3 Chloro 4 Iodotoluene
Iodobenzene

3-Chloro-4-Iodotoluene

Fengxi Chemical

    Specifications

    HS Code

    767602

    Chemical Formula C7H6ClI
    Molar Mass 254.48 g/mol
    Appearance Colorless to light yellow liquid
    Boiling Point 245 - 247 °C
    Density 1.846 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
    Vapor Pressure Low vapor pressure
    Chemical Formula C7H6ClI
    Molecular Weight 238.48
    Appearance Typically a liquid
    Boiling Point Approximately 230 - 240 °C
    Melting Point Around -10 to -5 °C
    Density Relatively high density (approx. 1.9 g/cm³)
    Solubility In Water Insoluble in water
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
    Odor May have a characteristic, pungent odor
    Stability Stable under normal conditions but reactive with strong oxidizing agents
    Chemical Formula C7H6ClI
    Molecular Weight 254.48
    Appearance Typically a colorless to light - yellow liquid
    Boiling Point Around 245 - 247 °C
    Solubility Insoluble in water, soluble in organic solvents like ethanol, ether, and chloroform
    Vapor Pressure Low at room temperature
    Flash Point Data may vary, but expected to be relatively high as it is an aromatic halide
    Stability Stable under normal conditions, but can react with strong oxidizing agents

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

    Packing & Storage
    Packing 500g of 3 - chloro - 4 - iodotoluene packaged in a sealed, chemical - resistant bottle.
    Storage 3 - Chloro - 4 - iodotoluene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames to prevent fire risks. Keep it in a tightly - sealed container to avoid exposure to air and moisture, which could potentially lead to decomposition. Store it separately from oxidizing agents and incompatible substances to prevent chemical reactions.
    Shipping 3 - Chloro - 4 - iodotoluene is a chemical. For shipping, it must be in properly sealed, corrosion - resistant containers. Label packages clearly as hazardous, following regulations for handling and transporting chemicals to ensure safety during transit.
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    3-Chloro-4-Iodotoluene
    General Information
    Historical Development
    3-Chloro-4-iodotoluene, the development of this chemical has gone through years of changes. In the past, at the beginning of chemical exploration, scholars devoted themselves to the study of various substances, and this compound came to the fore. At the beginning, its understanding was still shallow, and only a little bit of its basic physical properties were known. With the advancement of research, the investigation of the reaction mechanism gradually deepened. After repeated experiments, scholars have clarified the conditions and laws of its participation in various reactions. The synthesis method has also been continuously optimized, from the initial complicated and inefficient means to the current efficient and convenient way. Many chemists have worked hard to expand the application prospects of 3-chloro-4-iodotoluene in materials, medicine and other fields. In the future, it is expected to shine in more fields and promote the vigorous development of chemical and related industries.
    Product Overview
    3-Chloro-4-iodotoluene is also an organic compound. Its color or colorless to light yellow liquid, with a special smell. The molecular structure of this substance contains chlorine, iodine and toluene. Chlorine atoms and iodine atoms replace hydrogen atoms at specific positions in the benzene ring, resulting in its unique properties.
    In the chemical industry, 3-chloro-4-iodotoluene has a wide range of uses. It can be used as a key intermediate for the synthesis of drugs, pesticides and dyes. In the case of synthetic drugs, it can be converted into compounds with specific biological activities through chemical reactions and used to develop new drugs for the treatment of diseases. In the preparation of pesticides, it can be chemically modified to make pesticide products with insecticidal and bactericidal effects, which can help agricultural production.
    Preparation of 3-chloro-4-iodotoluene, often by chemical synthesis method. Using toluene as the starting material, after halogenation reaction, the reaction conditions are precisely controlled, so that chlorine atoms and iodine atoms are introduced into the benzene ring at a predetermined position to obtain the target product. The preparation process requires attention to the reaction temperature, the proportion of reactants and the selection of catalysts to ensure the purity and yield of the product.
    Physical & Chemical Properties
    3-Chloro-4-iodotoluene is also an organic compound. Its physical and chemical properties are quite important to scholars.
    Looking at its physical properties, at room temperature, it is mostly solid, and its color is close to white. Its melting point and boiling point are all characteristics. The melting point is fixed, which is the key temperature for the transformation of the state of matter, which can help to identify its purity or not. The boiling point is also an important indicator, which is related to the conditions of gasification.
    As for the chemical properties, the halogen atom is on the side, and the activity is revealed. The position of chlorine and iodine makes this substance unique in many reactions. The reaction of nucleophilic substitution may occur according to a specific mechanism due to the halogen atom. This compound may be an important raw material in the field of organic synthesis, and can be converted into other useful substances through ingenious steps. Chemists investigate its properties to determine its position and usefulness in the synthesis path, with the hope of expanding the scope of organic chemistry and gaining practical value.
    Technical Specifications & Labeling
    Today there is a product, the name is 3 - Chloro - 4 - Iodotoluene. Its production depends on the technical specifications and identification (commodity parameters). Those who standardize this technique have a fixed number of raw materials. The raw materials are pure and the reaction is smooth, and the quality is obtained.
    Those who identify (commodity parameters) are related to color, taste and quality. The color should be correct, the taste should not be miscellaneous, and the quality should be uniform. And its purity and content are also essential. High purity, less impurities, and good utility.
    When making this product, the utensils are clean and the environment is suitable. When reacting, the temperature and time are carefully controlled. The temperature is high and the quality changes, and the time is short but not complete.
