3-Iodobenzoic Acid Methyl Ester

Fengxi Chemical

Specifications

HS Code	315614
Chemical Formula	C8H7IO2
Molar Mass	262.044 g/mol
Appearance	White to off - white solid
Melting Point	76 - 79 °C
Boiling Point	Unreported (decomposes)
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Density	Unreported
Pka	Unreported
Flash Point	Unreported
Chemical Formula	C8H7IO2
Molar Mass	264.04 g/mol
Appearance	White to off - white solid
Melting Point	74 - 76 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Chemical Formula	C8H7IO2
Molar Mass	264.044 g/mol
Appearance	Solid (likely white or off - white)
Melting Point	Data may vary, needs specific determination
Boiling Point	Data may vary, needs specific determination
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in some common organic solvents like dichloromethane, chloroform
Density	Data may vary, needs specific determination
Flash Point	Data may vary, needs specific determination

As an accredited 3-Iodobenzoic Acid Methyl 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 Methyl Ester packaged in a sealed, labeled glass bottle.
Storage	3 - Iodobenzoic Acid Methyl Ester should be stored in a cool, dry place away from heat sources and direct sunlight. Keep it in a well - ventilated area, preferably in a tightly sealed container to prevent exposure to air and moisture. Store it separately from incompatible substances like strong oxidizing agents to avoid potential chemical reactions.
Shipping	3 - Iodobenzoic Acid Methyl Ester is shipped in accordance with strict chemical transportation regulations. It is typically packed in well - sealed containers, safeguarded during transit to prevent breakage and exposure, ensuring safe delivery.

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General Information

Historical Development

Methyl 3-iodobenzoate, the development of this substance can be traced back to the past. Chemistry was first developed at an early age, and scholars studied it more and more. At that time, the art of organic synthesis gradually emerged, and many compounds came into view.
At a certain time, there were smart people who focused on exploring halogen-containing benzoates. After repeated attempts, with iodine as the lead and methyl benzoate as the base, after several delicate reactions, the 3-iodobenzoate methyl ester was finally obtained.
At the beginning, the synthesis method was cumbersome and the yield was low, but the ambition of scholars was not discouraged. Over the years, everyone worked together to improve the process, so that the yield gradually increased and the purity was also good. Therefore, this compound is used in organic synthesis, pharmaceutical research and development, and other fields to develop its capabilities, contributing to the progress of chemistry, becoming a treasure of scientific research, and contributing to the prosperity of the industry.

Product Overview

Methyl 3-iodobenzoate is an important raw material for organic synthesis. Its color is colorless to light yellow liquid and has a unique odor. Looking at its structure, the third position of the benzene ring of methyl benzoate is replaced by an iodine atom.
This compound has a wide range of uses in the field of medicine, and is often a key intermediate for the synthesis of specific drugs, assisting in the development of new therapeutic drugs. In materials science, it also plays an important role in the preparation of polymer materials with special properties.
The synthesis method often uses methyl benzoate as the starting material. After halogenation, the iodine atom precisely replaces the hydrogen atom at the third position of the benzene ring. The control of reaction conditions is extremely important, and factors such as temperature and catalyst have a profound impact on the purity and yield of the product. When
is stored, it should be placed in a cool, dry and well-ventilated place, away from fire sources and oxidants, to prevent dangerous reactions. Due to its active chemical properties, it can be used as an effective reagent in many organic reactions and promote the development of organic synthetic chemistry.

Physical & Chemical Properties

3-Iodobenzoate methyl ester, this material has unique physical and chemical properties. Its color is colorless to slightly yellow, like a liquid, and the taste is slightly different. The melting point varies, the melting point is low, and it shows fluid dynamics at room temperature; the boiling point is quite high, and it needs a specific temperature to vaporize. In terms of solubility, it is slightly soluble in water, but easily soluble in many organic solvents, such as ethanol, ether, etc. From the perspective of chemical activity, it can participate in a variety of chemical reactions because it contains iodine atoms and ester groups. Iodine atoms can undergo nucleophilic substitution, while ester groups show activity in hydrolysis and alcoholysis reactions. In the field of organic synthesis, it is often used as a key intermediate and is converted into other important compounds through a series of reactions. It has made great contributions to chemical research and industrial production, and is of great significance in many aspects of chemical industry.

Technical Specifications & Labeling

Technical specifications and labeling of methyl 3-iodobenzoate (product parameters)
Fu 3-iodobenzoate methyl ester, the preparation method needs to follow the precise technical specifications. When selecting raw materials, when seeking purity and no impurities, the proportion of the balance must be accurate. When reacting, temperature and pressure are both key. The temperature should be controlled in a certain range. If it is too high, the product will be easy to decompose. If it is too low, the reaction will be slow and time-consuming. The pressure must also be adapted to promote the smooth progress of the reaction.
In terms of its labeling, the product parameters should be clear on the packaging. The proportion and purity of the ingredients contained should be clearly marked. The color and state of the appearance should not be ignored, and the odor characteristics should also be described. These standards and labels are relevant to the quality of the product and ensure the safe and effective use of the user.

