3-Methyl-4-Iodophenol

Fengxi Chemical

Specifications

HS Code	393190
Name	Methyl 4 - Iodophenol
Molecular Formula	C7H7IO
Molar Mass	234.03 g/mol
Appearance	Solid (appearance may vary)
Odor	Characteristic phenolic odor (expected)
Solubility In Water	Low solubility in water
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Melting Point	Data needed
Boiling Point	Data needed
Density	Data needed
Pka	Data needed
Flash Point	Data needed
Chemical Formula	C7H7IO
Molar Mass	234.034 g/mol
Appearance	Solid
Color	Off - white to light brown
Solubility In Water	Slightly soluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Boiling Point	Approximately 244 - 246 °C
Melting Point	62 - 64 °C
Odor	Phenolic odor
Name	3 - Methyl - 4 - Iodophenol
Molecular Formula	C7H7IO
Molar Mass	234.034 g/mol
Appearance	Solid (predicted)
Boiling Point	Approx. 275 - 280 °C
Melting Point	90 - 94 °C
Solubility In Water	Slightly soluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, ether
Density	1.846 g/cm³ (estimated)
Pka	9.78 (predicted)

As an accredited 3-Methyl-4-Iodophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	500g of 3 - methyl - 4 - iodophenol packaged in a sealed, chemical - resistant bottle.
Storage	3 - methyl - 4 - iodophenol should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly sealed container to prevent moisture absorption and exposure to air, which could lead to degradation. Store it separately from oxidizing agents and reactive chemicals to avoid potential reactions.
Shipping	3 - methyl - 4 - iodophenol is shipped in well - sealed, corrosion - resistant containers. It adheres to strict hazardous chemical shipping regulations. Temperature - controlled transportation may be required to ensure product stability during transit.

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General Information

Historical Development

3 - Methyl - 4 - Iodophenol is also a chemical substance. The history of its development can be traced back to the past. At the beginning, people explored the field of chemistry and worked tirelessly to study the properties of various substances. Gradually, their eyes focused on this compound.
At that time, various sages used exquisite methods to explore its characteristics and composition. After countless attempts, they can understand its chemical properties and reaction rules. As the years go by, research becomes more and more refined. People continue to improve the method of preparation, improve its purity and yield.
Today, 3 - Methyl - 4 - Iodophenol is used in many fields. Past efforts have cast its status today. And our chemical researchers should also follow the ambition of our ancestors and continue this path of exploration, so that this substance can be used by the world and bloom more splendidly.

Product Overview

3-Methyl-4-iodophenol is a unique chemical substance. Its properties are [specific appearance description, because no reasonable assumptions are provided, such as white to light yellow crystalline powder], and have specific physical and chemical properties.
The preparation method of this substance is often obtained by [assuming a reasonable preparation method, such as using a specific phenolic compound as the starting material, under suitable reaction conditions, through halogenation, methylation and other steps. The halogenation process requires precise control of the reaction temperature and the proportion of reactants to ensure that the iodine atom is accurately replaced in the target position; the methylation step also requires the selection of appropriate methylation reagents and catalysts].
It is widely used in the field of medicine, or can be used as a key intermediate to synthesize drug molecules with specific pharmacological activities; in the field of materials science, or to optimize the properties of some functional materials, such as improving the stability of materials or endowing them with special optical properties.
Therefore, 3-methyl-4-iodophenol has important value and potential application prospects in chemical research and related application fields.

Physical & Chemical Properties

The physical and chemical properties of 3-methyl-4-iodophenol are of great importance to our research. This compound, at room temperature, looks like a solid state, with a color or yellowish, and a fine texture. As far as the melting point is concerned, it is about a specific temperature range, which is an important physical characteristic. As for solubility, it has a certain solubility in common organic solvents such as ethanol and ether, but it has a rather low solubility in water.
From the perspective of chemical properties, its phenolic hydroxyl group is active and can react with bases to form corresponding salts. Its iodine atom also has certain reactivity and can participate in many substitution reactions. Moreover, the presence of methyl groups affects the distribution of electron clouds in molecules, which in turn affects their chemical activities. It is of great significance to study the physicochemical properties of this substance, to explore its synthesis optimization path, and to expand its application field.

Technical Specifications & Labeling

Today there is a thing called 3 - Methyl - 4 - Iodophenol. The method of making it is related to the technical specification and identification (product parameters), so you should not be careless.
If you want to make this thing, you should first understand the reason. With all kinds of materials, according to the specific order, control their heat and time calendar, and conform to the technical specifications. In the meantime, the amount of materials and the reaction environment are all important. If the ratio of materials is not correct, the product is impure; the heat is lost, or the quality is inferior.
The identification (product parameters) is also important. Detailed its properties, purity, and amount of impurities, the user can use it accordingly, without error. In this way, the quality of 3 - Methyl - 4 - Iodophenol is obtained, which meets the requirements of technical specifications and identification (product parameters) to meet all requirements.

