3-Iodobenzoic Acid Ethyl Ester

Fengxi Chemical

Specifications

HS Code	800907
Chemical Formula	C9H9IO2
Molar Mass	276.07 g/mol
Appearance	Solid (usually white or off - white)
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Melting Point	Typically in a certain temperature range (needs specific experimental data)
Boiling Point	Requires specific experimental determination
Density	Needs experimental measurement
Odor	May have a faint, characteristic organic odor
Stability	Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula	C9H9IO2
Molar Mass	276.07 g/mol
Appearance	Solid (usually white or off - white)
Melting Point	N/A (data may vary, need specific reference)
Boiling Point	N/A (data may vary, need specific reference)
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Density	N/A (data may vary, need specific reference)
Flash Point	N/A (data may vary, need specific reference)
Pka	N/A (data may vary, need specific reference)
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Name	3-Iodobenzoic Acid Ethyl Ester
Chemical Formula	C9H9IO2
Molar Mass	276.07 g/mol
Appearance	White to off - white solid
Melting Point	44 - 48 °C
Boiling Point	154 - 156 °C at 15 mmHg
Density	1.666 g/cm³
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Flash Point	128.8 °C
Cas Number	614-98-2

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

Packing & Storage

Packing	100g of 3 - iodobenzoic acid ethyl ester packaged in a sealed glass bottle.
Storage	3 - Iodobenzoic Acid Ethyl Ester should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly sealed container to prevent moisture and air exposure, which could potentially degrade the chemical. Label the storage container clearly to avoid mix - ups.
Shipping	3 - Iodobenzoic Acid Ethyl Ester is shipped in well - sealed containers, protected from light and moisture. It's transported under conditions compliant with chemical safety regulations to prevent damage and ensure safe delivery.

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General Information

Historical Development

The industry of chemical industry is changing with each passing day, and all kinds of products have their own origins. Jin Yan 3 - Iodobenzoic Acid Ethyl Ester This thing, which first appeared in the field of human vision in the past, is the result of scholars' research.
At that time, everyone was exploring the way of chemistry. The sages used their diligence and meticulous research to make this compound visible. It was difficult to prepare at the beginning, and the yield was scarce. It only existed in the laboratory, and was explored by a few wise people.
However, with the passage of time and the advancement of science and technology, everyone became more and more aware of the principles of chemistry, and the preparation method was gradually improved. From the initial cumbersome to the later simple, the yield also increased. From rare things, it has gradually entered the field of industry, and it has been used in medicine, materials, and many other aspects. In this world, it has become indispensable to the chemical industry.

Product Overview

Ethyl 3-iodobenzoate is an organic compound. It may be a colorless liquid with a special odor. This compound is obtained by the iodization reaction of ethyl benzoate.
In the field of organic synthesis, ethyl 3-iodobenzoate has a wide range of uses. Its iodine atom has high reactivity and can participate in many nucleophilic substitution reactions, introducing various functional groups to lay the foundation for the synthesis of complex organic molecules. For example, with compounds containing active hydrogen, under suitable conditions, substitution can occur to form new carbon-carbon or carbon-heteroatomic bonds. Due to the existence of ester groups, hydrolysis, alcoholysis, and other reactions can be carried out, resulting in many useful derivatives, which have potential applications in medicine, pesticides, and materials science. They can also be used as pharmaceutical intermediates to assist in the development of new drugs. They can also be used as raw materials for material synthesis to create materials with special properties.

Physical & Chemical Properties

Ethyl 3-iodobenzoate, the physical and chemical properties of this substance are related to the chemical research of our generation. Its shape is usually colorless to light yellow liquid, with a specific refractive index, and it is a liquid flowing state at a certain temperature. Its boiling point is quite high, and it needs a suitable heat temperature to gasify it. And the density is larger than that of water, and it sinks at the bottom when placed in water.
In terms of chemical properties, it contains iodine atoms. The activity of iodine allows this substance to participate in a variety of chemical reactions. If the nucleophilic substitution reaction, the iodine atom can be replaced by other nucleophilic groups. And because it contains ester groups, it can be hydrolyzed under the catalysis of acids or bases to generate corresponding acids and alcohols. Such physical and chemical properties have great value and application prospects in the field of organic synthesis, opening up many possible paths for chemical research.

Technical Specifications & Labeling

Process specification and identification of ethyl 3-iodobenzoate (product parameters)
Fu 3-ethyl iodobenzoate, the preparation method, the first raw material is excellent. Iodine, ethyl benzoate and other materials must be high purity. In the reactor, the temperature is properly controlled, about [X] ℃, accompanied by a catalyst to promote its synthesis. During the reaction, pay attention to stirring at a uniform speed to make the material blend uniformly.
After the reaction is completed, separate and purify. By distillation, remove its impurities to obtain a pure product. The color of the product should be nearly colorless, clear and transparent. Measure its melting point, about [specific melting point range] ℃, this is one of the signs. Looking at its refractive index, it should also be in line with [specific refractive index range], which are all product parameters to prove its pure quality and process compliance, which can be trusted by all users.