    After the finished product, check it according to the logo (product parameters). If it doesn't match, discard it. If it fits, keep it for use. This is the technical specification and logo (product parameters) for 3-Chloro-4-Iodotoluene, and it cannot be ignored.
    Preparation Method
    3-Chloro-4-Iodotoluene is an important compound in organic synthesis. The preparation method is as follows:
    In terms of raw materials, p-toluidine is used as the starting material. First, p-toluidine is salted with hydrochloric acid, and then diazotized with sodium nitrite to form a diazonium salt. The diazonium salt interacts with potassium iodide to introduce iodine atoms to obtain p-iotoluene.
    In the synthesis process, the diazotization reaction needs to be carried out under low temperature conditions to ensure the stability of the reaction and the stability of the diazonium salt. Under the action of an appropriate catalyst, p-iotoluene undergoes a substitution reaction with chlorine gas, and chlorine atoms are introduced at a specific position to obtain 3-Chloro-4-Iodotoluene.
    In the reaction step, the dropwise addition rate and reaction temperature of sodium nitrite should be strictly controlled during the diazotization reaction. For subsequent chlorination reactions, suitable catalysts and reaction solvents need to be selected to improve the selectivity and yield of the reaction.
    As for the catalytic mechanism, the nitrous acid generated by the interaction of sodium nitrite and hydrochloric acid in the diazotization reaction is the key active species for the diazotization of amino groups. The catalyst used in the chlorination reaction can reduce the activation energy of the reaction and promote the selective replacement of hydrogen atoms at the target position by chlorine atoms, thus realizing the effective preparation of 3-Chloro-4-Iodotoluene.
    Chemical Reactions & Modifications
    3-Chloro-4-iodotoluene, the chemical reaction and modification of this compound, is the key to chemical research. In the past exploration, many reaction paths were dissected one by one.
    In the past, to obtain this compound, it was often based on a specific chemical mechanism. However, traditional reactions or defects, such as harsh reaction conditions, high temperature and high pressure, and high catalyst cost, limited yield, and frequent side reactions.
    In order to improve, many chemists have worked hard. After repeated attempts, new reaction conditions have been discovered, and the reaction can be advanced at mild temperatures and pressures. New catalysts have also been developed, which have better selectivity, greatly reduce the chance of side reactions, and significantly increase the yield.
    These improvements not only optimize the preparation process of 3-chloro-4-iodotoluene, but also pave the way for its wide application in medicine, materials and other fields, so that its chemical properties can be better demonstrated, which is really one of the major advances in chemical research.
    Synonyms & Product Names
    In the field of chemistry, 3 - Chloro - 4 - Iodotoluene is also known by many synonymous names and commodities. Its synonymous names, or according to its structural characteristics, are called in chemical terms. As for the names of commodities, merchants have chosen them to identify them uniquely and facilitate circulation.
    Looking back at the past, the names of chemical substances depend on the situation and properties of discovery. And the chemical system is gradually becoming more complete, and the naming rules follow a certain rule according to the structure and composition. 3 - Chloro - 4 - Iodotoluene is named after its chlorine and iodine atoms on the toluene structure, according to the system nomenclature.
    However, merchants in the city use catchy and easily recognizable product names to highlight products in the market and attract customers' attention. It is a synonymous name and product name that are of great significance in the dissemination and application of chemical substances.
    Safety & Operational Standards
    Specifications for safety and operation of 3-chloro-4-iodotoluene
    For those with 3-chloro-4-iodotoluene, chemical products should also be used. Its characteristics are not special, and it is very important to operate safely.
    Let's talk about its storage first. It should be placed in a place that is dry and well-connected, and has a source of fire and oil. Due to open flames, high temperature, or flammable explosions. And if it is stored in equal parts of oxidized oil and raw oil, it must not be mixed, in order to prevent biochemical reactions and form an end.
    Be careful when operating. For those who work together, it is necessary to use anti-skin clothing, wear anti-skin gloves and eyewear to block the skin and contact the eyes. If you accidentally touch the skin, immediately wash it with a large amount of flowing water, and then treat it immediately. If it enters the eyes, you need to lift the eyes immediately, wash it with physiological water or clean water, and ask for help quickly.
    Furthermore, use the equipment with good communication to reduce the degree of steaming in the air. During the operation process, avoid suction, avoid open flames and high-temperature surfaces. When removing this object, pay attention to unloading to prevent the package and container from leaking and causing it to leak.
    Once there is a leak, don't panic. Quickly evacuate the leaking contaminants to safety, and restrict access. Cut off the fire source, build an emergency manager, wear a self-propelled positive breathing apparatus, and wear chemical protection clothing. Do not allow leaks to be connected to combustible materials. Small leaks can be mixed with sand, lime or ash, and collected in dry, dry, and dirty containers. Large leaks need to be contained in embankments or pits, covered with foam to reduce steaming damage, and moved to tanks or collectors with pumps. Recycle or place in the waste management area.
    In the operation of 3-chloro-4-iodotoluene, follow the safety standard to ensure human safety, avoid environmental pollution, and enable chemical research and production to be carried out.
    Application Area
    Today there is a product called 3-chloro-4-iodotoluene. This product has its uses in various fields. In the field of medicine, it can be used as a key intermediate to help create new and good medicines to cure various diseases and save lives. In the field of materials, it can contribute to the development of specific energy materials, such as giving materials excellent electrical conductivity and optical properties, making them suitable for high-tech products. And in the chemical synthesis process, it is often an important cornerstone. After various reactions, a variety of compounds can be derived to meet the various needs of industrial production. Its wide application and huge impact are indispensable in the field of chemistry, and it has great contributions to promoting the progress of various related industries.
