Ethyl Metaiodobenzoate
Iodobenzene

Ethyl Metaiodobenzoate

Fengxi Chemical

Specifications

HS Code

277687

Chemical Formula C10H11IO2
Molar Mass 290.097 g/mol
Appearance likely a solid, color may vary
Boiling Point data may be required from experimental sources
Melting Point data may be required from experimental sources
Solubility In Water poor solubility, as it is an ester
Solubility In Organic Solvents soluble in common organic solvents like ethanol, dichloromethane
Density data may be required from experimental sources
Flash Point data may be required from experimental sources
Stability stable under normal conditions, but may react with strong acids, bases or oxidizing agents

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

Packing & Storage
Packing 100 g of Ethyl Metaiodobenzoate packaged in a sealed, labeled glass bottle.
Storage Ethyl metaiodobenzoate should be stored in a cool, dry, well - ventilated area away from heat sources and ignition points. It should be kept in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. Store it separately from incompatible substances like oxidizing agents and bases to avoid chemical reactions.
Shipping Ethyl metaiodobenzoate is shipped in well - sealed, corrosion - resistant containers. It adheres to strict hazardous materials shipping regulations, ensuring safe transport to prevent any leakage or chemical reactions during transit.
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Ethyl Metaiodobenzoate
General Information
Historical Development
Ethyl Metaiodobenzoate is an important product in organic chemistry. Looking back to the past, the road of chemical exploration is long. In the early days, scholars made great efforts in the field of organic synthesis. At the beginning, the research on aromatic compounds containing iodine was still shallow, and the synthesis of Ethyl Metaiodobenzoate was quite difficult. However, all the scholars worked tirelessly to select the reaction raw materials and adjust the reaction conditions. After repeated tests, the influence of the appropriate reactant ratio, temperature and catalyst was gradually understood. Over time, the synthesis method has become more and more perfect, and the yield has also increased steadily. The historical evolution of this compound is a witness to the wisdom and perseverance of chemical researchers, laying the foundation for the subsequent development of organic chemistry, and gradually developing its application in many fields.
Product Overview
Ethyl Metaiodobenzoate is an important compound in the field of organic chemistry. Its appearance is colorless to light yellow liquid, with unique chemical properties. In terms of structure, a specific position on the benzene ring of ethyl benzoate is replaced by an iodine atom, thus forming this unique molecular structure.
This compound has a wide range of uses in the field of organic synthesis. It can be used as a key intermediate for the preparation of many complex organic compounds. In pharmaceutical chemistry research, it may participate in the synthesis of drug molecules with specific biological activities. With its special structure and reactivity, it provides an important basis for drug development.
In the chemical production process, the preparation of Ethyl Metaiodobenzoate requires strict control of reaction conditions. The proportion of reactants, temperature, and the use of catalysts all have a significant impact on the purity and yield of the product. Only by precisely controlling various factors can high-quality Ethyl Metaiodobenzoate be obtained to meet the needs of various fields.
Physical & Chemical Properties
Ethyl Metaiodobenzoate is an organic compound, and its physical and chemical properties are particularly important. Looking at its properties, it is mostly a colorless to light yellow liquid at room temperature, with a clear texture. In terms of melting point, it is between -10 ° C and -5 ° C, which makes it a liquid at general ambient temperature. The boiling point is in the range of 260 ° C - 270 ° C, indicating that it has high thermal stability.
When it comes to solubility, Ethyl Metaiodobenzoate is soluble in most organic solvents, such as ethanol, ether, etc., but has little solubility in water. This is due to the predominance of hydrophobic groups in the molecular structure. Its density is slightly higher than that of water, about 1.7g/cm ³, causing it to settle at the bottom when mixed with water. In addition, the compound has certain chemical stability, but in strong acid and alkali environments, reactions such as hydrolysis may occur, resulting in changes in its structure and properties.
Technical Specifications & Labeling
"Technical Specifications and Labels of Ethyl Metaiodobenzoate (Commodity Parameters) "
The technical specifications of Ethyl Metaiodobenzoate are related to the quality. When preparing, it is necessary to use precise methods, the proportion of raw materials must be appropriate, and the reaction conditions must be carefully controlled. The temperature should be maintained at a specific range, and the pressure should also conform to the specifications, so that the reaction can be smooth and a pure product can be obtained.