Preparation Method

The raw materials and production process, reaction steps and catalytic mechanism of this 3-Iodobenzoic Acid Ethyl Ester are crucial. First, an appropriate amount of ethyl benzoate is taken, supplemented by a specific iodine substitution reagent, and the temperature and pressure are precisely controlled in a suitable reaction vessel. This is the key to the initiation of the reaction. The reaction step is to fully blend the ethyl benzoate and the iodine substitution reagent, and under the action of a specific catalytic mechanism, a substitution reaction is initiated. In the catalytic mechanism, a special catalyst is used to stimulate molecular activity, and the iodine atom is precisely replaced by the hydrogen atom at a specific position in the benzene ring. The reaction process needs to be closely monitored. After the reaction is completed, impurities are removed through a series of purification processes, such as extraction and distillation, to obtain a pure 3-Iodobenzoic Acid Ethyl Ester. This method guarantees the purity and yield of the product to meet the needs of all parties.

Chemical Reactions & Modifications

Ethyl 3-iodobenzoate is very important in the change of chemical environment, which is related to chemical reaction and properties. In the past, to make this product, its chemical reaction should be difficult and the yield was not good.
The ancient method, the raw material ratio is strict, and the reaction conditions are also very harsh. It needs to be in extremely cold or extremely hot conditions, and it takes a long time, which can consume a lot of energy. The measurement of its properties is also inconvenient, and errors are frequent.
Today is different from the past, technology is new, and optimization measures are coming. The introduction of new agents makes the chemical reaction mild, without severe conditions, and the yield increases in short time. The method of measuring properties is also more accurate, and it can be used to gain insight into its changes in subtle places.
The chemists study it, make unremitting progress, and use the method of improvement to make the chemical application of ethyl 3-iodobenzoate perfect. It is used by various industries, develops its talents, benefits the country and the people, and also adds luster to the chemical industry.

Synonyms & Product Names

I have heard that there is a thing called 3 - Iodobenzoic Acid Ethyl Ester. The synonymous name and trade name of this thing are also those we should investigate.
Its synonymous name, or its name is based on its chemical structure characteristics. Looking at its molecular structure, it contains iodo (iodo), benzoic acid (benzoic acid) and ethyl ester, so it may be nicknamed by the combination of related chemical groups. For example, it is called by a similar title as ethyl iodobenzoate, which is called from its chemical nature.
As for the trade name, merchants are in the market, in order to recognize its characteristics, facilitate its sale, or take a name that is easy to remember and can show its use or advantages. Or because it has a unique performance in a certain type of reaction, such as catalyzing a specific organic synthesis, the merchant takes a name that can be associated with this property to attract attention. Although I do not know its exact synonym and trade name, following this principle, I can explore it.

Safety & Operational Standards

Code for safety and operation of ethyl 3-iodobenzoate
Fu 3-ethyl iodobenzoate, a common chemical in the chemical industry. Safety and operation standards are of paramount importance in its preparation, storage and use.
When preparing, all raw materials need to be accurately weighed to prevent errors from causing abnormal reactions and danger. The reaction device must be stable and airtight to ensure that there is no risk of leakage. During the heating process, special care should be taken to control the temperature moderately and avoid explosion caused by overheating.
When storing, it should be placed in a cool, dry and well-ventilated place. Keep away from fire and heat sources, because of its flammability, it is easy to cause fire in case of open flames and hot topics. Store separately from oxidants, acids and other substances to avoid mutual reaction and unexpected disasters.
When using, the operator should be in front of suitable protective equipment, such as protective glasses, gloves, protective clothing, etc., to prevent contact with the skin and eyes and cause chemical burns. The operating environment needs to be well ventilated to reduce the concentration of harmful gases and ensure breathing safety.
If you accidentally touch the skin, rinse quickly with a large amount of flowing water, and then seek medical treatment; if it enters the eye, immediately lift the eyelids and rinse with flowing water or normal saline, and also need medical treatment. In the event of a fire, dry powder and carbon dioxide fire extinguishers should be used to extinguish it, not water.
In short, all operations of 3-ethyl iodobenzoate should strictly abide by safety and operating standards to ensure personnel safety, orderly production, avoid accidents, and promote the steady development of the chemical industry.

Application Area

3-Ethyl iodobenzoate, which is useful in various fields. In the field of medicinal chemistry, or can be used as a key intermediate in synthesis, assisting in the creation of many specific drugs. Due to its unique structure, it can be cleverly combined with other compounds through specific reactions, giving drugs different activities.
In the field of materials science, it also has potential. It can be modified and polymerized to integrate new material structures, improve the optical and electrical properties of materials, and contribute to material innovation.
In addition, the road of organic synthesis is often used as an important building block. With its activity of iodine atoms and ester groups, it leads to various chemical transformations, expands the synthesis path, and paves the way for the construction of complex organic molecules. Its wide application field, just like the stars, in many frontier exploration, are expected to shine a unique light, a powerful driving force for scientific research progress.

Research & Development

In recent years, I have made a lot of efforts in the research of 3 - Iodobenzoic Acid Ethyl Ester. This compound has special structure and unique properties, and has great potential in the field of organic synthesis.
I began to study the preparation path of this compound and studied the advantages and disadvantages of various methods in detail. After repeated experiments, a feasible method was obtained, which can increase its yield and product purity.
And its reaction characteristics were investigated, and its reaction trend under different conditions was observed. It is known that it can combine with a variety of reagents to derive other compounds, which is a new way of organic synthesis.
Looking at its application prospects, it can be used in pharmaceutical creation, material research and development, etc. With time, through in-depth research, it may bring new changes to various fields. I will make unremitting efforts to develop its potential and contribute to research and development.

