3 4 Dichloroiodobenzene
Iodobenzene

3,4-Dichloroiodobenzene

Fengxi Chemical

    Specifications

    HS Code

    180597

    Chemical Formula C6H3Cl2I
    Molecular Weight 273.899
    Appearance Off - white to light yellow solid
    Boiling Point 258 - 260 °C
    Melting Point 43 - 47 °C
    Density 2.04 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like benzene, toluene
    Flash Point 110.4 °C
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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

    Packing & Storage
    Packing 100 - gram bottle of 3,4 - dichloroiodobenzene, securely sealed for chemical storage.
    Storage 3,4 - dichloroiodobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. Store it separately from oxidizing agents and incompatible substances to avoid chemical reactions.
    Shipping 3,4 - Dichloroiodobenzene is shipped in sealed, corrosion - resistant containers. It's carefully packaged to prevent leakage. Shipment follows strict chemical transportation regulations to ensure safety during transit.
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    3,4-Dichloroiodobenzene
    General Information
    Historical Development
    3,4-Dichloroiodobenzene is also an organic compound. At the beginning, the chemical sages studied and explored, and the first signs emerged in the corner of the experiment. At that time, the preparation method was still simple, and the yield was not abundant.
    As time goes by, science and technology advance, and new methods emerge one after another. Chemists think hard and improve the process, so that the yield gradually increases and the quality is better. This compound has emerged in the fields of medicine and materials, and its function is becoming more and more obvious.
    Looking at its historical evolution, from obscurity to clarity, depends on the diligent research of chemists of all dynasties. Therefore, the journey of 3,4-dichloroiodobenzene is becoming more and more prosperous, and it will surely bloom in the future scientific journey, contributing to human well-being.
    Product Overview
    3,4-Dichloroiodobenzene is also an organic compound. Its shape is either crystalline or light in color, which has special properties.
    This compound is widely used in the field of organic synthesis. It is often the key raw material for the synthesis of other complex organic molecules. Due to the characteristics of halogen atoms in its structure, it can combine with other reagents through many chemical reactions, such as nucleophilic substitution, coupling reactions, etc., and then construct novel organic structures.
    In the process of experimental preparation, it is necessary to strictly control the reaction conditions, such as temperature, ratio of reactants, type and dosage of catalysts, etc. Precise regulation of these factors can achieve higher yield and purity. Therefore, 3,4-dichloroiodobenzene plays an important role in the research and industrial production of organic chemistry.
    Physical & Chemical Properties
    3,4-Dichloroiodobenzene is an organic compound. Its physical properties, at room temperature, are solid, with a certain melting point and boiling point. Looking at the number of its melting boiling points, the strength of the intermolecular force can be known. Its density is related to the compactness of the substance.
    On its chemical properties, above the benzene ring, the substituents of chlorine and iodine make the electron cloud density of the benzene ring change, causing it to be active in the electrophilic substitution reaction. The electronegativity of the iodine atom and the chlorine atom is different, which affects the selectivity of the reaction check point. Due to the presence of halogen atoms in its structure,

    can participate in many organic reactions, such as coupling reactions, etc. It is quite useful in the field of organic synthesis and can be used as a key intermediate for the preparation of various complex organic compounds.
    Technical Specifications & Labeling
    "Technical Specifications and Labeling of 3,4-Dichloroiodobenzene (Product Parameters) "
    Fu 3,4-Dichloroiodobenzene is an important product of chemical research. Its technical specifications, the first choice of raw materials, must be pure, impurities need to be controlled in detail. The temperature of the reaction should be stable in a certain range, or at tens of degrees Celsius, according to a specific process, in order to obtain high-quality products.
    As for the label, the name of the product must be stated "3,4-Dichloroiodobenzene", and the key parameters should be listed in detail. Such as purity, it should reach a certain precise number, and the impurity composition and content should also be clearly marked. In this way, researchers and users can understand its characteristics and use them correctly, which will be of great benefit to chemical research and related applications.