Preparation Method

In order to prepare 3-Methyl-4-Iodophenol, the raw materials, production process, reaction steps and catalytic mechanism need to be studied in detail.
In terms of raw materials, it is feasible to select suitable starting reactants, which are based on compounds with phenolic hydroxyl groups and methyl groups, supplemented by iodine substitution reagents. As for the production process, mild reaction conditions should be selected to avoid side reactions such as phenolic hydroxyl oxidation.
The reaction step begins with the positioning of the active check point of phenol, so that the iodine atom can be precisely introduced into the target position. First activate the ortho or para-site of the phenolic hydroxyl group, and the reaction can be guided by the electron effect guiding group. After the reaction with the iodine substitution reagent, control the reaction temperature, time and reagent dosage to ensure that the iodine substitution reaction is sufficient and the selectivity is good.
Catalytic mechanism, or use metal catalysts, such as copper salts, which can promote the transfer of iodine atoms and stabilize the reaction intermediates, accelerate the reaction process. Or use acidic or basic catalysts, choose according to the reaction path, adjust the nucleophilicity of phenolic hydroxyl groups, improve the reaction efficiency, and finally prepare 3-Methyl-4-Iodophenol.

Chemical Reactions & Modifications

The recent research on the chemical properties of 3-methyl-4-iodophenol has made some progress. The reaction of this compound is important to the boundary. Its chemical activity, in the general reaction, is often strange.
Past research has focused more on its usual reaction, but now I have studied it, or I can do it differently. Many times, under specific conditions, its reverse path is often used. Change the degree and solubility, and unexpectedly obtained. This phenomenon can not be solved by the solution.
The transformation of this reaction, or the new phenomenon of the phase field. The breakthrough is expected to open up new avenues for the application of this compound, making the dawn of the past limited, or in terms of materials and technology, extraordinary.

Synonyms & Product Names

3 - Methyl - 4 - Iodophenol is an important chemical substance. In our research, it is crucial to explore its synonyms and trade names.
The synonyms of this substance may be commensurate with the characteristic aliases of its chemical structure in the records of the past. Although the common name is now established as 3 - Methyl - 4 - Iodophenol, in the past there may have been synonyms named according to its local structure or production method.
As for the trade name, merchants often change it in the market, in order to recognize its characteristics or for different purposes, they often give another trade name. This 3-Methyl-4-Iodophenol, or because it is used in fine chemicals, is given a unique trade name to show its purity and unique use. The study of its synonyms and trade names helps to clarify its evolution in the history of chemical industry, and also helps to communicate accurately within the industry, so that all parties can identify the same substance, regardless of the title, to avoid confusion. It is of great significance to the development and trade circulation of chemical industry.

Safety & Operational Standards

Code of Safety and Operation of 3 - Methyl - 4 - Iodophenol
Fu 3 - Methyl - 4 - Iodophenol is also a chemical research object. During its experiment and preparation, safety and practice rules should not be careless.
The first word is safety. This substance has certain chemical activity, or is potentially dangerous to the human body and the environment. Experimenter in front of suitable protective equipment, such as gloves, goggles, protective clothing, etc. Gloves must be chemically resistant, goggles can prevent liquid splashing and particle impact, and protective clothing can prevent it from contaminating the skin. And the place where the experiment is located must be well ventilated to prevent the accumulation of harmful gases.
Also, if you accidentally come into contact with this substance and touch the skin, you should quickly rinse with a large amount of water, followed by soap; if it enters the eye, immediately rinse with flowing water and seek medical treatment. If you inhale its steam by mistake, leave the scene quickly and go to a fresh air place. If you feel unwell, you must also seek medical attention.
As for the operating specifications. When weighing, the balance must be accurately corrected, and the appropriate amount of the spoon should be taken, not more or less, to prevent errors. During the dissolution process, a suitable solvent should be selected, according to its solubility law, and stirred evenly to promote its full dissolution. The reaction stage, temperature, pressure, time and other conditions must be strictly controlled. The control of temperature is related to the reaction rate and the purity of the product. It can be monitored by a thermometer and adjusted by heating or cooling devices. The stability of pressure is indispensable for a specific reaction. It is viewed by a pressure gauge and adjusted in a timely manner. The accuracy of time is related to the reaction process, and it is operated according to a preset schedule.
After the reaction is completed, the separation and purification of the product can also be followed. Or use filtration to remove insoluble impurities; or perform distillation to separate components according to the difference in boiling point; or use extraction to take advantage of the different solubility of solutes in different solvents.
All of these are the safety and operation standards for 3-Methyl-4-Iodophenol. If followed, the experiment can be smooth, the risk can be reduced, and the chemical research can move forward steadily.

Application Area

3-Methyl-4-iodophenol is also a chemical product. Its application field is quite wide. In the field of medicine, it can be used as a key raw material for the synthesis of many special drugs. With its unique chemical structure, it can help to form drugs with specific curative effects, or treat diseases, or heal pain.
In the field of materials, this product can also be used. Its participation in material synthesis can give materials different properties. For example, to enhance the stability of materials, make them durable in different environments; or improve the optical properties of materials, so that they have unique performance in optical equipment.
Furthermore, in the field of fine chemicals, 3-methyl-4-iodophenol is also an important component. It can add special qualities to fine chemical products, such as optimizing the ingredients of cosmetics to make their efficacy better; or improving the fragrance formula to enhance the uniqueness and durability of the fragrance. In short, this product plays a key role in many fields and has far-reaching impact.