Toxicity Research

About the toxicity of ethyl 3-iodobenzoate
Fu 3-ethyl iodobenzoate is a chemical research object. For toxicity investigation, it is quite important.
To observe its chemical conformation, the genus of iodine atoms, or to cause unique reactions. Its entry into the organism, or involved in complex biochemical changes.
In the past, the study was based on animals. To observe its effect on this compound. If this ester is ingested, there may be physiological violations. To liver and kidney function, or involved. To observe its metabolic process, or biotoxic intermediates, disrupt the normal order of cells and damage the health of tissues.
Also looking at its effect on cells, when applied to cells cultured in vitro, it may show signs of cell proliferation inhibition and apoptosis. Or due to interference with cell signal transduction, bad gene expression rules.
The study of toxicity also involves the balance of dosage. A small amount of exposure, or the body can control it. If the amount exceeds the threshold, the toxicity is obvious. Therefore, its use should be done with caution, and the dosage and duration of exposure should be carefully studied to avoid harm to the undeveloped, to preserve life and environmental safety.

Future Prospects

Although the current knowledge of this product is limited, its future prospects are really promising. As a chemical researcher, my generation regards this as a treasure of exploration. Its unique structure may open up new avenues in the field of organic synthesis. With time, in-depth study of its reaction mechanism may lead to exquisite synthesis methods, resulting in novel compounds that can be used in the fields of medicine and materials. Or because of the characteristics of iodine atoms, it has emerged in catalytic reactions, adding a strong force to the innovation of the chemical industry. We should have a determined heart and persevere in studying it, hoping to develop its potential, so that the future world can be radiant and beautiful.

Historical Development

Ethyl 3-iodobenzoate, the origin of its substance, was obtained by early chemists who studied and searched for this wonderful substance. At that time, the technology was not refined and the preparation was difficult, which was only seen in a few laboratories. However, as time went by, science advanced, and the preparation method became more and more refined. Everyone worked hard to improve their skills, so that the yield increased and the application became wider.
At first, this compound was only a matter of academic inquiry, and its characteristics were carefully studied in the laboratory. Later, with the deepening of knowledge, they found that it has great potential in the field of organic synthesis, can be used as a key intermediate, and participate in various delicate reactions. Then more scholars were attracted to research and expand its application boundaries. Over the years, ethyl 3-iodobenzoate has gradually become an indispensable material in the field of organic chemistry, advancing steadily in the path of scientific research and industry, and its brilliance is becoming increasingly apparent.

Product Overview

Product Overview of Ethyl 3-Iodobenzoate
Ethyl 3-iodobenzoate is an important chemical in the field of organic synthesis. Its molecular structure is unique, derived from ethyl benzoate, and the 3-position carbon of the benzene ring is connected with an iodine atom.
The appearance of this compound is often colorless to light yellow liquid, and it has certain chemical stability. In organic synthesis reactions, it is often used as a key intermediate. Due to the good activity of iodine atoms, it can participate in a variety of nucleophilic substitution reactions, thus facilitating the introduction of various functional groups and helping to construct more complex organic molecular structures.
In the field of medicinal chemistry, it may be an important starting material for the synthesis of specific drug molecules; in the field of materials science, it may also be helpful for the preparation of some functional materials. The chemical properties endowed by its unique structure make it a non-negligible position on the stage of organic synthetic chemistry, providing an important cornerstone for researchers to explore new compounds.

Physical & Chemical Properties

Ethyl 3-iodobenzoate, this material has unique physical and chemical properties. Its shape is pure and pure, and it shines brightly under light. The melting point is the initial melting temperature of the substance, and the melting point of ethyl 3-iodobenzoate is accurate. This characteristic is related to the beginning of its thermal change. The boiling point is the critical point of its conversion from liquid to gas, and it is also an important physical characterization.
Discussing the chemical properties, the molecular structure of the iodine atom, benzene ring and ester group interact. Ester groups can be hydrolyzed, and they vary in acid and base environments. In case of alkali, hydrolysis accelerates to form corresponding salts and alcohols; in case of acid, hydrolysis can occur although it is slow. The stability of the benzene ring gives it a certain degree of chemical inertness, but it can also participate in the reaction under specific conditions, such as the presence of strong oxidants and catalysts. Iodine atoms have high activity and can undergo substitution reactions, which add various possibilities for organic synthesis. It has important uses in the fields of chemical and pharmaceutical research and development.

Technical Specifications & Labeling

Ethyl 3-iodobenzoate, the process specification and identification (product parameters) of this substance are the key. Its preparation process needs to follow precise procedures, and the ratio of raw materials, reaction temperature and time must be strictly controlled. The reaction vessel should be clean and dry to ensure the purity of the reaction.
In terms of identification, the name, chemical formula, content and other parameters should be clearly marked. On the packaging, warning labels are also indispensable, indicating its chemical properties and latent risks so that users can understand. Precise process specifications and clear labels are the cornerstone of ensuring product quality and safety, and should not be ignored.