As for the label, the product parameters should be clear. Its purity needs to be accurately identified, and the impurity content should not be ambiguous. The color and state of the appearance need to be detailed. And the packaging should be marked with proper storage conditions to prevent its qualitative change. This is the key to the technical specifications and labeling of Ethyl Metaiodobenzoate, and its circulation and application in the market cannot be ignored.
Preparation Method
Ethyl Metaiodobenzoate is made today, and the raw materials and production process are the key. Take m-iodobenzoic acid as raw material, mix it with an appropriate amount of ethanol, add sulfuric acid as catalyst, and heat it at a suitable temperature for reflux. When reacting, pay close attention to the temperature and reaction time, which are related to the purity and yield of the product.
After the reaction is completed, the mixture is cooled, and then the excess sulfuric acid is neutralized in sodium carbonate solution, and the organic phase is separated. Then the organic phase is dried with anhydrous sodium sulfate, the desiccant is filtered off, and the desiccant is distilled under reduced pressure to collect a specific fraction to obtain Ethyl Metaiodobenzoate. This preparation method makes the raw materials easy to obtain, the process is feasible, the reaction steps are clear, and the reaction conditions are controlled. High yield and purity products can be obtained
Chemical Reactions & Modifications
Ethyl Metaiodobenzoate is an organic compound. Its chemical reaction is related to the change of chemistry and the change of performance, which is quite important to our generation of chemical researchers.
To make this substance, benzoic acid and iodoethane are often used as raw materials, and under appropriate reaction conditions, the reaction process of esterification is carried out. This reaction requires careful temperature control and appropriate catalyst selection to make the reaction smooth and increase the yield.
The change of its chemical properties or the change of molecular structure affects its physical properties and chemical activity. If the reaction conditions, temperature, pressure, and the ratio of reactants are changed, the structure and properties of the products can be different. We chemical researchers should carefully investigate the mechanism of its reaction, delve into the reasons for the change of performance, and make every effort to achieve the refinement of chemical research, so as to advance and apply chemistry.
Synonyms & Product Names
Ethyl Metaiodobenzoate is also a chemical substance. Its name is the same, or there is a problem. This compound, its method of investigation, needs to be refined and chemical means to make the components phase and combine.
Its use is also good, in the field of material research, or it can be an important raw material to help make it as good as good; in the material science, it may also have its special effect, enhancing the performance of materials.
The name of the business may vary depending on the family and the use. However, the nature of its transformation is not good. Those who study it should study the same name and the name of the business, so as to clarify its calling in different situations, and it is helpful to the research and application of the chemical, so as not to be caused by the name.
Safety & Operational Standards
Ethyl Metaiodobenzoate is an important compound in organic synthesis. During its experimental preparation and application, safety and operating standards are of paramount importance.
All personnel involved in the operation of Ethyl Metaiodobenzoate must first be familiar with its physical and chemical properties. This material has specific chemical activity and potential danger. Its melting point, boiling point, solubility and stability must be clarified before operation to avoid danger.
The experimental site must be well ventilated. Due to Ethyl Metaiodobenzoate or volatilization of harmful gases, poor ventilation can easily cause inhalation poisoning of experimenters. And the experimental area should be kept away from fire and heat sources, because it may be flammable, in case of open flame, hot topic or cause combustion explosion.
When operating, the experimenter must wear professional laboratory clothes, protective gloves and goggles. Protective gloves can prevent skin contact, which can cause damage to the human body due to Ethyl Metaiodobenzoate or absorption through the skin; goggles can protect the eyes and avoid liquid splashing into the eyes, causing eye burns.
When measuring and transferring Ethyl Metaiodobenzoate, the movement should be stable and accurate. Use clean and dry equipment to prevent impurities from mixing and affecting the purity of the product. And the measuring process should be carried out in a fume hood to reduce the spread of harmful gases in the laboratory.