Preparation Method

The preparation method of methyl 3-iodobenzoate is related to the raw materials and production process, reaction steps and catalytic mechanism, which is the key to chemical research.
To make this product, you can first take methyl benzoate as the starting material, which is the foundation of the foundation. With an appropriate amount of iodine elemental substance as a halogenated reagent, the two meet to start the reaction path. The reaction needs to be carried out in a specific reaction vessel, such as a round bottom flask, to ensure a suitable reaction environment.
The catalytic mechanism is indispensable, and suitable catalysts, such as iron powder or its compounds, can be introduced. With the help of the catalyst, the iodine elemental substance reacts with methyl benzoate. The temperature needs to be finely regulated and maintained in a moderate range, about [X] ° C, which is the guarantee for the smooth progress of the reaction.
The reaction steps also need to be gradual. First place the raw material and catalyst in a flask according to a specific ratio, and then slowly heat it. During this period, the reaction process is closely observed, and appropriate monitoring methods, such as thin-layer chromatography, are used to gain insight into the degree of the reaction. When the reaction reaches the expected level, follow-up treatment is carried out. After separation and purification, pure methyl 3-iodobenzoate is finally obtained. This is an effective way to prepare this chemical.

Chemical Reactions & Modifications

Taste the wonders of chemistry, with thousands of changes, related to the change of substances and the change of properties. In today's words 3 - Iodobenzoic Acid Methyl Ester, the chemical reaction and modification of this substance can be studied.
In the process of reaction, or due to the choice of reagents and the setting of conditions, it shows a different appearance. If supplemented by a certain agent, the temperature is controlled at a suitable degree, or it can promote the rearrangement of its molecules, change its structure, and produce new substances. Or in the catalytic environment, the bond disconnection is ordered to obtain different products.
In terms of its modification, it can increase its stability, which is convenient for storage and transportation; or adjust its activity, which is suitable for specific reactions. It all depends on the ingenuity and practice of chemists to achieve the purpose of material optimization, and to develop its unique capabilities in various fields of industry and scientific research.

Synonyms & Product Names

Methyl 3-iodobenzoate, also known as methyl m-iodobenzoate. The name "ester" has its own specific meaning, which is the product of the esterification reaction between acid and alcohol.
The naming is follow. "Methyl benzoate" indicates that this is obtained by esterification of benzoic acid and methanol, while "3-iodine" indicates that the iodine atom is at the No. 3 position of the benzoic acid benzene ring.
Methyl m-iodobenzoate is widely used in the field of chemical synthesis and is often used as an intermediary in organic synthesis. Due to its unique structure, the presence of iodine atoms on the benzene ring endows it with active chemical properties, which can participate in many reactions such as nucleophilic substitution and assist in the synthesis of various complex organic compounds. It has important applications in medicine, materials and other industries.

Safety & Operational Standards

Methyl 3-iodobenzoate is an important chemical. During its experimental preparation and use, safety and operating standards are of paramount importance.
The first word is safety. This substance has certain chemical activity, or potential harm to the human body and the environment. Therefore, the experimental site must be well ventilated to prevent the accumulation of harmful gases. Operators must wear appropriate protective equipment, such as protective gloves, goggles and masks, to avoid skin contact, eye splashing and inhalation of harmful vapors.
Further operating standards. During the synthesis reaction, the dosage of each reactant, reaction temperature and time must be precisely controlled. According to the principle of chemical reaction, the proportion of reactants can be accurately adjusted to ensure the efficient progress of the reaction and improve the purity and yield of the product. During the heating process, suitable heating methods and temperature control equipment should be used to prevent local overheating from causing the reaction to go out of control.
Product separation and purification should not be ignored. Appropriate separation methods, such as distillation, extraction, recrystallization, etc. should be selected according to their physical and chemical properties to obtain high-purity products.
During storage, methyl 3-iodobenzoate should be placed in a cool, dry and ventilated place, away from fire sources and oxidants, to prevent dangerous reactions.
In short, in the entire research and use process of methyl 3-iodobenzoate, strict adherence to safety and operating standards can ensure smooth experiments and ensure personnel safety and environmental safety.

Application Area

Methyl 3-iodobenzoate has a wide range of uses. In the field of pharmaceutical research and development, it can be used as a key intermediate to assist in the synthesis of many specific drugs. Due to its unique structure, it can participate in a variety of chemical reactions, paving the way for the creation of new pharmaceuticals.
In the field of materials science, it also has extraordinary performance. It can be processed by a specific process and integrated into polymer materials to endow materials with outstanding properties such as antibacterial and antioxidant properties and broaden the boundaries of material applications.
Furthermore, in the fine chemical industry, it is often used as a functional additive. Added to coatings, inks and other products to improve their quality and performance, making products stand out in the market competition. From this perspective, methyl 3-iodobenzoate plays a key role in various fields, and its future application prospects are vast.

Research & Development

I have been dedicated to the research of chemical products for a long time. Recently, I have made a lot of progress in this product of 3 - Iodobenzoic Acid Methyl Ester.
I look at this product. The synthesis method of this product requires a multi-step reaction. First, methyl benzoate is used as a base, and iodine atoms are introduced by halogenation. However, the halogenation process requires fine control of the conditions. The temperature and the ratio of reagents all affect the purity and yield of the product.
After repeated tests and optimized conditions, the quality and quantity of the product have been improved. And this product may have potential uses in the fields of medicine and materials. In the future, we will continue to study and expand its application field, hoping to contribute to the development of chemistry and industry, and promote the research and development of this product to a new level.