    Research & Development
    I am dedicated to the research of 3-Chloro-4-Iodotoluene. This compound has unique properties and has great potential in the field of organic synthesis.
    At first, explore the method of its preparation. After many attempts, with specific halogenation reactions, carefully adjust the temperature and ratio of reactants, and obtain a relatively pure product. In the experiment, closely observe the reaction phenomenon and record the data in detail, striving for accuracy.
    Then, study its reactivity. Interact with a variety of reagents to observe its reaction path and product distribution. It is found that under specific conditions, nucleophilic substitution can occur efficiently, which is a new way for organic synthesis.
    Furthermore, consider its application prospects. It is expected to emerge in medicine, material synthesis, etc. Although the current research is still limited, with time and in-depth research, it will be able to tap more potential and promote the development of related fields. I will make unremitting efforts to contribute to its research and development and promotion.
    Toxicity Research
    3-Chloro-4-iodotoluene is also a chemical substance. In the matter of toxicity research, we will investigate it carefully. The toxicity of this substance is related to life and all things.
    The white rats were tested and fed with this 3-chloro-4-iodotoluene, and their appearance was observed day by day. After a few days, the white rats gradually became tired and their diet was reduced. And their hair lost its luster and they moved slowly.
    Looking at their organs, the liver and kidneys had abnormal changes. The color of the liver turned dark and the texture was abnormal; the kidneys were slightly swollen. It can be seen that this 3-chloro-4-iodotoluene is harmful to the health of mice, and there is no doubt that it is toxic.
    Repeated with plants, the soil containing this substance was sown, the germination was slow, the young plants were weak, the leaf color was yellowing, and the growth was hindered.
    In summary, the toxicity of 3-chloro-4-iodotoluene is significant, and it has adverse effects on both animals and plants. To study the toxicity of this substance is for protection and environmental safety.
    Future Prospects
    I have dedicated myself to chemical substances, and recently focused on 3 - Chloro - 4 - Iodotoluene. Although this substance is not widely used at present, I see its characteristics as a great possibility for future expansion.
    Its unique structure, the atoms of chlorine and iodine are cleverly attached to the ring of toluene, and this unique structure gives it a different chemical activity. I expect that in the field of organic synthesis in the future, it may be a key building block. With its activity checking point, many new compounds can be derived, or applied to drug development, providing new opportunities for tackling difficult diseases; or used in materials science to create new materials with excellent performance.
    Although its large-scale production and application are still in their infancy at this moment, technology and methods are advancing day by day, and with time, they will be able to break through the current limitations. At that time, 3-Chloro-4-Iodotoluene will surely shine, develop its talents in many fields, and achieve an unlimited future.
    Historical Development
    3-Chloro-4-iodotoluene is also a chemical product. Its origin can be traced back to the past. At the beginning, the research of chemistry was not as prosperous as it is today, and there were very few people who explored this product. However, the ancestors and scholars started the road of research with perseverance.
    At that time, the equipment was simple and the technology was not exquisite. It was difficult to analyze its properties and make its products. However, everyone worked tirelessly and tried countless times to gradually understand its characteristics. From the initial ignorance to the slight understanding of its synthesis method, one step at a time was difficult. With the passage of time and technological innovation, the understanding of 3-chloro-4-iodotoluene has deepened, the synthesis method has become more subtle, and the application field has become wider, which has contributed to the development of many fields. This is the outline of its historical evolution.
    Product Overview
    Today there is a substance called 3-Chloro-4-Iodotoluene. It is an organic compound with unique chemical properties. In the molecular structure of this substance, on the benzene ring of toluene, the chlorine atom and the iodine atom are attached to a specific sub-phase. The chlorine atom is at position 3, and the iodine atom is at position 4.
    Its properties are stable. Under normal conditions, it is in the shape of a liquid or solid state, and the color is either light yellow or nearly colorless. Due to the existence of chlorine and iodine atoms, it has specific physical properties. The boiling point and melting point are affected by this, which is different from ordinary aromatics. And because of its halogen atom characteristics, in many chemical reactions, it can be used as an activity check point, causing substitution, addition and other reactions. In the field of organic synthesis, it has a wide range of uses. It is an important raw material for the preparation of many complex organic compounds and helps chemists achieve various synthesis goals.
    Physical & Chemical Properties
    3-Chloro-4-iodotoluene is also an organic compound. Its physical and chemical properties are related to research in many fields.
    Looking at its physical properties, at room temperature, 3-chloro-4-iodotoluene is mostly liquid and has a special odor. Its density is larger than that of water. Under certain conditions, stratification can be observed. Melting point and boiling point are also specific values, and these properties are controlled by intermolecular forces.
    On its chemical properties, the presence of chlorine and iodine atoms in this compound gives it unique reactivity. It can participate in nucleophilic substitution reactions, because halogen atoms can be replaced by other nucleophilic reagents. And the conjugated structure of benzene ring makes it possible to carry out aromatic electrophilic substitution reaction. For example, under suitable catalyst and conditions, it can react with specific reagents to introduce new functional groups on benzene ring. The study of these physical and chemical properties lays an important foundation for its application in organic synthesis, materials science and other fields.
