Methyl 3-Iodophenylacetate

Fengxi Chemical

Specifications

HS Code	446067
Chemical Formula	C9H9IO2
Molar Mass	262.07 g/mol
Appearance	Solid (usually white to off - white)
Solubility In Water	Insoluble (organic compound, non - polar nature)
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Vapor Pressure	Low at room temperature
Stability	Stable under normal conditions, but may react with strong oxidizing or reducing agents
Chemical Formula	C9H9IO2
Molar Mass	262.07 g/mol
Appearance	Typically a colorless to light - yellow liquid
Boiling Point	Around 277 - 279 °C
Density	Approx. 1.65 g/cm³
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Stability	Stable under normal conditions, but sensitive to light and air over time
Chemical Formula	C9H9IO2
Molar Mass	262.07 g/mol
Appearance	Liquid (usually)
Boiling Point	Around 270 - 275 °C (approximate)
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Odor	Characteristic organic odor

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

Packing & Storage

Packing	Methyl 3 - iodophenylacetate, 500g in a sealed, chemical - resistant glass bottle.
Storage	Methyl 3 - iodophenylacetate should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container to prevent leakage and exposure to air and moisture, which could potentially lead to decomposition or degradation of this chemical.
Shipping	Methyl 3 - iodophenylacetate, a chemical, is shipped in well - sealed, corrosion - resistant containers. Compliance with hazardous material regulations is ensured, with proper labeling for safe handling during transportation.

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General Information

Historical Development

Methyl 3 - Iodophenylacetate is an organic compound. Its initial discovery originated from the unremitting research of various scholars on organic synthesis. In the past, chemical research was just beginning, and everyone focused on expanding the variety of organic compounds. At that time, Zhu Xian explored new synthesis methods with exquisite experimental designs.
After years of hard work, this Methyl 3 - Iodophenylacetate was obtained. Early synthesis, the steps were complicated and the yield was quite low. However, scholars were not discouraged and continued to improve their skills. With the passage of time, the chemical theory and experimental methods have become more and more perfect, the method of synthesizing this compound has become simpler and more efficient, and the yield has also been greatly improved. It has gradually shown important value in the field of organic synthesis, laying the foundation for many subsequent studies and promoting the process of chemical development.

Product Overview

"Description of Compounds"
Today there is a thing called Methyl 3 - Iodophenylacetate. This is an organic compound with a molecular structure, which is cleverly named by the elements of carbon, hydrogen, oxygen and iodine. Among them, the benzene ring is the base, which is the genus of methyl acetate, and the iodine atom is also attached to the benzene ring.
Looking at its properties, it may be a colorless liquid at room temperature, with a slightly special odor. Its physical properties are related to the boiling point and melting point, and are also closely related to solubility. In organic solvents, such as ethanol and ether, it may be soluble; in water, it is slightly soluble or insoluble.
Its chemical properties are active, and iodine atoms are active and mobile, which can cause nucleophilic substitution. The structure of methyl acetate can also participate in many chemical changes, or hydrolysis, or esterification, and various changes. This compound is very useful in the field of organic synthesis and can be used as an intermediate to make other fine chemicals. It is used in medicine, materials and other industries.

Physical & Chemical Properties

There is a substance today called Methyl 3 - Iodophenylacetate. It has unique physical and chemical properties. Looking at its color, it is often colorless to light yellow liquid, clear and free of impurities. Smell it, it has a specific fragrance, light but not strong.
On its boiling point, it is about a few degrees Celsius, and it can be boiled and vaporized under a certain pressure. Its melting point is also fixed, and it is in a certain temperature range.
In terms of solubility, it is soluble in some organic solvents, but insoluble in water. This is due to the characteristics of the molecular structure. And its chemical properties are relatively stable. Under specific conditions, it can participate in a variety of chemical reactions, showing its unique chemical activity, laying the foundation for many chemical research and applications.

Technical Specifications & Labeling

The process specification and identification (product parameters) of Methyl 3-Iodophenylacetate are the key. The process must specify the ratio of raw materials and reaction conditions. The raw materials are pure and the proportion is accurate to ensure the quality. At the time of reaction, the temperature, pressure and duration must be strictly controlled, and the difference is very small, which is thousands of miles away.
On the label, in addition to its name, it is necessary to list the ingredients, properties, purity and other parameters in detail. The characteristics are clear at a glance if the color, state and taste; the purity is geometric, which is related to the use and efficacy. And there needs to be a safety label to show the attention of storage and use to prevent problems before they occur. In this way, the process is precise and strict, and the identification is detailed, so the quality and application of Methyl 3-Iodophenylacetate can be relied on.

Preparation Method

The method of preparing methyl 3-iodobenzoate is related to the raw materials, production process, reaction steps and catalytic mechanism. The raw materials need to be carefully selected, and the high-quality 3-iodobenzoic acid and methanol are the main reaction bases. In the production process, 3-iodobenzoic acid and an appropriate amount of methanol are placed in a clean reactor, sulfuric acid is added as a catalyst, and the temperature is raised to a suitable temperature to maintain this state so that the two can fully react. In this reaction step, the carboxyl group of 3-iodobenzoic acid and the hydroxyl group of methanol are dehydrated and condensed under the catalysis of sulfuric acid. After the reaction is completed, the temperature is lowered, and the product is purified through neutralization, extraction, distillation and other processes. The catalytic mechanism is that sulfuric acid provides protons to activate the carboxyl group of 3-iodobenzoate, accelerate the reaction with methanol, and improve the reaction rate and yield, so that methyl 3-iodophenylacetate can be obtained.