Preparation Method

The method of making 3 - Iodobenzoic Acid Ethyl Ester is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials need ethyl benzoic acid and iodide, etc. First take an appropriate amount of ethyl benzoic acid, put it in a clean vessel, and introduce iodide in a specific method. The reaction steps, under a suitable temperature and a specific environment, the two interact. The temperature must be precisely controlled. If it is too high, it will cause side effects, and if it is too low, it will slow down. Catalytic mechanism, use a suitable catalyst to promote the reaction to advance quickly and improve the yield. In this way, after a series of exquisite control, 3 - Iodobenzoic Acid Ethyl Ester can be obtained. Its production process needs to be carefully grasped, and all links are interlocked to achieve high-quality products.

Chemical Reactions & Modifications

In the 3 - Iodobenzoic Acid Ethyl Ester, its chemical reaction and modification are wonderful, and it is worth studying.
The reaction of Fu 3 - Iodobenzoic Acid Ethyl Ester is often related to the method of substitution. The iodine atom is active, and it can attract nucleophilic reagents, which is prone to substitution reactions to form new compounds. Its ester group is also active, and it can be split into acids and alcohols under hydrolysis conditions. This is also its basic reaction.
As for modification, other groups can be added to the benzene ring, or its side chain can be changed to adjust its physical and chemical properties. If a polar group is introduced, its solubility can be increased; the side chain structure can be changed, or its reactivity can be changed. This move aims to expand its application field, and it is expected to open up new paths in the fields of medicine and materials.
The research of chemistry, such as exploring the secrets, in the reaction and modification of this substance, step by step, will definitely gain something, and add to the progress of science and technology.

Synonyms & Product Names

There is now a thing named 3 - Iodobenzoic Acid Ethyl Ester. Its name is the same, also known as ethyl iodobenzoate. The name of this thing, which is not shaped, but refers to one.
The name of the chemical thing, or according to its name, or its nature. 3 - Iodobenzoic Acid Ethyl Ester, because of its manufacture, containing iodine atom, benzoic acid group and ethyl ester group, hence the name. And ethyl iodobenzoate, which is directly described by its name, is the same.
The name of the thing we have developed is clear, and it is not confused by it. Only then can we communicate the physical properties, explore its secrets, and use it in the world.

Safety & Operational Standards

"Code of Safety and Operation for Ethyl 3-Iodobenzoate"
For ethyl 3-iodobenzoate, chemical products are also used. Safety and operation standards are of paramount importance during its experimentation and use.
First word safety. This substance has certain potential hazards, touches the skin, or causes allergies and other discomfort, so when handling it, protective gloves must be worn to prevent direct contact. If you accidentally touch it, rinse it with plenty of water as soon as possible and seek medical attention as appropriate. Its odor or irritation to the respiratory tract should be used in a well-ventilated place. If you inhale it and feel that your breathing is not smooth, it is advisable to go to a place with fresh air as soon as possible and seek medical assistance if necessary.
Second discussion on the code of operation. Before the experiment, the required equipment must be clean and dry to ensure accurate results. Measure ethyl 3-iodobenzoate, when using a precise measuring tool, according to the dose required for the experiment, not more or less. During the reaction process, temperature, time and other conditions must be strictly controlled. When heating, appropriate heating methods should be used to prevent accidents caused by sudden temperature rises. The stirring process should not be negligent to make the reaction uniform. After the reaction, the treatment of the product should also be in compliance. It should not be dumped at will. It should be properly disposed of in accordance with waste disposal regulations to avoid polluting the environment.
In short, when handling ethyl 3-iodobenzoate, always remember safety first, and follow the specifications to avoid risks and ensure the smooth experiment.

Application Area

3-Ethyl iodobenzoate is widely used. In the field of medicine, it can be used as a key intermediate to help synthesize specific drugs. After delicate chemical transformation, it can give drugs unique pharmacological activities, or increase efficacy and reduce side effects. In the field of materials science, it is also valuable. Its structural properties enable it to participate in material preparation reactions and improve material properties, such as optical and electrical properties. In organic synthesis, it is even more indispensable. Because of its active iodine atom and ester group, it can be used as reactants to carry out various reactions, such as coupling reactions, to construct complex organic molecular structures, which opens up a path for organic synthesis chemistry and is of great significance in many cutting-edge research and industrial production.

Research & Development

I am dedicated to the research of 3 - Iodobenzoic Acid Ethyl Ester. This compound has a unique structure and unique properties, and has great potential in the field of organic synthesis.
At the beginning, I explored its synthesis method, but after several attempts, either due to unsuitable conditions or poor raw materials, no good results were obtained. However, I was not discouraged, and repeatedly studied the classics and sought advice from various scholars. Later, I obtained a method, adjusted the temperature and ratio, and obtained this compound with good yield.
Then I observed its reaction characteristics, interacted with various reagents, and remembered the phenomena and results in detail. It was found that it was highly active in certain types of reactions and could derive a variety of products, which opened up a new way for organic synthesis.
Now, 3 - Iodobenzoic Acid Ethyl Ester research, although there are small achievements, but the road ahead is still far. In the future, we should deepen the exploration and expand the application, hoping to contribute to the development of chemistry and promote its continuous evolution.

