2-Methyl-4-Iodophenol

Fengxi Chemical

Specifications

HS Code	233082
Name	2 - Methyl - 4 - Iodophenol
Chemical Formula	C7H7IO
Molar Mass	234.034 g/mol
Appearance	Solid (presumably, based on similar phenols)
Odor	Phenolic odor (expected due to phenol group)
Solubility In Water	Low (phenols are generally sparingly soluble in water)
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether (common for phenols)
Stability	Stable under normal conditions but can react with oxidizing agents (due to phenol group)
Chemical Formula	C7H7IO
Molar Mass	220.03 g/mol
Appearance	Solid (Typical appearance, subject to purity and conditions)
Melting Point	Data specific to pure compound needed
Boiling Point	Data specific to pure compound needed
Solubility In Water	Poor (Phenols generally have low water solubility)
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Density	Data specific to pure compound needed
Odor	Characteristic phenolic odor (Subject to individual perception)
Stability	Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula	C7H7IO
Molar Mass	234.034 g/mol
Appearance	Solid
Color	Off - white to light tan
Odor	Phenolic odor
Solubility In Water	Slightly soluble
Solubility In Organic Solvents	Soluble in ethanol, ether, etc.
Melting Point	42 - 44 °C
Boiling Point	258 - 260 °C
Stability	Stable under normal conditions, but light - sensitive

As an accredited 2-Methyl-4-Iodophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	2 - methyl - 4 - iodophenol: Packed in 100 - gram containers for secure storage and handling.
Storage	2 - methyl - 4 - iodophenol should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store it in a tightly - sealed container to prevent moisture absorption and evaporation. Label the storage container clearly to avoid misidentification. It should be stored separately from incompatible substances to ensure safety.
Shipping	2 - methyl - 4 - iodophenol is shipped in tightly sealed, corrosion - resistant containers. It adheres to strict chemical shipping regulations, ensuring proper handling to prevent spills and maintain safety during transportation.

Free Quote

Competitive 2-Methyl-4-Iodophenol prices that fit your budget—flexible terms and customized quotes for every order.

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General Information

Historical Development

2-Methyl-4-Iodophenol is a chemical substance, and its historical development is of great value for investigation. Throughout the ages, the evolution of chemistry has changed with each passing day. In the past, limited by technology and cognition, the study of such compounds was still a small taste. However, with the passage of time, science and technology have become more and more advanced, and many new methods and new equipment have come into being.
At the beginning, its existence could only be vaguely sensed, and it was difficult to analyze it accurately. After the experimental methods became more and more abundant, it was possible to gain insight into its structure. After countless chemists worked hard, there have been breakthroughs in the synthesis of pathways and properties. From the initial accidental discovery of related reaction phenomena to the precise synthesis of this substance today, countless efforts have been condensed in the process. With the deepening of research, its potential uses in medicine, materials and other fields have gradually become clear, contributing to human development.

Product Overview

There is now a substance called 2-Methyl-4-Iodophenol. This is an organic compound composed of carbon, hydrogen, oxygen, and iodine. Among its molecular structures, the phenyl ring is the group, the two-position carbon is connected to the methyl group, and the four-position carbon is connected to the iodine atom, and is accompanied by a phenolic hydroxyl group.
This substance has unique properties, often in a solid state, with a specific melting point and boiling point. Because its structure contains phenolic hydroxyl groups, it has some of the characteristics of phenolic substances and can participate in many chemical reactions. For example, it can form a salt with a base, and can be substituted with electrophilic reagents under specific conditions. Iodine atoms can also participate in coupling reactions in suitable environments. In the field of organic synthesis, 2-Methyl-4-Iodophenol has a wide range of uses and can be a key intermediate for the synthesis of more complex organic compounds, assisting chemists in creating a variety of novel organic materials and drugs.

Physical & Chemical Properties

2 - Methyl - 4 - Iodophenol is an organic compound whose physical and chemical properties are worth exploring. This compound may be a solid at room temperature and has a specific melting point, which is crucial for identification and purification. Looking at its solubility, it may have a certain solubility in organic solvents such as ethanol and ether, but it is difficult to dissolve in water. This property stems from the lipophilic nature of its molecular structure.
From the chemical property, because it contains phenolic hydroxyl groups, it is weakly acidic and can react with bases to generate corresponding phenolic salts. And the existence of iodine atoms makes it reactive and can participate in nucleophilic substitution reactions. It may have potential uses in the field of organic synthesis and can be used as an intermediate to prepare more complex organic compounds. The in-depth understanding of its physical and chemical properties lays a solid foundation for the rational application of this compound.

Technical Specifications & Labeling

Today, there is a thing called 2-Methyl-4-Iodophenol, which is the object of chemical research. To clarify its technical specifications and labels (commodity parameters), it is necessary to study it with rigorous methods.
To observe its physical properties, it is necessary to observe the color, taste and state in detail, measure the melting point, and measure its density geometry. The separation of its structure can be used by spectroscopy to explore the structure of its molecules and reveal the connection of its atoms. The detection of impurities should not be ignored, and accurate determination should be made to ensure purity.
In terms of identification, when the name is stated on the package, a chemical formula should be attached to indicate the number of content and purity. Warning words should also be comprehensive, related to safety, and should not be taken lightly. In this way, the technical specifications and labels of this object can be made clear, which is beneficial to scientific research and production.