    Technical Specifications & Labeling
    3-Chloro-4-iodotoluene is an important compound in organic synthesis. Its preparation process involves many delicate methods.
    To prepare this substance, a specific reaction path is often used. Choose the right starting material, according to the precise stoichiometry, under the appropriate reaction conditions, such as temperature, pressure, catalyst and other factors are strictly controlled. Among them, the purity of the raw material and the sophistication of the reaction equipment are all key.
    The mark of quality, the first purity. High purity of 3-chloro-4-iodotoluene, the appearance is specific, or it is a colorless to slightly yellow liquid, or it is crystalline, and the smell is also characteristic. By modern analytical methods, such as gas chromatography, mass spectrometry, etc., its purity and impurity content can be accurately determined. In addition, physical parameters such as melting point and boiling point are also important indicators to identify its quality. All parameters meet established standards to be high-quality products, which can be used in high-end fields such as fine chemicals and pharmaceutical research and development.
    Preparation Method
    To prepare 3-Chloro-4-Iodotoluene, the method is as follows: First take toluene as raw material, use an appropriate chlorination agent, and perform chlorination reaction under specific reaction conditions. Among them, the reaction temperature, time and amount of chlorination agent need to be precisely controlled. After chlorination, a chlorine-containing toluene derivative is obtained.
    Then, use the derivative as the substrate and react with an iodine reagent. During the reaction process, adjust the pH, temperature and other conditions of the reaction environment to promote the precise replacement of iodine atoms in specific positions.
    When preparing, a reasonable monitoring mechanism needs to be set up. For example, the reaction process is monitored by thin-layer chromatography, and the reaction conditions are adjusted in time to achieve the best reaction effect. At the same time, the product can be separated and purified by column chromatography or recrystallization to obtain high purity 3-Chloro-4-Iodotoluene. In this way, it can be prepared.
    Chemical Reactions & Modifications
    3-Chloro-4-iodotoluene is also an organic compound. Its chemical reaction is related to the change of chemical properties and is very important.
    This compound can be obtained by halogenation. The introduction of halogen atoms changes the distribution of its electron cloud, resulting in very different chemical activities. For example, nucleophilic substitution reactions, due to the presence of chlorine and iodine atoms, the reaction check point and rate are different.
    To optimize the reaction, you can start from multiple ends. The choice of catalyst is crucial. A suitable catalyst can reduce the activation energy of the reaction and accelerate the reaction process. The reaction conditions cannot be ignored. The regulation of temperature and pressure has a great impact on the yield and purity of the product.
    And the chemical modification of this compound can expand its application. Modifying functional groups or giving them new properties has potential value in materials science, medicinal chemistry and other fields, and is an important direction of chemical research.
    Synonyms & Product Names
    Today there is a thing, named 3 - Chloro - 4 - Iodotoluene. In the field of my chemical research, it has many nicknames, and it is also important for commerce, and it runs in the city under different names.
    The name of this thing is also synonymous with its name, which is determined by chemists to recognize its chemical nature and structure. Chemists give it a precise title according to the group and bonding of its atoms. It is expected to be correct and clear in academic exchanges.
    As for the name of the commodity, it involves the business plan and the needs of the market. Merchants want their objects to be made public and easy to remember, so they take their names. Either seek its simplicity, or seek its specificity, hoping to attract the eyes of customers and promote the prosperity of transactions.
    In this way, the name of synonymy emphasizes academic certainty, and the name of commodity emphasizes commercial effectiveness. Although the two are different ways, they are both signs of 3-Chloro-4-Iodotoluene's movements in the world, each of which is used to participate in the grand scene of chemistry and commerce.
    Safety & Operational Standards
    3-Chloro-4-iodotoluene is an important chemical compound in chemical research. In terms of experimental operation and safety assurance, it is necessary to follow specific norms.
    When operating, make sure that the experimental environment is well ventilated. Because of its volatility, if the ventilation is not smooth, the gas will accumulate, or cause damage to the health of the experimenter. When taking 3-chloro-4-iodotoluene, use clean and dry equipment to prevent impurities from mixing and affecting its chemical properties and experimental results.
    In addition, the protection of the experimenter should not be ignored. Wear laboratory clothes, suitable protective gloves and goggles. This compound may be irritating to the skin and eyes, and protective equipment can effectively reduce the risk of injury.
    For storage, 3-chloro-4-iodotoluene should be kept in a cool, dry place away from sources of ignition. Because it encounters open flames or high temperatures, it may be dangerous to burn or even explode. At the same time, it should be stored separately from oxidants, acids and other substances to avoid chemical reactions.
    If you accidentally come into contact with this compound during the experiment and splash it on the skin, you should immediately rinse it with a large amount of flowing water, and then seek medical treatment. If it enters the eyes, rinse it quickly with normal saline, and also seek medical attention in time.
    In conclusion, when conducting research operations on 3-chloro-4-iodotoluene, strict follow of safety and operating standards can ensure the smooth progress of the experiment and ensure the personal safety of the experimenters.
    Application Area
    Today there is a product called 3-Chloro-4-Iodotoluene. This product is useful in many fields.
    In the field of medicine, it can be used as a key intermediate. With its unique structure and delicate reaction, it can make special drugs to treat various diseases and eliminate diseases for the world.
    In the world of materials, it is also indispensable. It can participate in material synthesis and give materials specificity, such as enhancing its stability, changing its optical properties, etc., making materials suitable for various scenarios, or for high-end electronic devices, or as special protective coatings.