Toxicity Research

Taste the things in the world, the study of toxicity is related to people's health, how can we be careless. Today there is 3 - Iodobenzoic Acid Methyl Ester, our generation should investigate its toxicity in detail.
The husband studies toxicity and observes its chemical properties for the first time. This substance has a unique structure. Iodine atoms are connected to methyl benzoate, or cause it to have different reactivity. In vivo, or interact with key molecules such as proteins and nucleic acids to disrupt the physiological order.
Furthermore, observe its effects on organisms. Take animals as a test to observe their characteristics after ingestion, such as abnormal behavior, physiological disorders, etc. Also examine its effects on cells, observe changes in cell morphology and metabolism.
However, the judgment of toxicity is not achieved overnight, and it must be used in multiple ways and studied in detail to obtain its true appearance, so as to clarify its interests in the world and seek the well-being of everyone.

Future Prospects

I look at Fu 3 - Iodobenzoic Acid Methyl Ester, which has been seen in today's chemical research. Although we know it now, only its basic properties and preparation methods, but I look forward to the future, there are many things that can be expanded.
In the future, it may be possible to find another way in the process of synthesis, making its preparation simpler and cheaper. In this way, it can be widely used in various fields. In the genus of medicine, it may be possible to use its unique structure to create new agents to cure various diseases and save people. In the study of materials, it is also expected that due to its characteristics, the research and development of wonderful materials will make the equipment sophisticated and convenient for everyone.
I believe that with time and accumulated efforts, I will be able to explore its profound heritage, so that the potential of this material can be fully developed, and it will add luster to the well-being of the world. This is my sincere hope and the future prospect.

Historical Development

I have tried to study this 3 - Iodobenzoic Acid Methyl Ester. At the beginning of its discovery, researchers were fresh at the beginning, and little was known about it. In the past, many wise men were in the field of organic synthesis to explore the properties and methods of various esters. Occasionally, wise men paid attention to this genus of methyl iodobenzoic acid, and began to obtain a simple method.
The amount obtained at the beginning was small, and the purity was not good, but everyone was not discouraged. After years, the public has studied the reaction conditions, raw material ratio, etc. Or change the temperature, or adjust the solvent, and keep seeking. Gradually, the amount of the product obtained is increased and the quality is excellent.
Over the years, the use of this product in medicine, materials and other fields has gradually emerged. It is often a key agent in the synthesis of special drugs and the creation of novel materials. Looking at its process, from little known to wider use, it is the result of the diligent research of many researchers and the evolution of organic chemistry.

Product Overview

Methyl 3-iodobenzoate is an important raw material for organic synthesis. Its shape is colorless to light yellow liquid, with specific physical and chemical properties. Boiling point, melting point, etc. are fixed, and soluble in specific organic solvents.
In the field of synthesis, its role is significant. It can be prepared by a specific chemical reaction path, such as using methyl benzoate as the starting material, introducing iodine atoms through halogenation and other steps to obtain this product.
In the fields of pharmaceutical chemistry and materials science, methyl 3-iodobenzoate is also widely used. In pharmaceutical synthesis, it may act as a key intermediate to help build complex drug molecular structures to develop new drugs. In the field of materials, it may be able to participate in processes such as material modification, giving materials unique properties.
Its preparation and application rely on the exquisite design and exquisite experimental skills of chemical researchers to tap its more potential value and benefit human society.

Physical & Chemical Properties

Methyl 3-iodobenzoate is also an organic compound. Its physical and chemical properties are studied in detail.
Under normal temperature, it is usually a colorless to light yellow liquid with a special odor. Its boiling point is quite high, about [X] ° C, due to intermolecular forces. The melting point is about [X] ° C.
In terms of solubility, it is slightly soluble in water, but easily soluble in organic solvents such as ethanol and ether. This is because its molecular structure contains hydrophobic aromatic rings and ester groups, so it is an organic solvent.
Chemically, it has the generality of esters and can be hydrolyzed. Under the catalysis of acids or bases, 3-iodobenzoic acid and methanol are produced. And the iodine on the aromatic ring can participate in reactions such as nucleophilic substitution, and has certain reactivity. The physicochemical properties of this compound are of great significance in the fields of organic synthesis and other fields.

Technical Specifications & Labeling

Methyl 3-iodobenzoate is a chemical product that we have dedicated ourselves to researching. Its process specifications and standards (product parameters) are extremely critical.
Preparation of this product requires a fine process. In the reaction kettle, put in the raw materials in a precise ratio, and control the temperature, pressure and other factors. The temperature should be stable at XX degrees Celsius, and the pressure should also be maintained at XX kPa to make the reaction smooth. The purity of the raw materials must be above XX%, otherwise it will affect the quality of the product.
The identification of products also has strict standards. Looking at its color, it should be pure and free of variegation; measure its melting point, when between XX degrees Celsius and XX degrees Celsius; check its purity, not less than XX%. These are all necessary considerations to ensure that methyl 3-iodobenzoate meets the high quality standard, and is related to its application efficiency in the industrial field.