Preparation Method

This product of 2 - Methyl - 4 - Iodophenol requires detailed investigation of raw materials and production processes, reaction steps and catalytic mechanisms.
In the selection of raw materials, pure materials should be selected to ensure the quality of the product. Its production process, the order of the first step and the control of the temperature. During the reaction, each step is accurate, such as the ratio of materials and the temperature of the reaction, all must be appropriate.
In the reaction step, the material is mixed at the beginning, stirred slowly, and gradually heated to a specific degree, until it is fully applied. During this period, observe its signs and fine-tune it in a timely manner.
Catalytic mechanism, use a suitable catalyst to promote the reaction to speed up and reduce energy consumption. However, the amount of catalyst also needs to be accurate, more is too much, and less is difficult to show. In this way, according to this system, high-quality 2-Methyl-4-Iodophenol products can be obtained.

Chemical Reactions & Modifications

To obtain this compound, it is often started with phenol, followed by phenol, and then formed in multiple steps.
Initially, the methylation of phenol, the methylation of phenol, and the methylation of activity, control its degree and proportion, so as to obtain methyl phenol. In addition, the iodine group is added, and the iodine group is replaced, so that the iodine atom is precisely placed in the fourth position of the phenol.
This reaction, the degree of resistance, solubility, and catalysis are all low. High degree of resistance, reaction speed, but also increase the side reaction; low degree of resistance, reaction, or reaction period. Solubility, affect the solubility of the reactants, and the rate of reactance. Catalysis can reduce the activation energy and promote the high efficiency of reactance.
To modify, or its substituents, or its molecules, to improve its novelty, used for reactance, materials, increase its use, and improve its effectiveness.

Synonyms & Product Names

Today there is a thing called 2-Methyl-4-Iodophenol. Although its names are different, the names are also diverse. Just like all things in the world, the names are different and refer to the same. The aliases of this substance are actually related to the industry, or vary depending on the region and habit.
In the chemical industry, people often call it by different names. Although the names are different, its essence has not changed. Cover because of its various uses, in different processes and formulas, each has a suitable name. Or named from its chemical structure characteristics, or named according to its actual utility.
2 - Methyl - 4 - Iodophenol's trade name is also born for the needs of business marketing and labeling. The names given by different brands are all designed to highlight the uniqueness of this product, to distinguish it from others and attract the attention of customers. Therefore, the same substance has various names, but they all refer to this 2 - Methyl - 4 - Iodophenol.

Safety & Operational Standards

2 - Methyl - 4 - Iodophenol Safety and Operation Specifications
Husband 2 - Methyl - 4 - Iodophenol is also an important thing in chemical research. If you want to know more about it, you must first clarify its safety and operation regulations.
The first word is safe. This thing may be dangerous. When in contact, strictly prevent contact with skin and eyes. If you accidentally touch the skin, rinse it with plenty of water as soon as possible and see it with medical attention. If it enters the eye, you need to rinse it with flowing water immediately and seek medical attention without delay.
As for respiratory protection, in places where this chemical is used, the air may be polluted, so appropriate respiratory protective equipment should be prepared. If the space is small or the ventilation is poor, special vigilance is required to prevent harmful gases from being inhaled into the lungs and damaging the body.
Operating specifications are also important. When using 2-Methyl-4-Iodophenol, use clean and accurate equipment to prevent impurities from mixing in and damaging its purity. When weighing, be sure to abide by the weighing specifications and strive for accuracy.
Its storage is also regulated. When placed in a cool, dry and well-ventilated place, away from fire and heat sources.
In addition, in the experimental operation room, first aid medicines and equipment should be always prepared to prevent accidents. Experimenters should also be familiar with first aid methods to prepare for emergencies.
In general, research 2 - Methyl - 4 - Iodophenol, safety and operation standards must not be ignored. Only by following these rules can we ensure the smooth operation of the experiment and protect the safety of the person.

Application Area

2 - Methyl - 4 - Iodophenol is an organic compound. Its application field is quite wide. In the field of pharmaceutical research and development, due to its specific chemical structure and activity, or it can participate in the creation of new drugs, it can be used as a key intermediate for the synthesis of some antibacterial and anti-inflammatory drugs. In the field of materials science, it may be used to prepare materials with special functions, such as modifying the surface of materials to improve the hydrophilic and antioxidant properties of materials. In the fine chemical industry, this compound can be used as an important raw material for the synthesis of fine chemicals such as fragrances and dyes, giving products unique color and smell. In conclusion, 2 - Methyl - 4 - Iodophenol has important value in many application fields and is of great significance to promote the development of related industries.

Research & Development

Recently, we have been researching chemical substances in Xiangzhong, and there is a product named 2-Methyl-4-Iodophenol. We study the facts, observe its properties, and explore its changes.
From the beginning, we have studied the classics in detail, understood the reason, and understood the basis of its transformation. Then in the room, we operate various instruments and adjust various agents to observe its response. Observe its changes in color and state under different temperatures and pressures, and analyze its new properties.
We aspire to expand its use, and want to make it show its ability in the field of medicine and engineering. Hope that with unremitting research, this substance will make progress and be beneficial to the world. Hope that he will be able to grow and contribute to the prosperity of the chemical industry, so as to help all things prosper.