    In the path of scientific research and exploration, it is an important reagent. Helping researchers explore the mysteries of chemistry and solve unknown problems can play a key role in organic synthesis, reaction mechanism research, etc., and lead chemical research to continue to advance.
    From this perspective, although 3-Chloro-4-Iodotoluene is small, it has a wide range of applications and far-reaching influence. It is actually one of the important substances in the field of chemistry.
    Research & Development
    In recent years, I have focused on the research of 3-Chloro-4-Iodotoluene. This compound has a unique structure and great potential in the field of organic synthesis.
    At the beginning, the preparation method was often constrained, the yield was low, and impurities were plagued. I worked hard, searched ancient books, learned from ancient methods, and participated in new ideas. Improve the reaction conditions, adjust the proportion of reagents, and after repeated trials, we can optimize the way. The yield is gradually increasing, and the quality is also excellent.
    Then, explore its reaction mechanism. With precise instruments, observe the process of the reaction in detail, and understand the change of the bonding and the migration of electrons. We are well aware of its specificity in nucleophilic substitution and coupling reactions.
    Looking to the future, we hope to expand the creation of new materials based on this. Hope that it can emerge in the fields of optoelectronics and medicine, adding new colors and promoting development for the academic and industry, and becoming a grand event.
    Toxicity Research
    3-Chloro-4-iodine toluene is also a chemical substance. Yu is a chemical researcher and often studies the toxicity of various substances. The toxicity of this substance should not be ignored.
    Looking at its structure, chlorine and iodine atoms are attached to toluene. Chlorine and iodine are both chemically active, or react with various molecules in the body. After experiments, in white mice, if exposed to this 3-chloro-4-iodine toluene, the fur may change, and the action is slightly slow, as if the nervous system is disturbed.
    Another study was on cells. When this substance was added to cultured cells, the cell growth rate slowed down, and some cell morphologies were abnormal. All this shows that 3-chloro-4-iodotoluene is toxic and has adverse effects on the physiological functions of organisms. Researchers should be careful to prevent its harm to themselves and the surrounding environment.
    Future Prospects
    Fu 3 - Chloro - 4 - Iodotoluene is also an organic compound. Looking at the structure of its molecules, chlorine and iodine atoms are placed on the toluene ring, making it unique.
    In the future, its use will surely increase. In the field of chemistry, new substances are often relied on to open up new avenues. This compound may play a great role in drug synthesis. With its unique structure, or it can be a key raw material for new agents, it can heal various diseases and save people from diseases.
    Or it has emerged in material science. With ingenious modifications, it endows materials with specific properties, such as photoelectric sensitivity and structural strength, adding wings to the transformation of materials.
    Although its application may still be limited at present, over time, it will shine like a pearl, making immeasurable contributions to the advancement of science and technology and the benefit of people's livelihood in the future.
    Historical Development
    3-Chloro-4-iodine toluene, the research and development process of this substance is really meaningful. In the past, when organic chemistry was still in its infancy, all the sages were diligent in the field of halogenated aromatics. At first, only a little knowledge of the method of introducing halogen atoms into aromatic hydrocarbons, but precise positioning and efficient synthesis were still difficult.
    At that time, the exploration of toluene derivatives was gradually deepened, and there was no cure for 3-chloro-4-iodine toluene. After generations of chemists unremitting search, testing thousands of paths, or changing the reaction conditions, or changing the type of reagent. At the beginning of traditional halogenation methods, the results were not obvious, the products were complicated, and the separation was difficult.
    Post-organic synthesis techniques are becoming increasingly sophisticated, and new catalysts and new methods are emerging frequently. With the help of emerging metal-catalyzed coupling reactions, after repeatedly adjusting parameters and optimizing the process, 3-chloro-4-iodotoluene can finally be accurately prepared. Its research and development process is like a long road, from ignorance to clarity, relying on the wisdom and dedication of chemists of successive generations to achieve today's results.
    Product Overview
    3-Chloro-4-iodine toluene is also an organic compound. Its color or light, like a crystalline powder, has a specific taste. The structure of this substance, chlorine and iodine atoms are respectively connected to specific positions in the toluene benzene ring.
    The method of preparation often involves the magic of organic synthesis. Or starting from toluene and halogenating it, chlorine and iodine atoms are introduced in sequence, but this process requires fine regulation of reaction conditions, such as temperature, reagent ratio and catalyst, etc., to obtain higher yields.
    It is active and widely used in the field of organic synthesis. It can be used as a key intermediate for the preparation of other complex organic compounds, or involved in drugs, pesticides, materials and other industries.
    It should be used with caution, as it is toxic and irritating, and strict safety procedures must be followed during operation to prevent harm to people and the environment.
    Physical & Chemical Properties
    3-Chloro-4-iodotoluene is also an organic compound. Its physical and chemical properties can be investigated. Looking at its shape, under normal conditions, it is either a colorless to light yellow liquid or a crystalline state, depending on the ambient temperature and pressure. It has a special smell, but it is not a pungent and unpleasant genus.
    In terms of its physical properties, the melting point is quite regular. The melting point is moderate, and it can melt into a liquid state in a specific temperature range. The boiling point is also fixed, and it can be gasified into a gaseous state under the corresponding pressure. Its density is different from that of water, and it is not compatible with water. The two meet and can stand in layers.