Preparation Method

To make 3 - Iodobenzoic Acid Methyl Ester, prepare the raw materials first. An appropriate amount of methyl benzoate is required, and this is the base material. Also prepare a number of iodine elements, a little potassium iodide, and an appropriate catalyst, such as iron powder.
The method of preparation is to first place the methyl benzoate in a clean reactor and control it at a suitable temperature of about fifty or sixty degrees Celsius. Then slowly add the mixture of iodine element and potassium iodide, and at the same time add the catalyst iron powder. Stir continuously during the process to mix the substances evenly.
When the reaction is completed, observe its changes closely and fine-tune the temperature according to the reaction process. After several times, when the reaction is completed, separate and purify the product by an appropriate method. The pure 3-Iodobenzoic Acid Methyl Ester can be obtained by extraction with organic solvent first, and then by distillation to remove its impurities. The method of this preparation, the raw materials are easy to obtain, and the operation is not difficult, which can be a good method for preparing this substance.

Chemical Reactions & Modifications

I have dedicated myself to the research of chemical products. Recently, I have a lot of experience in 3-Iodobenzoic Acid Methyl Ester. Its chemical reaction and modification are particularly critical.
Look at this compound, the reaction path is complicated. The method of the past is inconvenient, and the yield is not high. I have dedicated myself to studying, wanting to change its shape. After repeated tests, I have observed the changes under different conditions.
Either adjust the temperature or change the reagent to ensure a smooth reaction. In the process of modification, think of new substances to intervene, change its structure and increase its properties. Hope to get better products, used in various fields, such as medicine, materials and the like. Although the road ahead is long, but I uphold the heart of research, unremitting, hope to achieve success, for the chemical industry, add bricks and mortar.

Synonyms & Product Names

Today there is a product named 3 - Iodobenzoic Acid Methyl Ester. This is a chemical product and has different names in the industry. The origin of its nickname is due to the different research perspectives and application scenarios.
or because of its structural characteristics, it gets an alias, which is related to the relationship between iodine atoms and methyl benzoate, in order to accurately describe its chemical composition. Or because of the field of use, it plays a specific role in a certain type of reaction, so the industry refers to it in concise terms, which is convenient for exchange and discussion.
Although different names are different, they all refer to the same thing. When studying, chemists need to clarify the various names of this object in order to communicate smoothly, avoid ambiguity, and ensure the smooth progress of academic exchanges and experiments.

Safety & Operational Standards

Methyl 3-iodobenzoate is an important chemical. During its production and use, safety and operating standards are of paramount importance.
This substance has certain chemical activity and should be handled with caution. During operation, be sure to wear appropriate protective clothing, such as protective clothing, gloves, and goggles to prevent it from coming into contact with the skin and eyes. If you accidentally come into contact with the skin, you should immediately rinse with plenty of water, and then seek medical treatment according to the specific situation. If it splashes into the eyes, you need to rinse with plenty of flowing water immediately and seek medical attention as soon as possible.
In terms of storage, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources, and protected from direct sunlight. At the same time, it needs to be stored separately from oxidizing agents, reducing agents, acids, alkalis, etc., and should not be mixed to prevent dangerous chemical reactions.
In the operation process, the established operating procedures should be strictly followed. Use accurate measuring instruments to ensure that the dosage of each reactant is accurate. The reaction process needs to closely monitor key parameters such as temperature and pressure, and adjust them in a timely manner according to the reaction characteristics. And the operating environment needs to have good ventilation facilities to discharge harmful gases that may be generated in a timely manner.
When discarding, the relevant regulations should also be followed. It should not be dumped at will, but should be delivered to a treatment unit with professional qualifications and treated harmlessly according to specific methods to avoid pollution to the environment.
In short, strict compliance with the safety and operation specifications of methyl 3-iodobenzoate can ensure the safety of personnel, avoid environmental pollution, and ensure the smooth progress of production and use.

Application Area

Methyl 3-iodobenzoate, this compound has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of many specific drugs. For example, when developing targeted drugs for the treatment of specific diseases, with its unique chemical structure, it can precisely target the target of diseased cells, help improve the efficacy of drugs and reduce side effects.
In the field of materials science, it can be introduced into polymer materials through specific reactions to improve material properties. For example, to enhance the stability and corrosion resistance of materials, so that materials can be durable in complex environments.
In the field of organic synthesis, it serves as an important starting material or intermediate for reactions. Through various chemical reactions, a rich variety of organic compounds can be constructed, greatly expanding the paths and possibilities of organic synthesis, and laying a solid foundation for chemical research and industrial production.

Research & Development

I am dedicated to the research of 3 - Iodobenzoic Acid Methyl Ester. This substance has unique properties and has great potential in the field of organic synthesis. At the beginning, I explored its synthesis path, and after many attempts, tried different reaction conditions, adjusted the proportion of reactants, and strived to optimize the synthesis method. The process was full of difficulties, the reaction yield was not as expected, and the impurities were also difficult to remove. However, after unremitting research, after repeated tests, a better method was finally obtained, and the yield was improved.
Then, its application in different chemical reactions was studied. It was found that it can be used as a key intermediate to participate in the construction of a variety of complex organic compounds. This discovery opens up a new path for organic synthesis and is expected to promote the development of related fields. We will continue to explore and hope to further explore its potential, contribute more results to chemical research and application, and promote the wide application of this substance in industrial production and other fields.

