1 4 Iodophenyl Ethanone
Iodobenzene

1-(4-Iodophenyl)Ethanone

Fengxi Chemical

    Specifications

    HS Code

    305542

    Chemical Formula C8H7IO
    Molar Mass 248.044 g/mol
    Appearance Yellow - brown solid
    Melting Point 86 - 88 °C
    Boiling Point 154 - 156 °C (12 mmHg)
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
    Density 1.807 g/cm³
    Flash Point 110.8 °C
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Chemical Formula C8H7IO
    Molecular Weight 248.04
    Appearance Solid
    Color Yellow to off - white
    Odor Characteristic
    Melting Point 98 - 100 °C
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, chloroform
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Chemical Formula C8H7IO
    Molar Mass 246.044 g/mol
    Appearance Solid
    Melting Point 88 - 92 °C
    Boiling Point 300.8 °C at 760 mmHg
    Density 1.78 g/cm³
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
    Flash Point 135.7 °C
    Purity Typically high - purity (>95%) in commercial products
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    Packing & Storage
    Packing 100g of 1-(4 - iodophenyl)ethanone packaged in a sealed, chemical - resistant container.
    Storage 1-(4 - iodophenyl)ethanone should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly closed container to prevent exposure to air and moisture, which could potentially cause degradation. Place it on shelves at a suitable height for easy access and avoid storing near incompatible substances.
    Shipping 1-(4 - iodophenyl)ethanone, a chemical, is shipped with strict adherence to safety regulations. It's carefully packaged in suitable containers to prevent leakage and damage during transit, ensuring safe delivery.
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    1-(4-Iodophenyl)Ethanone
    General Information
    Historical Development
    The historical development of 1- (4-iodophenyl) ethyl ketone
    In the past, the exploration and research of various chemical substances relied on the efforts of many scholars. 1- (4-iodophenyl) ethyl ketone was originally hidden in the source of chemical mysteries. At that time, the tools for chemical research were still simple, and scholars used their keen insight and unremitting practice to find traces in the complex reactions.
    With the passage of time, chemical skills became more and more exquisite. The precision of instruments has gradually increased, and the synthesis methods have also become more and more diverse. Researchers have increasingly accurately analyzed the structure of 1- (4-iodophenyl) ethyl ketone, and the synthesis method has gradually evolved from the initial complexity to the efficient and concise. This substance has emerged in the field of organic synthesis, laying the foundation for many subsequent studies and opening a new chapter in chemical exploration. Its historical development is a vivid portrayal of chemical progress.
    Product Overview
    1- (4 'iodophenyl) ethyl ketone is a key intermediate in organic synthesis. It has a unique chemical structure, with an iodine atom attached at position 4 above the benzene ring and an acetyl group.
    This compound is widely used in many fields. In the field of medicinal chemistry, it is often the starting material for the synthesis of specific drug molecules. With the activity of iodine atoms, it can participate in a variety of nucleophilic substitution reactions, introducing the required functional groups to construct structures with specific pharmacological activities. In the field of materials science, it may also be an important building block for the preparation of functional materials, giving special photoelectric properties to materials.
    There are many ways to synthesize 1- (4 -iodophenyl) ethyl ketone. Common ones are obtained by iodization with acetophenone as the starting material. During operation, attention should be paid to the precise control of reaction conditions, such as temperature, reagent dosage, etc., to improve the purity and yield of the product. In-depth study of it will provide more possibilities and directions for the development of organic synthesis chemistry.
    Physical & Chemical Properties
    1- (4 - Iodophenyl) Ethanone is also an organic compound. Its physical and chemical properties are worth studying. Looking at its physical properties, at room temperature, it is in the shape of a solid state, with a color or nearly white, and has a specific melting point and boiling point. This is the key evidence when separating and purifying. Its melting boiling point value may vary slightly due to environmental factors. Regarding chemical properties, the presence of iodine atoms and carbonyl groups in this compound gives it unique reactivity. Iodine atoms can involve nucleophilic substitution reactions, while carbonyl groups can interact with many nucleophilic reagents, or add, or condensate. In case of a suitable base, carbonyl α-hydrogen can be taken away, initiating a series of reactions. These physicochemical properties, in the field of organic synthesis, are the cornerstone of the preparation of complex compounds and contribute significantly to the development of organic chemistry.
    Technical Specifications & Labeling
    The process specifications and identification (product parameters) of this product of 1- (4 - Iodophenyl) Ethanone are the key. The process specifications need to specify the reaction conditions, such as temperature, pressure, duration, material ratio, and operation details of each step. There must be no omission. The reaction temperature should be controlled at XX degrees, the pressure should be maintained at XX Pa, and the time length is about XX, and the material ratio should be accurate.
    In terms of identification, the product parameters must be detailed. Its purity should reach XX%, the impurity content should not exceed XX%, the appearance should be XX shape, and the color should be XX color. On the packaging, the name, specification, purity, production date, etc. should be clearly marked. In this way, the process specifications and labels of this product can be made clear and used for all purposes.
    Preparation Method
    1- (4 - Iodophenyl) Ethanone is an important compound in organic synthesis. The method of its preparation, the selection of raw materials is very important. Usually 4-iodobenzene and acetylation reagent are used as starting materials. In the synthesis process, the reaction steps need to be gradual.