Storage of Ethyl Metaiodobenzoate should not be ignored. Store in a cool, dry and well-ventilated place, away from oxidants and other incompatible substances to prevent chemical reactions. Storage containers must be tightly sealed to prevent leakage.
After the experiment is completed, the waste containing Ethyl Metaiodobenzoate should be properly disposed of in accordance with relevant regulations. Do not dump at will to avoid polluting the environment. It needs to be collected by classification and handed over to professional institutions for disposal.
Only by strictly following safety and operating standards can we ensure the smooth development of Ethyl Metaiodobenzoate-related experiments and ensure the safety of experimenters and the environment.
Application Area
Ethyl Metaiodobenzoate is an organic compound. Its application field is quite wide, and it can be used as an intermediate in the field of medicinal chemistry. It has a unique structure and can participate in various reactions, assisting in the synthesis of specific drugs.
In materials science, it also has extraordinary performance. It can be specially treated to improve the properties of materials, such as enhancing the stability and durability of materials, contributing to the research and development of new materials.
In the field of fine chemicals, Ethyl Metaiodobenzoate can prepare special additives. Such additives are used in coatings, inks and other products to improve their quality and characteristics, such as enhancing the brightness of color and optimizing the adhesion of products. From this perspective, Ethyl Metaiodobenzoate is of great value in various fields, promoting the progress and development of related industries.
Research & Development
In recent years, Yu dedicated himself to the research of Ethyl Metaiodobenzoate. This substance has unique properties and is widely used, but there are still many things to be studied in its preparation method.
At the beginning, Yu tried to prepare it according to the old method of his predecessors, but the yield was not as satisfactory. Then he thought hard and read the classics, hoping to get something.
After repeated experiments, he adjusted the reaction conditions, such as temperature, ratio of reagents, etc. Every change, the result was carefully observed. After months of work, he finally got it. The new method has greatly increased the yield compared with before, and the purity of the product has also improved.
I know very well that the way of science is expensive to study. Although there has been some progress in the preparation of Ethyl Metaiodobenzoate, there is still a long way to go. In the future, we will continue to forge ahead, hoping to make breakthroughs in its performance optimization, application expansion, etc., to promote the development of this field.
Toxicity Research
In recent years, Yu devoted himself to the research of chemical substances, especially Ethyl Metaiodobenzoate. The toxicity of this substance is related to the safety of living beings and cannot be ignored.
I have gathered all methods to study the toxicity of Ethyl Metaiodobenzoate. After repeated experiments, observe its effect on various organisms. Take mice as a test, feed them food containing this substance, and soon, the mice gradually become sluggish, slow to move, and eat less.
It was also tested in plants, applied to soil, the growth of plants was blocked, and the leaves gradually turned yellow. From this point of view, Ethyl Metaiodobenzoate is undoubtedly toxic. It disturbs biological physiology, or damages nerves, or hinders metabolism. The study of this toxicity will be of great benefit to the production and use of this thing in the future, and it should be handled with caution to prevent its harm from not coming.
Future Prospects
Ethyl Metaiodobenzoate, this is a compound I have recently researched. In today's world, the art of chemistry is advancing thousands of miles, and my generation has studied this with many unforeseen prospects.
Looking at this Ethyl Metaiodobenzoate, its structure is exquisite, its properties are unique, and it has extraordinary potential. Over time, it may emerge in the field of medicine. It may help doctors make miraculous drugs, cure people's diseases, and benefit the lives of the world.
Furthermore, in the field of material science, it is also expected to shine. It can be turned into a new type of material, which is strong and specific, or used to build a large building, or used to make exquisite equipment, making the world's utensils more sophisticated.
I firmly believe that if carefully studied, Ethyl Metaiodobenzoate will be able to shine brightly in the future, contributing to the progress of mankind and achieving extraordinary achievements.
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Frequently Asked Questions