    As for the chemical properties, because of the chlorine and iodine atoms in its structure, it is active. It can react with many reagents, such as the reaction of nucleophilic substitution, and the halogen atom can be replaced by other groups, and then new compounds can be derived. It has a wide range of uses in the field of organic synthesis and is valued by chemical researchers.
    Technical Specifications & Labeling
    Today there is a product, the name is 3 - Chloro - 4 - Iodotoluene. To clarify its technical specifications and identification (commodity parameters), it is necessary to study it in detail.
    To observe its shape and quality, it is necessary to ensure that its color is correct, the taste is pure, and there is no variegated odor. The standard of its purity should reach a very high level, and the impurities should be minimal, so that it fits well.
    When it comes to the logo, the name of the product should be obvious on the package, and the ingredients and content must be accurate. The production time, batch, etc. should also be recorded in detail as evidence for traceability. And the logo should be in accordance with common regulations, clear and recognizable, and will not fade for a long time.
    In the technical specifications, the number of melting points and the state of solubility are all key. It is necessary to make all parameters conform to the established standards before it can be said that the quality of this thing is excellent, and it can be used in various applications to achieve its effectiveness and live up to expectations.
    Preparation Method
    In order to prepare 3-Chloro-4-Iodotoluene, the raw materials and production process, reaction steps and catalytic mechanism are crucial.
    To prepare this product, toluene should be used as the initial raw material. First, toluene is reacted with chlorine under specific conditions. This step requires precise temperature control and catalysts. Chlorine atoms replace hydrogen on the toluene benzene ring to form a mixture of chlorotoluene isomers. After separation and purification, the target chlorotoluene product is obtained.
    Then, the obtained chlorotoluene and iodine are reacted in the presence of suitable solvents and catalysts. The reaction steps need to be carefully operated in a specific order. In this process, the catalytic mechanism is crucial, and the efficient catalyst can promote the reaction to proceed efficiently and improve the yield and purity of the product.
    After this series of steps, 3-Chloro-4-Iodotoluene can be obtained. However, each step of the reaction needs to be carefully controlled to achieve the desired production effect.
    Chemical Reactions & Modifications
    Today there is a chemical substance called 3-Chloro-4-Iodotoluene. In the field of chemistry, its reaction and modification are the most important things for us to study.
    To study its reaction, we should investigate the structure of its molecules. In this substance, chlorine and iodine atoms are attached to the ring of toluene, which gives it unique chemical properties. In the case of nucleophiles, chlorine or iodine atoms can be substituted, because they have a certain activity. For example, with appropriate nucleophiles, such as alkoxides or amines, and 3-Chloro-4-Iodotoluene, under suitable conditions, such as temperature and solvent selection, substitution reactions can be induced to obtain new compounds.
    As for modification, its properties can be adjusted by chemical means. Or introduce new functional groups to change its physical and chemical properties. If a specific reaction is used to increase the hydroxyl or carboxyl groups on the ring, its solubility and reactivity can be changed. This is all in chemical research, exploring the reaction and modification of 3-Chloro-4-Iodotoluene, hoping to obtain new chemical results, which are used in various fields.
    Synonyms & Product Names
    3-Chloro-4-iodotoluene, in the field of chemical industry, although its name is the same, it is also known as many. In the theory of Fangjia, it is often called by the name of synonym and the name of commodity.
    Due to the science of chemical industry, the title varies a lot. Some are given synonymous names because of their chemical structure characteristics, so as to facilitate academic research and process description. If it is a wonderful structure, or it is called by the name of a similar chemical concept, in recognition of its nature.
    As for the name of the product, it is in response to the needs of the market. In order to make the product logo unique and fit the marketing activities, the merchant will also establish a separate product name. This 3-chloro-4-iodotoluene, or in different trade names, has different trade names to show its differences, in response to the requirements of all parties.
    Therefore, the synonymous name and the name of the product, in terms of 3-chloro-4-iodotoluene, are both important for chemical exchanges and business exchanges, helping people in the industry to understand their products and use their materials.
    Safety & Operational Standards
    Safety and Handling Specifications for 3-Chloro-4-Iodotoluene
    For those with 3-chloro-4-iodotoluene, it is also an important substance in chemical preparation. To use it properly, safety and operating standards are the key.
    The first word is safety. This substance has a certain chemical activity and comes into contact with the skin or causes irritation. Therefore, when handling, it is necessary to wear protective clothing, such as gloves, goggles, etc., to prevent accidental contact. If the skin touches occasionally, rinse quickly with a lot of water and still feel unwell, seek medical attention. Its volatile gas, or harmful to breathing, is suitable for working in a well-ventilated place. If in a confined space, set up ventilation equipment to prevent gas accumulation. And this product is flammable, away from fire and heat sources, and the storage place must also be dry, cool, and fireproof.
    The second discussion on the operating specifications. When weighing, use a precise weighing instrument and measure according to the experimental requirements, not more or less. When dissolving, choose a suitable solvent, slow in in sequence, and stir moderately to help it disperse evenly. During the reaction process, strictly control temperature, pressure and other conditions. Monitor with a thermometer and a pressure gauge, and fine-tune according to the reaction process. If heating is required, use a suitable heating device, and the temperature control is stable to prevent overheating from causing the reaction to go out of control. After the reaction is completed, the product is separated and purified, and the established steps are followed to ensure purity.
    Waste disposal should not be ignored. Waste containing 3-chloro-4-iodotoluene shall be disposed of in accordance with environmental regulations and shall not be discarded at will. Or hand it over to professional institutions, or degrade it by chemical methods to avoid polluting the environment.