    First mix 4-iodobenzene with an appropriate amount of acetylation reagent in a specific reaction vessel. Controlling the temperature and reaction time is the key to the success of the reaction. Generally speaking, the reaction needs to be heated under mild conditions for several days to be sufficient.
    The catalytic mechanism cannot be ignored. The selection of suitable catalysts can significantly improve the reaction rate and yield. Such as some Lewis acid catalysts, it can effectively promote the reaction process.
    After the reaction is completed, after subsequent separation and purification steps, impurities can be removed to obtain high-purity 1- (4 - Iodophenyl) Ethanone products. This preparation method can provide important reference for related research and production.
    Chemical Reactions & Modifications
    To observe the transformation of 1- (4-Iodophenyl) Ethanone, its reaction and change, is the weight of chemical study. The method of the past may not be good, the yield is not perfect, and the side effects should be mixed.
    In order to find a good strategy, the researchers have worked hard. After many trials, the influence of different conditions was observed. If the temperature rises and falls, the proportion of the agent is related to the reaction path.
    Then there is a new way, change the reaction environment, choose the appropriate medium, and adjust the temperature to the appropriate level. As a result, the production of 1- (4-Iodophenyl) Ethanone can be increased, and the side effects should also be reduced.
    This is not only beneficial to the system of 1- (4-Iodophenyl) Ethanone, but also to the transformation of other things, showing a clear way. Let us know that in the research of transformation, we can always seek change and progress, so that we can obtain good results and meet the needs of the world.
    Synonyms & Product Names
    1- (4-iodophenyl) ethyl ketone, which has many other names. Its synonyms and trade names are also reflected in past literature records.
    In ancient books, the names of chemical substances often change depending on the region and era. 1- (4-iodophenyl) ethyl ketone, or named for its characteristics and structure. Although there was no precise nomenclature at that time, chemists also named it according to their observations and understanding.
    It may be commensurate with the part, because the iodine atom is attached to the specific position of the phenyl group, and the structure of ethyl ketone, the predecessors may have given it a different name. Although it is not as standard as today, it also has the logic of that time. The name of the product may vary depending on the use and production process. This reflects the evolution of the naming of chemical substances, as well as the trajectory of scientific development. It is of great significance for the study of past chemical achievements.
    Safety & Operational Standards
    1 - (4 - iodophenyl) ethyl ketone, this chemical substance is related to safety and operation standards, and is extremely important. Today's detailed discussion is to ensure the smooth operation of the experiment and the safety of personnel.
    All operations involving 1 - (4 - iodophenyl) ethyl ketone, the experimenter should strictly abide by the procedures. The first protection must be fitted with protective clothing, gloves, and goggles to prevent it from coming into contact with the skin and eyes. Because it may be irritating, if it is not careful, it will cause injury.
    The place where the operation is located must be well ventilated. If the volatile gas of this chemical gathers in the room and is inhaled into the human body, it may damage health. The ventilation equipment is turned on to quickly expel harmful gases and keep the air fresh.
    Take 1 - (4 - iodophenyl) ethanone, when using a precise measuring tool, according to the required amount of the experiment, not more or less. After the amount is completed, properly seal it to avoid exposure to air for too long and cause qualitative change.
    During the experiment process, closely monitor the reaction conditions. Temperature, pH and other factors can affect the direction of the reaction, and are also related to safety. If the reaction is out of control, or an accident occurs.
    Waste disposal should not be ignored. Waste containing 1 - (4 - iodophenyl) ethanone should be collected in accordance with regulations and handled by professional institutions. It must not be discarded at will, and the environment should be free from pollution.
    When storing, choose a cool, dry and ventilated place, away from fire and heat sources. Isolate from oxidants, acids, etc., to prevent danger caused by interaction.
    In short, the safety and operation specifications of 1- (4-iodophenyl) ethyl ketone are the key to the experiment. Experimenters keep it in mind and practice it cautiously, so that they can be safe and promote the steady progress of scientific research.
    Application Area
    Today there is a substance named 1- (4 - Iodophenyl) Ethanone. This chemical substance has its uses in many fields.
    In the field of medicine, it can be used as a key intermediate. Doctors want to make special drugs to treat various diseases, and this substance may help. Its unique structure can lead to the precise action of drug molecules on the lesion, such as a sharp blade to break bamboo, making the drug more effective.
    In material research, it cannot be ignored. Craftsmen want to create strange materials with unique optical and electrical properties. 1- (4 - Iodophenyl) Ethanone may be the key to opening the door to new materials. It can adjust the molecular arrangement of materials, resulting in its extraordinary characteristics and application in high-end technology products.
    And in fine chemicals, it can make special fragrances and pigments. Fragrance masters get it, which can endow fragrances with unique charm and fragrance; painters use it to make pigments gorgeous and lasting. From this point of view, 1- (4 - Iodophenyl) Ethanone is widely used and has a deep impact, which cannot be underestimated.
    Research & Development
    In recent years, I have focused on the research of 1- (4 - Iodophenyl) Ethanone. This compound has a unique structure and unique properties, and has great potential in the field of organic synthesis.
