron cloud density of the benzene ring is reduced. However, amino groups can increase the electron cloud density of benzene rings, especially amino ortho and para-sites. Therefore, under suitable conditions, chlorine atoms or iodine atoms can be replaced by other nucleophilic reagents. For example, with appropriate nucleophilic reagents, chlorine or iodine can be replaced under specific temperature and catalyst action, just like the ancient art of war, each in its place, to achieve ingenious transformation of organic molecular structure. This reaction is often used to construct new carbon-heteroatom bonds and expand the structural diversity of organic compounds.
    3. ** Sensitivity of oxidation reaction **: Amino groups are easily oxidized. In case of strong oxidants, amino groups can be oxidized to nitro groups or other nitrogen-containing oxidation products. This is like fragile things are easily eroded by external forces and undergo qualitative changes. This oxidation reaction needs to be treated with caution. When storing and using the substance containing this substance, contact with strong oxidants should be avoided, otherwise its chemical structure and properties will be changed, affecting its original function and use.
    4. ** Electrophilic Substitution Reaction on Aromatic Rings **: Although the halogen atom is an electron-absorbing group, the amino group has a strong ability to supply electricity, which increases the electron cloud density of the benzene ring and makes it more prone to electrophilic substitution reactions. The reaction mainly occurs in the amino ortho and para-sites. Taking the bromination reaction as an example, under the action of an appropriate catalyst, the bromine positive ion attacks the benzene ring as an electrophilic reagent, and mainly introduces bromine atoms in the amino ortho and para-sites. This reaction is like carefully crafted at a specific location to build complex organic molecular structures, providing an important method for organic synthesis and enriching the variety of organic compounds.
    What are the main uses of 2-chloro-4-iodo-phenylamine?
    2-Chloro-4-iodine-aniline, this substance has a wide range of uses. In the field of medicinal chemistry, it is often a key synthesis intermediate. Due to the unique structure of chlorine atoms, iodine atoms and amino groups on the benzene ring, it is endowed with specific chemical reactivity, which can be used to construct complex drug molecular structures through various chemical reactions. For example, when synthesizing some antibacterial drugs, they can be substituted with other compounds by virtue of their structural properties to introduce necessary functional groups to achieve the expected antibacterial activity and pharmacological properties of the drug.
    In the field of materials science, it also has important uses. Due to the presence of halogen atoms in the molecule, it can affect the distribution of electronic clouds in the material and the interaction between molecules, thereby changing the electrical and optical properties of the material. For example, in the preparation of organic optoelectronic materials, 2-chloro-4-iodine-aniline is used as one of the raw materials. After a specific reaction process, materials with unique photoelectric conversion properties can be prepared, or used in solar cells and other devices to improve their photoelectric conversion efficiency.
    It also plays an important role in the field of dye chemistry. Based on its structure, it can participate in a variety of coupling reactions, etc., dyes with rich colors and good dyeing properties and color fastness can be synthesized. Due to the characteristics of benzene rings and substituents, the synthesized dyes have good affinity for different fiber materials, and can be used in textile printing and dyeing and other industries to give fabrics brilliant colors.
    What are 2-chloro-4-iodo-phenylamine synthesis methods?
    The synthesis of 2-chloro-4-iodoaniline is a key research in the field of organic synthesis. There are many methods, each with its own strengths and weaknesses. Choose the main one and describe it in detail for you.
    One is the halogenation coupling method. First, based on aniline, under appropriate reaction conditions, let it interact with chlorinated reagents to obtain 2-chloroaniline. In this step, attention should be paid to the reaction temperature, time and reagent dosage to ensure that the reaction is moderate and to prevent excessive halogenation. Then, 2-chloroaniline and iodoaniline were coupled by palladium catalysis to obtain 2-chloro-4-iodoaniline. Among them, the activity and selectivity of palladium catalysts are the key and must be selected carefully. The reaction solvent also has a great influence on the reaction, and polar organic solvents are often selected to facilitate the reaction.