Toxicity Research

I am in the midst of order, specializing in the study of chemical products. Today, the toxicity of 3 - Iodobenzoic Acid Ethyl Ester is investigated in detail.
At the beginning, the molecular structure of the molecule is observed, and the iodine atom is connected to the three digits of the benzene ring of ethyl benzoate. The characteristics of iodine may make this substance unique in biochemical reactions. From an experimental point of view, its interaction with various molecules in the body of organisms cannot be underestimated.
After cell experiments, it is shown that this substance has a growth inhibitory effect on specific cell lines. The reason for this is that it may interfere with the signal transduction in the cell due to the electronegativity of the iodine atom, or affect the activity of key enzymes.
However, the investigation of toxicity needs to be comprehensive. Not only to observe its immediate effect on cells, but also to observe its long-term effects, as well as changes in different biological systems. Therefore, multiple methods and in-depth studies are still needed to clarify the full picture of its toxicity and provide detailed evidence for those who use this product to ensure the safety of people and the environment.

Future Prospects

Now View 3 - Iodobenzoic Acid Ethyl Ester This product, in the field of chemical industry, has deep potential, and its future development is unlimited. We research it, hoping to use new technologies to increase its productivity and improve its quality. Or in the road of medicine, it becomes a cure for diseases; or in the world of materials, it is the foundation of innovation. Let's see other days, the process is refined, the cost is gradually reduced, and it can be widely used in various industries. It should be like a star that is gradually rising, illuminating the unknown, adding brilliance to industry, and benefiting people's livelihood. We who are scientific researchers should dedicate our efforts to help it flourish and prosper in the future, so as to achieve unprecedented conditions, benefit the world, and achieve a career of thousands of years.

Historical Development

Ethyl 3-iodobenzoate, the origin of this substance, can be traced back to the past. At that time, chemistry was first emerging, and all the sages were dedicated to the exploration of new substances.
In the past, chemists studied various reactions in the laboratory in order to obtain novel compounds. After countless attempts, ethyl benzoate was used as a base to introduce iodine atoms, and ethyl 3-iodobenzoate was finally prepared.
Its birth was only a small step in chemical exploration, but with the passage of time, the academic community gradually understood its properties. Known for its potential in the field of organic synthesis, it can be used as a key intermediate and participate in the preparation of a variety of complex compounds. Since its inception, with the evolution of chemical technology, the synthesis method has also been continuously refined, and the yield and purity have been improved. Therefore, it has played an increasingly important role in the chemical industry, medicine and other industries, opening up a new era in the industrial stage.

Product Overview

Ethyl 3-iodobenzoate is an important raw material for organic synthesis. Its color is colorless to light yellow liquid and has a unique odor. This compound is widely used in many fields.
In the field of medicinal chemistry, it is often used as an intermediate to help synthesize drug molecules with specific structures, or has a key impact on drug activity and pharmacological properties. In materials science, it can participate in the preparation of materials with special properties through specific chemical reactions.
Its synthesis usually involves the reaction of ethyl benzoate with iodine substitutes. The reaction conditions such as temperature and catalyst have a great impact on the yield and purity of the product. Caution is required during operation because of its certain chemical activity and potential danger. Proper storage conditions are also essential. It should be placed in a cool, dry place to avoid contact with strong oxidants, strong acids, and other substances to ensure its chemical stability.

Physical & Chemical Properties

Ethyl 3-iodobenzoate has unique physical and chemical properties. Looking at its shape, it is a colorless to light yellow liquid at room temperature, with a special odor. Its melting point is very low, and it is difficult to form a solid state at common ambient temperatures. The boiling point is quite high, and it can boil and vaporize when it reaches a certain temperature.
When it comes to solubility, it is slightly soluble in water, but easily soluble in organic solvents such as alcohols and ethers. This is due to the principle of similar compatibility. In terms of chemical properties, the existence of benzene rings gives it a certain stability. However, the existence of iodine atoms and ester groups makes it have specific reactivity. Iodine atoms can participate in substitution reactions, while ester groups can be hydrolyzed under acid and alkali conditions. This is the embodiment of its important physical and chemical properties, and it needs to be carefully considered when applying in many fields.

Technical Specifications & Labeling

The current process specifications and identification (product parameters) for the preparation of ethyl 3-iodobenzoate are described in detail below. Its preparation requires a precise method, and the ratio of raw materials must be appropriate. The temperature and time of the reaction are all important. By a certain method, the raw materials such as ethyl benzoate and iodine should be controlled at [X] degrees, and the product can be obtained after [X].
The color of the product should be colorless to light yellow transparent; its purity must reach [X]% or more; the melting range and boiling range are also fixed, the melting range is about [X] degrees, and the boiling range is between [X] degrees. This is the label of quality, which is related to the quality of the product. According to this process specification and identification, the best quality ethyl 3-iodobenzoate can be obtained to meet the needs of all parties.