    I first investigated its physicochemical properties and explored its reaction rules in detail. After repeated experiments, I found that it can form new bonds or change configurations under different conditions. If it encounters a certain reagent, under a specific temperature and pressure, it can produce different products. This is a new way for organic synthesis.
    However, the road to research is full of thorns. The rate of reaction was not as expected; the removal of impurities is also a problem. I thought about it day and night, consulted the classics, and visited colleagues. After many attempts, the method of optimization was finally obtained, the yield was improved, and the product was purified.
    Looking at this research now, although there are small achievements, the road ahead is still far away. In the future, I hope to expand its application in the fields of medicine and materials, and make great achievements for the development of the academic community.
    Toxicity Research
    Taste the essence of medical science, and observe the advantages and disadvantages of physical properties. In today's chemical substances, there are 1- (4-Iodophenyl) Ethanone, and the investigation of its toxicity cannot be ignored.
    Although this substance has chemical uses, its toxicity is hidden. The ancient people studied medicine with caution, observing its properties, testing its effectiveness, and preventing its harm. In 1- (4-Iodophenyl) Ethanone, it is necessary to examine its entry into the body in detail, or damage the organs, or disrupt qi and blood.
    In order to study its poison, it is necessary to observe its sympathies with other things in a rigorous way, and observe its changes in different environments. If it is efficacious in life, carefully examine its symptoms, and record it in detail, it will be possible to clarify the depth of its toxicity. Those who use this thing for future generations will be cautioned to avoid its harm and take advantage of it, and to ensure the safety of all living beings.
    Future Prospects
    The prospect of the future is related to (1- (4-Iodophenyl) Ethanone) this thing. We study it, hoping that it will develop extraordinary capabilities in the field of knowledge. In the world of knowledge, we hope that it will become the foundation of new knowledge, or help relieve diseases, and save the disease of life. In the world of materials, we hope that it will be the source of new materials, the characteristics of new materials, and the field of expansion. We are now researching it well, but our hearts are determined, and we are not afraid of the road ahead. It is expected that in the near future, we can improve its delicacy, so that (1- (4-Iodophenyl) Ethanone) can be used greatly, and the world will add more and more tiles. This is the grand scene we hope to see in the future.
    Historical Development
    1- (4-Iodophenyl) ethyl ketone did not have its name in ancient times, but the method of its preparation has gradually emerged over the years. In the past, organic synthesis was not yet prosperous, and such compounds were little known. And the evolution of science, many sages have delved deeper and deeper.
    At the beginning, scholars explored its synthesis in the laboratory with exquisite methods. After countless trials and errors, an effective recipe was obtained. Using acetophenone as a base to introduce iodine atoms, the process is very difficult. It is necessary to precisely control the temperature and select the appropriate reagents.
    However, the fearless ancestors, with perseverance and excellent wisdom, finally made the preparation of 1- (4-iodophenyl) ethyl ketone mature. Therefore, this compound has gradually developed its use in medicine, materials and other fields, opening a new chapter and laying the foundation for future development.
    Product Overview
    1- (4 -iodophenyl) ethyl ketone is a key compound in organic synthesis. Its properties are crystalline, white to light yellow in color, and have a special odor. This substance is widely used in scientific research and chemical production.
    From the perspective of chemical structure, the iodine atom on the benzene ring is cleverly connected to the acetyl group, giving it unique chemical activity. In organic reactions, iodine atoms are often the activity check point of nucleophilic substitution reactions, which can react with many nucleophilic reagents, and then derive a variety of organic products.
    In terms of synthesis paths, it is often prepared by a series of reactions such as halogenation and acylation of specific aromatic hydrocarbons. During the preparation process, the reaction conditions need to be carefully controlled, such as temperature, the proportion of reactants, and the choice of catalyst, which all have a great impact on the purity and yield of the product.
    1- (4-iodophenyl) ethyl ketone has good stability, but when storing, it is still necessary to avoid light and high temperature to prevent its decomposition or deterioration, and ensure that it can play its due role in subsequent use.
    Physical & Chemical Properties
    1- (4 'iodophenyl) ethyl ketone, an organic compound. Its physical and chemical properties are worth exploring. Looking at its properties, under normal temperature, it is often solid, white or nearly white. Its melting point has a fixed number, about a certain temperature range. This property is of great significance for the identification and purification.
    When it comes to solubility, it has a certain solubility in common organic solvents such as ethanol and ether, but it is insoluble in water. This is due to the characteristics of molecular structure. Its chemical properties are very active because it contains carbonyl and iodine atoms. Carbonyl can lead to the reaction of nucleophilic addition, and iodine atoms can perform substitution reactions under appropriate conditions. This is an important path for organic synthesis. The physical and chemical properties of this compound can provide a solid foundation for applications in organic synthesis, medicinal chemistry, and other fields.
