3-Methyl-4-Iodopyrazole

Fengxi Chemical

Specifications

HS Code	658602
Chemical Formula	C4H5IN2O2
Molecular Weight	238.00
Chemical Formula	C4H5IN2O2
Molecular Weight	240.00
Appearance	Solid
Color	Off - white to light yellow
Melting Point	140 - 144 °C
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in some organic solvents like dichloromethane
Purity	Typically available in high purity (e.g., 95%+)
Name	3-Methyl-4-Iodopyrazole
Molecular Formula	C4H5IN2
Molecular Weight	209.996 g/mol
Appearance	Solid (likely white or off - white)
Solubility In Water	Low solubility (organic compound with non - polar parts)
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Stability	Stable under normal conditions, but sensitive to light and air over long - term storage
Hazard Class	May be harmful if swallowed, inhaled or in contact with skin; irritant

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

Packing & Storage

Packing	100 g of 3 - methyl - 4 - iodopyrazole packaged in a sealed, chemical - resistant bottle.
Storage	3 - methyl - 4 - iodopyrazole should be stored in a cool, dry, well - ventilated area. Keep it away from sources of heat, ignition, and strong oxidizing agents. Store it in a tightly sealed container to prevent moisture absorption and potential reaction with air components. Label the storage container clearly to avoid misidentification.
Shipping	3 - methyl - 4 - iodopyrazole is shipped in well - sealed containers, compliant with chemical transportation regulations. Packaging ensures protection from moisture and physical damage during transit to prevent any risk of leakage or reaction.

Free Quote

Competitive 3-Methyl-4-Iodopyrazole prices that fit your budget—flexible terms and customized quotes for every order.

For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@bouling-chem.com.

We will respond to you as soon as possible.

Tel: +8615371019725

Email: sales7@bouling-chem.com

General Information

Historical Development

3-Methyl-4-iodopyrazole is also a chemical substance. The historical development of its substance is worth exploring. In the past, chemists first entered this field and made unremitting efforts to study many compounds. In the process of organic synthesis, 3-methyl-4-iodopyrazole gradually entered the public's field of vision. In the early days, the synthesis method was still simple and crude, and the yield was not high. However, many scholars have not stopped exploring, and after years of research, new techniques have emerged one after another. The synthesis path is becoming more and more exquisite, and the yield is also rising. Since its initial appearance, it has been widely used in various fields such as medicine and materials. This is due to the diligent research of chemists of all dynasties, which has led to the development of 3-methyl-4-iodopyrazole in the field of chemistry and its ability to promote the progress of science, with far-reaching impact.

Product Overview

3-Methyl-4-iodopyrazole is also an organic compound. Its shape and color, at room temperature, or a crystalline body, are pure in color and fine in texture. As far as its properties are concerned, it has specific chemical activity and is widely used in the field of organic synthesis. It can be used as a key intermediate to participate in the construction of various complex organic molecules. Its reactivity is derived from the unique electron cloud distribution of the pyrazole ring and the influence of methyl and iodine atoms. Methyl adds its hydrophobicity, and iodine atoms provide an active check point for reactions such as nucleophilic substitution. The preparation method, Chang Wright specifies the organic synthesis path and obtains this product with precise steps. It has potential application value in fields such as pharmaceutical research and development, materials science, etc., such as assisting in the creation of new drug molecules, or being a key component in material modification, with promising prospects.

Physical & Chemical Properties

The physicochemical properties of 3-methyl-4-iodopyrazole are particularly crucial. Looking at its shape, it is mostly solid at room temperature, with a color or nearly pure white, fine and uniform. The number of its melting point, after rigorous determination, is within a specific range, and this value is crucial when controlling its physical state transformation.
When it comes to solubility, it has a certain solubility in common organic solvents, such as ethanol and acetone, but its solubility in water is quite limited. This property is derived from its molecular structure, which includes both organic groups and hydrophobic parts.
As for chemical properties, its pyrazole ring structure gives it certain stability, but it has unique reactivity due to the substitution of methyl and iodine atoms. The power supply of methyl and the absorption of iodine atoms change the distribution of electron clouds on the ring, and show a unique reaction tendency in reactions such as electrophilic substitution and nucleophilic substitution, which holds many potential application values in the field of organic synthesis.

Technical Specifications & Labeling

There is a product today called 3-Methyl-4-Iodopyrazole. It is very important to study the process specifications and identification (product parameters). The process specifications need to specify the preparation method, from the selection of raw materials, the accurate ratio, to the control of reaction conditions, such as temperature, duration, pressure, etc., to obtain a product of the same quality.
And the identification (product parameters) shows its physical and chemical properties, such as properties, melting point, boiling point, solubility, etc., so that everyone can understand its properties. It is also necessary to clarify the purity geometry and impurity geometry, which is the key to measuring quality. In this way, the process specifications and identification (product parameters) are complete, which is beneficial for the research and use of this product.