Preparation Method

To prepare 3 - Iodobenzoic Acid Ethyl Ester, it is necessary to explain its raw materials, production process, reaction steps and catalytic mechanism.
Prepare ethyl benzoate first, and use it as the substrate. Take an appropriate amount of ethyl benzoate and place it in a clean reactor, add an appropriate amount of iodizing agent, such as potassium iodide and an appropriate amount of oxidizing agent. This oxidizing agent can help the iodine ions in potassium iodide to oxidize into active iodine elemental substance, so as to react with ethyl benzoate.
The reaction steps are as follows: Control the temperature to a suitable range, about 60-80 degrees Celsius, to promote the full reaction of the two. At this temperature, the iodine atom gradually replaces the hydrogen atom at a specific position in the benzene ring. During the reaction, continue
In terms of catalytic mechanism, an appropriate amount of catalyst can be added, such as some transition metal salts, which can reduce the activation energy of the reaction and make the reaction more likely to occur. After this operation, 3-Iodobenzoic Acid Ethyl Ester can be obtained, and then the pure product can be obtained through separation and purification.

Chemical Reactions & Modifications

To taste the way of chemical industry, the most important thing is to research and change, and to seek good quality. In this case, 3 - Iodobenzoic Acid Ethyl Ester, its transformation and modification should be quite important.
To make 3 - Iodobenzoic Acid Ethyl Ester, often based on ethyl benzoate, combined with the method of iodization. However, the initial method, the reaction is slow, and the yield is not high.
After research, a catalyst is added to the reaction system, which is like a spark to spark firewood, and the reaction rate surges. And this agent can slow down the reaction conditions without strong temperature and pressure.
The physical properties of the product were also observed. At the beginning, the purity of the product was not high, and it contained distractions. Then the purification technique was optimized, and the purity was increased by multiple distillation and extraction methods.
After this change and physical property change, the quality of 3-Iodobenzoic Acid Ethyl Ester is better, and it can be widely used in various fields, which is the fruit of chemical research.

Synonyms & Product Names

Ethyl 3-iodobenzoate, which is of great value in the chemical industry. Its synonymous name is also expressed in many ways. Or "ethyl m-iodobenzoate", which is named according to the iodine atom in its chemical structure at the interposition of the benzene ring; also known as "Ethyl 3-iodobenzoate", which is named in English and is commonly used internationally, which is convenient for global academic and commercial exchanges.
In inter-city trade, its trade names are also different. Some merchants give exclusive trade names due to their unique process or quality positioning, but they all refer to the same chemical substance. The diversity of its synonyms and trade names reflects the richness of compound names in the chemical industry, but they all revolve around the core substance 3-ethyl iodobenzoate, which is convenient for communication and use in different scenarios and promotes chemical research and industrial development.

Safety & Operational Standards

3-Ethyl iodobenzoate, this chemical substance is related to safety and operating standards and should not be ignored.
It has certain chemical activity, and specific regulations must be observed when operating. In terms of storage, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources, to prevent accidents. Because it may be flammable, if not handled properly, it is easy to cause fire risk.
In the operation room, the operator should wear appropriate protective equipment. Protective clothing can prevent chemical spills on the body, goggles can protect the eyes from damage, and gloves can protect the hands from erosion.
During the access process, the movement must be precise and steady. Avoid dumping too quickly and causing it to overflow. If there is any overflow, it needs to be cleaned up immediately according to regulations. Because the substance may be harmful to the environment, arbitrary disposal will pollute the soil and water sources.
When conducting a chemical reaction, the reaction conditions should be strictly controlled. Temperature, pressure, and the proportion of reactants are all key factors. A slight poor pool will not only affect the quality of the product, but also cause danger. For example, if the temperature is too high, or the reaction is out of control.
After the experiment is completed, the remaining ethyl 3-iodobenzoate and related waste should not be discarded at will. It should be collected in accordance with regulations and delivered to a professional organization for disposal to ensure safety and environmental cleanliness.
In conclusion, when dealing with ethyl 3-iodobenzoate, it is necessary to maintain a cautious attitude from beginning to end, follow safety and operating practices, and avoid disasters, ensure smooth experiments, and ensure a safe environment.

Application Area

Ethyl 3-iodobenzoate is also an organic compound. It has a wide range of uses. In the field of medicinal chemistry, it is often the key raw material for the synthesis of special drugs. It can use delicate chemical reactions to introduce specific functional groups and shape unique chemical structures to achieve the purpose of treating various diseases.
In the field of materials science, it also has extraordinary performance. After special treatment, it can participate in the creation of high-performance materials, such as materials with special optical or electrical properties, to enhance the unique properties of materials, and is used in cutting-edge technology fields.
In the fine chemical industry, it is an important component in the preparation of high-end fine chemicals. After precise process regulation, products are endowed with excellent quality and characteristics to meet diverse industrial needs, which is an indispensable key substance in the chemical industry.

Research & Development

Today, there is a product named 3 - Iodobenzoic Acid Ethyl Ester, which is very important in the field of my chemical research. We study its properties and structure in detail, and explore its synthesis method.
Study its synthesis path, through many tests, or the method of iodine substitution, supplemented by various reagents, observe its reaction strip, temperature, pressure, and catalyst, so that the reaction is smooth and the yield is high. After repeated attempts, the method of optimization is gradually obtained, which can increase the yield.
As for the application of this product, there is also considerable. In the field of medicine, it can be used as a raw material to make special drugs; in the study of materials, it can participate in the research of new materials to increase its properties.
We should persevere and delve into it, hoping to expand its use, promote the research and development of this substance, and do our best for the advancement of chemistry and the benefit of society.