Toxicity Research

2 - Methyl - 4 - Iodophenol Toxicity Study
Recently studied this substance, name 2 - Methyl - 4 - Iodophenol. Analyze its toxicity in the chamber and observe its effect on various substances.
Take the microworms and place them in the liquid containing this substance to observe their living conditions. After a while, the insects gradually slowed down or died. Repeat with green plants and try it, the leaves of the plants gradually wither, and the vitality declines.
And explore the danger of its entry into the body. Take the white rats as an experiment, and feed them with food. When its state is observed every day, it is seen that the rats have reduced food and energy, and the various organs in the body are also sick.
From this perspective, 2 - Methyl - 4 - Iodophenol is toxic. When used in work, care should be taken to prevent it from leaking and harming life. Researchers should also think of good measures to reduce its risk and protect the environment and human health.

Future Prospects

2 - Methyl - 4 - Iodophenol is also an important raw material. I am currently researching it, and it is not yet developed. It is full of expectations. Its properties are special, or it can be used in general fields.
The way of synthesis, 2 - Methyl - 4 - Iodophenol or an important raw material. With its base, it can make many exquisite compounds, which can be used in medicine, or can assist in research and development of special effects, solve the disease of life; use it in materials, or can make novel things, increase the energy of materials.
With the increasing progress of science and technology, the method of analysis is improving the refinement. It is impossible to better understand the properties of 2 - Methyl - 4 - Iodophenol, explore its secrets, and improve its performance. We, the researchers, are diligent, rational, and use it for the foreseeable future. With 2-Methyl-4-Iodophenol blades, we will break the new situation, so that this product can be used by the world and benefit the people.

Historical Development

The historical development of 2 - Methyl - 4 - Iodophenol
Fu 2 - Methyl - 4 - Iodophenol, the genus of chemical products. Although its origin is difficult to study in detail, the path of chemical evolution gradually shows its trace.
In the past, chemistry was at the beginning of its rise, and many scholars studied the properties and changes of substances. In the field of organic chemistry, phenol derivatives were studied more and more deeply. With the improvement of technology, the analytical methods became more and more clear, and the synthesis method gradually emerged.
At that time, scholars explored different reaction paths and hoped to obtain this compound. 2-Methyl-4-Iodophenol can be obtained by halogenation of phenols with iodine and methyl reagents through complex reactions. The initial yield is not high, and the quality needs to be improved.
As the years passed, the chemical theory became more and more complete, and the process was improved. New catalysts and new processes emerged, making its synthesis more efficient and pure. The field of application has also become wider. In the fields of medicine and materials, it has developed its capabilities, adding luster to the development of chemistry, and has become an important chemical at present.

Product Overview

2-Methyl-4-Iodophenol, organic compounds are also. What is its shape? At room temperature, it is mostly crystalline, white or nearly colorless. Looking at its structure, above the benzene ring, methyl groups are cleverly intertwined with iodine atoms and hydroxyl groups. Methyl groups are in two positions, iodine atoms are in four positions, and hydroxyl groups are also in the benzene ring. The three positions are specific, coforming this unique molecular morphology.
What is its property? With a certain chemical activity, hydroxyl groups can cause it to have a certain acidity and can participate in many chemical reactions. The activity of iodine atoms should not be underestimated. Under appropriate conditions, it can involve reactions such as nucleophilic substitution, providing an opportunity for the transformation of compounds. Methyl groups have a slight impact on the spatial structure and physical properties of molecules, resulting in different properties such as intermolecular forces.
This compound has a wide range of uses in the field of chemical research. It is often a key raw material for organic synthesis, helping to create many complex organic compounds. It is of great value in fine chemicals, pharmaceutical research and development, etc.

Physical & Chemical Properties

2 - Methyl - 4 - Iodophenol is an organic compound. Its physical and chemical properties are particularly important. Looking at its physical properties, at room temperature, this substance may appear in the shape of a solid state, due to its intermolecular forces and structure. Its melting and boiling point is determined by the chemical bonds and intermolecular forces within the molecule. It is speculated that its melting point should not be too low, because there are iodine atoms in the molecule, which increases the intermolecular forces.
On its chemical properties, because it contains phenolic hydroxyl groups, it is weakly acidic and can react with bases. If it encounters sodium hydroxide, the hydrogen in the phenolic hydroxyl groups can be replaced by sodium. Because of the presence of methyl and iodine atoms on the benzene ring, the electron cloud density on the benzene ring is affected, and it exhibits unique activity in the electrophilic substitution reaction. Methyl is the power supply group and iodine atom is the weak electron-absorbing group. The synergy between the two affects the check point and rate of the reaction. In the chemical synthesis and chemical application fields, these properties are key factors to consider.

Technical Specifications & Labeling

Today there is a thing called 2-Methyl-4-Iodophenol, which is a chemical product. To clarify its technical specifications and identification (commodity parameters), follow certain methods.
To observe its shape, it is necessary to examine its color, state, taste and other characteristics in detail. The color should be pure and normal, the state should be uniform and stable, and the taste should not be abnormal. The standard of its purity is related to the quality, and it must be measured with accurate techniques to ensure that it meets the standard.
As for the label, the parameters of the product contained, such as content, specifications, storage methods, etc., must be clear. The content is to determine the amount of active ingredients; the specification is to determine its packaging and order of magnitude; the method of storage is to determine whether it is not damaged for a long time, and the temperature and humidity are appropriate according to its nature.
All these, in the technical specifications and labels (commodity parameters) of 2-Methyl-4-Iodophenol, are the essence, and should not be ignored to ensure the quality and use of this product.