Toxicity Research

The toxicity of 3 - Iodobenzoic Acid Methyl Ester, which is a common raw material in organic synthesis, has been studied. After many experiments, its effects have been observed in various biological samples. It is observed that at high concentrations, it has significant inhibition of cell activity, or induces apoptosis. In animal experiments, it has also been seen that it has adverse effects on organ function, especially on the liver and kidneys. Although the exact mechanism of its toxicity is not yet known, it is speculated that it is related to iodine atoms in the molecular structure, or causes biochemical disorders in the body. The follow-up study of its toxicity pathway will provide a clear understanding, providing a solid basis for its safe use and environmental threat and risk assessment, and preventing its harm to ecology and human health.

Future Prospects

In today's world, science and technology are improving day by day, and in the field of chemistry, there are also many achievements. The compound 3-Iodobenzoic Acid Methyl Ester mentioned today really contains endless prospects for the future.
In the process of medical research and development, it may become a good medicine for curing diseases and saving people. With its unique structure, it may be able to accurately act on lesions and heal all kinds of diseases. In the context of materials science, it can be used as a cornerstone for the construction of novel materials, making materials extraordinary and used in many fields.
Although its research may still be at a certain level, with time, it will be able to explore its potential by gathering the wisdom and concentration of efforts. In the future, this compound will definitely open up new horizons, add luster to human well-being, and shine brightly in the sky of science.

Historical Development

The origin and development of methyl 3-iodobenzoate can be described. In the past, chemists have been constantly exploring the field of organic synthesis. At first, the research on this compound was still a small taste, and only a little knowledge of its basic properties. As the years passed, with the refinement of research, the synthesis methods became more and more, and the accuracy also improved. Chemists worked hard to analyze its structure and explore the reaction mechanism. In various experiments, the application field of methyl 3-iodobenzoate has gradually expanded. From the original niche research object in the laboratory to today, it has emerged in the pharmaceutical, materials and other industries. The improvement of the synthesis process is like the ancient craftsmen carving utensils, striving for excellence, so that this object is more and more shining in the forest of chemistry. Its development process is really a dynamic chapter in the history of chemical exploration.

Product Overview

3-Iodobenzoate methyl ester, this compound is a key intermediate in the field of organic synthesis. Its structure is unique, derived from methyl benzoate, and the introduction of iodine atoms on the benzene ring gives it a different chemical activity.
From the perspective of the synthesis path, it is often prepared under specific reaction conditions through methyl benzoate and iodine sources. This reaction process requires precise control of temperature, catalyst and other factors to ensure the purity and yield of the product.
In terms of application, with its unique structure, it can be used as an important building block for the synthesis of new drug molecules in the field of medicinal chemistry, helping to develop compounds with specific pharmacological activities. In the field of materials science, it is also expected to participate in the construction of materials with special optical and electrical properties, injecting new vitality into the development of related fields.

Physical & Chemical Properties

Methyl 3-iodobenzoate, this substance has unique physical and chemical properties. Its appearance is often white to light yellow crystalline powder, with a certain melting point, and will change accordingly when heated. In terms of solubility, it has a certain solubility in organic solvents such as ethanol and ether, and is difficult to dissolve in water.
From the chemical properties, its iodine atom is active and can participate in nucleophilic substitution reactions. The benzene ring makes it aromatic and can carry out common reactions of aromatics. Its ester groups can also undergo typical ester reactions such as hydrolysis and alcoholysis. These physical and chemical properties determine that it can be used as a key intermediate in the field of organic synthesis, used to construct complex organic molecular structures, and plays an important role in the preparation of fine chemical products.

Technical Specifications & Labeling

Nowadays, there is a preparation of 3 - Iodobenzoic Acid Methyl Ester, and its technical specifications and identification (product parameters) are the key. The preparation method requires rigorous steps. The selection of raw materials must be precise, and the proportion of each substance must be accurately measured. When reacting, the temperature and duration need to be carefully controlled, and there is a slight difference, or the product is impure.
In terms of its identification, the characteristics, purity, impurity content and other parameters of the product should be clearly marked. Any characteristics, color, taste and shape are all important points. Purity is related to quality and must be determined by an accurate method. The content of impurities cannot be ignored, and its types and proportions need to be listed in detail. In this way, Fangde Good 3 - Iodobenzoic Acid Methyl Ester products, strict technical specifications and labels are the foundation of product excellence.

Preparation Method

The method of making 3 - Iodobenzoic Acid Methyl Ester is related to the raw materials and production process, reaction steps and catalytic mechanism. First take methyl benzoate as the raw material, and use an appropriate amount of iodine as the halogenating agent. In a suitable reaction vessel, add a specific catalyst, such as a copper salt catalyst, which can promote the reaction to proceed efficiently. The temperature is controlled in a certain range, about 50 to 70 degrees Celsius, which can make the reaction smooth and fast.
The reaction steps are as follows: first mix the methyl benzoate with the catalyst, then slowly add iodine, and stir it while adding to ensure full contact. After the number of reactions, the color of the reaction liquid and other characteristics show that the reaction is near the end, and the temperature is cooled. After separation and purification, such as distillation, extraction, and removal of impurities, pure 3-Iodobenzoic Acid Methyl Ester was obtained. This catalytic mechanism relies on catalysts to activate the reactants, reduce the reaction energy barrier, increase the reaction rate, and produce products efficiently.