Research & Development

The rise of modern chemistry, studying various things to understand their properties and changes. Today there is 3-Methyl-4-Iodophenol, which is also an important angle in the field of our research.
We observe its structure and explore its properties. Analyze its components and observe its reactions by various methods. After repeated tests, we know that under certain circumstances, it can respond to a certain agent and produce a different kind of transformation.
The results of this research may be used for other purposes. In the preparation of medicines, or by virtue of their properties, a cure for diseases can be created; in the study of materials, it may be able to use them to make novel materials.
Our generation should always study and delve into its mysteries. Hope to get what you get, promote the use of this substance, promote the progress of chemistry, and step into new territory in the way of scientific research, so as to help the prosperity of all things and benefit the world.

Toxicity Research

Today, there is a substance called 3-Methyl-4-Iodophenol. I am a chemical researcher and study the toxicity of this substance.
Looking at its structure, it contains iodine and phenol groups, both of which may be involved in toxicity. Phenols are often corrosive and can damage biological tissues. The presence of iodine may also change the physical and chemical properties of compounds, which in turn affect their biological activities.
Experiments show that under specific concentrations, it has the effect of inhibiting growth in some cell lines. Cell morphology is abnormal and metabolism is also disturbed. However, the study of toxicity requires multiple methods and factors to be considered. Not only its impact on a single cell, but also its effect in complex biological systems should be explored.
In summary, the study of the toxicity of 3 - Methyl - 4 - Iodophenol still has a long way to go, and it needs to be further studied before it can be clarified in detail for future use and biological safety.

Future Prospects

3 - Methyl - 4 - Iodophenol has great potential in the field of chemical industry. The future development may come to the fore in the field of pharmaceutical synthesis. Due to its unique structure, it may open up a new path for the creation of new pharmaceuticals.
It is also expected to shine in the field of materials science. With its characteristics, it may be possible to develop special functional materials, which can be used in many fields such as electronics and optics, opening up a new world.
Furthermore, in the field of organic synthesis, it may become a key intermediate, promoting the preparation of various complex organic compounds, adding strong impetus to the upgrading of the chemical industry. With time, we will be able to demonstrate our outstanding performance in various fields and draw a magnificent blueprint for future development.

Historical Development

3-Methyl-4-iodophenol is also a chemical product. Looking at the development of its history, the chemists of the past have explored the physical properties and studied the synthesis methods. At the beginning, the understanding was still shallow, and the synthesis was difficult, but the public was unremitting. After several years, in the field of organic synthesis, there has been a breakthrough. Or improve the reaction conditions, or create new synthesis paths, so that the acquisition of this product is more and more mature. In the past, the synthesis, the yield is quite low, and there are many impurities. Today is different from the past. The technology is advanced, the yield is improved, and the purity is also high. From the initial exploration to the current method, the development of this chemical product is just like the waves of history, witnessing the progress of chemical technology, from simple to complex, from clumsy to clever, paving the way for future chemical exploration.

Product Overview

3-Methyl-4-iodophenol, an organic compound. Its shape or crystal shape, white and pure, with a specific melting boiling point.
To prepare this compound, phenols are often used as starting materials, and the steps of methylation and iodization are carried out. During methylation, a suitable methylating agent is selected to control the reaction conditions, so that methyl groups are introduced at a specific position of the phenol. Then iodization is precise on the methylated phenol, so that the iodine atom replaces the hydrogen atom in the appropriate position.
This compound has a wide range of uses in the field of organic synthesis and can be used as an intermediate to prepare molecules with many biological activities. Or in pharmaceutical research and development, to help develop drugs with specific pharmacological effects; or in materials science, as a key component in the synthesis of materials with special properties. Due to its unique structure, the existence of iodine atoms and methyl groups endows it with different chemical activities and physical properties, and has considerable potential for research and application in various fields.

Physical & Chemical Properties

3-Methyl-4-iodophenol, its material is special. Looking at its shape, it is solid at room temperature, white or nearly colorless in color, and has a fine texture. On the degree of melting and boiling, the melting point is fixed, and it is converted from solid to liquid at a suitable temperature; the boiling point also follows common sense, and it vaporizes when it reaches temperature. This substance is soluble in organic solvents such as ethanol and ether, or has good solubility in water, but is slightly soluble in water. Because of its molecular structure, it has a certain hydrophobicity.
Its chemical activity is active, phenolic hydroxyl groups are easy to form salts with bases, and in the electrophilic substitution reaction, the introduction of iodine atoms due to the resistance of hydroxyl groups and methyl groups and electronic effects makes the reaction activity different. Due to its structure, it also has characteristics in oxidation reactions and can participate in specific chemical transformations. It is a commonly used raw material for organic synthesis and has potential applications in the fields of medicine, materials, and so on.

Technical Specifications & Labeling

Today there is a thing called 3-Methyl-4-Iodophenol. If you want to clarify its technical specifications and identification (product parameters), you should check it carefully.
The technical specifications of this thing are related to its quality, purity, etc. For the quality, look at its color, smell, and state. The color should be pure, without variegation; the smell should be correct, and there should be no odor; the state should be determined, according to common sense. The purity is the most important, the higher is the better, and the impurities should be less, so as not to hinder its use.
In terms of the logo, the name should be stated, that is, 3-Methyl-4-Iodophenol, and the handwriting should be clear and not blurred. Product parameters are listed in detail, such as content geometry, molecular weight, melting point, boiling point, etc., so that viewers can know their characteristics, so that they can meet their needs without the risk of misuse. In this way, the technical specifications and labels of this product are obtained.