    Preparation Method
    If you want to make 3,4-dichloroiodobenzene now, you need to study the method of its preparation in detail. First of all, when discussing the raw materials, you need to prepare appropriate reactants, such as compounds containing chlorine and iodine, as the foundation. The production process first allows chlorine-containing substances to introduce chlorine atoms at specific positions in the benzene ring in a suitable way, or through substitution, addition and other reactions. Then, iodine atoms are introduced in an ingenious way.
    The reaction step first carefully regulates the conditions of the chlorine-containing reaction, such as temperature, pressure, catalyst, etc., so that the chlorine atoms fall precisely at the 3 and 4 positions of the benzene ring. When the chlorine substitute is formed, then iodine atoms are introduced. In this step, you need to pay attention to the control
    As for the catalytic mechanism, it is necessary to find a suitable catalyst to promote the efficient progress of the reaction. The catalyst may reduce the activation energy of the reaction and allow the reaction to occur under milder conditions. In this way, through rigorous raw material selection, exquisite production process, orderly reaction steps and reasonable catalytic mechanism, it is expected to produce 3,4-dichloroiodobenzene.
    Chemical Reactions & Modifications
    Yu tried to study the reaction and chemical properties of 3,4-Dichloroiodobenzene. The method of preparation often starts with halogenated aromatic hydrocarbons and is obtained by iodization.
    At the beginning, the reaction conditions are not good, the yield is quite low, and impurities are clustered. Yu repeatedly inferred, and observed the proportion of reactants, temperature changes, and the effect of catalysts. Change to precise measurement, temperature control is appropriate, and the catalyst is selected. The reaction is smooth, the yield is greatly increased, and the product is also pure.
    Its chemical properties were also explored. In the nucleophilic substitution reaction, 3,4-Dichloroiodobenzene has excellent iodine atom activity, which can quickly react with various nucleophilic reagents and produce various derivatives. This characteristic makes it widely used in the field of organic synthesis. After many tests, it has been proved that it can be used as a key material in the way of organic synthesis, and it can lead to new paths.
    Synonyms & Product Names
    I heard that there is a substance called 3,4-dichloroiodobenzene. This substance is very important in our chemical research. There are also many synonyms, such as those who may be called by other names, all refer to the same thing.
    In today's world, chemical refinement, this 3,4-dichloroiodobenzene has its uses in various fields. It is either a key raw material for the synthesis of new substances, or plays a unique role in reactions. Its trade name is also well known in the industry, and it is favored by many researchers because of its excellent quality and outstanding performance.
    We often explore its characteristics and reaction mechanism, hoping to expand the boundaries of its application, so as to promote the development of chemistry and hope to seek more benefits for the world. In the laboratory, repeated studies are conducted to ensure a more thorough understanding of it, with the hope of leveraging its strength to create a new environment and contribute to the prosperity of chemistry.
    Safety & Operational Standards
    Safety and Operation Specifications for 3,4-Dichloroiodobenzene
    Fu 3,4-Dichloroiodobenzene is also a substance commonly used in chemical research. If you want to make good use of this substance, you must first clarify its safety and operation specifications, so as to ensure that everything goes smoothly and there is no risk.
    #1. Storage Requirements
    3,4-Dichloroiodobenzene should be placed in a cool, dry and well-ventilated place. Avoid open fires and hot topics to prevent accidents. Its properties may change due to changes in temperature and humidity, so the temperature and humidity of the storage must be strictly controlled. And it should be stored separately with oxidants, strong bases and other substances to avoid their interaction and cause harm.
    #2. Rules for Access
    When taking 3,4-dichloroiodobenzene, it must be fully equipped. Dress in experimental clothes, wear protective gear on your hands, and cover your face with eye protection glasses to prevent it from touching your skin and eyes. When taking it, your movements should be slow and steady. Use clean utensils and take it according to the amount. Do not spill it. If it is accidentally spilled, quickly take it with an appropriate object, clean it, and do not leave hidden dangers.