    Technical Specifications & Labeling
    1- (4 'iodophenyl) ethyl ketone, the process specification and identification (product parameters) of its preparation are the key to our research. To obtain this product, first take an appropriate amount of raw materials, and after careful weighing, the proportions of each substance are accurate. In the clean reactor, put in the raw materials in sequence, control the temperature moderately, so that the reaction can proceed steadily. During the reaction, pay close attention to the changes in temperature and pressure, which are essential for the smooth reaction. After the reaction is completed, the pure 1- (4' iodophenyl) ethyl ketone can be obtained after separation and purification. The label should specify the product parameters, such as purity, molecular weight, melting point, boiling point, etc., and should be clearly marked for identification and access. This is necessary to ensure product quality and application.
    Preparation Method
    The preparation method of 1- (4 'iodophenyl) ethyl ketone is related to the raw materials and production process, reaction steps and catalytic mechanism. The selection of raw materials is very critical, and iodobenzene and acetylation reagents can be used. At the beginning of the reaction step, iodobenzene and an appropriate amount of acetylation reagents are placed in a certain ratio in the reactor. Then, a specific catalyst is added to create a suitable reaction environment, such as controlling temperature and pressure. In the catalytic mechanism, the catalyst accelerates the reaction process and promotes the effective combination of the phenyl ring of iodobenzene and the acetyl group. After this series of operations, the pure 1- (4' iodophenyl) acetone product can be obtained through subsequent processes such as separation and purification. This preparation method is of great significance in the chemical industry and can optimize the process to improve yield and purity.
    Chemical Reactions & Modifications
    The technique of modern chemistry is increasingly refined, and there are many reasons for the change of various substances. Today's discussion on the chemical reaction and modification of 1- (4-Iodophenyl) Ethanone.
    The way of its reaction may involve nucleophilic substitution, and the iodine activity of the halogen atom is quite good. It is often replaced by other groups, which causes the structure to change. Or there is a response to oxidation and reduction, and the carbonyl group can be changed, which affects its chemical properties.
    As for modification, other groups can be introduced to adjust its polarity and stability. If an alkyl group is extended, its lipid solubility is increased; if a hydrophilic group is added, its solubility is changed. This can be required to suit different applications. The study of its reaction and modification is of great use in the fields of materials and medicine, and can open up new avenues for the industry.
    Synonyms & Product Names
    1- (4 -iodophenyl) ethyl ketone, which is also known as many other names. Although ancient chemistry is not as accurate as it is today, it also has related names for such substances.
    Its name is "iodoacetophenone", which directly describes the relationship between the iodine atom and acetophenone in its structure, to indicate its characteristics concisely. Or "p-iodoacetophenone", the word "pair" indicates the opposite position of the iodine atom in the benzene ring to indicate its structure.
    Although there was no current scientific system at that time, our ancestors were in the chemical exploration, and they also gave matter names with their wisdom. Although it was not as accurate and complete as it is today, it was also the cornerstone of chemical development, allowing future generations to continue to explore its principles, clarify its characteristics, and apply it to the world.
    Safety & Operational Standards
    1- (4 - Iodophenyl) Ethanone is an important chemical product. In the preparation and use of this product, safety and operating practices are of paramount importance.
    First of all, in terms of safety, this chemical may be toxic and irritating. Be sure to take protective measures at the time of contact. The experimenter should wear professional laboratory clothes and protective gloves to avoid direct contact with the skin. At the same time, eye protection is also indispensable. Wear goggles to prevent it from splashing into the eyes and causing damage to the eyes.
    Furthermore, in terms of operating practices, relevant operations should be carried out in a well-ventilated environment. Because the product may produce harmful gases during some reactions, good ventilation can discharge harmful gases in time to protect the health of the experimenter. When conducting chemical reactions, strictly follow the established reaction conditions and operating procedures. For example, control the reaction temperature, reaction time and the proportion of reactants. If the temperature is not properly controlled, or the reaction is too violent, causing safety accidents; and the proportion of reactants is out of balance, it may affect the purity and yield of the product.
    When storing this product, it should be placed in a cool, dry and ventilated place. Avoid mixing with oxidants, acids and other substances to prevent chemical reactions. Regularly check the storage environment and product status, and take appropriate measures in time if any abnormalities are found.
    In summary, for 1- (4 - Iodophenyl) Ethanone products, strict adherence to safety and operating practices is necessary to ensure the smooth conduct of experiments and the safety of personnel and the environment.
    Application Area
    1- (4-iodophenyl) ethyl ketone is also an organic compound. It has a wide range of uses in the field of medicinal chemistry. It is often a key raw material for the synthesis of special drugs, and helps chemists produce antibacterial and anti-inflammatory medicines.
    In materials science, 1- (4-iodophenyl) ethyl ketone can also be used. It can be transformed into a material with special photoelectric properties through specific reactions and used in electronic devices, such as optimizing display performance, increasing its clarity and stability.
    In organic synthesis chemistry, this compound is an important intermediate. Chemists take advantage of the activity of iodine atoms to construct complex and functional organic molecules through many reactions, paving the way for the development of new functional materials and drugs. Therefore, 1- (4-iodophenyl) ethyl ketone plays an indispensable role in many application fields.
    Research & Development
    Today there is a thing named 1- (4 - Iodophenyl) Ethanone. We study this thing carefully with the key of research and development.
    Examine its properties in detail, explore the beauty of its structure, and study the rules of reaction. On the road of experimentation, we tried many times to understand its changes under different conditions. After repeated trial and error, we gradually obtained the essentials.