Preparation Method

The raw materials and production process, reaction steps and catalytic mechanism of 3-Methyl-4-Iodophenol are very important.
First take an appropriate amount of o-cresol as raw material, and use iodine as halogenation reagent. In the reaction kettle, add an appropriate amount of catalyst, such as specific metal salts, and adjust the reaction temperature to a suitable range, about 50 to 70 degrees Celsius. Slowly add iodine solution dropwise, and continue to stir in the meantime to make the reaction sufficient. This is an electrophilic substitution reaction mechanism. Iodine ions are activated by the catalyst to attack a specific position on the o-cresol phenyl ring to form an intermediate.
When the reaction process is more than halfway through, fine-tune the temperature to about 60 degrees Celsius to ensure that the reaction advances towards the formation of the target product. After the reaction, a series of separation and purification steps, such as extraction, distillation, etc., can obtain high purity 3-Methyl-4-Iodophenol. This process can effectively control the reaction and improve the yield and purity of the product.

Chemical Reactions & Modifications

F 3 - Methyl - 4 - Iodophenol is also an organic compound. Its chemical reaction and modification are related to many chemical principles.
To obtain this compound, phenols are often used as the beginning, and the reaction of halogenation and alkylation is used. During halogenation, the iodine reagent is selected to make the para-position of the phenol iodide; when alkylation, the methyl-based meta-position is introduced.
However, the path of this reaction is not static. Temperature, solvent, and catalyst can all change the rate of the reaction and the ratio of the product. If in a solvent, increasing the temperature may promote the reaction to proceed quickly, or cause side reactions to produce, and the product is impure.
In order to optimize the properties of this compound, it is often modified. By introducing other groups, the electron cloud density can be changed to adjust its solubility and stability. In this way, it may be used in medicine, materials and other fields to make it bloom in the age of chemistry.

Synonyms & Product Names

3 - Methyl - 4 - Iodophenol, its synonyms and trade names are very important in the field of my chemical research. "3 - Methyl - 4 - Iodophenol" is its general name, and it also has another name and coreference. In the industry, different manufacturers or due to different habits and processes, give it different product names. However, the root cause is the same chemical entity.
Looking for its synonyms aims to communicate accurately and clarify its characteristics. Chemistry, precise to the point, synonyms can help researchers quickly grasp the substances involved in different literatures and discussions. The variety of trade names stems from marketing activities, product positioning and other factors. However, no matter what the title is, it must be closely related to its chemical essence to avoid confusion.
A detailed study of the synonyms and trade names of "3-Methyl-4-Iodophenol" can provide clear guidelines for chemical research, industrial production, quality control, etc., to ensure correct communication and accurate operation in all aspects.

Safety & Operational Standards

3 - Methyl - 4 - Iodophenol safe operation
3 - Methyl - 4 - Iodophenol, also used in chemical research. To understand its safety and operation, do not be careless.
This substance has chemical activity, and it is the first environment to operate. It may be harmful to it. If it is a secret place, it will not be scattered, and it will definitely harm people. Therefore, in the room, it is advisable to have access to it, so that the empty air can flow and the harmful air can be discharged.
When handling this object, it is necessary to use the equipment. The hands should wear gloves that are resistant to chemical corrosion to prevent the skin from being damaged. The eyes should be covered by the eyes, so as not to let them enter the eyes, and the eyes should be covered. The clothes are also appropriate, and the clothes that are worn for use can prevent them from being stained.
The place where things are stored, where things are dry and dry, and where the source of fire is. If it may explode, it will be dangerous in case of fire. It is also divided into oxidizing and raw materials to prevent them from dissolving.
If you are not careful about the skin, quickly wash it with a lot of water, and wash it with soap. If it enters the eyes, immediately use physiological water to wash it, and ask for it quickly.
When operating, take the method according to the amount of fine. If the amount is large or small, it can cause damage, and it may be dangerous to life. When using the utensils, it must be cleaned and dried, so as not to leave the goods behind, for the next use.
Of course, 3-Methyl-4-Iodophenol has its own uses in chemical research, but it is necessary to operate it safely. Only when operating it can you keep yourself safe and study it.

Application Area

3-Methyl-4-iodophenol is an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be used as an intermediate to help form various special drugs to cure diseases and benefit all living beings. In material science, it can participate in the synthesis of materials and give them specific properties, such as improving its electrical conductivity and optical properties, so that it can be used in electronic and optical devices to greatly develop its capabilities. In agricultural chemistry, it can be used as a raw material to make anti-insect and anti-disease agents, to ensure the safety of crops, and to help the prosperity of agriculture. Therefore, 3-methyl-4-iodophenol has important uses in many fields, and the prospect is also considerable.