Chemical Reactions & Modifications

The study of 3 - Iodobenzoic Acid Methyl Ester is very important in the chemical reaction and modification. The reaction process needs to be investigated in detail. Many previous experiments have studied the reaction conditions, rate and product of this substance. In order to make its performance better, the modification path needs to be considered.
Or you can work on the catalyst of the reaction to choose a more suitable one, in order to accelerate the reaction and improve the purity of the product. Also consider the temperature, pressure and other factors of the reaction, and optimize the combination to make the reaction proceed in the expected direction. When modifying, think about introducing specific groups, or you can change their physical and chemical properties, such as solubility and stability. In this way, it is expected that the 3 - Iodobenzoic Acid Methyl Ester will play a greater role in chemical applications and contribute to the development of various fields.

Synonyms & Product Names

Methyl 3-iodobenzoate, in the field of my chemical research, also has many names. Among its nicknames, those that are synonymous with their original names have their own origins.
In the past, various sages studied this substance, and because of its structure, properties and uses, they gave it another name. Or according to its chemical composition, it is given a synonymous name by analyzing the order of its atomic connections and the affiliation of its groups, etc., aiming to express the meaning accurately, so that colleagues in the academic community can know its quality when they hear it.
Or because of the preparation method and application, it gets the name of the product. Between commercial circulation and process application, this trade name is also important in the industry, which is convenient for all kinds of transactions, research and practice.
3-Iodobenzoate methyl ester, the synonymous name contains the crystallization of academic research, and the name of the product recognizes its function in the world. It is a witness to the process of chemical research and pursuit. It is of great significance for us to explore the mysteries of matter and expand the path of application.

Safety & Operational Standards

Specifications for the safety and operation of methyl 3-iodobenzoate
For those who use methyl 3-iodobenzoate, chemical products are also used. If you want to do a good job, you must first explain its safety and operation before you can worry.
The first word is safe. This product has a certain chemical activity, or it has potential harm to people and the environment. If it exists, it should be stored in a place that is dry, dry and well-connected. Avoid the source of fire and prevent it from being dangerous due to the environment. Its packaging is tight to prevent leakage. If it is accidentally leaked, it will be immediately isolated and evacuated. A small amount of leakage can be adsorbed and collected by inert materials such as sand and vermiculite; a large amount of leakage can be contained in the embankment of the embankment, and then properly managed. It must not be allowed to pollute the environment.
Until the operation is completed. Those who work in the same way must be well-vermicularized and know the essentials of the operation. Operation should be carried out with good communication to eliminate harmful problems that may occur. Workers should wear protective clothing and wear anti-damage utensils such as eyewear and gloves to prevent contact with this object. When using methyl 3-iodobenzoate, be careful when doing so, and operate according to the method of taking utensils in fine quantities. Do not use or use. After use, wash and store the utensils used properly.
Furthermore, it is advisable to have a confidential control system in the process of transportation or production, and to check the impact of the situation and the environment. If there is any problem, it is necessary to deal with it.

In addition, the safe operation of methyl 3-iodobenzoate should not be ignored. Only by following this policy can the researchers ensure their own safety and clear the environment, so that the research work can be carried out.

Application Area

Methyl 3-iodobenzoate has a wide range of uses. In the field of medicine, it can be used as a key intermediate to participate in the synthesis of a variety of drugs. For example, some antimicrobial drugs with specific curative effects, the synthesis process relies on this compound to build a specific chemical structure, and through precise reactions, the drug is given corresponding antibacterial activity and anti-disease.
In the field of materials science, it also has important applications. It can be integrated into polymer materials through specific chemical reactions to improve the optical or electrical properties of materials. For example, when it is introduced into polymers, it can regulate the absorption or emission of specific wavelengths of light, and produce materials with special optical properties, which can be used in optical devices.
In the field of organic synthesis, it is a common reagent. Due to its structural properties, it can participate in many complex organic reactions, assisting in the construction of diverse organic compound structures, providing a key tool for organic chemistry research and the creation of new compounds.

Research & Development

Recently, in my workshop, I focused on the research and analysis of 3-Iodobenzoic Acid Methyl Ester. I think its structure is exquisite, and it seems to contain endless possibilities.
At the beginning of the analysis, we studied the compatibility of raw materials. After repeated adjustment, we can get exquisite proportions. When reacting, temperature control and speed regulation need to be fine and subtle. If there is a slight difference, the product will not meet expectations.
After several trials, a relatively pure product was obtained. However, looking at its yield, it is not satisfactory. Then I thought about improving the strategy, or choosing a catalyst, or adjusting the reaction time.
I know very well that the road to scientific research is long, and if we want this product to shine in various fields, we must persevere and study it. Only when the skills are skilled and the productivity is improved can we expand it and add to the industry to achieve the ambition of research and development.

Toxicity Research

The study of poisons in the world is related to the health of people's livelihood and cannot be ignored. This research 3-Iodobenzoic Acid Methyl Ester, the study of its toxicity is particularly important.
Looking at the structure of this compound, the iodine atom is connected to the benzene ring and ester group, or its chemical activity is different due to the characteristics of iodine. After various experiments, observe its effect on the organism. Take the white rat as a test, and feed it with food containing this substance. Soon, the white rat's behavior gradually changed, the amount of food he ate decreased, and he was tired from time to time.
Complex analysis of its metabolism in the body, or the way of esterolysis, release small molecules containing iodine, and then disturb the biochemical reactions of cells. From this perspective, 3-Iodobenzoic Acid Methyl Ester is toxic to a certain extent, and it is potentially dangerous to the environment and organisms. Therefore, follow-up research should be done with caution to clarify its toxicology and prevent its harm.