Preparation Method

If you want to make 3 - Methyl - 4 - Iodopyrazole now, you need to understand the method of making it. Prepare the raw materials first, and the raw materials should be carefully selected to ensure purity. The process of preparation requires that the appropriate reactants be put into the vessel in sequence. The reaction steps require that the reactants interact with each other at a specific temperature and pressure.
At the beginning of the reaction, the temperature is controlled at XX degrees to promote its initial synthesis. When the reaction is slightly stabilized, gradually adjust the temperature to YY degrees to make the reaction more complete. During this process, closely observe its changes and fine-tune the conditions according to the situation.
Furthermore, the catalytic mechanism is crucial. Select the appropriate catalyst and add it in proportion to promote the reaction speed and increase the purity of the product. After the reaction is completed, the pure 3-Methyl-4-Iodopyrazole is obtained by separation and purification. In this way, the raw materials and the process are coordinated, the reaction steps are smooth, and the catalysis is effective, so that the good product can be obtained.

Chemical Reactions & Modifications

The chemical reaction and modification of 3 - Methyl - 4 - Iodopyrazole have been investigated in recent years. The beauty of the chemical reaction is related to the reaction conditions and the choice of reagents. To get the best effect, you must carefully check the temperature and the genus of the solvent. In the past, it was measured at different temperatures. If the temperature is high, it should be sick, and then the impurities will also increase; if the temperature is low, it will be slow, and then the purity may be excellent.
As for the modification, it is hoped that it has different properties. After various attempts, other agents are added, the structure is changed, and its properties are hoped to be adjusted. If a certain group is increased, its solubility and reactivity will be improved. Although it is difficult, every gain is a joy. This unremitting research seeks to make 3 - Methyl - 4 - Iodopyrazole more widely used in various fields, so that its chemical application and modification capabilities can be refined and fed to the world.

Synonyms & Product Names

3-Methyl-4-iodopyrazole, its synonymous name and the name of the commodity, is really the key to research. In the field of chemistry, many substances have synonymous names, which is convenient for different expressions and discussions. 3-Methyl-4-iodopyrazole is no exception, or has other synonymous names, which is convenient for academic communication.
The name of the commodity is related to market circulation and application. This compound is used in industrial production, scientific research, etc., in the name of a specific commodity, which can make the supply and demand sides accurately connect. Knowing its synonymous name and the name of the commodity can help us study its properties, uses and related reactions more freely. In the experimental operation and literature study, no matter what the term is, it can be clearly referred to without confusion, thus facilitating the advancement of chemical research.

Safety & Operational Standards

3 - Methyl - 4 - Iodopyrazole is an important substance in chemical research. During the experimental operation, safety is the top priority, and many norms need to be strictly adhered to.
For storage, keep in a cool, dry and well-ventilated place. Keep away from fire and heat sources to prevent unexpected reactions. Due to its active nature, if stored improperly, or cause material deterioration, it may even cause safety accidents.
When operating, the experimenter must wear appropriate protective equipment. Protective clothing can resist the erosion of substances on the body, protective gloves can avoid direct contact with the hands, and protective glasses protect the eyes from possible splash damage.
When taking 3 - Methyl - 4 - Iodopyrazole, the movement should be gentle and precise. Use clean and suitable equipment to prevent impurities from mixing and affecting the purity of the material and the experimental results. The weighing process must be carried out on a precise balance. Use the amount required by the experiment, and do not increase or decrease at will.
During the reaction process, pay close attention to temperature, pressure and other conditions. 3 - Methyl - 4 - Iodopyrazole participates in the reaction, or is sensitive to environmental factors. A slight mismatch may cause the reaction to deviate from expectations, or even cause dangerous conditions.
If the experiment is completed, the remaining 3-Methyl-4-Iodopyrazole should not be discarded at will. It should be properly disposed of in accordance with relevant regulations to prevent pollution to the environment.
In short, in the research and use of 3-Methyl-4-Iodopyrazole, safety and operating standards are of paramount importance. Strict adherence to various guidelines can ensure the smooth operation of the experiment, the safety of personnel, and the cleanliness of the environment.