    #3. How to operate
    Operate 3,4-dichloroiodobenzene in a fume hood to avoid the accumulation of harmful gases. When operating, be familiar with the reaction mechanism, follow the established steps, and do not change it without authorization. When heating, control its temperature, step by step, and avoid sudden temperature rise. The speed of stirring should also be moderate to make the reaction uniform. If the reaction is severe, be prepared for emergency measures to prevent dangerous situations.
    #4. Emergency measures
    If 3,4-dichloroiodobenzene touches the skin, rinse quickly with plenty of water, followed by fine soap. If it enters the eye, rinse immediately with flowing water or normal saline, and seek medical attention immediately. If there is a fire, choose an appropriate fire extinguisher according to its nature, and do not do it blindly.
    In general, in the research operation of 3,4-dichloroiodobenzene, safety is the first, and norms are the most important. Strictly adhere to this approach, so that the research can be smooth, and the safety of people and the environment can be ensured.
    Application Area
    Those who have heard of 3,4-dichloroiodobenzene are chemical materials. Its application field is quite wide. In the way of pharmaceutical research and development, it can be a key intermediate to help create new drugs to treat various diseases and relieve people's pain. In the context of material science, it can participate in the synthesis of materials with specific properties, such as those with good optoelectronic properties, for electronic devices, so that the performance of devices is better. In the way of organic synthesis, it is an important building block, which can build complex organic molecular structures and expand the variety of organic compounds. From this point of view, 3,4-dichloroiodobenzene has its uses in various fields, and it is a chemical substance that cannot be underestimated.
    Research & Development
    In recent years, Yu has dedicated himself to the research of 3,4-dichloroiodobenzene. This compound has a unique structure and has great potential in the field of organic synthesis. At the beginning, I explored its synthesis method, tried many times, and encountered many obstacles. The choice of raw materials and the conditions of the reaction all need to be carefully considered.
    After repeated experiments, a feasible path was finally achieved. Starting with a specific halogenated aromatic hydrocarbon and after several steps of reaction, this product was obtained. Although the yield is not perfect, it has research value.
    Looking at its application, it can be used as an intermediate to participate in various reactions and synthesize complex organic molecules. Looking to the future, if the synthesis process can be optimized, the yield and purity can be improved, and 3,4-dichloroiodobenzene will shine in the fields of materials science and drug research and development, promoting the progress of related industries and contributing to the development of scientific research and industry.
    Toxicity Research
    The industry of chemical industry is related to people's livelihood, but the study of poisons in it is crucial. Now, the study of the toxicity of 3,4-dichloroiodobenzene should not be ignored.
    In the laboratory, observe its properties carefully. Try it with all kinds of creatures and observe its reaction. See the skin it touches, or there is a burning pain; enter the body, the viscera may be disturbed by it. After repeated investigation, it is known that it affects the state of cells and the activity of enzymes.
    Although this substance is used in chemical synthesis, its toxicity is well known, and it should be used with caution. Users must strictly abide by the procedures to prevent leakage. Where to store, you must choose a proper place. In this way, we can avoid its harm and promote its benefits, ensuring the safety of the living and protecting the tranquility of the environment.
    Future Prospects
    Wuguanfu 3,4 - Dichloroiodobenzene This product has unique properties and has great potential in various fields of chemical industry. Although it is in the process of research and development today, the prospect of the future is really promising.
    The structure of this product is exquisite, and it may be used to create new drugs and cure various diseases. In the field of materials, it can also be the foundation of advanced materials, helping its performance to be outstanding. Or in the art of catalysis, it can develop extraordinary effects, accelerate the reaction process, and increase the amount of products produced.
    Although there may be thorns in the current road ahead, we chemical researchers should have a determined heart and explore more. With time, it will be able to explore its endless potential, be used by the world, and become a treasure for future development, benefit all people, promote the progress of science and technology, and prosper in various industries, so as to move towards a bright future.
    Where to Buy 3,4-Dichloroiodobenzene in China?
    As a trusted 3,4-Dichloroiodobenzene 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 3,4-Dichloroiodobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of 3,4-dichloroiodobenzene?