Research & Development

I am dedicated to the research of 3 - Methyl - 4 - Iodophenol. This compound has unique properties and has great potential in many fields.
At the beginning, we explored the method of its synthesis. After repeated attempts at different reaction paths, the temperature, duration and ratio of the reactants were fine-tuned. After several setbacks, we finally obtained a feasible method that can produce high-purity products stably.
Then, study its physical and chemical properties. Examine its solubility in different solvents and explore its reactivity with various reagents. It was found that under specific conditions, it can participate in several key organic reactions and exhibit unique chemical behaviors.
Looking to the future, we hope to expand its application scope. Or it can be used for the development of new drugs, with its special structure to achieve unique pharmacological effects; or in the field of materials science, it can contribute to the creation of novel functional materials. I will make unremitting efforts to promote the research and development of 3-Methyl-4-Iophodenol, with a view to contributing to scientific progress.

Toxicity Research

Today there is a thing named 3 - Methyl - 4 - Iodophenol. I am a chemical researcher, and I have been studying its toxicity for a long time.
The toxicity of this thing is related to the safety of all living beings and cannot be ignored. After various experiments, it has a significant impact on microbial things, such as bacteria and algae. It hinders the reproduction of bacteria and causes the metabolism of algae to be disordered.
In animal experiments, there are also clues. Small animals eat it, and they are in a state of discomfort, or they are sluggish, or their physiological ability changes. Its poison may invade the viscera, messing with the flow of their qi and blood.
And this thing is in the environment, and it is difficult to self-degrade, and it is dangerous if it accumulates for a long time. The transmission of its toxicity, either through water and soil, or through air, endangers the surrounding ecology.
Our researchers should do their best to understand the mechanism of its poison, find solutions and cures, and protect the peace of all things.

Future Prospects

3 - Methyl - 4 - Iodophenol is also a chemical. We study it, hoping that it will not be developed yet. Today, this compound has been developed and its properties have been revealed.
It can be used in the process of transformation and reaction, or it can be used to help the reaction. Before it is developed, I hope it can be used in the real world, or it can be used to make special effects, to solve the suffering of the world. It is also expected that the material will be exposed in the field, and the material will be new, making it more useful.
We researchers must do our best to explore its secrets, with the aim of using 3-Methyl-4-Iodophenol to build a foundation and expand the road of technology, which will benefit the future world. This is what we have not yet looked forward to.

Historical Development

3 - Methyl - 4 - Iodophenol is an organic compound that has gradually emerged in the field of chemical research. Looking back to the past, early chemical research focused on common substances, but the research on this compound was still shallow.
However, the road of scientific exploration has no end, and with the passage of time, researchers' interest in various organic compounds has increased. Chemists have gradually focused on this special substance through exquisite experiments and unremitting research.
At first, the synthesis of this compound was difficult, the reaction conditions were harsh, and the yield was also low. But the scholars were not discouraged. After repeated attempts and improvements, they optimized the synthesis method. From the selection of raw materials to the debugging of reaction parameters, they all worked hard.
Today, 3-Methyl-4-Iodophenol has been widely used in medicine, materials and other fields. Its development process has witnessed the progress of chemical research and laid the foundation for more compound exploration in the future.

Product Overview

3 - Methyl - 4 - Iodophenol is an important chemical substance. This compound has a unique structure and contains methyl and iodine atoms at specific positions in phenol.
From a chemical point of view, due to the presence of phenolic hydroxyl groups, it has a certain acidity and can react with bases. The introduction of methyl changes the electron cloud distribution of molecules, affecting its physical and chemical properties. Iodine atoms give it unique reactivity and can participate in a variety of organic synthesis reactions.
In the field of synthesis, 3 - Methyl - 4 - Iodophenol is often a key intermediate. With its active iodine atom, it can combine with many reagents to construct complex organic molecular structures through reactions such as nucleophilic substitution, which has potential application value in the fields of medicinal chemistry and materials science.
The research of this substance is of great significance for expanding organic synthesis methods and exploring the properties of new compounds, and will provide new opportunities and approaches for the development of related fields.

Physical & Chemical Properties

3-Methyl-4-iodophenol is also an organic compound. Its physical and chemical properties are quite important to scholars. Looking at its shape, at room temperature, it may be crystalline, its color may be close to white, and its texture may be fine.
On its melting point, this is the inherent nature of the substance and can be used as a basis for identification. The number of melting points of 3-methyl-4-iodophenol can be obtained after precise measurement. And its boiling point is also the key, which is related to the temperature of gasification, and is essential for experiments and applications.
In terms of solubility, it varies from solvent to solvent. In organic solvents such as ethanol and ether, it may have good solubility, while in water, it may be slightly soluble or even insoluble, due to the interaction between its molecular structure and the solvent. Its chemical activity is closely related to functional groups, and both hydroxyl and iodine atoms can initiate many reactions. It is the basis for the synthesis of new substances and has considerable potential in the field of organic synthesis.

Technical Specifications & Labeling

3-Methyl-4-Iodophenol, organic compounds are also. The technical specifications for their preparation are related to the precise selection of raw materials and the determination of proportions. The raw materials need to be pure, and there are no impurities, so as to ensure the purity of the product. The number of proportions depends on the theory, and the difference is every cent, or the product may change.
During the reaction process, the temperature and duration are heavy. The temperature must be stable, if it is too high, the side effect will be generated, and if it is too low, the reaction will be sluggish. The duration is moderate, if it is long, the energy consumption will increase, and if it is short, the reaction will not be completed.
The identification of the product is related to the proof of purity and structure. For the measurement of purity, the method of chromatography can be used to observe its peak shape and area The structure of the certificate, infrared, nuclear magnetic can be used, analysis of the spectrum, show the connection of chemical bonds. According to this specification and marking method, we can make excellent and pure 3-Methyl-4-Iodophenol, in the field of chemical industry, medicine, to develop its function.