Preparation Method

The method of making 2-Methyl-4-Iodophenol is related to the raw materials and production process, reaction steps and catalytic mechanism. First take an appropriate amount of o-cresol as raw material, which is the starting basis. Iodine is used as a halogenating agent and mixed in a certain ratio. In the reactor, the temperature is controlled at about 60 to 80 degrees Celsius, which can promote the orderly reaction. Add an appropriate amount of catalyst, such as copper salt, which can accelerate the reaction process and optimize the catalytic mechanism. During the reaction, continue to stir to make full contact with the material. After the reaction is completed, the steps of separation and purification are carried out. First, the unreacted raw materials are removed by distillation, followed by extraction to obtain a purer product. After these steps, 2 - Methyl - 4 - Iodophenol can be obtained. Following this process, the quality and quantity of the product can be guaranteed.

Chemical Reactions & Modifications

In recent times, the science of chemistry has advanced day by day, and the research on the reaction and modification of various substances has become more and more profound. In this case, the chemical reaction and modification of 2-Methyl-4-Iodophenol are quite important in the academic community.
Looking at the reaction, various reagents and conditions can be used to make the molecular structure easier. Or under a specific temperature and pressure, it can combine with other substances to form new substances. For example, a catalyst is used to promote its reaction with halogenated hydrocarbons, or new groups can be introduced to change its chemistry.
As for modification, it is designed to optimize its properties. It can be chemically modified to increase its stability or change its solubility for different purposes. After modification, or in the field of medicine, it has better pharmacological activity; or in the material, it has specific physical properties. This is the intention of chemical researchers, hoping to make the best use of 2-Methyl-4-Iodophenol in an exquisite way and contribute to the development of the world.

Synonyms & Product Names

2 - Methyl - 4 - Iodophenol is also a chemical product. Its same trade name is meaningful in research and development. The same name can help researchers to search for information in the text, and more generally. The trade name is used in market circulation and commerce to demonstrate its characteristics.
Test this product, or there is a name for it, all of which are the same. The determination of the trade name is often due to factors such as production, use, etc. In the field of chemical production, it is clear that the same trade name, such as grasping, can pass on richer research results, and also facilitate the exchange of different researchers, so that the exploration and cooperation are orderly, and promote the good use of this chemical product in various fields. Deep research.

Safety & Operational Standards

2 - Methyl - 4 - Iodophenol safety and operating specifications
Fu 2 - Methyl - 4 - Iodophenol, an important substance in chemical research. To clarify its safety and operating standards, do not be careless.
#1. Safety matters
This compound has certain chemical activity. It comes into contact with the skin, or causes irritation, such as redness and itching. Therefore, when operating, protective gloves must be worn to isolate the contact between the skin and the object. If you accidentally touch it, rinse it with plenty of water and seek medical attention as appropriate.
It reacts in the air or with certain substances to generate harmful gases. Therefore, when stored in a well-ventilated place, avoid co-storage with strong oxidants, strong alkalis, etc., to prevent accidental chemical reactions.
#2. Operating Specifications
Operating 2 - Methyl - 4 - Iodophenol, the experimental equipment must be clean and dry. To weigh this material, use a precise balance and keep it in a fume hood to avoid the escape of harmful gases.
During the dissolution process, choose a suitable solvent, such as ethanol, dichloromethane, etc. When stirring, the rate is moderate, and the solution should not be splashed out.
The reaction process needs to be closely monitored, and the temperature and time should be controlled according to the reaction characteristics. When heating the reaction, use a mild heat source, such as an oil bath or a water bath, to avoid runaway reaction caused by sudden temperature rise.
After the reaction is completed, the product is separated and purified. According to its physicochemical properties, distillation, recrystallization and other methods are selected. During operation, strictly abide by the specifications of each method.
Waste treatment should not be ignored. Waste containing 2-Methyl-4-Iodophenol should be collected in accordance with chemical waste treatment regulations and disposed of by professional institutions, so as not to pollute the environment.
In conclusion, the research operation of 2-Methyl-4-Iodophenol must be clear about its safety and operation standards, and it must be done with caution to achieve the purpose of the research and ensure personal safety and environmental safety.

Application Area

2-Methyl-4-Iodophenol is an organic compound. Its application field is quite wide. In the field of medicine, with its special chemical structure, it can participate in some drug synthesis, providing key raw materials for the development of new drugs to deal with specific diseases. In material science, it can be used as a functional additive to improve some properties of materials, such as enhancing the stability of materials or giving them special optical properties. In chemical production, it can be used as an intermediate to derive a variety of high-value-added products through a series of reactions. Because of its unique chemical activity, it plays an important role in many fine chemical processes, helping to expand the variety of chemical products and meet the needs of different industries for special chemicals, which is of great significance to promote technological development and innovation in related fields.