    3,4-Dibromobenzoic acid is a crucial raw material in organic synthesis. Although it is not directly described in books such as Tiangong Kaiwu, its use can be analyzed based on the evolution of ancient chemical technology and the principles of organic synthesis.
    First, in the field of drug synthesis, its role is remarkable. The construction of many drug molecules requires the introduction of specific functional groups to give drugs specific pharmacological activities. The bromine atom and carboxyl group contained in 3,4-dibromobenzoic acid can be cleverly spliced with other organic molecules through organic reactions. For example, carboxyl groups can be bound to alcohols through esterification reactions, and bromine atoms can participate in nucleophilic substitution reactions, which are indispensable for building complex drug molecular structures. Through these reactions, drugs with antibacterial and anti-inflammatory effects can be prepared.
    Second, in the field of materials science, 3,4-dibromobenzoic acid also has important value. It can be used as a monomer to participate in the synthesis of polymer materials. Carboxyl groups can be condensed with compounds containing hydroxyl groups or amino groups to form polymers, and bromine atoms can change the physical and chemical properties of polymers, such as improving the flame retardancy of materials. In this way, the synthesized polymer materials can be used in fields with strict requirements for flame retardancy, such as packaging materials for electronic devices and building materials.
    Third, in the field of dye synthesis, 3,4-dibromobenzoic acid can be used as a key intermediate. Through a series of organic reactions, chromophore groups are introduced to construct dye molecules with specific colors and properties. Because of the bromine atoms and carboxyl groups in the structure, it can have a significant impact on the color, light resistance, washable properties and other properties of the dye. By rationally designing the reaction path, dyes that meet different dyeing needs can be synthesized and used in textile, printing and dyeing industries.
    What are the physical properties of 3,4-dichloroiodobenzene?
    3% 2C4-dibromothiophene is one of the organic compounds. Its physical properties are quite characteristic, let me talk about them one by one.
    Looking at its appearance, it is often colorless to light yellow liquid, pure in color, or transparent under light. The boiling point of this substance is about a specific temperature range, because of the force between molecules, it needs to reach the corresponding heat to make the molecule break free from bondage and change from liquid to gaseous state. Its boiling point is very important in separation, purification and other processes. According to this characteristic, it can be precisely separated from the mixture by distillation.
    Furthermore, the melting point is also its important physical property. Under certain low temperature conditions, the substance will solidify from liquid to solid state, and this temperature is the melting point. The value of the melting point reflects the stability of its solid structure and the closeness of the molecular arrangement. Understanding the melting point is helpful to reasonably control the temperature conditions during storage and transportation to ensure that its morphology is stable and its quality and performance will not be affected by temperature changes.
    The density of 3% 2C4-dibromothiophene is also a significant physical property. Its density value is specific, and it is either light or heavy compared with other substances. This property has important applications in experiments and industrial processes involving liquid-liquid mixing, delamination, etc. With the difference in density, it can be separated from other substances with different densities by means of liquid separation.
    In addition, solubility is also a property that cannot be ignored. It may have good solubility in some organic solvents, but poor solubility in water. This solubility characteristic is related to the choice of reaction medium in organic synthesis reactions. Choosing an appropriate solvent can make the reactants fully contacted, promote the smooth progress of the reaction, and also help the separation and purification of the product.
    In short, the physical properties of 3% 2C4-dibromothiophene, such as appearance, boiling point, melting point, density, solubility, etc., are related to each other, and together determine its application in chemical industry, scientific research and many other fields. For relevant practitioners, knowing its properties is the key to making good use of this substance.
    Is the chemical property of 3,4-dichloroiodobenzene stable?
    The chemical properties of 3% 2C4-dihydroxybenzoic acid are quite stable. In its molecular structure, the hydroxyl group is connected to the benzene ring, which gives it a certain stability.
    The hydroxyl group has active chemical properties, but in 3% 2C4-dihydroxybenzoic acid, it forms a conjugate system with the benzene ring. The benzene ring is a stable ring structure. The formation of the conjugate system makes the electron cloud more uniform, reducing the energy of the molecule, thereby enhancing its stability.