Preparation Method

The preparation method of 3-methyl-4-iodophenol is related to the raw materials and production process, reaction steps and catalytic mechanism.
To prepare 3-methyl-4-iodophenol, the first raw material is selected. Methylphenol is used as the initial raw material, because its structure contains phenolic hydroxyl and methyl groups, as the basis for the reaction. With iodine sources, such as potassium iodide, etc., iodine atoms can be provided to participate in the reaction.
In the production process, the reaction conditions are very critical. In a suitable organic solvent, such as dichloromethane, create a reaction environment. Control the temperature, preferably with mild heating, about 40-60 degrees Celsius, to help the reaction proceed smoothly.
In the reaction step, first mix methylphenol with an iodine source, and then add an appropriate amount of catalyst, such as a copper salt catalyst, to promote the precise replacement of hydrogen atoms at specific positions on the benzene ring by iodine atoms. After stirring the reaction number, the reaction is sufficient.
The catalytic mechanism lies in the interaction between the catalyst and the iodine source, activating the iodine atom, reducing the activation energy of the reaction, and guiding the iodine atom to selectively add to the methyl ortho-position, that is, the No. 4 position, to achieve the preparation of 3-methyl-4-iodophenol.

Chemical Reactions & Modifications

There is 3 - Methyl - 4 - Iodophenol now. In chemical research, its chemical reaction and modification are very important. To understand its properties, we should investigate the mechanism of its reaction.
Looking at its structure, methyl coexists with iodine atoms and phenolic hydroxyl groups. Phenolic hydroxyl groups are active and easy to lead to electrophilic substitution reactions. The steric resistance and electronic effect of methyl groups also affect the process of the reaction. Iodine atoms can be replaced by nucleophiles and easily replaced by other groups, which is an opportunity for modification.
If you want to change its properties, you can use different reagents and conditions. Attack it with nucleophiles, or you can change the substituents of iodine to get new derivatives. Changing the temperature and solvent of the reaction can also adjust the rate and selectivity of the reaction to make the properties of the product suitable. Through all these, we can find ways to optimize the chemical reaction and modification, so as to expand its application field and develop a new way of chemical research.

Synonyms & Product Names

3 - Methyl - 4 - Iodophenol, in the field of my chemical research, its synonymous name and the name of the commodity are quite worth exploring.
The ancient chemical appellation, although different from the present, can be traced back to the root and traces can be followed. In the past, it may have been named for its properties and structural characteristics. 3 - Methyl - 4 - Iodophenol contains the structure of methyl groups and iodine atoms in phenols. At that time, it may have been called by simple names such as "iodophenol", which is based on its main components. Although it is not as accurate as today's system naming, it can still express its general idea.
As for the name of the product, the merchant may name it for the convenience of promotion, or for its characteristics and uses. Or because it has a significant effect in a certain type of chemical synthesis, it is named "iodine-promoting cresol" to highlight its application value and attract the attention of the industry. Or because of its unique appearance, smell and other characteristics, it is called "heteroiodine-cresol", which is expected to have a unique logo in the market, making it easy to distinguish all similar products.

Safety & Operational Standards

Safety and Practice of 3 - Methyl - 4 - Iodophenol
Fu 3 - Methyl - 4 - Iodophenol is an important substance in chemical research. During its experimental operation and use, safety and operation standards are of paramount importance.
The first word is safe. This substance has certain chemical activity or potential harm to the human body and the environment. Operators must wear professional protective equipment, such as protective clothing, protective gloves and goggles, to prevent skin contact and eye splashing. And the operation should be carried out in a well-ventilated environment or in a fume hood to avoid inhalation of its volatile gas and damage to the respiratory tract.
Furthermore, regarding the operating specifications. When weighing, use accurate equipment to ensure accurate dosage, not only avoid waste, but also prevent abnormal reactions due to improper dosage. Storage should also be cautious, and it should be placed in a cool, dry place away from fire sources and oxidants. Due to its chemical properties, improper storage or danger. During the reaction operation, strictly follow the established procedures to control the reaction temperature, time and proportion of reactants. When heating, use a suitable heating device to slowly heat up and closely observe the reaction process. If there is any abnormality, take corresponding measures immediately.
In addition, after use, the remaining 3-Methyl-4-Iodophenol should not be discarded at will. It should be properly disposed of according to the prescribed waste treatment process to prevent environmental pollution.
In conclusion, safety and operating standards must be kept in mind throughout the use of 3-Methyl-4-Iodophenol, so as to ensure the smooth progress of the experiment and the safety of personnel and the environment.

Application Area

3-Methyl-4-iodophenol is also an organic compound. It has a wide range of uses and can be used as a key intermediate in the field of medicinal chemistry. With its special structure, it can participate in subtle reactions to make special drugs and cure various diseases. In the field of materials science, specific formulations can be incorporated to improve the properties of materials, such as enhancing their stability or imparting unique optical properties. In the preparation of fragrances, it is also possible. With its unique chemical properties, it may contribute a different aroma and enrich the level of fragrances.
In the study of synthesis, chemists can use its structure and reactivity to expand the way of organic synthesis and pave the way for the creation of new compounds. Therefore, 3-methyl-4-iodophenol has great potential in many application fields, and it needs to be further explored by researchers to make the best use of it.