Chemical Reactions & Modifications

Recently, the chemical reaction and modification of Methyl 3-Iodophenylacetate (Methyl 3-Iodophenylacetate) have been studied with much consideration.
In the past, the reaction path of this chemical followed the conventional method, but the results were not high. Its yield often fluctuates, and the purity of the product is not perfect.
I think it is better to change the reaction conditions. Or adjust the temperature and control the temperature to make the molecules collide in an orderly manner; or change the solvent and choose the appropriate one to help the reaction run smoothly. As for modification, new groups can be introduced to observe the change of its structure and performance. With this, we can optimize the reaction, improve the quality of the product, and add a new chapter to chemical research. We also hope to inspire future generations' thinking and achieve a long-term goal in chemistry.

Synonyms & Product Names

Methyl 3 - Iodophenylacetate is also a chemical substance. Its trade name is the same as the field of transformation, and it also represents the gist.
The same name of this substance can be used in ancient books. As far as it is concerned, it may be called in the name of its transformation and creation. And the name of the product depends on the business of production and the positioning of the market.
In the process of chemical research, knowing the same trade name is essential. It can help researchers to find out the important information in the text. It is not to explore the method of its synthesis, or to study its properties and uses. The same trade name can be used as a guide. It can make researchers involved in the material, without naming it, and miss the results of the investigation. It is based on the same trade name as Methyl 3 - Iodophenylacetate, and has been studied in order to promote the research process of chemistry.

Safety & Operational Standards

"Code of Safety and Operation of Methyl 3-Iodophenylacetate"
Methyl 3-iodophenylacetate is an important chemical. Safety and operation standards are of paramount importance in its experimental and production process.
Safety in the first place. This chemical has certain potential hazards and must be properly stored. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources to prevent fire or other safety accidents. Because it may cause harm to the human body, protective measures must be taken when contacting. Experimenters should wear suitable protective clothing, gloves and goggles to avoid direct contact between skin and eyes. In case of accidental contact, rinse with plenty of water immediately and seek medical attention according to the specific situation.
In terms of operating specifications, it is necessary to conduct a comprehensive inspection of relevant instruments and equipment before use to ensure that they are in normal operation. In experimental operations, strictly follow the established procedures. When weighing, strive to be accurate and avoid errors. The reaction process should closely monitor key parameters such as temperature and pressure to prevent the reaction from getting out of control.
In addition, after use, the remaining methyl 3-iodophenylacetate and related waste must be properly disposed of in accordance with regulations, and must not be discarded at will to avoid pollution to the environment.
In short, only by strictly observing safety and operating regulations can we ensure the smooth development of methyl 3-iodophenylacetate-related work, while ensuring the safety of personnel and the environment from damage.

Application Area

In modern times, chemistry has flourished, and the properties and uses of all things have been investigated in detail. Methyl 3-Iodophenylacetate has its uses in various fields.
In the way of medicine, it can be used as a raw material for medicine, to assist in the research of new drugs, and to treat human diseases. With its characteristics, or the ability to adjust the body, it can cure diseases.
In the industry of spices, it can add a unique fragrance. Its taste is elegant and pleasant, adding a different style to the fragrance, making all kinds of fragrances, pleasing to the sense of smell.
In the field of materials, it can also be used. Or it can participate in the synthesis of materials, change the properties of materials, make them stronger and tougher, and apply them to equipment, utensils, etc., to increase their practical use. From this perspective, Methyl 3-Iodophenylacetate has a wide range of applications and has made great contributions to the development of this world.

Research & Development

In recent years, I have been focusing on the preparation and development of Methyl 3 - Iodophenylacetate in the field of organic synthesis. This compound has a unique structure and has potential applications in many fields such as medicine and material synthesis.
At the beginning, I explored its synthesis path and encountered many difficulties. The harsh reaction conditions and the delicate ratio of raw materials all need to be carefully weighed. After repeated experiments, a suitable method was finally obtained to improve the yield and purity.
Then, expand its application scope. In collaboration with colleagues, it was introduced into the construction of new drug molecules, and positive results were initially achieved. Also explore the possibility of synthesis of functional materials, hoping to open up new frontiers.
In the future, we want to deepen the research of this compound. Optimize the synthesis process, reduce costs and increase efficiency; explore more application scenarios, promote its progress from laboratory results to practical applications, and contribute to the development of the chemical industry.

Toxicity Research

I have heard the research of various sages on poisons, and now I will study Methyl 3-Iodophenylacetate. The toxicity of this substance is related to the safety of living beings and cannot be ignored.
Examine its properties in detail, and observe its effect on all living beings between experiments. Or see that after it enters the body, the viscera and meridians are infested by it. Looking at the genus of insects, if you touch it, it will stop abnormally and your vitality will gradually decrease.
And if you are in the environment, it is not safe and harmless. Spreading between water and soil, it may cause ecological changes. Although the amount is small, it can also cause harm.
Therefore, when studying the toxicity of this substance, we should exhaust its source, investigate its changes, and clarify its harm, so as to prepare preventive measures, protect the safety of all living beings, and protect the peace of nature.