    Examine the field of its application, or we can make progress in the research of medicine and materials. Although the road ahead is difficult, we will continue to study with perseverance. Ji can take advantage of the research of this product to create something, contribute to the development of the industry, and in the future, show its extraordinary use, and become a grand event of research and development.
    Toxicity Research
    Recently, I studied the properties of poisons in my room, involving 1- (4-Iodophenyl) Ethanone. The toxicity of this substance is really the core of my research.
    Looking at its properties, it made me think deeply. After exploring ancient books in many ways, I followed up with my own experiments. Its effect in the body, or disturbing the movement of qi and blood, messing with the functions of the viscera. Although no ancient books have written directly about its poison, it is deduced from similar things, or there is potential harm.
    I studied its structure in detail, analogous to known poisons, and expected it to enter the body, or injure the liver and spleen, causing qi and blood to stagnate. Thinking about the ancients said: "The nature of things must be characterized." Therefore, when experimenting, be cautious. Test it with small animals, observe their behavior, eating, and mental changes, and explore the toxicity of this 1- (4-Iodophenyl) Ethanone, providing detailed evidence for future generations to use this substance or avoid its harm.
    Future Prospects
    The prospect of the future concerns the product of 1- (4-iodophenyl) ethyl ketone. This chemical product still has a wide way to go in the way of scientific research. We will use our diligent techniques to increase its yield and improve its quality. Hope to explore its novelty and develop its potential application in the field of medicine, or as a cure for diseases; in the world of materials, or as a cornerstone of creation. With time, we will surely be able to use technological progress to break through the current barriers, expand its application, and contribute to the well-being of the world.
    Historical Development
    1- (4-iodophenyl) ethyl ketone, the birth of this substance is really a chapter in chemical evolution. In the past, chemists studied and searched, and in the field of organic synthesis, they made great efforts.
    At that time, many talents focused on the reaction of iodine aromatics and ketones. After countless attempts, or the choice of solvents, or the adjustment of temperature and temperature, or the exploration of catalytic aids.
    At the beginning, there was little effect, but everyone was not discouraged. After unremitting research, we finally achieved a delicate method. With suitable reagents and precise conditions, the iodine atom cleverly fell in a specific position of the phenyl group and was connected to the acetone structure. Since then, 1- (4-iodophenyl) ethyl ketone has made its mark on the chemistry stage, paving a new path for subsequent organic synthesis, drug research and development, and opening a different chapter.
    Product Overview
    1- (4 'iodophenyl) ethyl ketone, this compound is a key raw material for organic synthesis. Its appearance is white to light yellow crystalline powder, with specific physical and chemical properties. In the field of organic chemistry, with its unique molecular structure, it is often a core participant in many reactions.
    The synthesis process can be achieved by following a specific organic reaction path. It plays an important role in organic synthesis and can be carefully prepared through a series of steps such as halogenation reaction and acylation reaction. When preparing, precise control of the reaction conditions is critical, such as temperature and catalyst dosage, which all affect the purity and yield of the product.
    1- (4-iodophenyl) ethyl ketone is widely used in the fields of medicinal chemistry and materials science. In medical research, it can be used as a key structural fragment of lead compounds to develop new drugs through structural modification and optimization. In the field of materials science, it may participate in the construction of specific functional materials, endowing materials with unique properties.
    Physical & Chemical Properties
    1- (4-iodophenyl) ethyl ketone, which has unique physical and chemical properties. From the perspective of physical properties, it takes a specific form at room temperature, or is crystalline, with a certain color and appearance. Its melting point, boiling point and other parameters related to the change of physical state are crucial to determine its physical stability. In terms of chemical properties, because its structure contains iodine atoms and carbonyl groups, it is active in many chemical reactions. Iodine atoms can participate in nucleophilic substitution reactions, while carbonyl groups can perform addition reactions. This compound has a wide range of uses in the field of organic synthesis. With its unique physical and chemical properties, it can be used as a key intermediate to prepare a variety of complex organic compounds, providing an important basis for chemical research and industrial production.
    Technical Specifications & Labeling
    1- (4 - Iodophenyl) Ethanone, the thing that transforms is also. The quality of the technology of its creation is the most important. First, it shows the quality of its materials, and the quality of the materials used must be high, so as to obtain a good quality. In terms of the quality of the reaction, the quality and the force of the reaction, the precision of the control. If the quality is not good, the speed or speed of the reaction will be guaranteed.
    The method of determination cannot be ignored. It can be determined that its appearance, color and shape are uniform. In addition, the equipment, such as the external light, can be determined by its function, and the molecular weight of the fragments can be known. The combination of the two can improve the accuracy of 1- (4 - Iodophenyl) Ethanone, making the product suitable for the needs of business, for the purpose of engineering and scientific research.
    Preparation Method
    To prepare 1- (4 - Iodophenyl) Ethanone, the first raw materials are iodobenzene and acetyl chloride. The preparation process is to mix iodobenzene with anhydrous aluminum trichloride, which is the key to the Fu-Ke acylation reaction. Slowly drop acetyl chloride and stir the reaction at a suitable temperature. During the reaction, an anhydrous and oxygen-free environment needs to be maintained to prevent side reactions from breeding. After the reaction is completed, quench with ice water, and then separate and purify the product through extraction, washing, drying, distillation and other steps. In this process, precise temperature control, raw material ratio and reaction time are all elements for obtaining high-purity products, so that 1- (4 - Iodophenyl) Ethanone can be prepared.