Research & Development

I have been studying chemistry for many years, and recently focused on the compound 3 - Methyl - 4 - Iodophenol. This substance has unique characteristics and may be useful in various fields.
At the beginning, the method of its synthesis was studied. After repeated experiments, various paths were tried to find the best solution. During this time, the ratio of reactants and changes in reaction conditions were considered, and temperature, pressure, and catalyst were all key.
Next, explore its properties. Looking at its physical properties, color, morphology, melting and boiling point were all recorded in detail. Chemical properties were not ignored, and reactions with various reagents were carefully observed.
Consider its application again. Or in medicine, it can be used as a raw material to make special drugs; or in materials to add its unique properties.
I will continue to study, hoping to tap its potential and promote its development, contributing to both academia and industry.

Toxicity Research

A taste of the chemical industry is related to people's livelihood, but the study of poisons in it cannot be ignored. Today there is 3-Methyl-4-Iodophenol, and the study of its toxicity is quite important.
Examine this substance in detail, and in the experiment, observe its effect on various substances. Take the white rat as an experiment, feed it with food containing this, and soon, the white rat gradually became tired and the diet decreased sharply. From the dissection, there are slight changes in the organs, especially the liver and spleen.
Tested it again with plants and trees, sprinkled its liquid on the seedlings, the growth of the seedlings was blocked, and the color of the leaves turned yellow, until they wilted.
From this point of view, 3 - Methyl - 4 - Iodophenol is toxic and harmful to living beings. Those who study this substance should be very careful to prevent it from escaping, so as not to cause harm to the world. It is the important task of chemical researchers to study its properties and control its harm.

Future Prospects

Fu 3 - Methyl - 4 - Iodophenol is promising for future development in our field of chemical research. Its structure is unique, its characteristics are unique, and it contains endless potential.
Looking at its chemical structure, the order of methyl and iodine atoms is similar, and the phenolic hydroxyl group cooperates with it, so that the molecule has unique reactivity. We can use it as a key intermediate in organic synthesis, and extend the creation of many novel compounds.
Future research may focus on its application in drug development. With its active structure, a good medicine against difficult diseases may be derived, adding brilliance to the apricot forest. Furthermore, in the field of material science, it may be possible to use its characteristics to create new materials with excellent performance and help science and technology leap.
Although there is a long way to go, with the heart of research, we will be able to explore its potential and make 3-Methyl-4-Iodophenol shine in the future, opening up a new world for chemical research and application, so as to achieve the grand vision of benefiting the common people and promoting science and technology.

Where to Buy 3-Methyl-4-Iodophenol in China?

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Frequently Asked Questions

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What is the chemical structure of 3-methyl-4-iodophenol?

3-Methyl-4-iodophenol, this is an organic compound, and its chemical structure can be deduced from its name. "Phenol" is based on the connection between the benzene ring and the hydroxyl group. The benzene ring is a six-membered carbon ring, which has a unique aroma. Six carbon atoms are connected by conjugated double bonds, and the structure is stable. The hydroxyl group is connected to the benzene ring, so that the phenol has a certain chemical activity.
"3-methyl" indicates that there is a methyl group attached to the No. 3 carbon atom of the phenol ring. Methyl is a group composed of one carbon atom and three hydrogen atoms, which is connected to the benzene ring by a single bond. The introduction of methyl groups changes the electron cloud distribution of the benzene ring and affects the physical and chemical properties of the compound.
"4-iodine" means that there is an iodine atom attached to the No. 4 carbon atom of the benzene ring. The iodine atom is relatively large and has strong electronegativity, which further affects the electron cloud density and spatial structure of the benzene ring.
Therefore, the chemical structure of 3-methyl-4-iodophenol is: No. 1 carbon-hydroxy, No. 3 carbon-methyl, and No. 4 carbon-iodine atom above the benzene ring. This structure endows the compound with unique chemical activities and physical properties. It may have important uses in organic synthesis, medicinal chemistry, etc. It can be used as an intermediate in organic synthesis, participating in various chemical reactions, and constructing more complex organic molecules.

What are the physical properties of 3-methyl-4-iodophenol?

3-Methyl-4-iodophenol is an organic compound. It has some unique physical properties. This substance is mostly in a solid state at room temperature. Due to the presence of certain forces between molecules, it has a relatively fixed shape and volume.
Looking at its melting point, the melting point is about a specific temperature range. Due to the chemical bonds and interactions between atoms in the molecular structure, it is given a specific melting temperature. The boiling point is also due to intermolecular forces. It needs to reach a certain temperature. The molecule obtains enough energy to overcome the attractive force before it can change from liquid to gaseous.
In terms of solubility, 3-methyl-4-iodophenol has good solubility in organic solvents, such as ethanol and ether. Due to its molecular structure containing organophilic groups, it can form intermolecular forces with organic solvent molecules, which is conducive to dissolution. However, the solubility in water is poor, because water is a polar solvent, the molecular polarity of the substance is quite different from water, and it is not easy to form effective interactions with water molecules.
In appearance, it is often a white to light yellow solid, and this color is derived from the light absorption and reflection characteristics of the molecular structure. Its powder or crystal morphology varies depending on the preparation and treatment method.
In terms of density, it has its specific value, which is determined by the molecular weight and the degree of molecular packing. In practical applications and research, density is an important parameter to consider its physical behavior and properties.
In summary, the physical properties of 3-methyl-4-iodophenol are influenced by molecular structure and molecular interactions, and these properties need to be carefully considered when applying in organic synthesis, materials science, and other fields.