Future Prospects

Guanfu methyl 3-iodophenyl acetate, its future prospects, is the heart of our chemistry researchers. This compound has a unique structure and seems to contain endless potential.
We expect it to shine in the field of organic synthesis. It may pave the way for the creation of new drugs. With its characteristics, it may be able to precisely connect with lesions and bring good news to patients.
Or in materials science, emerging. It can improve the properties of materials, make them more tough and durable, and be used in aviation, electronics and other fields to promote the progress of science and technology.
Furthermore, in the catalytic reaction, it can be used as an efficient catalyst to improve the rate and yield of the reaction, save resources, and benefit the development of green chemistry.
The future of methyl 3-iodophenyl acetate is like a star. Although it is out of reach, its light can be learned, and it will definitely lead our generation on the road of chemistry, continue to move forward, and explore the unknown.

Historical Development

Methyl 3 - Iodophenylacetate is an organic compound. It originated when chemists first explored various reaction paths in the field of organic synthesis. At that time, the chemical technology was not as exquisite as it is today, and the synthesis method was complicated and inefficient.
With the passage of time, science has evolved, and various new technologies and theories have emerged. Chemists have made the synthesis of Methyl 3 - Iodophenylacetate easier and more efficient with better reaction conditions and catalytic systems. In the past, it could only be prepared in small quantities in a few specific laboratories, but now it can be produced on a large scale. Its application has also expanded from its initial limitations to various fields such as medicine and materials. It has gradually become a shining star in the long river of organic chemistry, promoting the continuous progress of the chemical field and contributing to the improvement of human life.

Product Overview

Product Overview about Methyl 3-Iodophenylacetate
There is a product today called Methyl 3-Iodophenylacetate. This is an important raw material for organic synthesis and has key uses in many fields. Its properties are colorless to light yellow liquids with unique chemical structures.
From the perspective of chemical composition, it contains iodine atoms and methyl phenylacetate structures, giving it special reactivity. The iodine atom is active and can participate in many nucleophilic substitution reactions. It can be used as a key check point when constructing complex organic molecular structures. The structure of methyl phenylacetate makes it both the stability of the benzene ring and the reaction characteristics of the ester group.
In the field of medicinal chemistry, this product is often a key intermediate for the synthesis of specific drug molecules, helping to develop new drugs to cure diseases. In the field of materials science, it can also contribute to the creation of new functional materials.
In summary, Methyl 3-Iodophenylacetate occupies an important position in the field of modern chemical synthesis due to its unique chemical properties and structure, and has great potential for future development.

Physical & Chemical Properties

Methyl 3 - Iodophenylacetate is an organic compound. Its physical properties, at room temperature, are mostly liquid, with a specific color and smell. Looking at its density, it is heavier than water, insoluble in water, but soluble in various organic solvents. Regarding its boiling point, due to the force between molecules, it can be boiled and volatilized at a certain temperature. Its chemical properties are active, iodine atoms have high activity, and are prone to nucleophilic substitution reactions. The benzene ring structure also gives it the characteristics of aromatic compounds, which can undergo reactions such as halogenation and nitrification. In the field of organic synthesis, it is often used as a key intermediate to prepare a variety of complex organic molecules, and has great potential for applications in medicine, materials and other fields.

Technical Specifications & Labeling

Today there is a substance called Methyl 3-Iodophenylacetate. Its production method depends on the exquisite process regulations. Prepare all kinds of raw materials first, according to the precise proportion, such as the ratio of materials, all have a fixed number. In clean utensils, put them in sequence. Use a suitable temperature, or slow heat, or hot fire to promote melting, so that the materials are fused.
Its quality identification is related to color, purity, etc. The color should be pure, and no miscellaneous colors should be mixed in between. The purity must meet the parameters of the commercial goods, and the impurities must not exceed the limit. After this process specification and quality identification, high-quality Methyl 3-Iodophenylacetate can be obtained, so as to meet the needs of all parties, used in all kinds of wonderful places, and live up to the meaning of fine craftsmanship.

Preparation Method

The method of making Methyl 3 - Iodophenylacetate is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials are selected to be pure to ensure the quality of the product. First take an appropriate amount of 3 - iodobenzoic acid and absolute ethanol, use concentrated sulfuric acid as the catalyst, and mix the two in a round bottom flask in a certain proportion.
Put a stirrer in the flask and a reflux condenser to control the stability of the reaction. Slowly raise the temperature to about 70 - 80 degrees Celsius, this temperature can promote the esterification reaction to proceed quickly. In the reaction, concentrated sulfuric acid catalyzes the dehydration and condensation of the two to form Methyl 3 - Iodophenylacetate.
After several hours, when the reaction is near the end, pour the mixture into the separation funnel, wash with saturated sodium carbonate solution to remove the remaining acid. Then dry with anhydrous magnesium sulfate to remove its moisture. After distillation under reduced pressure, a specific boiling range fraction is collected to obtain pure Methyl 3 - Iodophenylacetate. This product has high purity and meets the regulations of chemical production.