    Chemical Reactions & Modifications
    In modern times, chemistry has flourished, exploring the changes of various things to benefit people's lives. Today there is 1- (4 - Iodophenyl) Ethanone, and its chemical reaction and modification are quite important to us.
    To obtain this substance, it is often prepared by various reactions. The reaction method used in the past may have the disadvantages of being complicated and inefficient. For example, the old method has complicated steps and the yield is not ideal.
    We then think about changes and seek new things, and improve the reaction method. After repeated experiments, new reagents and optimized conditions have been used to make the reaction simpler and the yield has been greatly improved. And after modification, this substance is more usable in the fields of medicine and materials.
    The way of chemistry is changing with each passing day. Our chemists, like the wise men of ancient times, continue to explore, and strive for excellence in the way of reaction and modification, so as to achieve the great cause of chemistry and benefit the world.
    Synonyms & Product Names
    1- (4-iodophenyl) ethyl ketone, also known as p-iodoacetophenone. Its other names include 4-iodoacetophenone, etc. P-iodoacetophenone is widely used in the chemical industry. It can be used as an intermediary in organic synthesis and is used in the pharmaceutical, dye and other industries.
    Looking at its naming, "1- (4-iodophenyl) ethyl ketone" is determined according to the chemical naming rules. According to this rule, the position and name of the substituent are marked first, that is, "4-iodophenyl", and then the main structure is "acetone". The title of "p-iodoacetophenone" is based on the customary nomenclature of the relative position of the benzene ring substituent. P-iodoacetophenone, because of its structural properties, has specific chemical properties and can participate in many chemical reactions, playing a key role in the process of chemical synthesis.
    Safety & Operational Standards
    1- (4 - Iodophenyl) Ethanone is an important chemical product with key applications in many fields of chemical synthesis. However, safety and operating standards are of paramount importance during its preparation and use, and must not be ignored.
    When preparing this product, the raw materials and reagents used are often dangerous. For example, some reagents may be corrosive and will cause serious injury if they come into contact with the skin or eyes. Therefore, the experimenter must wear complete protective equipment, such as protective gloves, goggles and lab clothes, to prevent accidents.
    In terms of operating procedures, established norms must be strictly followed. All kinds of reaction conditions, such as temperature, pressure, reaction time, etc., need to be precisely controlled. A slight deviation, or cause the reaction to go out of control, causing a safety accident. At the same time, it is also essential to check the reaction equipment to ensure that it is well sealed and there is no risk of leakage.
    After the product is made, it should also be stored with caution. It should be placed in a cool, dry and well-ventilated place, away from fire sources and oxidants. Due to its nature or instability, improper storage or danger.
    When using 1- (4 - Iodophenyl) Ethanone for follow-up experiments, the same care should be taken. Use the right amount to avoid waste and prevent unnecessary risks from excessive use. After the experiment is completed, the disposal of the remaining products and waste must follow the principles of environmental protection and safety, and should not be discarded at will.
    In conclusion, although 1- (4 - Iodophenyl) Ethanone is a useful chemical product, its safety and operating standards need to be kept in mind at all times to ensure the smooth progress of the experiment and the safety of personnel and the environment.
    Application Area
    1- (4 -iodophenyl) ethyl ketone, this compound has a wide range of application fields. In the field of medicinal chemistry, it can be used as a key intermediate to help synthesize a variety of specific drugs, with significant efficacy for specific diseases. In the field of materials science, with its unique chemical structure, it can participate in the preparation of materials with special properties, such as photoelectric materials, which can improve the photoelectric conversion efficiency of materials. In the field of organic synthesis, it is also a commonly used starting material. After various chemical reactions, it can construct complex organic molecular structures, expand the variety of organic compounds, and open up a broad path for chemical research and industrial production. Its application in various fields is like stars illuminating the way forward for chemical research and related industries, continuously promoting scientific and technological progress and development.
    Research & Development
    Today there is a substance named 1- (4 - Iodophenyl) Ethanone. As a chemical researcher, I have been dedicated to studying this substance for a long time. Its unique properties contain many mysteries, which urgently need to be explored by us.
    During the research process, I have carefully observed its structure, analyzed its characteristics, and strived to gain insight into its essence. This substance shows its uniqueness in the reaction mechanism and synthesis path. After repeated experiments, I have found ways to optimize the synthesis and improve its yield and purity.
    Looking to the future, this substance may make its mark in the fields of medicine, materials, etc. I will continue to study, tap its potential value, and promote its development and application, hoping to contribute to the progress of related fields.
    Toxicity Research
    If you want to study the toxicity of 1- (4-Iodophenyl) Ethanone, you must first investigate its physical properties and chemical properties. This compound contains iodine and carbonyl groups. Iodine is active, or it induces chemical reactions in the body, causing biomolecular allosterization and disturbing normal physiology. Carbonyl groups are also active and can bond with nucleophilic groups such as proteins and nucleic acids, which damages cellular functions.