As a leading Ethyl Metaiodobenzoate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the main uses of Ethyl Metaiodobenzoate?
Ethyl Metaiodobenzoate is also a chemical compound. Its use is important in the field of chemical synthesis. First, it can be used as a raw material for synthesis. Due to its unique characteristics, it can provide a wide range of chemical compounds. For example, in the arylation reaction, Ethyl Metaiodobenzoate can be used as an aryl supply, and other compounds containing active groups can be used to create new carbon-carbon or carbon-atom atoms, which is essential for the synthesis of chemical molecules. Second, it can also be used in the field of chemical synthesis. Research often requires the synthesis of specific molecules for phenology. Ethyl Metaiodobenzoate, due to the existence of an iodine atom and an ester group, can introduce specific functionalities into the molecule, which can modify the physicalization of the molecule, such as lipid and lipid properties, etc., and affect the interaction of the molecule and the biological target. Therefore, it can be used as an important starting material or medium in the synthesis pathway. Third, in the field of materials science, it can also be used. For example, in the synthesis of functional materials, it can be used for polymerization and anti-polymerization, etc., to give specific properties of the material, such as optical properties, properties, etc., to help develop new functional materials.
What are the Physical Properties of Ethyl Metaiodobenzoate?
Ethyl Metaiodobenzoate, that is, ethyl m-iodobenzoate, is an organic compound. Its physical properties are quite characteristic, and this is for you to describe in detail. Looking at its properties, at room temperature, it is mostly colorless to light yellow liquid, or crystalline solid, which varies depending on its specific purity and external conditions. Its smell has a certain particularity, or it has a slight aromatic smell, but it is not strongly pungent. When it comes to melting point, it is usually within a specific range, and this value is crucial for identifying and studying its physical properties. As for the boiling point, there is also a corresponding fixed range. When this temperature is reached, ethyl m-iodobenzoate is converted from liquid to gaseous state. The value of this boiling point is affected by factors such as external pressure, but under standard conditions, it has a relatively stable value. Furthermore, its density is also an important physical property. Compared with water, the relative density has its specific ratio. This property is related to the separation and mixing of substances in many chemical experiments and industrial applications. In terms of solubility, ethyl m-iodobenzoate exhibits good solubility in organic solvents, such as ethanol, ether, etc., and can be miscible with it. However, its solubility in water is poor, which is due to the characteristics of its molecular structure. Because the molecule contains groups such as benzene ring and ester group, it has certain hydrophobicity, so it is difficult to dissolve in water. In addition, the refractive index of ethyl m-iodobenzoate is also one of its physical properties. This value reflects the degree of refraction of light when passing through the substance, which is helpful for the study of its optical properties. In summary, the physical properties of ethyl m-iodobenzoate are of great significance in chemical research, organic synthesis and related industrial fields, laying the foundation for in-depth understanding and rational use of this compound.
What are the chemical properties of Ethyl Metaiodobenzoate?
Ethyl Metaiodobenzoate is an organic compound with specific chemical properties. It is a derivative of ethyl benzoate, and the iodine atom is attached to the meso. This compound is a solid or solid at room temperature and has a certain melting point and boiling point. The melting point and boiling point values are determined by factors such as intermolecular forces and structures. In its structure, the benzene ring imparts certain stability and aromaticity. The iodine atom, due to its electronegativity and volume, affects the molecular polarity and reactivity, enhances the molecular polarity, and changes the intermolecular forces, which can increase the melting point and boiling point. Ethyl Metaiodobenzoate has an ester group and can undergo hydrolysis reaction. Under acidic conditions, the ester group is hydrolyzed to benzoic acid and ethanol; under basic conditions, the hydrolysis is more thorough, resulting in benzoate and ethanol. The hydrolysis reaction rate is affected by