Chemical Reactions & Modifications

In recent years, I have studied methyl 3-iodophenyl acetate, and I have gained a lot of experience in the reaction and modification of this compound. The initial reaction of this compound is based on the usual method, and the effect is not good. Observe its shape, think carefully, and read the ancient method or can be referred to.
Then try to change its agent, adjust its temperature, and observe its response. At first, methyl ether is used as a solution, and zinc powder is added, but the yield is not up to expectations. Later, it is easy to use ethanol and copper salt as a catalyst, and the reaction is gradually smooth, and the yield also rises.
As for the modification, I want to increase its stability and strengthen its properties. Before adding alkenyl groups to the side chain, I did not get good results. I also tried to introduce hydroxyl groups from the benzene ring, and it was actually achieved. The stability and activity of
After all kinds of tests, the reaction and modification of Minghua cannot be achieved overnight. It is necessary to be sensitive and know the details in order to make progress and get what you want.

Synonyms & Product Names

Today there is a product called Methyl 3 - Iodophenylacetate. This is a product of fine chemicals and has a wide range of uses in the field of organic synthesis. Its aliases are also numerous, all of which vary according to the situation and industry practice. Or call it a similar name according to its structural characteristics; or start from its function and give it another name.
Guanfu This product has a unique chemical structure. The iodine atom is cleverly connected to methyl phenylacetate, giving it a special chemical activity. Because of its active nature, it is an indispensable raw material in many fields such as pharmaceuticals and materials research and development. When making a drug, it can participate in key reactions to help generate active ingredients; when developing materials, it can also improve material properties and improve quality.
So all the aliases revolve around the name of this core product. Although the names are different, they all refer to the same thing, Methyl 3 - Iodophenylacetate is also. In the process of scientific research and production, knowing its synonyms can be handy and unimpeded.

Safety & Operational Standards

Code of Safety and Operation of Methyl 3 - Iodophenylacetate
Methyl 3 - Iodophenylacetate is an important chemical compound in chemical research. If you want to use this substance, you must first clarify its safety and operation specifications to ensure the smooth operation of the experiment and the safety of personnel.
This substance has certain chemical activity. In case of open flame, hot topic or contact with oxidant, there is a risk of combustion and explosion. Therefore, when storing, it should be placed in a cool and ventilated warehouse, away from fire and heat sources. The storage temperature should not exceed 30 ° C. Keep the container sealed. It should be stored separately from oxidants and food chemicals, and should not be mixed. The storage area should be equipped with leakage emergency treatment equipment and suitable containment materials.
When operating, the experimenter needs to wear appropriate protective clothing, gloves and goggles. Avoid direct contact with skin and eyes. If contact is inadvertent, rinse immediately with a large amount of flowing water and seek medical attention in a timely manner. Operate in a well-ventilated environment to prevent steam leakage into the air of the workplace.
In the event of a leak, personnel from the contaminated area of the leak should be quickly evacuated to a safe area and quarantined to strictly restrict access. Cut off the source of fire. It is recommended that emergency personnel wear self-contained positive pressure breathing apparatus and anti-toxic clothing. Do not come into direct contact with the leak. Cut off the source of the leak as much as possible. Prevent it from flowing into restricted spaces such as sewers and drainage ditches. Small leakage: mix with sand, dry lime or soda ash. It can also be scrubbed with an emulsion made of a non-flammable dispersant, and the lotion is diluted and placed into the wastewater system. Large amount of leakage: build a dike or dig a pit for containment. Cover with foam to reduce vapor disasters. Transfer to a tanker or a special collector with an explosion-proof pump, recycle or transport to a waste treatment site for disposal.
In short, in the process of using Methyl 3 - Iodophenylacetate, it is necessary to strictly observe safety and operating practices, and do not slack in the slightest, in order to achieve the purpose of the experiment and ensure safety.

Application Area

In the field of organic synthesis, it is often used as a key intermediate. With its unique structure, a variety of compounds with special properties can be derived through various chemical reactions, such as for the creation of new medical drugs. Physicians make good medicines, relying on such intermediates to build active molecular structures, hoping to cure various diseases. In the field of materials science, it also has its use, or can help synthesize materials with special functions, adding new materials for the manufacture of devices and appliances, making them have unique properties. From this point of view, methyl 3 - iodophenyl acetate has a value that cannot be ignored in various application fields, and is actually an important thing in chemical research and industrial production.

Research & Development

In recent years, many people have studied methyl 3-iodophenyl acetate. This compound has unique properties and is widely used, and it has shown its ability in various fields.
We have devoted ourselves to studying and exploring the method of its synthesis. At first, with conventional techniques, the effect is not obvious, and the yield is quite low. Then think about changes, adjust the conditions of the reaction, and choose exquisite reagents. After repeated trials, a good method can be obtained, which can increase its yield, and the product is pure.
Restudy the properties of this substance, and investigate its changes in different environments. It is known that it is sensitive to temperature, light, and catalysts. According to this, it shows the importance of its application, can be used in the preparation of medicine, and can also help the research of materials.
Methyl 3-iodophenylacetate has broad prospects. We should continue to study it, expand its use, and promote its progress in various industries, hoping to contribute to the development of the world, promote the research and progress of this compound, and reach a new level.