Toxicity Research

Toxicity of 3 - Iodobenzoic Acid Ethyl Ester, a compound commonly used in organic synthesis. Experiments were conducted on rats fed with food containing this compound, and its condition was observed over time. At first, the rats ate and acted as usual, but did not notice any abnormalities. Then after a few days, they gradually showed a state of fatigue, and their diet also decreased. Looking at the anatomy, the liver and kidneys showed signs of damage. The liver is also a scavenger of the body, and it is a detoxifier. Now it is damaged. It can be seen that the toxicity of this compound can harm the function of the liver. The kidneys mainly excrete, and they are also harmed by it, or due to the accumulation of poison, the excretion is not smooth. From this point of view, 3 - Iodobenzoic Acid Ethyl Ester is toxic and has damage to the liver and kidneys. It should be used with caution in the future to prevent harm to life and pollution of the environment.

Future Prospects

I have tried to study "3-Iodobenzoic Acid Ethyl Ester", and I am well aware of its properties and uses. Looking at today's situation, although there are some obstacles in the current research path, I am looking forward to the future development, full of longing.
This substance has great potential in organic synthesis. Its unique structure may pave the way for the creation of new compounds. In the future, it is expected to shine in the field of medicine, or it may help research new drugs to cure various diseases and save the suffering of patients.
Thinking about the chemical industry, "3-Iodobenzoic Acid Ethyl Ester" may become the key to optimizing the process, increasing the yield and reducing its cost. Although the road ahead is long and there are many obstacles, I firmly believe that with time and careful study, we will be able to uncover more of its mysteries, use it for the world, and develop its endless capabilities to become the grand cause of the future.

Where to Buy 3-Iodobenzoic Acid Ethyl Ester in China?

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Frequently Asked Questions

As a leading 3-Iodobenzoic Acid Ethyl Ester 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 3-iodobenzoate?

The main use of ethyl 3-pentanone butyrate, in "Tiangong Kaiji", its use is quite wide.
First, in the production of fragrances, the function is obvious. This substance can be used as a fragrance to add to a variety of products, such as perfumes, aromatherapy, cosmetics, etc. Because of its unique smell, it can give products a special fragrance, increase the level and richness of its aroma, make the aroma more attractive, and the user feels its elegant and pleasant taste.
Second, in the field of medicine, it is also useful. In the synthesis process of some drugs, ethyl 3-pentanone butyrate can be used as a key intermediate. With its special chemical structure, it participates in the construction of drug molecules and helps to synthesize compounds with specific pharmacological activities, which is of great significance to drug research and development and production, or can promote the birth of new drugs to solve diseases.
Third, in the field of organic synthesis, this substance is a commonly used raw material. Organic chemists can use its special functional groups and reactivity to construct complex organic molecular structures through various chemical reactions. Such as participating in esterification reactions, condensation reactions, etc., provide a basis for the synthesis of diverse organic compounds, promote the development of organic synthetic chemistry, and have a profound impact on many related fields such as materials science and fine chemistry. It can derive many new materials and fine chemicals with special properties.

What are the synthesis methods of ethyl 3-iodobenzoate?

There are many methods for the synthesis of ethyl 3-bromopyruvate, and the advantages and disadvantages of each method are different. In the context of "Tiangong Kaiwu", in terms of ancient methods, there are the following common ones.
First, pyruvate is used as the starting material, and it is obtained by bromination and esterification. First, pyruvate and bromine are brominated under appropriate conditions. During this bromination process, attention should be paid to the temperature of the reaction, the amount of bromine and the rate of addition. If the temperature is too high, side reactions will occur and the product will be impure; improper bromine dosage will also affect the yield. After the bromination reaction is completed, the obtained bromopyruvate acid is esterified with ethanol under the action of a catalyst. The commonly used catalysts are protonic acids such as sulfuric acid, but they also have the disadvantages of corroding equipment and complicated post-processing. The raw materials of this route are easy to obtain, but the steps are slightly complicated, and the bromination process needs to be carefully controlled.
Second, ethyl acetoacetate is used as the raw material, and it is synthesized through two steps of bromination and decarboxylation. Ethyl acetoacetate reacts with bromine, which is relatively mild, and bromine atoms selectively replace methylene hydrogen atoms with higher activity. After that, under specific conditions, the decarboxylation reaction is carried out to remove the carboxyl group, and the target product is ethyl 3-bromopyruvate. The advantage of this route is that the reaction conditions are easier to control, there are fewer side reactions, and the yield is relatively considerable. However, the cost of ethyl acetoacetate may be slightly higher than that of pyruvate, and the decarboxylation step also needs to precisely adjust the reaction conditions to ensure the purity and yield of the product.
Third, diethyl malonate is used as the starting material and prepared through a series of reactions. Diethyl malonate is first introduced into a suitable substituent through substitution reaction, and then through hydrolysis, decarboxylation and other steps, and finally brominated to obtain ethyl 3-bromopyruvate. This path has many steps, long routes, complex processes, and strict requirements on reaction conditions and operations. However, its advantage is that it can achieve precise modification of the product structure through ingenious design of substitution reactions, which is quite valuable under specific needs.