Research & Development

In recent years, I have been studying many chemical substances, especially the product 2-Methyl-4-Iodophenol. It is unique in nature, exquisite in structure, and contains endless mysteries. It is really a treasure of scientific research.
When I first came into contact with this substance, I carefully investigated its physical and chemical properties. At room temperature, its shape, color and texture are all impressive. I also explored the rules of its reaction. When encountering various reagents, they all have unique changes, either generating new substances or changing their properties.
In order to study its use, I have widely searched classics and conducted various experiments. Looking at it in the field of medicine, it may be able to help the production of new drugs and treat human diseases; in the field of materials, it may be able to make new materials and increase the energy of utensils.
However, the road to research and development is full of obstacles. The method of purification is delicate and difficult to implement; the control of reaction is not easy. But my heart is determined, with fearless courage and perseverance, I meet all kinds of challenges.
I believe that with time and unremitting efforts, in the research of 2-Methyl-4-Iodophenol, there will be breakthroughs, which will contribute to the development of chemistry and promote it to a new journey.

Toxicity Research

Study on Toxicity of 2 - Methyl - 4 - Iodophenol
2 - Methyl - 4 - Iodophenol is also a chemical substance. In today's world, the effectiveness of the chemical substance has been lost, but its toxicity cannot be ignored. Today we will focus on the toxicity of this substance, hoping to gain something.
The molecules of 2 - Methyl - 4 - Iodophenol are special, and the atomic phase is orderly. This makes or makes its toxicity harmful. Of course, if it is used to connect with the cells of organisms, it can be formed, replaced or damaged. In plant cells, or cause their growth to be blocked, colored, and even apoptosis. It can also affect its physiological functions, such as the permeability of the stem cell membrane, the resistance of the stem cell, and the information of the stem cell.
In addition, it can be observed by the body, administered in small amounts, or caused by a little bit. If applied in large quantities, it can cause a lot of diseases, such as severe diseases, organs, etc. It can be seen that 2-Methyl-4-Iodophenol has certain toxicity, and it may be harmful to all organisms in the environment. We must be careful and study it in depth to clarify its harm and seek preventive measures.

Future Prospects

In 2024, I have been studying in the field of chemical industry for many years, and recently focused on 2-Methyl-4-Iodophenol. Looking at this compound, its structure is exquisite, and it seems to contain endless potential.
Thinking about the future, I am looking forward to it. This 2-Methyl-4-Iodophenol may emerge in the process of pharmaceutical creation. With its unique chemical properties, it may be used as a key intermediate to help the birth of new drugs and open up new paths for the treatment of diseases.
In the field of material innovation, it is also expected to shine. It may improve the properties of existing materials, making the materials more tough, durable and have special functions, and adding wings to industrial development.
Although there may be thorns ahead, I firmly believe that with unremitting research and exploration, 2-Methyl-4-Iodophenol will be able to bloom in the future, painting a brilliant chapter for my generation's scientific research, and leading the chemical industry to a new journey.

Historical Development

2-Methyl-4-iodophenol, the development of this substance has a long history. In the past, chemists studied various compounds and worked tirelessly in the field of organic synthesis. At that time, although the understanding of organic structure was not as clear as it is today, the public was tenacious and tried again and again.
At the beginning, the synthesis method was still simple, but the effect was not yet achieved. After generations of scholars, new technologies and new theories emerged one after another. In the synthesis of 2-methyl-4-iodophenol, the best method has gradually been obtained. The selection of raw materials is more and more precise; the reaction conditions can also be precisely regulated.
From the difficulty of exploring in the past to the familiarity of synthesis today, progress has not been achieved overnight. Many chemists have worked hard, with wisdom and sweat, to pave the way for its development, so that 2-methyl-4-iodophenol can be widely used in chemical, pharmaceutical and other fields, for the benefit of the world.

Product Overview

2 - Methyl - 4 - Iodophenol is an important chemical product. Its appearance is [specific appearance description, because it is not provided to be supplemented], and it has specific physical properties. In terms of chemical structure, methyl and iodine atoms are substituted at specific positions in the benzene ring, giving them unique chemical activities.
This product is widely used in the field of organic synthesis. It can be used as a key intermediate to participate in the preparation of many complex organic compounds. Because of its high activity of iodine atoms, it can undergo nucleophilic substitution reactions and introduce other functional groups; the presence of methyl affects the distribution of molecular electron clouds and affects the selectivity of the reaction.
Preparation of 2 - Methyl - 4 - Iodophenol often requires delicate chemical synthesis paths. Through precise control of reaction conditions, such as temperature, reactant ratio, catalyst type, etc., to achieve high yield and purity. However, the synthesis process may face challenges such as impurity generation and harsh reaction conditions, requiring fine operation and optimization.

Physical & Chemical Properties

2 - Methyl - 4 - Iodophenol is also an organic compound. Its physical and chemical properties are related to chemical research. This substance is at room temperature or in a solid state, with a specific melting point, and its purity can be determined. Its melting point is the critical temperature at which a substance changes from solid to liquid state, which is of great significance for identification and purification.
In terms of chemical properties, because it contains phenolic hydroxyl groups and iodine atoms, phenolic hydroxyl groups are weakly acidic and can be neutralized with bases. Iodine atoms make the compound active in nucleophilic substitution reactions. And because of its methyl group, it affects the intermolecular force, which in turn affects its boiling point. For boiling point, the temperature at which a substance changes from liquid to gas state is related to its separation and purification. Only by studying these physical and chemical properties can researchers make good use of 2-Methyl-4-Iodophenol in the fields of organic synthesis and drug development, which will contribute to scientific progress and practical applications.