    In summary, the use of 3-chloro-4-iodotoluene must be observed in accordance with safety and operating standards in order to achieve the purpose of the experiment and ensure the safety of people and the environment.
    Application Area
    3-Chloro-4-iodotoluene is also an organic compound. Its application field is quite wide. In the field of pharmaceutical synthesis, it is often a key intermediate. The properties of chlorine and iodine on the benzene ring make it easier for compounds to participate in various chemical reactions to produce specific drugs.
    In the field of materials science, it also has important uses. Because of its unique chemical structure, it can help to develop new functional materials, such as photoelectric materials. Through specific reactions, it is integrated into the material system to give the material unique optical and electrical properties.
    In the fine chemical industry, it is a raw material for the preparation of special chemicals. With its chemical activity and clever reaction path, high value-added fine chemicals can be produced to meet the special needs of many fields. All these show that 3-chloro-4-iodotoluene has an indispensable position in many application fields.
    Research & Development
    3-Chloro-4-iodotoluene is an important compound in organic chemistry. I have been studying this compound for a long time. The synthesis method requires many delicate reactions. The choice of initial raw materials is crucial, and it is related to the purity and yield of the product.
    During the experiment, the control of the reaction conditions should not be lost. Temperature, pH, and reaction time are all key factors affecting the results. After repeated experiments, a better synthesis path was found, which could improve the yield.
    Looking forward to its development, 3-chloro-4-iodotoluene has great application potential in the fields of medicine, materials, etc. It may become a key intermediate for new drugs and lay the foundation for the synthesis of high-performance materials. I will continue to study and strive to expand its application scope and contribute to the progress of the chemical field.
    Toxicity Research
    Since modern times, chemical refinement has led to the emergence of various compounds in an endless stream. In today's 3-Chloro-4-Iodotoluene, the study of toxicity is crucial.
    Examine this substance in detail, its molecular conformation is unique, and chlorine and iodine atoms are attached to the ring of toluene. The electronegativity of chlorine can shift the electron cloud, or cause its chemical activity to be different. The heavy atom effect of iodine atoms may also affect its reaction path.
    On the basis of toxicity, or because of its structure, it can interact with various molecules in organisms. After it enters the organism, it may combine with the activity check point of proteins, interfering with normal biochemical reactions; or affecting the permeability of cell membranes, causing cell dysfunction.
    Although the relevant toxicity research is still in the process of evolution, its potential harm should not be underestimated based on chemical principles. In the future, scientific methods should be used to study its toxicological mechanism in depth to provide a solid basis for protection and application.
    Future Prospects
    I have dedicated myself to the study of 3 - Chloro - 4 - Iodotoluene. Although the current research has only seen one or two of it, my heart is looking to the future, full of hope.
    Looking at its properties, its structure is unique and contains mysteries. In terms of its ability to react, it may have the potential to open up new paths. With time and careful investigation, we will be able to learn more about its characteristics and explore its unseen functions.
    In the future, we hope to optimize its preparation method, improve its purity, and increase its yield. Or apply it to medicine to aid in healing techniques; or use it in materials to promote its performance. The road ahead is long and full of thorns, and we will continue to move forward. With wisdom and perseverance, I have achieved brilliant results in the research of 3-Chloro-4-Iodotoluene, contributing to the academic and industry, and paving the way for a bright future.
    Where to Buy 3-Chloro-4-Iodotoluene in China?
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    Frequently Asked Questions

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    What is the chemistry of 3-chloro-4-iodotoluene?
    3-Chloro-4-iodotoluene is also an organic compound. Its chemical properties are unique and valuable to explore.
    In this compound, the presence of chlorine atoms and iodine atoms endows it with specific reactivity. Chlorine and iodine are both halogen elements and have certain electronegativity. Chlorine atoms can reduce the electron cloud density of the benzene ring due to their electronegativity, which can change the activity of the electrophilic substitution reaction of the benzene ring. In the electrophilic substitution reaction, chlorine atoms are ortho and para-sites, which have an important influence on the choice of the reaction check point.
    Iodine atoms also have characteristics. Although their atomic radius is large, they have unique performance in some reactions when they are left groups. For example, in the nucleophilic substitution reaction, the iodine ion is easy to leave, which can promote the reaction to proceed in the direction of product formation.
    The methyl group of 3-chloro-4-iodotoluene is the power supply group, which can increase the electron cloud density of the benzene ring, especially in the ortho and para-positions. This interaction with the chlorine atom determines the regioselectivity of the substitution reaction on the benzene ring.
    In the oxidation reaction, the methyl group can be oxidized to an oxygen-containing functional group such as a carboxyl group, but this process requires specific reaction conditions and oxidizing agents. The halogen atom can undergo many reactions such as substitution and elimination under certain conditions. The chemical properties of this compound are complex and interesting, and its reaction properties offer many possibilities for the field of organic synthesis, which can be used to prepare various organic compounds with unique functions.
    What are the physical properties of 3-chloro-4-iodotoluene?
    3-Chloro-4-iodotoluene is one of the organic compounds. Its physical properties are quite important and are detailed as follows:
    First of all, its appearance, under room temperature and pressure, 3-chloro-4-iodotoluene is mostly colorless to light yellow liquid, with a clear texture. It can be seen that its fluidity is good, like smart water, but it also has its own unique state.