    Furthermore, its carboxyl group also interacts with the benzene ring. Although the carboxyl group is acidic, its acidity and reactivity are also changed due to the electronic effect of the benzene ring. This interaction further stabilizes the molecular structure.
    In common chemical environments, 3% 2C4-dihydroxybenzoic acid can resist a certain degree of chemical changes. In mild acid-base environments, without specific catalysts or severe reaction conditions, its structure is not easily damaged. That is, in the case of weak bases, although carboxyl groups can react with them, the reaction rate is slow; in the case of weak acids, the molecular structure remains basically unchanged.
    However, if placed under extreme conditions of high temperature, strong oxidation or strong reduction, its stability will also be challenged. High temperature can cause the vibration of intramolecular chemical bonds to intensify. When the energy reaches a certain level, the chemical bonds can be broken. Strong oxidants may attack the electron cloud on the benzene ring, causing oxidation reactions and changing the molecular structure. Strong reducing agents may also react with carboxyl groups or benzene rings, destroying their original stable structure.
    In general, the chemical properties of 3% 2C4-dihydroxybenzoic acid are relatively stable in general chemical scenarios, but it is another matter in case of extreme conditions.
    What are the synthesis methods of 3,4-dichloroiodobenzene?
    The synthesis method of 3,4-dibromofuran is much ingenious. I will describe it in ancient French.
    First, furan can be used as the beginning, and bromine is added. However, furan is active, and the reaction of bromine with it often requires careful control of conditions. In a low temperature and quiet place, bromine is slowly added into the furan solution, such as spring breeze and rain, dripping into it. At this time, the temperature must be checked, and it should not be overly dramatic to prevent side reactions from clumping. In this way, the product of 3,4-dibromofuran may be obtained.
    Second, other methods can also be used. Based on a compound with a furan structure, first modify its side chain to activate a specific part. After encountering bromine again, it is like finding an old friend and combining it in an appropriate place. This approach requires detailed study of the structure of the compound and insight into its reactivity, in order to choose the right one, so that the bromine atom can fall at the position of 3,4 as desired.
    Third, there is still an idea. Take other ring-like substances containing heteroatoms as the starting material, and after several steps of transformation, reshape the structure of the ring and introduce bromine atoms to the desired place. This process is like a craftsman's carving, step by step carefully. First, the starting material is ingeniously changed to build an environment conducive to bromination, and then treated with bromine in a timely manner, and finally 3,4-dibromofuran is obtained.
    Synthesis methods, although each has its own unique path, all require a clear understanding of the reaction mechanism and control of the conditions. Every step is related to success or failure, so the experimenter needs to be in awe and cautious in order to obtain this target product.
    What is the price range of 3,4-dichloroiodobenzene in the market?
    The price of 3,4-dibromotoluene in the market often varies due to factors such as quality, supply and demand, and season, and it is difficult to determine the exact number. However, I can give an approximate price range according to common sense and past market conditions.
    In today's city, if 3,4-dibromotoluene is of ordinary industrial grade with a purity of about 98%, the price per kilogram may be between 200 yuan and 500 yuan. This grade is mostly used for general industrial manufacturing, such as the synthesis of specific organic compounds, pharmaceutical intermediates, etc. If it is of high purity, the purity is more than 99%, and it is mostly used in the research and development of fine chemicals and high-end medicines. The price per kilogram may rise to 500 yuan to 1000 yuan, or even higher.
    In addition, market supply and demand are also the main factors affecting its price. If there are many people seeking at a time, the supply is difficult to respond to the demand, and the price will rise; on the contrary, if the supply exceeds the demand, the price may fall. And different seasons, production and transportation costs are also different, such as cold winter and extreme summer, transportation and storage are more difficult, the cost rises, and the price also changes. And different origins and manufacturers, due to the difference in process and cost, the price is also different. When purchasing, it is advisable to inquire and compare multiple parties to get a suitable price.