Technical Specifications & Labeling

There is a substance today, called 2-Methyl-4-Iodophenol. To clarify its technical specifications and identification (commodity parameters), it is necessary to observe it in detail.
Viewing its shape, pure color and uniform quality, this is the basis of the product phase. Its purity must be very high, and the impurities must be fine. As for the physical constants such as melting point and boiling point, it must also be accurate, which is the key to considering its quality.
On the label, the name is clear, and the molecular formula and structural formula are correct, so that the person who sees it can clarify its chemical quality. The commodity parameters are detailed, and the origin, batch, and preservation methods are all prepared to ensure its stability and suitability. In this way, 2 - Methyl - 4 - Iodophenol technical specifications and labels (commodity parameters) are also good.

Preparation Method

To prepare 2-Methyl-4-Iodophenol, it is necessary to explain its raw materials and production process, reaction steps and catalytic mechanism.
In terms of raw materials, o-cresol can be used as a starting material, which is a common chemical raw material. The production process is based on halogenation reaction, so that o-cresol reacts with iodine reagents.
The reaction steps are as follows: First, the o-cresol is placed in an appropriate solvent. The solvent should be stable and does not interfere with the reaction. Then, under a certain temperature and stirring conditions, the iodine reagent is slowly added. The temperature needs to be precisely controlled. If it is too high, the side reactions will increase, and if it is too low, the reaction will be slow.
In the catalytic mechanism, specific catalysts, such as certain metal salts, can be selected to accelerate the reaction process, reduce the activation energy of the reaction, and make the iodine atom more likely to replace the hydrogen atom of the phenolic hydroxyl ortho-position, so that 2-Methyl-4-Iodophenol can be efficiently prepared.

Chemical Reactions & Modifications

In recent years, the method of chemical research has focused a lot on 2-Methyl-4-Iodophenol. Its transformation is wonderful, and it is related to the yield and quality, and all workers have carefully studied it.
The method of the past, the transformation should be more inconvenient. If you use a certain method, although you can get it, the yield is quite low, and the quality is not high. The disturbance of impurities is also a serious problem, making it difficult to adapt to all needs.
All researchers think about changes and seek new things, hoping to improve the method of adaptation. Or adjust the temperature at the time, or use the agent easily, hoping to get better results. After repeated trials, there are ways to increase its yield and improve its quality. The amount of impurities has dropped sharply, and the purity of 2-Methyl-4-Iodophenol has increased, which can be used by various industries.
Our generation should continue this ambition, and we should make unremitting efforts to improve the chemical, hoping to go to the next level, so that this chemical will emit greater light and heat in the world.

Synonyms & Product Names

2 - Methyl - 4 - Iodophenol, the name of the thing that is transformed. The same as the trade name, it is important to study. The same can help us to clarify the name of the product, and the trade name indicates the market.
Examine the past, the name of the thing that is transformed, often because of the place. 2 - Methyl - 4 - Iodophenol, or there is a different context. In the research, the same can promote communication, so as not to confuse the name. As in the ancient books, the name of the same thing has a special name, but the study of it, one by one.
As for the name of the product, it involves the field of commerce. Merchants sell their products, each special name. This name is not only convenient, but also contains business. Therefore, the same product name is necessary for the research and application of 2-Methyl-4-Iodophenol. To be able to understand these two, it is even more important for this thing.

Safety & Operational Standards

2 - Methyl - 4 - Iodophenol Safety and Operation Code
2 - Methyl - 4 - Iodophenol is a chemical commonly used in chemical research. During the research process, safety and standard operation are of paramount importance.
Its chemical properties are lively, and it is easy to cause combustion or even explosion in case of open flames, hot topics or oxidants. Therefore, when storing, it must be placed in a cool and well-ventilated place, away from fire and heat sources, and should be stored separately from oxidants. Do not mix storage. When taking it, handle it with care to avoid damage to packaging and containers.
During operation, researchers must strictly protect. It is necessary to wear a self-priming filter dust mask to protect the respiratory system; wear chemical safety glasses to protect the eyes; wear anti-poison infiltration work clothes to prevent skin contact; wear rubber gloves to avoid hand contamination. The experimental operation should be carried out in a fume hood to ensure air circulation and reduce the concentration of harmful gases.
If you accidentally touch the skin, you should immediately remove the contaminated clothes, rinse with a lot of flowing water for at least 15 minutes, and then seek medical attention. If it splashes into the eyes, you need to immediately lift the eyelids, rinse thoroughly with a lot of flowing water or normal saline for at least 15 minutes, and seek medical attention as soon as possible. If you inhale accidentally, you should quickly leave the scene to a fresh air place to keep the respiratory tract unobstructed. If you have breathing difficulties, give oxygen, stop breathing, and immediately perform artificial respiration and seek medical attention. In case of fire, dry powder, carbon dioxide, sand and other fire extinguishing agents can be used to extinguish the fire, and water must not be used.
2 - Methyl - 4 - Iodophenol is a tool for research assistance, but only by following safety and operating standards can researchers be kept safe and the research work can be carried out smoothly.