Toxicity Research

I have heard physicians talk about drugs. The nature of poisons is related to human life, and it must be observed. Today there is Methyl 3 - Iodophenylacetate, and I will conduct detailed toxicity studies.
After various experiments, its effects on organisms were observed. Enter the body of a white rat and observe its diet, movement, and mental state. At first, the white rat showed a little fatigue, and then the diet gradually decreased. Over time, the physiological functions were different, and the organs were also damaged.
It was also tested in cell experiments. It was found that it inhibited the activity of cells and caused apoptosis. It can be seen that Methyl 3 - Iodophenylacetate is toxic and harmful to the health of organisms. When using it, be careful and study its safe dosage in detail to prevent it from harming the living beings and causing endless harm.

Future Prospects

Methyl 3 - Iodophenylacetate has great potential in the field of chemical industry. Although it is currently used or not widely used, the future prospects are really promising.
Its unique structure may lead to novel reaction paths, opening up a new path for organic synthesis. In the field of pharmaceutical research and development, it may be cleverly modified to be turned into new drugs with unique curative effects.
In the field of materials science, it is also expected to develop high-performance functional materials by virtue of its characteristics. Although the road ahead may encounter technical bottlenecks, cost constraints and other obstacles, scientific researchers are determined to study.
I firmly believe that with time, through unremitting exploration and innovation, Methyl 3-Iodophenylacetate will be able to bloom in various fields, contribute to future development, and create extraordinary achievements.

Historical Development

The origin of Methyl 3 - Iodophenylacetate can also be investigated. In the past, the name of this substance was not first heard in the study of chemistry. However, with the passage of time, various sages have diligently explored the way of chemistry, analyzed micro-observations, and gradually gained something.
In the early years, various craftsmen studied various reactions in the field of organic synthesis to figure out the formation of new substances. After repeated trials, under specific conditions and ingenious formulations, Methyl 3 - Iodophenylacetate was finally obtained. Its initial appearance, or just one of the various achievements, is not significant. However, with the deepening of research, it has been found to have potential uses in medicine, materials and many other aspects. Then it attracted the attention of many scholars and studied Yiqin, making it gradually appear in the world from nowhere, leaving a unique track in the long river of chemical development, and becoming an indispensable part of today's chemical field.

Product Overview

Today there is a product called Methyl 3-Iodophenylacetate. It is an important raw material for organic synthesis and has applications in many fields. The preparation of this product requires a multi-step reaction, and the raw materials and conditions are very critical. Its properties are colorless to light yellow liquid, with a specific odor and density.
In terms of structure, it contains iodine atoms, benzene rings and ester groups, and its unique structure gives it special chemical properties. In the reaction, iodine atoms are active and can participate in reactions such as nucleophilic substitution, providing the possibility to construct new chemical bonds. Ester groups also have their own characteristics, such as hydrolysis and alcoholysis.
Due to its unique properties, it can be used in the synthesis of compounds with specific biological activities in the field of medicinal chemistry; in materials science, or as a key intermediate for the preparation of new materials. The research and development of this compound has broad prospects, and many chemists are working to explore more potential uses and reaction pathways.

Physical & Chemical Properties

"Physicalization of Methyl 3-Iodophenylacetate"
Methyl 3-Iodophenylacetate is an important substance for chemical research. Its physical properties, the external color is often in the color to light color liquid, and it is often determined under normal conditions. With a specific melting temperature, the melting temperature is low, and it is often in the liquid state, so it is easy to operate for many times. The boiling force varies slightly according to the environment, but it is roughly within a certain range.
As far as the chemical properties are concerned, the existence of the iodine atom ester group in the molecule gives this compound a special chemical activity. The iodine atom is easy to be replaced and reversed, and can be replaced by multiple nuclei, changing the molecular transformation. Ester groups can undergo hydrolysis, alcoholysis, and other reactions, and under different catalytic components, generate phase acid and alcohol compounds. Such physicalization properties are of great importance in the fields of synthesis and chemical research.

Technical Specifications & Labeling

Today there is a product called Methyl 3 - Iodophenylacetate. The preparation of this product is related to the process specification and identification (product parameters), which is the most important thing. To make this product, you need to follow the precise method. The choice of raw materials must be pure and the proportion should be in accordance with the rules. When reacting, factors such as temperature and duration must be strictly checked.
After being made, the logo should not be ignored. Detail its properties, content and other parameters to prove the excellence of quality. The process specification makes the process orderly, and the identification is accurate, so that everyone can understand its characteristics. In this way, only the excellent Methyl 3 - Iodophenylacetate products can be used in all fields without error.