    Melting point and boiling point, the melting point is about -20 ° C. At this temperature, this substance gradually turns from liquid to solid, like a temporary break in life. The boiling point is between about 240 ° C and 250 ° C. When the temperature rises, the liquid boils, and the substance converts to a gaseous state, opening a new physical state.
    Then there is the density, which is heavier than water, about 1.8g/cm ³. If it is placed in a container with water, it can be seen that it sinks to the bottom of the water, such as stone entering the water, which is clearly identifiable.
    Solubility is also a key property. 3-chloro-4-iodotoluene is insoluble in water. It is like an isolated island in water, and it is difficult to blend with water. However, it is soluble in many organic solvents, such as ethanol, ether, benzene, etc. In such solvents, it can be evenly dispersed, just like a fish entering water and swimming freely.
    In terms of volatility, its volatility is relatively low. It evaporates slowly in a room temperature environment, and a special smell can be smelled in the air. However, it is not pungent and intolerable, and it can be detected only by paying attention.
    The physical properties of 3-chloro-4-iodotoluene are of great significance in many fields such as organic synthesis and chemical production, and are used by relevant practitioners to play a unique value.
    What are the main uses of 3-chloro-4-iodotoluene?
    3-Chloro-4-iodotoluene is also an organic compound. It has a wide range of uses and is involved in various fields of chemical industry.
    First, it can be used as an intermediary for organic synthesis. In the process of organic synthesis, such halogenated aromatics are often relied on as starting materials. After various chemical reactions, such as nucleophilic substitution reactions, its chlorine or iodine atoms can be replaced by other functional groups. Reacting with alcohols or amines can introduce hydroxyl, amino and other functional groups to build more complex organic molecules, paving the way for the preparation of compounds with specific structures and functions. In the field of medicinal chemistry, lead compounds with unique pharmacological activities can be synthesized.
    Second, it is also useful in the field of materials science. It can be polymerized and copolymerized with other monomers to introduce its structural units into the main chain or side chain of polymer materials. Because of its halogen atom properties, it may endow materials with special properties, such as improving the solubility and thermal stability of materials, and even affecting the optical and electrical properties of materials, playing an important role in the preparation of special polymer materials.
    Third, it is also indispensable in the manufacture of fine chemicals. It can be used to synthesize fine chemicals such as fragrances and dyes. With its structural characteristics, it can endow fine chemicals with unique molecular structures, which in turn affect their color, aroma and other characteristics, and improve product quality and added value.
    In summary, 3-chloro-4-iodotoluene, with its intermediary properties, is an important chemical raw material in the fields of organic synthesis, materials science, and fine chemical manufacturing, promoting the development and innovation of various fields.
    What are 3-chloro-4-iodotoluene synthesis methods?
    The synthesis methods of 3-chloro-4-iodotoluene vary widely, depending on various chemical techniques and materials. One method is to take toluene as the base first, and use chlorination to make chlorine atoms connect to the toluene benzene ring to obtain chlorine-containing derivatives. This chlorination method often requires the selection of suitable catalysts, such as iron filings or anhydrous iron trichloride. Under a specific temperature and reaction atmosphere, toluene meets chlorine gas, and the chlorine atoms can enter the benzene ring in the appropriate position according to the positioning rules to obtain m-chlorotoluene.
    The method of re-iodization of m-chlorotoluene is obtained. When iodizing, the iodine element is often used as the source, and an appropriate oxidant, such as hydrogen peroxide or nitric acid, is used to promote the iodine atom to connect to the benzene ring and form a position adjacent to the chlorine atom, resulting in 3-chloro-4-iodotoluene. This process requires fine temperature control, and attention to the reaction process. The strength and dosage of the oxidant are all related to the effectiveness of the reaction and the purity of the product.
    There are other methods, which can be used to iodize toluene first, and then chlorinate it. First, by means of iodization, the iodine atom is connected to the toluene-benzene ring, and then according to the chlorination process, the chlorine atom However, in this order, the reaction conditions also need to be carefully observed, because the activity and localization effects of iodization and chlorination affect each other, so that the two can cooperate to obtain the target product. All kinds of synthesis methods require the experimenter to study the physical properties and be familiar with the skills in order to achieve the effect and obtain pure 3-chloro-4-iodotoluene.
    What are the precautions in storage and transportation of 3-chloro-4-iodotoluene?
    3-Chloro-4-iodotoluene is also an organic compound. When storing and transporting, be sure to pay attention to many things.
    First, store this compound in a cool, dry and well-ventilated place. Because it is sensitive to heat, high temperature can easily cause it to decompose or cause other chemical reactions, so it is the first thing to keep away from heat and fire sources. Furthermore, it should be placed separately from oxidizing agents, strong bases and other substances, because 3-chloro-4-iodotoluene is prone to chemical reactions with such substances, or is dangerous. And the storage place should be clearly marked to inform everyone of its chemical properties and potential hazards.
    As for transportation, it should not be ignored. The transportation equipment must be tightly sealed to prevent leakage. Because of its certain toxicity and irritation, if it leaks outside, it may pose a threat to the environment and personal safety. During transportation, strict temperature control is required to avoid excessive temperature fluctuations. At the same time, transportation personnel should be familiar with their emergency treatment methods. In case of leakage and other accidents, they can quickly take effective measures, such as evacuating crowds, containing leaks, and adsorbing with appropriate materials, etc., to minimize the harm. And transportation documents should record the quantity, nature and other key information of the compound in detail for inspection. In this way, the safety of storage and transportation is guaranteed.