Application Area

Today there is a product called 2 - Methyl - 4 - Iodophenol. This product is used in many fields.
In the field of medicine, it can be used as a raw material to help develop new drugs. Due to its special chemical structure, or antibacterial, anti-inflammatory and other effects, it is expected to relieve the pain of patients.
In the chemical industry, it can participate in the synthesis of special materials. Based on it, polymers with unique properties can be prepared for high-end material manufacturing to improve product quality and performance.
In scientific research and exploration, it provides researchers with key reagents. Help them explore the mechanism of chemical reactions, expand the boundaries of chemical cognition, and promote the progress of chemistry. It is actually widely used and of great value to all parties.

Research & Development

In modern times, chemistry has flourished, and the study of the properties and changes of various things has become more and more refined. Today there is a thing called "2-Methyl-4-Iodophenol", and we devote ourselves to studying it.
First study its structure, explore the shape of its atomic connections and bonds, and know the state of its molecules. Also observe its properties. Under different circumstances, observe its degree of melting and boiling, the state of fusion, and know how it should be with other things.
Study the method of its production, seek the way of high efficiency and purity. Improve the old technique and explore innovative methods, hoping to reduce its consumption and increase its production.
And think about its use, in the fields of medicine and chemical industry, it is expected to develop its growth. Or as a raw material for medicine, or as a chemical agent, the future is quite broad.
We should study unremittingly, hoping to understand its arcane, expand its use, promote the development of this chemical product, and contribute to the world.

Toxicity Research

Recently, the toxicity of 2 - Methyl - 4 - Iodophenol was studied in the laboratory. The appearance of this substance is unique, and its properties are unknown, so it needs to be investigated in detail.
Take an appropriate amount of this substance and observe it with various experiments. First observe its reaction with other substances, and see that when it encounters a certain liquid, its color changes and its state changes, which seems to be violent. Repeat with small animals and feed them with food containing this substance. Soon, the behavior of small animals is erratic, or irritable or tired, which shows that it has a disturbance to the state of living things.
The influence of it on the environment was also explored. When placed in water and soil, the nature of water and soil gradually changed, and plant growth was also hindered by it.
In summary, 2 - Methyl - 4 - Iodophenol is toxic and harmful to both organisms and the environment. Follow-up studies should be conducted on its toxicology and ways to avoid harm in order to preserve the safety of life and the environment.

Future Prospects

2 - Methyl - 4 - Iodophenol is also a chemical substance. I have no high hopes for my research yet.
This compound is unique, or can be used in multiple domains. In the way of research, it may be able to assist in research and development, so as to cure diseases and save lives. The field of materials, or the source of new materials, makes it solid and durable, and its use is low.
And the method of synthesis, if it can be refined, it will definitely improve the amount and reduce the cost. Not yet, we will reveal its secrets, and explore its possibilities with the method of science. Hope to be able to create this compound, which is the best step in the world, and make the world better. It is the heart of our researchers.

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Frequently Asked Questions

As a leading 2-Methyl-4-Iodophenol supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What is the chemical structure of 2-methyl-4-iodophenol?

2-Methyl-4-iodophenol, the analysis of its chemical structure is related to the category of organic chemistry. This compound is made of benzene ring as the base, and the benzene ring is a common six-membered ring structure in organic chemistry, with unique stability and chemical activity.
On the benzene ring, there are several substituents. One is methyl (-CH 🥰), which is connected to the No. 2 position of the benzene ring. Methyl is one of the alkyl groups, which has an electron-pushing effect and can affect the electron cloud density of the benzene ring, which in turn has an effect on the chemical properties of the compound. The other is the iodine atom (-I), which is located at the No. 4 position of the benzene ring. The iodine atom is relatively heavy and has a certain electronegativity. Its existence also affects the electron cloud distribution of the benzene Furthermore, there are phenolic hydroxyl groups (-OH), which are characteristic functional groups of phenolic compounds and are connected to the benzene ring. The hydrogen atom of the phenolic hydroxyl group has a certain acidity. Because of the high electronegativity of the oxygen atom, the O-H bond electron cloud is biased towards the oxygen atom, and the hydrogen atom is easily dissociated in the form of protons.
Overall, in the chemical structure of 2-methyl-4-iodophenol, the phenyl ring is the core, and the methyl group, iodine atom and phenolic hydroxyl group are used as substituents. Each of their properties and interactions jointly determine the chemical properties and reactivity of this compound. It may show unique application value in many fields such as organic synthesis and medicinal chemistry.

What are the main uses of 2-methyl-4-iodophenol?

2-Methyl-4-iodophenol has a wide range of uses. In the field of medicine, it is often a key intermediate for the synthesis of many drugs. For example, some drugs with antibacterial and anti-inflammatory effects, in the synthesis process, 2-methyl-4-iodophenol can participate in key reaction steps by virtue of its specific chemical structure. After a series of transformations, it lays the foundation for the generation of drug molecules with precise pharmacological activity.
In the field of materials science, it also shows unique value. It can be used as a starting material for the synthesis of polymer materials with specific functions. Through clever chemical means, it is connected to the polymer chain segment to give the material special optical, electrical or thermal properties. For example, through polymerization, it becomes one of the parts of photochromic materials, so that when the material is exposed to specific light, the color changes reversibly, and it has broad application prospects in the field of intelligent optical materials.
Furthermore, in organic synthetic chemistry, it is an extremely important building block. Chemists can use the activity of its phenolic hydroxyl and iodine atoms to carry out various classical organic reactions, such as nucleophilic substitution, coupling reactions, etc. By carefully designing reaction routes, organic compounds with complex structures and diverse functions are constructed with them as the core, which contributes an important force to the creation of new compounds and the development of organic synthesis methodologies.
In addition, in the fragrance industry, although it is relatively rarely used, the special smell derived from its unique chemical structure, when properly blended and modified, may provide novel ingredients for the development of new fragrances, enriching the variety and aroma level of fragrances.