Preparation Method

The method of making Methyl 3 - Iodophenylacetate is related to the raw materials and production process, reaction steps and catalytic mechanism. First take an appropriate amount of 3 - iodobenzoic acid and methanol as raw materials, and the ratio of the two needs to be precisely controlled. In the reaction kettle, add an appropriate amount of concentrated sulfuric acid as a catalyst, concentrated sulfuric acid can promote the reaction rate.
Control the temperature to about 60 - 80 degrees Celsius, this temperature range is conducive to the forward reaction. Turn on the stirring device to fully mix the raw materials with the catalyst. The reaction process is closely monitored after several hours. After the reaction is completed, cool down, neutralize the excess sulfuric acid with sodium bicarbonate solution, and then separate the liquid to obtain the organic phase. Methyl 3 - Iodophenylacetate was obtained by distillation and purification of the organic phase. In this process, the catalyst accelerated the esterification reaction, and the ratio of raw materials and temperature control were the key factors, which affected the purity and yield of the product.

Chemical Reactions & Modifications

The chemical reaction and modification of 3-iodophenylacetate is an important topic in chemical research. In the field of organic synthesis, halogenation and esterification reactions are often involved in the preparation of this compound.
In the halogenation reaction, the iodine reagent interacts with the corresponding phenyl compound, so the control of the reaction conditions is the key. Temperature and the choice of solvent all affect the substitution check point and reaction rate of iodine atoms. If the conditions are not suitable, side reactions may be caused, and the product is impure.
In the esterification reaction, the halogenated product is esterified with acetic acid or its derivatives. The type and dosage of catalysts in this process also affect the reaction process. Choosing a high-efficiency catalyst can increase the reaction activity and improve the product yield.
In order to optimize this chemical synthesis, new reaction paths should be explored and existing conditions improved. Such as finding mild and efficient halogenation reagents, developing green and environmentally friendly esterification methods to modify chemical synthesis and improve the synthesis efficiency and quality of methyl 3-iodophenylacetate.

Synonyms & Product Names

In the field of chemical industry, new substances have emerged one after another. Today there is Methyl 3 - Iodophenylacetate. Although its name is different, similar substances may have other names. This compound is an important material for organic synthesis and is widely used in the fields of medicine and materials.
Looking at its naming, according to the rules of chemistry, its structure and composition are explained. However, between the market and the well, or because of its characteristics and uses, it is commonly known. Just like the ancient Dansha, the scientific name is mercury sulfide, but the alchemist and pharmacist have their own names. Methyl 3 - Iodophenylacetate is also the same. Industry exchanges, or there is a convenient name, to replace its traditional name, this is the industry custom, for the convenience of telling and remembering. Although the names are different, the nature of natural things has not changed, and they are all the cornerstones for promoting the progress of chemical industry.

Safety & Operational Standards

Methyl 3 - Iodophenylacetate (Methyl 3 - Iodophenylacetate), the product of the chemical, in the experimental and production environment, must follow the safety and operation standards to ensure that everything goes smoothly and there is no risk of harm.
#1. Storage
This material should be placed in a cool, dry and well-ventilated place. Avoid open flames and hot topics to prevent unexpected explosions. Storage places should be kept away from fires and heat sources, and the temperature should not be too high to cover high temperatures or cause their physical properties to mutate, causing danger. It also needs to be stored separately with oxidants, strong alkalis and other substances to avoid chemical reactions and cause disaster.
#2. Rules for Access
When taking methyl 3-iodophenyl acetate, it is necessary to wear suitable protective equipment. Wear protective gloves to prevent the skin from being invaded by it; wear safety goggles to protect your eyes in case. The device used must be clean and dry to prevent impurities from mixing in, which will damage its purity and affect the result of the reaction. When measuring, when using a precise measuring tool, according to the needs of the experiment, be careful to measure the number, not more or less, to ensure the accuracy of the experiment.
#Third, the mode of operation
It is appropriate to operate in the fume hood, so that the volatile gas can be quickly discharged from the outside, so as not to gather in the room and harm the human body. The operator must be skilled in the process and careful. When stirring, the speed is moderate, do not overdo it and cause the liquid to splash out. Heat the reaction, control the temperature in an orderly manner, follow the nature of the reaction, choose the right heat source, and do not rashly heat up, causing the danger of loss of control. If there is a spill, stop immediately and clean up the scene. Small spills can be adsorbed by sand, vermiculite and other substances, properly collected, and handed over for special disposal; if a large amount of spills, people need to be evacuated, and warning signs should be set up, which will be handled by professionals.
#4. Emergency measures
If you accidentally touch the skin, quickly rinse with plenty of water, and then wash with soap. If it enters the eye, immediately open the eyelids, rinse with flowing water or normal saline, and seek medical treatment. In case of fire, choose carbon dioxide or dry powder fire extinguishers to put out as appropriate. Do not use water to prevent the fire from spreading and causing even more damage.
The safety and operation of methyl 3-iodophenyl acetate are related to personal safety, the success or failure of the experiment, and all kinds of norms. It should not be ignored. It should be kept in mind and practiced.

Application Area

Methyl 3 - Iodophenylacetate is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be used as a key intermediate to help synthesize specific drugs, or treat difficult diseases, and save patients from pain. In the field of materials science, it can participate in the creation of novel materials, endow materials with specific properties, such as enhancing their stability and improving their optical properties, so that materials can be used in various high-end technologies. In the field of fine chemicals, it is also an important raw material, which can be used to make high-end fragrances, additives, etc., to increase the quality and value of products. All these show that Methyl 3 - Iodophenylacetate has an indispensable position in many fields and has made great contributions to promoting the development of related industries.