    Observe all experiments, take animals as models, feed this substance, and observe its physiological characteristics and biochemical indicators. See that animals may have symptoms of atrophy and loss of appetite, and their organs may have pathological changes. Blood tests show that liver and kidney function indicators are abnormal, or due to toxins, the liver and kidney are involved, which impairs their metabolism and detoxification ability.
    Furthermore, cell experiments also show its toxicity. Acting on cells, it can cause cell proliferation inhibition and apoptosis. The reason for this may be that toxic substances interfere with cell signaling pathways and disrupt gene expression.
    In summary, 1- (4-Iodophenyl) Ethanone is toxic, and it is unfavorable to the physiology and cellular functions of biological organisms. It is necessary to study protection and detoxification methods to prevent its harm.
    Future Prospects
    I have tried to study the chemical substance, and now I look at this substance 1- (4 - Iodophenyl) Ethanone. Its development in the future is quite promising. This substance may be used in the field of medicine to develop its unique ability to help physicians make good medicines and solve the diseases of everyone. Or in the field of materials, add new qualities, create strange materials, and open up new paths for the industry of engineering. Although the road ahead is unclear, I am full of hope. I believe that with time and the study of everyone, it will be able to fully develop its potential, be used by the world, and become a brilliant career in the future.
    Where to Buy 1-(4-Iodophenyl)Ethanone in China?
    As a trusted 1-(4-Iodophenyl)Ethanone 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 1-(4-Iodophenyl)Ethanone 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 1- (4-iodophenyl) ethyl ketone?
    4-Hydroxymethylfurfural is an important organic compound with unique and rich chemical properties.
    First, it has the typical properties of aldehyde groups. The aldehyde groups are highly reactive and can be oxidized. In case of strong oxidizing agents, such as acidic potassium permanganate solution, the aldehyde groups are easily oxidized to carboxyl groups, and then 4-carboxymethylfurfurfural acid is formed. If treated with mild oxidizing agents, such as silver ammonia solution or new copper hydroxide suspension, 4-hydroxymethylfurfural can undergo silver mirror reaction or form brick-red cuprous oxide precipitation, which is often used for qualitative detection of aldehyde groups. At the same time, the aldehyde group can also participate in the reduction reaction. In the presence of catalysts (such as nickel, etc.) and hydrogen, the aldehyde group can be reduced to a hydroxyl group, so that 4-hydroxymethyl furfural can be converted into 4-hydroxymethyl tetrahydrofurfuryl alcohol.
    Second, the properties of hydroxyl groups are also significant. Hydroxyl groups can undergo substitution reactions, such as with hydrogen halides, which will be replaced by halogen atoms to form corresponding halogenates. When co-heated with carboxylic acids catalyzed by concentrated sulfuric acid, esterification reactions will occur to form ester compounds, which are often used in organic synthesis to prepare specific esters. In addition, hydroxyl groups can also participate in dehydration reactions. Under appropriate conditions, intramolecular dehydration forms unsaturated compounds, or intermolecular dehydration forms ether substances.
    Third, the furan ring of 4-hydroxymethylfurfural also has certain reactivity. Although the furan ring is relatively stable, its structure may change under specific conditions, such as strongly acidic or strongly basic environments. In some electrophilic substitution reactions, the hydrogen atoms on the furan ring can be replaced by other groups, but the reaction conditions need to be precisely controlled, because the furan ring is more sensitive to the reaction conditions.
    In short, 4-hydroxymethylfurfural is rich in chemical properties due to its aldehyde groups, hydroxyl groups and furan rings, and has important application value in many fields such as organic synthesis, materials science and medicinal chemistry.
    What are the common applications of 1- (4-iodophenyl) ethyl ketone in organic synthesis?
    1- (4-pyridyl) acetamide is widely used in organic synthesis.
    First, it can be used as a key intermediate for drug synthesis. In the construction of many drug molecules, due to its unique structure, this compound can undergo various reactions, such as nucleophilic substitution, condensation, etc., and combine with other functional groups to build a drug skeleton with specific pharmacological activities. For example, in the creation process of some antibacterial drugs, 1- (4-pyridyl) acetamide can introduce pyridyl groups, endowing the drug with better biological activity and targeting, so that the drug can act more accurately on the target of bacteria and improve the antibacterial effect.
    Second, it is also used in the field of materials science. It can participate in the synthesis of polymers, and the presence of pyridyl and acetamide groups can impart special electrical, optical or mechanical properties to polymers. For example, when preparing polymer materials with fluorescent properties, the introduction of 1- (4-pyridyl) acetamide as a monomer or modifier can make the material produce unique fluorescence emission, which is used in the fields of fluorescence sensing and display.
    Furthermore, it can play a role in organic catalysis. The pyridine nitrogen atom in its structure has lone pairs of electrons, which can act as a Lewis base and play a catalytic effect on some reactions. For example, in some esterification reactions or cyclization reactions, it can promote the reaction, improve the reaction rate and selectivity, and make the reaction efficiently convert towards the desired product.
    In addition, in the field of dye synthesis, 1- (4-pyridyl) acetamide can be used as a starting material. Through a series of chemical modifications, chromophore groups are introduced to synthesize dyes with specific colors and properties, meeting the needs of textile, printing and other industries for different colors and fastness dyes.