What are the physical properties of 2-methyl-4-iodophenol?

2-Methyl-4-iodophenol, this is an organic compound. Looking at its physical properties, it often takes the form of a solid state at room temperature. Its melting point is within a specific range, about [X] ° C. The value of this melting point varies depending on factors such as specific purity.
When it comes to appearance, it is mostly white to light yellow crystalline powder. The subtle difference in its color is also related to the purity and impurities contained.
Its solubility is quite critical. In organic solvents, such as ethanol, ether, etc., it exhibits good solubility. This is due to the specific interaction between the molecular structure and the molecules of the organic solvent, which makes the two easily miscible. However, in water, its solubility is relatively low, because water is a polar solvent, and the polarity of 2-methyl-4-iodophenol molecule is not highly matched with water, so it is difficult to dissolve in water.
Furthermore, its volatility is relatively weak. Due to the influence of intermolecular forces, it is difficult to convert from solid or liquid to gaseous and escape at room temperature and pressure.
In addition, its density also has a specific value, about [X] g/cm ³. This density value is the inherent property of the compound, which is of important reference value for the measurement and separation of substances in related experiments and industrial applications.
The physical properties of 2-methyl-4-iodophenol have important applications in many fields such as organic synthesis and drug development, providing a basic basis for researchers to carry out relevant research and practice.

What are 2-methyl-4-iodophenol synthesis methods?

The synthesis method of 2-methyl-4-iodophenol, although the ancient book "Tiangong Kaiwu" does not contain the specific synthesis method of this compound, it can be deduced by referring to the principles and methods of organic synthetic chemistry at present.
First, 2-methylphenol is used as the starting material, and the iodine atom at the 4th position is to be introduced. The electrophilic substitution reaction characteristics of phenolic compounds can be exploited. The phenolic hydroxyl group is a strong donator group, which increases the electron cloud density of the phenyl ring and the para-position, which is conducive to the attack of electrophilic reagents.
The combination of iodine element ($I_2 $) and an appropriate oxidizing agent can be selected. If hydrogen peroxide ($H_2O_2 $) is used as an oxidizing agent, under acidic conditions, hydrogen peroxide can oxidize iodine ions to iodine positive ions ($I ^ + $), which is a strong electrophilic reagent and can attack the 4 position of the 2-methylphenol phenyl ring. Electrophilic substitution reaction occurs to generate 2-methyl-4-iodophenol. The reaction steps are as follows: in the reaction vessel, add 2-methylphenol, an appropriate amount of iodine elemental substance and solvent, such as glacial acetic acid, under low temperature stirring, slowly add hydrogen peroxide solution dropwise, control the reaction temperature and time, and after the reaction is completed, the target product is obtained through separation and purification.
Second, it can also be started from 4-iodoaniline. First, through the diazotization reaction, the amino group is converted into a diazonium salt, such as reacting with sodium nitrite in the presence of hydrochloric acid to form a diazonium salt. Then through the Sandmeier reaction or similar reactions, the cyanyl group is substituted for the diazonium group, and then the cyanyl group is hydrolyzed to the carboxyl group. Then through the decarboxylation reaction, the methyl group is introduced in combination with the methylation step to finally synthesize 2-methyl-4-iodophenol. This route is a bit complicated, but it is also a feasible method. During the synthesis process, the control of the reaction conditions at each step, the trade-off of the amount of reagents, and the separation and purification of the product are all key, which

2-methyl-4-iodophenol What are the precautions during storage and transportation?

2-Methyl-4-iodophenol is an organic compound. When storing and transporting, many matters need to be paid attention to.
First talk about storage. This compound is quite sensitive to light and heat, and should be stored in a cool and dark place. Due to light and high temperature, it can decompose and deteriorate, damaging its quality. The temperature of the warehouse should be strictly controlled, and it should not exceed 30 ° C, and it should be kept dry to avoid moisture, because moisture may also cause reactions and affect purity.
Furthermore, this compound has certain toxicity and irritation. When storing, it must be separated from oxidants, acids, bases, etc., and cannot be mixed. Because it encounters with these substances, or reacts violently, it causes safety hazards. At the same time, the warehouse should set up obvious warning signs to remind people entering and leaving to pay attention to protection.
As for transportation, it is necessary to ensure that the packaging is intact. Packaging materials should have good sealing and corrosion resistance to prevent leakage. During transportation, vehicles should also run smoothly to avoid bumps and vibrations and prevent packaging from breaking.
Transportation personnel should also be professionally trained to be familiar with the dangerous characteristics of 2-methyl-4-iodophenol and emergency treatment methods. In case of leakage during transportation, emergency measures should be taken immediately to evacuate people, isolate contaminated areas, and properly dispose of leaks to ensure the safety of personnel and the environment from pollution.
In summary, the storage and transportation of 2-methyl-4-iodophenol are subject to strict requirements in terms of temperature, humidity, light, packaging and personnel operation, so as to ensure its safety and quality.