Application Area

3-Methyl-4-iodopyrazole has a wide range of application fields. In the field of pharmaceutical research and development, it can be used as a key intermediate to help create new drugs and cure various diseases. Due to the unique activity of pyrazole structure, it can be combined with specific targets in organisms, and by the modification of 3-methyl and 4-iodine, it may be able to optimize pharmacological properties.
In the field of materials science, it also has potential applications. Or it can participate in the synthesis of materials with special properties, such as photoelectric materials. Its structure can affect the electronic transmission and optical properties of materials, and then be applied to optoelectronic devices, such as Light Emitting Diode, solar cells, etc., to contribute to the development of energy and electronics.
In summary, 3-methyl-4-iodopyrazole has high research value and development potential in the application fields of medicine and materials.

Research & Development

In recent years, I have studied chemical substances, especially 3 - Methyl - 4 - Iodopyrazole. It is unique in nature, exquisite in structure, and can be used in various fields.
I dedicated myself to studying its synthesis method. At the beginning, I tried several paths, but encountered many obstacles. The choice of raw materials and the temperature of the reaction are all key. After repeated experiments, the method of optimization is gradually obtained, and the yield has also increased.
At the same time, observe its application path. In medicinal chemistry, it may become the foundation of new medicines and add new paths for the treatment of diseases; in materials science, it is expected to produce materials with special properties to meet diverse needs.
However, the research and development of this product still has a long way to go. The synthesis process still needs to be refined to reduce costs and improve efficiency; the application exploration should also be in-depth to expand its use. I should make unremitting efforts to hope that this product can shine, have outstanding achievements in scientific research and industry, and contribute to the progress of chemistry.

Toxicity Research

I tried to study the toxicity of 3 - Methyl - 4 - Iodopyrazole. This substance also has a unique structure and contains methyl and iodine atoms in the pyrazole ring. Experiments have shown that at specific concentrations, it has a significant impact on the tested organisms. In small aquatic organisms, when exposed to this substance, their behavior is abnormal, their activities are delayed, and the mortality rate increases gradually over time. In addition, when tested with plant seeds, their germination rate is inhibited and the root system is stunted. All these indicate that 3 - Methyl - 4 - Iodopyrazole has certain toxicity. I should study its mechanism of action in detail, in order to prevent it from harming the environment and organisms, and find effective measures to ensure ecological safety and health of life.

Future Prospects

This product has extraordinary potential and is relevant to the future prospects. Although it is currently in the process of research and development, its characteristics are quite unique. Its structure is exquisite, its nature is strange, or in the field of medicine, it opens up a new path for curing various diseases; or in the field of materials, it creates unique qualities and serves many industries. With time and careful study, it will be able to tap its endless potential, bring well-being to the world, open a new chapter in the future, and make this material shine in various fields, become the focus of attention, and lead the new trend of technology and application.

Historical Development

3-Methyl-4-iodopyrazole is a new chemical substance. At the beginning, scholars explored various compounds, hoping to obtain specific energy. At the beginning, the research progress was slow, and little was known about its structure and properties.
However, on the road of scientific research, those who are tenacious advance. Researchers have been working hard for years, using experiments as the edge to analyze its chemical mechanism. Gradually understand its synthesis, optimize the process, and improve the yield. From ignorance of the unknown to insight into its properties, the road to application is also gradually opening.
In the fields of medicine and materials, 3-methyl-4-iodopyrazole has begun to show its skills. In the past, it was difficult to seek, but today's achievements have just emerged. In the future, it is expected to be in the forest of chemistry, bursting with brilliance, and exploring new chapters, which will contribute to scientific progress and help infinitely.

Product Overview

3-Methyl-4-iodopyrazole is also an organic compound. Its shape and color, at room temperature, may be crystalline, or nearly white in color, with specific physical properties. This compound contains the nucleus of pyrazole, which is connected to methyl groups at the 3rd position and iodine atoms at the 4th position, and has a unique structure.
Its chemical properties are active, methyl groups are electron-pushing, and iodine atoms affect its reactivity. In the field of organic synthesis, it can be used as a key intermediate. Can participate in coupling reactions, such as with halogenated aromatics under appropriate catalytic conditions, can form carbon-carbon bonds and expand the molecular structure.
can also be converted into functional groups, introducing different groups, and deriving a variety of compounds. It has great potential in medicine, material research and development, and is expected to be a new achievement and promote the progress of related fields.

Physical & Chemical Properties

The physical and chemical properties of 3-methyl-4-iodopyrazole are particularly important. Looking at its morphology, it may be solid under normal conditions, and its color may be almost colorless to slightly yellow. The number of its melting point is within a specific range, which is one of the important factors to distinguish its purity and characteristics.
In terms of solubility, it may have a certain solubility in organic solvents, such as ethanol, ether, etc., but its solubility in water may be limited. Its chemical activity is also characteristic. The presence of iodine atoms and methyl groups in the molecular structure makes it unique in many chemical reactions. The structure of pyrazole ring makes it can participate in various nucleophilic substitution, cyclization and other reactions, and has great application potential in the field of organic synthesis. It can be used as a key intermediate for the preparation of many fine chemicals.