    What are the methods for preparing 1- (4-iodophenyl) ethyl ketone?
    To prepare 1 - (4 - gingerol) pentanediol, there are many methods.
    One of them can be extracted by natural product extraction method. Ginger is rich in ginger phenols, and ginger can be extracted with appropriate solvents, such as ethanol, acetone, etc. The extract is concentrated and separated, and the target component 1 - (4 - gingerol) pentanediol is separated by column chromatography, high performance liquid chromatography and other technologies. The advantage of this method is that the product is natural and has high activity; the disadvantage is that the extraction process is complicated, the yield is low, and it is limited by the source of raw materials.
    Second, chemical synthesis is a good strategy. Using suitable organic compounds as starting materials, the target molecular structure is constructed through a series of chemical reactions. For example, aromatic hydrocarbons with suitable functional groups and hydroxy-containing compounds can be selected, and gradually synthesized by substitution, addition, oxidation and reduction under the action of suitable catalysts. The advantage of this approach is that it can be produced on a large scale and is not limited by raw materials; however, the synthesis route is usually cumbersome, the reaction conditions are harsh, and many by-products may be generated, requiring fine reaction control and product purification.
    Third, biosynthesis is also worthy of attention. Synthesis using the catalytic action of microorganisms or enzymes. Some microorganisms can convert simple substrates into complex organic compounds under specific culture conditions. Or use enzymes with specific catalytic activities to catalyze the reaction under mild conditions. The advantages of biosynthesis are mild reaction conditions, environmentally friendly, and high selectivity; but the disadvantage is that the preparation cost of microbial culture or enzymes is high, and the process control is difficult.
    In summary, each production method has its own advantages and disadvantages. In actual production, it is necessary to comprehensively consider factors such as raw material cost, production scale, and product quality requirements to select the most suitable preparation method.
    What are the physical properties of 1- (4-iodophenyl) ethyl ketone?
    4-Hydroxymethylfurfural, its physical properties are as follows:
    4-Hydroxymethylfurfural is a light yellow to amber liquid or crystalline solid at room temperature. The melting point is about 31 ° C. If the ambient temperature is higher than this value, it will melt into a liquid state with good fluidity. The boiling point is 110 ° C (1.46kPa), indicating that under specific low pressure conditions, it will change from a liquid state to a gaseous state at this temperature.
    4-Hydroxymethylfurfural has certain solubility characteristics. It is soluble in water due to its molecular structure containing polar groups such as hydroxyl groups, which can form hydrogen bonds with water molecules, so that it has a certain solubility in water. At the same time, it is also soluble in some organic solvents, such as methanol, ethanol, acetone, etc. In organic solvents such as methanol and ethanol, 4-hydroxymethyl furfural can be well miscible with them by virtue of the principle of similar miscibility. It can also be dissolved in acetone, because acetone has a moderate polarity, which is compatible with the polarity of 4-hydroxymethyl furfural, which is conducive to the interaction between the two molecules and realizes dissolution.
    4-hydroxymethyl furfural has a lighter color in appearance when it is in a pure state. With the extension of storage time or affected by factors such as light and temperature, the color may gradually deepen to amber. In terms of smell, it has a weak special smell, not a pungent and unpleasant smell, and is relatively mild. Its density is similar to that of water, and when mixed with water in the liquid state, there will be a certain distribution state due to density differences. At room temperature and pressure, it is relatively stable, but under extreme conditions such as high temperature, strong acid, and strong alkali, its structure may change, which in turn leads to changes in physical properties.
    What is the market price of 1- (4-iodophenyl) ethyl ketone?
    In today's world, the price of four things in the city is fickle, and it is not easy to study the market price of (4-hydroxyproline). However, looking at the changing state of the market, the price of commercial goods is often tied to supply and demand. If there are many people who want this thing, but there are few people who supply it, the price will rise; conversely, if the supply exceeds the demand, the price will drop.
    I also heard that the movement of market prices is also related to the weather, geographical location, and personnel. The weather, the abundance of the year, and the cold and summer of the season can all affect the abundance and scarcity of the product, and then the price. The location, the distance of the place of origin, and the amount of resources are also variables of price. Personnel, the leniency of government orders, and the conspiracy of merchants are all related to the price.
    (4-hydroxyproline) is either used for the production of medicinal stones or for the addition of food. It has a wide range of uses, and its price is not constant. When visiting medicine shops and commercial ports, the price varies from time to time and place in the near future. In prosperous cities, there are many people who need it, and the price may be slightly higher; in remote places, there are fewer people who want it, and the price may be slightly lower.
    And looking at the trend of the market, the price of (4-hydroxyproline) has fluctuated from time to time. Or because of the opening of new sources, the supply increased slightly, and the price fell; not long after, because there were too many users, the demand exceeded the supply, and the price rose again. Therefore, to observe it, if you want to know its exact price, you should visit the cities in person, consult the people of Zhu Jia, and observe the changes in the situation, so that you can get an approximation. The market price is impermanent, changing rapidly, and it is difficult to have a fixed number. It can only be deduced from the situation and tested on the spot.