Research & Development

I have dedicated myself to the research of Methyl 3 - Iodophenylacetate. When I first saw this thing, I felt that its structure is exquisite and must have unique characteristics. Then I explored it in various ways, observed its reaction, and observed its changes.
At the beginning, the experiment encountered many obstacles, and the yield was not as expected. However, I was not discouraged, so I repeatedly studied ancient books, referred to the methods of the sages, and improved the steps of the experiment. After months of hard work, I finally got something. The yield gradually increased, and the quality of the product was also good.
In this process, I well know the way of research, and the most important thing is persistence and innovation. Every failure is the foundation of success. In the future, we should continue to make progress and expand the application of this product, with the hope of contributing to the development of chemistry, in order to reach new frontiers and benefit everyone.

Toxicity Research

I have heard that the sages have talked about the nature of poisons, which is related to people's health. I would like to say Methyl 3-Iodophenylacetate. This chemical substance is quite important for toxicological investigation.
Looking at its structure, iodine atoms are connected to benzene rings, and there is an ester group structure. Toxicological properties, or involve its metabolic pathway into the body. Ester groups can be hydrolyzed, and the generated substances may interact with biochemical reactions in the body. The presence of iodine may cause disorders in cellular physiological processes.
After various experiments, its effects on organisms are observed. In animal experiments, it can be seen that it affects the function of the nervous system and causes abnormal behavior. Or it can damage the liver, kidneys and other organs, causing their function to decline. All of these indicate the terrible toxicity of Methyl 3-Iodophenylacetate, which needs to be investigated in detail to clarify its harm and find good measures for protection and treatment.

Future Prospects

Methyl 3-Iodophenylacetate is not widely known today, but I can see its properties and use it in the future development. Its structure is exquisite and its characteristics are unique. If it can be well studied, it will surely shine in the fields of medicine and materials.
The way of medicine may use its characteristics to make a good medicine with special effects and treat diseases in the world. The way of materials may also be due to its characteristics, innovative materials, and meet the needs of the times. Although there may be thorns in the road ahead, the progress of science is fearless and dangerous.
I firmly believe that over time, Methyl 3-Iodophenylacetate will be able to break through the limitations of the present, demonstrate its endless potential, create a new world for our generation, and realize the unfinished business. This is my eagerness for its future development.

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Frequently Asked Questions

As a leading Methyl 3-Iodophenylacetate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the chemical properties of Methyl 3-iodophenylacetate?

Methyl 3-iodophenylacetate, an organic compound, has unique chemical properties. Its physical properties are usually liquid or solid at room temperature, depending on the force between the substituent and the molecule. Its melting and boiling point is relatively high due to the large size of the iodine atom and the strong van der Waals force.
In terms of solubility, as an ester, it is slightly soluble in water, because water is a polar molecule, and the polarity of the compound is weak. According to the principle of "similar miscibility", it is more soluble in organic solvents, such as ethanol, ether, etc. These organic solvents can form van der Waals forces or weak interactions with its molecules.
Chemically active, ester groups can be hydrolyzed, and under acidic or alkaline conditions, the hydrolysis rate is different. In an alkaline environment, 3-iodophenylacetate and methanol are hydrolyzed, which is irreversible because hydroxide continues to consume the hydrolyzed acid. Under acidic conditions, hydrolysis is reversible, resulting in 3-iodophenylacetic acid and methanol.
The iodine atom endows it with the properties of halogenated aromatics, which can undergo nucleophilic substitution reactions. Affected by the electronic effect of the benzene ring, the iodine atom can be replaced by nucleophilic reagents, such as reacting with sodium alcohol to form corresponding ethers. At the same time, the benzene ring can undergo electrophilic substitution reactions. Because iodine is an ortho-para-site group, new substituents are mostly introduced into the ortho or para-site of the iodine atom.
In addition, the compound may also participate in the reverse reaction of esterification reaction, generating new esters and methanol with alcohol under acid catalysis. This process is reversible, and the reaction direction and degree can be adjusted by controlling the reaction conditions, such as temperature, proportion of reactants, and removal of products.

What are the preparation methods of Methyl 3-iodophenylacetate?

The method of preparing methyl 3-iodophenylacetate often follows several paths. First, it can be started from 3-iodophenylacetic acid, and it can be esterified with methanol under the condition of acid catalysis. Sulfuric acid, p-toluenesulfonic acid, etc. are commonly selected for acid. During the reaction, 3-iodophenylacetic acid and methanol are mixed in a reaction bottle in an appropriate proportion, and the catalyzed acid is added to heat the reflux number. After the reaction is completed, pure methyl 3-iodophenylacetate is obtained through neutralization, separation, distillation and other steps.
Another method uses 3-iodobenzoic acid as raw material to first reduce to 3-iodobenzyl alcohol. Strong reducing agents such as lithium aluminum hydride can be selected. Then 3-iodobenzyl alcohol reacts with methyl iodoacetate under the catalysis of alkali, such as potassium carbonate. In the reaction system, the two are fully mixed, heated and stirred, and the reaction is complete. After separation and purification, the target product is obtained.
Furthermore, 3-iodobromobenzene is used as the starting material and interacts with magnesium chips to prepare Grignard's reagent 3-iodophenyl magnesium bromide, and then reacts with methyl glyoxylate to generate the corresponding alcohol. After oxidation and esterification steps, methyl 3-iodophenyl acetate can also be obtained. Each method has its own advantages and disadvantages, and the practical operation needs to be comprehensively weighed according to factors such as raw material availability, cost, and difficulty of reaction conditions. The most suitable method is selected.