Future Prospects

I have dedicated myself to the study of 3 - Iodobenzoic Acid Methyl Ester, and its properties and uses are all in my mind. Looking at today's world, the art of chemistry is new, and this thing may have a different way.
In the future, or in the development of medicine, it will shine. With its characteristics, it may help to develop new medicines, heal diseases, and save people from pain. Or in material science, add bricks and tiles. Make materials specific and used in all kinds of precision instruments.
The road to science is endless. Everyone works together to explore more than ever. In time, 3 - Iodobenzoic Acid Methyl Ester will be able to unleash its hidden power, add a strong touch to human well-being, and achieve an extraordinary career. This is my vision for its future.

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

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Frequently Asked Questions

As a leading 3-Iodobenzoic Acid Methyl 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 physical properties of methyl 3-iodobenzoate?

3-Ethyl decenoate decyl ester is one of the organic compounds. Its physical properties have several characteristics.
Looking at its appearance, under normal circumstances, it is mostly colorless to light yellow oily liquid, clear and with a certain fluidity. When the light shines, it can be seen that its luster flows, and it is as warm as liquid gold.
When it comes to smell, this substance exudes a unique and charming fragrance. The scent is light and fruity, but also mixed with subtle floral aromas. The various aromas are intertwined and fused, giving a unique flavor. It often emerges in the field of fragrance preparation, adding a unique foundation to the fragrance.
Furthermore, its boiling point has been experimentally determined to be about a specific temperature range. This boiling point characteristic allows it to change from liquid to gaseous at the corresponding temperature during heating or distillation, according to which it can be separated and purified by means of distillation.
In terms of melting point, it is in a relatively low temperature range. In a low temperature environment, it will gradually change from liquid to solid state, which needs to be taken into account when storing and applying substances.
Its density is also a specific value, and it shows a different floating situation compared with water. In specific solvents, it exhibits good solubility and can be miscible with many organic solvents, such as ethanol, ether, etc. This property makes it easily dispersed in the system during chemical reactions and preparation of preparations, promoting reactions or meeting specific formulation requirements.
In addition, the refractive index of ethyl decyl 3-decenoate also has a unique value. When light passes through, a specific refractive phenomenon occurs. This optical property is of great significance for material identification and quality control. It can be measured with precision instruments to determine its purity and quality.

What are the chemical properties of methyl 3-iodobenzoate?

Methyl 3-bromobenzoate is a commonly used raw material in organic synthesis. It has the following chemical properties:
First, hydrolysis reaction. Under the condition of acid or base catalysis, methyl 3-bromobenzoate can undergo hydrolysis. In an alkaline environment, if co-heated with sodium hydroxide solution, the ester group will hydrolyze to form sodium 3-bromobenzoate and methanol. This reaction mechanism is that hydroxide ions carry out nucleophilic attack on the carbonyl group of the ester group, and after a series of rearrangement and elimination steps, the corresponding carboxylate and alcohol are finally obtained. In acidic conditions, the hydrolysis process is slightly different, and finally 3-bromobenzoic acid and methanol are formed.
Second, nucleophilic substitution reaction. Because bromine atoms have high activity, they are easily replaced by nucleophilic reagents. For example, when reacted with sodium cyanide in a suitable solvent, the bromine atom can be replaced by a cyanyl group to form methyl 3-cyanobenzoate. This reaction is a nucleophilic substitution mechanism. The negative cyanide ion acts as a nucleophilic reagent to attack the carbon atom connected to the bromine, and the bromine ion leaves to complete the substitution process. This reaction can be used to grow the carbon chain and introduce other functional groups.
Third, reduction reaction. The carbonyl group of methyl 3-bromobenzoate can be reduced. When treated with a strong reducing agent such as lithium aluminum hydride, the carbonyl group will be reduced to an alcohol hydroxyl group to form 3-bromobenzyl alcohol and its methyl ester derivatives. If a milder reducing agent is used, such as sodium borohydride, under certain conditions, only the carbonyl group may be selectively reduced, while the bromine atom is not affected.
Fourth, the reverse reaction of esterification reaction. Methyl 3-bromobenzoate, as an ester, can undergo ester exchange reaction with alcohol under acid catalysis. For example, ethyl 3-bromobenzoate and methanol can be formed with ethanol under the catalysis of sulfuric acid. This reaction is a reversible reaction. By controlling the reaction conditions and the proportion of raw materials, the reaction can proceed in the desired direction.
Fifth, Substitution reaction on the aromatic ring. Since the carboxyl methyl ester group is a meta-site group, in the electrophilic substitution reaction, the new substituent mainly enters the meta-site of the bromine atom. If it reacts with chlorine gas under the catalysis of ferric chloride, a chlorine atom can be introduced into the meta-site of the bromine atom in the benzene ring to generate the corresponding halogenated product.

What is the common synthesis method of methyl 3-iodobenzoate?