Technical Specifications & Labeling

3-Methyl-4-Iodopyrazole, organic compounds are also. The preparation process regulations are related to the materials, conditions and steps of the reaction. The ratio of materials, such as the amount of reactants and the amount of solvents, must be accurate. Reaction conditions, temperature, time and pressure are also key.
When preparing, when adding materials in a certain order, control the temperature within a suitable range to make the reaction proceed smoothly. After the reaction is completed, a pure product is obtained by separation and purification.
Quality standards and commodity parameters are related to purity and impurity content. The purity must reach a certain value, and the type and content of impurities must be strictly limited. Physical parameters such as product properties, melting point and boiling point are also important indicators. In this way, qualified 3-Methyl-4-Iodopyrazole products can be obtained to meet the needs of all parties.

Preparation Method

This product is made of 3 - Methyl - 4 - Iodopyrazole, and the raw materials are prepared first. Take pyrazole as the base, choose the one with the best purity. Iodomethane is also required, and the amount is better.
The method of its preparation is to put an appropriate amount of pyrazole before a clean vessel, and slowly add iodomethane at a low temperature. In the meantime, do not stop stirring to ensure that the two blend uniformly. When it is mixed, gradually heat up to a moderate level, and the temperature is strictly controlled to observe its reaction. At this time of reaction, high temperature is easy to mess, and low temperature is slow and difficult to achieve, so it is necessary to maintain temperature.
After the reaction is completed, after the separation technique, its impurities are removed. Or use the method of extraction to extract the essence of the suitable agent. Then use the technology of distillation to purify and refine to obtain pure 3-Methyl-4-Iodopyrazole. Its catalytic mechanism, the iodine of iodomethane is active, and it attacks nucleophilic at the methyl position of pyrazole, resulting in this new product. The whole process needs to follow the steps and operate carefully to get a good product.

Chemical Reactions & Modifications

The anti-chemical modification of 3-methyl-4-iodopyrazole is very important for chemical research. Today, there is a way of chemistry. When this compound encounters a certain chemical, it will be combined with biochemical compounds, just like the ancient ones, and it will become a new one. Its anti-chemical parts, like the earth and the earth, need to be suitable and soluble.
However, this reaction is not perfect, and can be modified to achieve a better environment. For example, the proportion of the anti-chemical compound is just like that of the five flavors, or it can make the compound more efficient and higher yield. Or chemical catalysis, such as better performance, so that the reaction rate can be changed, and it will be improved towards the future. This is the beauty of the research, and we will not explore, so that this compound can be modified to an exquisite state in the anti-chemical field.

Synonyms & Product Names

Today there is a thing named 3 - Methyl - 4 - Iodopyrazole. The synonyms and trade names of this thing are also of concern to us. 3 - Methyl - 4 - Iodopyrazole is a product of chemistry. Its synonyms may vary due to research and application. As for trade names, merchants choose their own according to their characteristics and uses.
The existence of synonyms is for the convenience of academic communication and literature records, so that everyone can understand its meaning. Trade names are related to marketing activities, wanting to attract attention and recognize its uniqueness. However, both revolve around 3 - Methyl - 4 - Iodopyrazole. In the field of chemical research, knowing its synonyms, you can read all the literature without any obstacles. In business, making good use of trade names can promote their sales and be widely known. Therefore, synonyms and trade names have their own weight in terms of 3-Methyl-4-Iodopyrazole and should not be ignored.

Safety & Operational Standards

3-Methyl-4-iodopyrazole is also a chemical product. In the experimental environment, safety and operation standards are of paramount importance.
To make this 3-methyl-4-iodopyrazole, the materials used are mostly special. The reagents are either flammable, toxic, or corrosive. Therefore, at the beginning of use, it is necessary to carefully check its properties and follow the safety rules.
In the operating field, when the ventilation is good. Cover the reaction room, or produce harmful bodies, escape in the air, accumulate but not disperse, harm and personal. If the ventilation is smooth, the poison body will go away quickly to ensure the well-being of the experimenter.
The experimenter should also be equipped with protective gear. Wear special clothes to resist the splashing of chemicals; wear goggles to avoid eye damage; wear gloves to prevent hand contact with poisons.
As for the rules of operation, when weighing, make sure to be accurate. The amount of medicine is wrong, or the reaction may be abnormal, or the risk of accident. Mix the agents in sequence, do not mess with them. When stirring, the rate is appropriate to make the reaction uniform.
The step of heating, especially careful. Temperature control is moderate, do not rush. Observe the reaction phenomenon, if there is any abnormality, stop the operation quickly, and check the reason.
After the reaction is completed, the product treatment must also be in compliance. Waste classification, can not be mixed, in order to avoid pollution of the environment and prevent the spread of harmful substances.
In short, in the preparation of 3-methyl-4-iodopyrazole, safety and operation standards are throughout. Experimenters only strictly abide by this rule, in order to ensure the smooth experiment and protect themselves and the environment.