What are the applications of Methyl 3-iodophenylacetate?

Methyl 3-iodophenylacetate, this substance has wonderful uses in many fields. In the field of pharmaceutical and chemical industry, it is often the key raw material for the synthesis of exquisite drugs. The unique chemical activity of the benzene ring with iodine atoms and ester groups can build a complex drug molecular structure through various chemical reactions. For example, when creating some anti-cancer drugs with specific targeting properties, it can combine with specific targets through precise chemical reactions to exert therapeutic effects.
In the field of materials science, it also has its uses. Or it can participate in the synthesis of special materials, with its unique structure, endowing materials with novel properties. For example, in optical materials, it may affect the optical properties of the material, making the material exhibit unique performance in light absorption and emission, and opening up a path for the research and development of new optical materials.
In the field of organic synthesis, it plays an important role. As a building block of organic synthesis, with its iodine atoms prone to nucleophilic substitution reactions, ester groups can participate in hydrolysis, alcoholysis and other reactions, chemists can use it to construct rich and diverse organic compounds, expand the structure types of organic molecules, and promote the vigorous development of organic synthetic chemistry. It can be described as a wide range of uses, and it is an indispensable important chemical substance in various scientific research and industrial production fields.

What is the market price of Methyl 3-iodophenylacetate?

The market price of methyl 3-iodophenylacetate is difficult to sum up in a single word. The price of methyl 3-iodophenylacetate is influenced by many factors, which seem to be changing and elusive.
First, the price of raw materials is of great significance. Iodobenzene, methyl acetate, etc. are the raw materials for this product. If the price is high, the cost of methyl 3-iodophenylacetate will rise, and its price will rise. If the price of raw materials is low, the cost will decline, and the price may also be lowered. It is the fluctuation of the raw material market that is like the wind moving at the end of Qingping, which drives the price of finished products.
Second, the difficulty and cost of the preparation process are also the key. If the process is complicated, many instruments and equipment are required, and the manpower consumption is huge, or it is accompanied by high energy consumption, all of these will push up the production cost, resulting in the product being sold at a high price in the market. However, if the process is advanced and the cost is controlled, the price may be close to the people.
Third, the situation of market supply and demand is the core of determining the price. If the market has strong demand for this product, but the supply is limited, just like there are few porridge monks and many monks, the price will inevitably rise. Businesses are all eager to make profits, and when the supply is in short supply, the price will be difficult to suppress. On the contrary, if the market demand is low and the supply is excessive, it is like a mountain of goods and no one cares about it. In order to get rid of it, the price may drop again and again.
Fourth, the market competition situation should not be underestimated. There are many products of the same type, and merchants compete for market share or make a fuss about the price. Where the competition is intense, some merchants may attract customers with low-price strategies, which will also make the price of methyl 3-iodophenylacetate fluctuate.
Furthermore, policies and regulations and the international trade situation also affect the price. The rise and fall of tariffs and the tightness of environmental protection policies can invisibly change the cost of products and market circulation, which in turn affects the price.
In order to know the exact market price, it is necessary to carefully investigate the raw material market dynamics, process progress, changes in supply and demand, competition situation, policies and regulations, and many other aspects, and must be in the professional chemical products trading platform, market survey institutions to inquire about, in order to obtain more accurate price information.

What are the storage conditions for Methyl 3-iodophenylacetate?

Methyl 3-iodophenylacetate is an organic chemical substance. Its storage conditions are quite important, and it is related to the quality and properties of this substance.
When hiding, it should be placed in a cool place. Cover heat can cause its chemical properties to change, or it can cause decomposition and damage its quality. A cool place can slow down the movement of its molecules and maintain the stability of its structure.
And it must be stored in a dry place. Water is often a medium for the reaction of various reactions. If moisture invades it, or causes hydrolysis, it will cause the substance to deteriorate. In a dry environment, there is no water to disturb, and the molecules are settled, and the quality is complete.
It should also be avoided from encountering light. Light contains energy, or stimulates the molecules of this substance, which initiates the reaction of light and causes its structure to break and its properties to change. Hidden in a dark place, the road to cut off light can reduce the risk of photochemical transformation.
Furthermore, it should be sealed and stored. Sealing can isolate the gas, dust, etc. from the outside world, so as to prevent it from coming into contact with foreign objects, and prevent volatilization, so as to ensure the accuracy of its content.
This substance may be dangerous to a certain extent. When hiding, it should be stored in isolation from other objects according to its characteristics and in accordance with relevant regulations to prevent unexpected changes. In this way, according to the requirements of cool, dry, dark and sealed, and following the rules, methyl 3-iodophenylacetate can be well stored and its quality can be maintained for a long time.