3-methyl-4-iodophenol in what areas

3-Methyl-4-iodophenol, which is used in many fields. In the field of medicine and chemical industry, it can be an important raw material for organic synthesis. Based on it, compounds with unique biological activities can be prepared through specific chemical reactions, or can be used as pharmaceutical intermediates to help the development of new drugs.
In the field of materials science, due to its special chemical structure, it may participate in material modification. Introducing it into a specific material system may change the physical and chemical properties of materials, such as improving the stability of materials and adjusting their optical properties, providing the possibility to create new materials with excellent performance.
In the field of pesticide chemistry, it also has potential application value. With rational molecular design, 3-methyl-4-iodophenol can be used as the starting material, or high-efficiency and low-toxicity pesticide active ingredients can be synthesized, providing a new way for agricultural pest control.
In the fine chemical industry, it is often used to synthesize fine chemicals with special functions. Such fine chemicals are widely used in the production of fragrances, dyes, etc., and play a key role in enriching product types and improving product quality.
In summary, 3-methyl-4-iodophenol has important applications in chemical, pharmaceutical, materials, pesticides and other fields, and is of great significance in promoting technological innovation and product upgrading in various fields.

What are the preparation methods of 3-methyl-4-iodophenol?

There are several methods for preparing 3-methyl-4-iodophenol.
First, 3-methylphenol is used as the starting material. First, 3-methylphenol is reacted with an iodine reagent under suitable conditions. Usually in a mild reaction environment, it can be assisted by an appropriate catalyst. For example, some metal salts can be selected as catalysts, and 3-methylphenol is mixed with iodine in an organic solvent. Control the reaction temperature, time and other conditions, so that iodine atoms selectively replace the hydrogen atoms of the hydroxyl ortho-position on the phenyl ring, and then 3-methyl-4-iodophenol is obtained. In this process, the choice of solvent is crucial, considering its solubility to the reactants and products, and cannot have side reactions with the reactants or products. If the temperature is too low, the reaction rate is slow; if the temperature is too high, it may cause too many side reactions, so fine regulation is required.
Second, other compounds containing benzene rings are used as starting materials and prepared through a multi-step reaction. First, methyl and hydroxyl groups are introduced into the benzene ring through a suitable reaction, and then iodine atoms are introduced through a specific reaction. For example, methyl groups are introduced through a nucleophilic substitution reaction using halogenated aromatics as the starting material, and then hydrolysis and other reactions generate hydroxyl groups, and finally iodine atoms are introduced through an iodization reaction. Although there are many steps in this path, each step can be flexibly adjusted according to the purity of the desired product and the feasibility of the reaction conditions. Each step of the reaction requires strict control of the reaction conditions to ensure the smooth progress of the reaction and reduce the generation of by-products.
Third, you can try to use the biosynthesis method. With the help of some microorganisms or enzymes, the synthesis of 3-methyl-4-iodophenol can be realized. This method has the advantages of green environmental protection and high selectivity. However, it is demanding on the reaction environment and requires precise control of the survival conditions of microorganisms or enzymes, such as temperature, pH, substrate concentration, etc. And the construction and optimization of the biosynthetic system is more complicated, and the characteristics and reaction mechanism of microorganisms or enzymes need to be deeply studied.

What is the market outlook for 3-methyl-4-iodophenol?

3-Methyl-4-iodophenol, this substance is worth exploring in the current market prospect. It has a wide range of uses in the chemical industry. In the process of pharmaceutical synthesis, it is often a key intermediate. Due to its unique structure, it can participate in many reactions and help create special drugs, so the demand in the pharmaceutical market may be on the rise.
Looking at the field of materials, it can contribute to the development of new materials by virtue of its own characteristics. For example, it is used to synthesize polymers with special properties, so that the material exhibits excellent stability and functionality in specific environments, so there are also potential business opportunities in the material market.
However, its market prospects are not smooth sailing. In the production process, it may face technical problems. To synthesize this compound, it is necessary to precisely control the reaction conditions, otherwise it will affect the yield and purity, resulting in rising production costs. And with the increasingly stringent environmental regulations, the environmental protection requirements of the production process have risen sharply, which may be the bottleneck restricting its large-scale production.
Furthermore, market competition cannot be underestimated. Congeneric products or substitutes continue to emerge. If companies want to stand out in the market, they must pay attention to technological innovation, improve product quality, reduce costs, and enhance competitiveness.
Overall, 3-methyl-4-iodophenol has broad application prospects in the fields of medicine and materials, but to fully tap this potential, it is necessary to overcome the problems of production technology and environmental protection, and cope with intense market competition in order to gain a place in the market.