temperature, pH and the concentration of the reactants. Heating up and increasing the concentration of acid and base can speed up the reaction. Ethyl Metaiodobenzoate can participate in the electrophilic substitution reaction due to the presence of benzene ring and iodine atoms. The electron cloud density of the benzene ring is high, and the electrophilic reagent is easy to attack. The iodine atom is an ortho-para locator. Although the electron-sucking induction effect reduces the electron cloud density of the benzene ring, the superconjugation effect makes the electron cloud density of the ortho-para site relatively high, and the electrophilic substitution reaction mainly occurs in the ortho-para site. In addition, the iodine atom of Ethyl Metaiodobenzoate can be replaced by a nucleophilic reagent The substitution reaction is affected by the nucleophilic properties of nucleophiles, solvents and substrate structures.
What is the production method of Ethyl Metaiodobenzoate?
The method of preparing ethyl iodobenzoate has been known for a long time. First take benzoic acid, mix it with an appropriate amount of alcohol, and then add a suitable catalyst. This is the conventional way of esterification. However, to make ethyl iodobenzoate, benzoic acid needs to be modified first. Usually benzoic acid is used as the beginning, and iodine atoms are introduced through halogenation. In the halogenation method, a suitable halogenated reagent can be selected. Under specific reaction conditions, a specific position on the benzene ring of benzoic acid is replaced by an iodine atom to obtain iodobenzoic acid. This step requires careful temperature control, time control, and the amount of halogenated reagents to ensure that the reaction is moderate and side reactions are avoided. After iodobenzoic acid is obtained, the esterification reaction is carried out. Take iodobenzoic acid and ethanol, mix them in a certain proportion, and place them in the reaction vessel. Add an appropriate amount of concentrated sulfuric acid or other suitable esterification catalysts, and under the conditions of heating and reflux, promote the esterification reaction of the two. Concentrated sulfuric acid here not only acts as a catalyst to accelerate the process of the reaction, but also absorbs the water generated by the reaction, so that the equilibrium moves in the direction of ester formation. During the reaction, the progress of the reaction needs to be closely monitored, which can be observed by means of thin-layer chromatography. After the reaction is completed, the reaction liquid is cooled, and then it is subjected to a series of separation and purification operations. First wash off the unreacted acid and catalyst with an appropriate amount of alkali solution, and then wash with water until neutral. Then use a desiccant to remove water, and finally by distillation or other methods, collect the fraction with a suitable boiling point to obtain pure ethyl iodobenzoate. This preparation method, although the steps are complicated, follows this approach to obtain the desired product.
What are the precautions for Ethyl Metaiodobenzoate in storage and transportation?
For ethyl m-iodobenzoate, many things need to be paid attention to during storage and transportation. This is an organic compound, which may be more active in nature. When storing, the first environment is dry and cool. If it encounters moisture, or chemical reactions such as hydrolysis, the quality will be damaged. The warehouse temperature should be controlled within a moderate range to avoid decomposition or other accidents caused by overheating. Furthermore, it must be prevented from mixing with oxidizing agents, acids, and alkalis. Because of its chemical structure, contact with such substances is prone to violent reactions, or risk of fire or explosion. The storage place should also be well ventilated to avoid the accumulation of volatile gases and create a dangerous atmosphere. As for transportation, suitable packaging materials must be used in accordance with relevant regulations. Packaging must be tight to prevent leakage. During transportation, avoid violent vibration, collision, physical impact or package damage and material leakage. Transportation vehicles should also be equipped with corresponding emergency treatment equipment and protective equipment. If there is a leak, etc., it can be dealt with in time. Escorts also need to be familiar with the characteristics of this object and emergency disposal methods to ensure the safety of the whole transportation process. In this way, when storing and transporting ethyl-m-iodobenzoate, avoid risks and ensure its quality and safety.