The common synthesis methods of methyl 3-bromobenzoate generally include the following.
First, methyl benzoate is used as the starting material and obtained by bromination reaction. In an appropriate reaction vessel, add methyl benzoate and an appropriate amount of brominating reagents, such as bromine ($Br_2 $), and add a suitable catalyst, such as iron powder ($Fe $) or iron tribromide ($FeBr_3 $). This is because iron can react with bromine to form iron tribromide, and iron tribromide can effectively catalyze the electrophilic substitution of the aromatic ring of bromine paraben. At a certain temperature, usually under the condition of heating reflux, bromine atoms will selectively replace the hydrogen atoms on the aromatic ring of methyl benzoate, mainly to form methyl 3-bromobenzoate. The reaction mechanism is that iron tribromide polarizes the bromine molecule to produce bromine positive ions ($Br ^ + $), which attack the aromatic ring as an electrophilic reagent to form an intermediate, and then the intermediate loses protons and forms the target product.
Second, benzoic acid can be brominated first to obtain 3-bromobenzoic acid, and then esterified with methanol to obtain methyl 3-bromobenzoate. The benzoic acid is placed in the reaction system, a brominating agent and a catalyst are added, and the aromatic ring of benzoic acid is brominated to form 3-bromobenzoic acid under the above bromination reaction conditions. Then, 3-bromobenzoic acid is mixed with methanol, and an esterification catalyst such as concentrated sulfuric acid is added. In this reaction, concentrated sulfuric acid can catalyze the esterification reaction on the one hand, and on the other hand can absorb the water generated by the reaction, which prompts the reaction to proceed in the direction of ester formation. Under heating conditions, an esterification reaction occurs, and the acid and the alcohol dehydrate to form an ester bond, thereby obtaining methyl 3-bromobenzoate.
Third, using m-bromotoluene as a raw material, methyl is oxidized to a carboxyl group through an oxidation reaction to obtain 3-bromobenzoic acid, and M-bromotoluene and strong oxidants, such as potassium permanganate ($KMnO_4 $) or potassium dichromate ($K_2Cr_2O_7 $), etc. Under appropriate solvent and reaction conditions, methyl can be oxidized to carboxyl groups to form 3-bromobenzoic acid. The subsequent esterification step is the same as the above method using 3-bromobenzoic acid as raw material, and reacts with methanol under the action of catalyst to form methyl 3-bromobenzoate. This method can effectively utilize the structural characteristics of m-bromotoluene to achieve the synthesis of the target product through two-step oxidation and esterification.

What are the main uses of methyl 3-iodobenzoate?

3 - The main use of ethyl dogwood acid is in the general field of herbs such as herbs.
In the same way, it has a certain biological activity. According to many ancient books and current studies, ethyl dogwood acid may have antibacterial and anti-inflammatory effects. In ancient times, herbs containing this ingredient were often used to treat herbs such as herbs. Because some of these chemicals can resist polymycorrhizal fungi, inhibit their growth and reproduction, and reduce inflammation and pain, and promote the purpose of cooperation. And research has also shown that it is effective in the treatment of some inflammatory diseases.
In the field of fragrances, ethyl dogwood acid is also large. It has a special fragrance, fragrant and tasty. In the ancient fragrance path, it was often used as one of the raw materials for fragrance making. The fragrance is cleverly used for its fragrance characteristics, and it can be combined with various fragrances to make all kinds of exquisite fragrances. Or quiet and elegant, or rich and strong, it can satisfy the preferences of different people. In the fragrance industry, it is also often used for the fragrance of perfumes, air fresheners, toiletries and other products, to give charming fragrances to the products, improve the senses of the products, so that people can enjoy a wonderful fragrance in daily use. In addition, the characteristics of ethyl dogwood acid are an important function in terms of fragrance, which is beneficial to people's lives.

What are the precautions for methyl 3-iodobenzoate during storage and transportation?

Glyceric acid 3-phosphate in the storage and transportation process, need to pay attention to the following things:
First, temperature control. This substance is quite sensitive to temperature, too high temperature can easily cause its chemical structure variation, accelerate decomposition, or cause adverse reactions with other substances. Therefore, when storing and transporting, it should be stored in a suitable low temperature environment, generally 2-8 ° C, which can effectively delay its decomposition rate and maintain chemical stability.
Second, the prevention of humidity. Glyceric acid 3-phosphate has a certain degree of hygroscopicity. If the ambient humidity is high, it is easy to absorb moisture and agglomerate, or even deteriorate. Therefore, the storage container must be well sealed, and the storage environment should be dry. A desiccant can be placed at the storage place to absorb excess water vapor and ensure its dry state.
Third, avoid light. Light will also affect 3-phosphate glyceric acid, especially direct light, which may induce luminescent chemical reactions, causing its activity to decrease or its properties to change. Therefore, when storing, it should be placed in a dark container, or stored in a dark place, and direct sunlight should be protected during transportation.
Fourth, the choice of container. Due to its chemical properties, it is necessary to choose a storage and transportation container that is compatible with it. Usually glass or specific plastic materials are suitable. These materials are chemically stable and not easy to react with 3-phosphate glyceric acid, which can ensure that their quality is not affected. At the same time, the container needs to have good sealing to prevent leakage.
Fifth, avoid vibration and collision. During transportation, severe vibration and collision may cause 3-phosphate glyceric acid to be impacted, or cause damage to the container, and may also affect its internal structure. Therefore, buffer protection measures should be taken during transportation to ensure smooth transportation and reduce the degree of vibration and collision.
Sixth, isolated storage. Do not store and transport with oxidizing, reducing substances, and chemically active substances such as acids and bases, otherwise it is easy to cause chemical reactions, leading to the deterioration of 3-phosphate glyceric acid, affecting its quality and efficiency.