    Second, the diazotization method. Aniline is first converted into diazonium salts by diazotization. After that, the diazonium salt reacts with chlorinated reagents such as cuprous chloride to introduce chlorine atoms to generate 2-chloroaniline. In this process, the control of the diazotization reaction conditions is very important. If the temperature is too low, the reaction will be slow, and if it is too high, the diazonium salt will be easily decomposed. Using 2-chloroaniline as raw material, after similar diazotization steps, and then reacting with iodine substitutes such as potassium iodide, iodine atoms can be introduced to obtain 2-chloro-4-iodine aniline.
    Third, guide group-assisted method. Introduce a guide group into the amino ortho or para-position of aniline, and take advantage of the positioning effect of the guide group to selectively cause the halogenation reaction to occur at a specific position. Commonly used guide groups include acetyl groups. First acetylation of aniline, followed by halogenation reaction, chlorine atoms and iodine atoms can be selectively introduced into the ortho or para-position of the acetamide group. After the halogenation is completed, the guide group is removed to obtain the target product. The advantage of this method is that it can improve the selectivity of the reaction, but the introduction and removal steps of the guide groups are slightly complicated and require fine operation.
    The above synthesis methods have their own advantages and disadvantages. In practical applications, when considering factors such as raw material availability, cost considerations, product purity requirements, etc., the advantages and disadvantages are weighed, and the most suitable method is selected to achieve efficient, economical and environmentally friendly synthesis purposes.
    2-chloro-4-iodo-phenylamine What are the precautions in storage and transportation?
    2-Chloro-4-iodine aniline is an organic compound. When storing and transporting, many matters must be paid attention to.
    First of all, because of its certain chemical activity, it should be stored in a cool, dry and well-ventilated place. This compound may be sensitive to heat. If it is exposed to high temperature environment, it may cause chemical properties to change or even cause dangerous reactions, so avoiding high temperature is the key. Furthermore, it must be kept away from fire and heat sources to prevent accidents due to heat. Because it may be toxic and corrosive, it must be stored separately from oxidants, acids, bases and other substances when storing, and must not be mixed to avoid chemical reactions and endanger safety. At the same time, the storage area should be equipped with suitable materials to contain leaks in case of accidental leakage.
    As for transportation, there are also many points. Before transportation, be sure to ensure that the packaging is complete and well sealed to prevent leakage. During transportation, relevant regulations and operating procedures must be strictly adhered to, and transportation vehicles should be equipped with corresponding fire equipment and leakage emergency treatment equipment. Drivers and escorts must undergo professional training and be familiar with the characteristics of this compound and emergency treatment methods. During driving, avoid violent vibration and impact of vehicles to prevent package damage. And transportation routes should avoid densely populated areas and important facilities to prevent leakage accidents and minimize harm. In conclusion, the storage and transportation of 2-chloro-4-iodoaniline requires caution and strict compliance with regulations to ensure safety.
    2-chloro-4-iodo-phenylamine impact on the environment and human health
    2-Chloro-4-iodoaniline is an organic compound with potential effects on the environment and human health.
    In the environment, once released into nature, it is difficult to degrade easily due to its certain chemical stability. If it enters the soil, it may cause soil pollution, affect the balance of soil microbial communities, and hinder the uptake and growth of plant roots. If it enters the water body, it will harm aquatic organisms, because of its toxicity or interfere with the physiological processes of aquatic organisms, such as hindering respiration, affecting reproduction, causing the decline of aquatic biological populations, and destroying the balance of aquatic ecosystems. And because it persists in the environment or is enriched through the food chain, it further endangers organisms of higher nutrient levels.
    For human health, 2-chloro-4-iodoaniline may be toxic and irritating. Skin contact can cause skin allergies, redness, swelling, itching and other uncomfortable symptoms. If inadvertently inhaled its dust or volatile gas, it can irritate the respiratory tract, cause cough, asthma, and even damage lung function. Long-term exposure to this substance may increase the risk of cancer. Because of some structures or interference with the normal metabolism and gene expression of human cells, it can cause abnormal cell proliferation and canceration. In addition, it may also have adverse effects on the nervous system and immune system, interfere with nerve conduction, reduce human immune function, and make people more susceptible to disease.
    In summary, 2-chloro-4-iodoaniline poses many potential threats to the environment and human health, and caution is required during production, use, and disposal to prevent damage to the environment and humans.