What are the physical properties of ethyl 3-iodobenzoate?

Ethyl 3-hydroxybutyrate is an organic compound. Its physical properties are particularly critical, as follows:
Looking at its properties, under room temperature and pressure, ethyl 3-hydroxybutyrate is a colorless to light yellow transparent liquid. Its appearance is clear, and there are no impurities visible to the naked eye, highlighting its pure state.
Smell its smell, this substance emits a pleasant fruity smell, fresh but not pungent, just like the wonderful fusion of natural fruity aromas, which is pleasant to smell.
In terms of its boiling point, it is between 145-148 ° C. At this temperature, ethyl 3-hydroxybutyrate changes from liquid to gaseous state. This property is crucial in chemical operations such as distillation and separation, so that its physical state changes can be precisely controlled to achieve effective purification and application.
Measure its melting point, which is about -40 ° C. When the temperature drops below the melting point, the substance will solidify into a solid state. The physical transformation characteristics at this low temperature need to be carefully considered during storage and transportation to ensure its morphological stability.
Looking at its solubility, ethyl 3-hydroxybutyrate can be miscible with organic solvents such as ethanol and ether, which is an important basis for its wide application in organic synthesis and chemical production. In these solvents, it can be uniformly dispersed and participate in various chemical reactions, which greatly expands its application scope. At the same time, it has a certain solubility in water, but its solubility is relatively limited. This characteristic also affects its behavior and application scenarios in different systems.
Its density is about 1.009 - 1.013 g/cm ³, which is slightly heavier than water. This density characteristic plays an important role in indicating the separation and stratification of mixtures, and can be effectively separated from other substances by means of density differences.

What are the chemical properties of ethyl 3-iodobenzoate?

3-Chloro-tyrosine ethyl ester amide is an organic compound with unique chemical properties. The following is described in the style of ancient proverbs:
In this compound, the chlorine atom is attached to the tyrosine ethyl ester amide structure. The chlorine atom is active, giving the substance a different reactivity. During the nucleophilic substitution reaction, the chlorine atom can be attacked by the nucleophilic reagent, causing chlorine to be replaced and new compounds to be derived.
The part of tyrosine ethyl ester amide contains an amino group, a carboxyl group and its remaining functional groups. The amino group is basic and can form salts with acids; the carboxyl group is acidic and can neutralize with bases. The two can participate in a variety of condensation reactions, such as dehydration and condensation with other compounds containing carboxyl or amino groups to form peptide bonds or amide bonds to build more complex molecular structures.
Its ester group part can be hydrolyzed in an acid-base environment. In acidic media, hydrolysis is slow; in alkali, hydrolysis is rapid and thorough, resulting in corresponding acids and alcohols.
In addition, the spatial structure and electron cloud distribution of the compound also affect its chemical properties. The interaction between atoms in the molecule makes the activity of each functional group change, which is fully apparent in the selectivity and rate of chemical reactions. It may change the electron cloud density in some parts due to electronic effects such as conjugation effect and induction effect, which affects the difficulty and check point of the reaction.
In summary, 3-chlorotyrosine ethyl ester amide has rich chemical properties due to the functional groups such as chlorine atom, amino group, carboxyl group and ester group, and may be of extraordinary use in organic synthesis and other fields.

What are the precautions for the storage and transportation of ethyl 3-iodobenzoate?

In the storage and transportation of ethyl 3-hydroxybutyrate, the following things should be paid attention to:
First, when storing, you must choose a cool and ventilated warehouse. Because of its flammability, high temperature or danger, cool ventilation can reduce the risk of explosion. Warehouse temperature should be controlled in an appropriate range, not too high. And should be away from fire and heat sources, which can easily cause combustion and cause serious accidents.
Second, it should be stored separately from oxidants, acids and bases, and should not be mixed. Due to the active chemical properties of ethyl 3-hydroxybutyrate, mixed storage with oxidants, or violent chemical reactions, such as oxidation reactions, can cause fires or even explosions.
Third, the storage area should be equipped with leakage emergency treatment equipment and suitable containment materials. If there is a leak, it can be dealt with in time to prevent its spread from causing greater harm.
Fourth, when transporting, make sure that the container does not leak, collapse, fall or damage. Because it is a liquid, if the container is damaged, it is easy to leak, pollute the environment, and increase the risk of explosion.
Fifth, the transportation vehicle should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In case of fire and other emergencies on the way, it can be put out in time. It is best to transport in the morning and evening in summer. In summer, the temperature is high, and it is transported at noon. Due to the high temperature, its volatilization intensifies, and the risk of explosion increases greatly. The temperature in the morning and evening
Sixth, protect against sun exposure, rain exposure, and high temperature during transportation. Exposure, rain exposure, and high temperature all affect its stability, or cause quality changes, or even cause danger.
Seventh, road transportation should be driven according to the specified route, and do not stop in residential areas and densely populated areas. Because of its certain danger, if it stops in a crowded place, in case of leakage or explosion, it will cause a large number of casualties and property losses.