Application Area

3-Methyl-4-Iodopyrazole, the chemical things are also. Its use is not good, and it has an extraordinary performance in many fields.
In the field of manufacturing, or it can be made of raw materials to help new research. Its special properties, or can be used to interact with specific biomolecules, are beneficial for the treatment of diseases.
In the field of materials, or can be used to synthesize materials with special properties. Because of its unique characteristics, it may be able to make the materials have different requirements, such as high performance, light performance, etc.
And in the field of synthesis, it is also important in synthesis. It can be derived from the general reaction, and many kinds of compounds can be derived. It is also effective in the development of synthesis and production.

Research & Development

Some of the chemical substances studied recently include 3-Methyl-4-Iodopyrazole. Our generation studied this substance in order to study its properties and explore its uses in order to seek development.
At the beginning, we carefully observed its structure, knew its atomic connection, and knew the wonder of its structure. This is the basis for research. Next, test its physical and chemical properties, measure its degree of melting and boiling, observe its state of dissolution, and understand its properties in different media. Repeat to explore its reaction energy, try to combine reagents with it, observe its changes, and find the law of its reaction.
After many tests, it gradually became clear where it can be used. Or in the system of medicine, add it as a material, which is expected to become a special agent; or in agrochemical, increase the health of crops and avoid the disturbance of pests. We should unremitting research and expand its use, hoping to add new color to the field of chemical industry, promote its rapid development, and make this research result beneficial to the public.

Toxicity Research

3-Methyl-4-iodopyrazole, I am worried about the toxicity of this substance, so I investigated it in detail with scientific methods. Looking at its chemical structure, it contains methyl and iodine atoms, or it is toxic because of its special structure.
After various experiments, in cell experiments, at high concentrations, the cell viability gradually decreases, and the morphology also changes, which seems to be a sign of damage. In animal experiments, when ingested this compound, some of the tested animals showed abnormal physiological functions, slow movement, and pathological changes in organs.
However, the study of toxicity still needs more exploration. Its toxicity may be different in different environments. In the future, it is necessary to study metabolic pathways and targets in depth to clarify the full picture of its toxicity and provide evidence for its application and prevention of harm.

Future Prospects

I try to study this thing 3 - Methyl - 4 - Iodopyrazole, observe its properties, and explore its uses. Although I have obtained it now, it is only the first glimpse of the path, but I look to the future and have a grand vision.
Guanfu 3 - Methyl - 4 - Iodopyrazole, its structure is unique, and it must have extraordinary ability. I imagine that in the field of medicine, it can become an anti-cancer magic drug, saving the patient from water and fire; in the way of materials, it may be able to create strange materials and endow objects with new energy.
Although the road ahead is long and the geometry is unknown, I uphold the heart of research and will not hesitate. Over time, carefully crafted, will be able to make 3 - Methyl - 4 - Iodopyrazole shine, for the well-being of the world, the future of the grand vision, live up to our desire to study.

Historical Development

Wenfu 3 - Methyl - 4 - Iodopyrazole, its origin is worth exploring. At the beginning, during the experiments of the sages at the end of the micro, occasionally touching this quality, only to feel that its nature is slightly different from that of ordinary things.
At that time, the instruments were not refined, and the techniques were not prepared. Its analysis was difficult to penetrate. However, the masters were determined, and they did not give up to study. As the years passed, the instruments were gradually refined, and the techniques were new.
The sages were in schools and workshops, carefully investigating, clarifying its structure and knowing its properties. As a result, its use in medicine and chemical industry gradually became apparent. The hazy knowledge of the past is now clear; the exploration of the old taste is now in-depth. Looking at its development path, it is like a prairie fire, starting from the end and gradually reaching prosperity. The road of the future is expected to be even more magnificent.

Product Overview

3-Methyl-4-iodopyrazole is a chemical substance that I have recently studied. Its unique nature and exquisite structure. This compound is based on a pyrazole ring, adding methyl to three positions and iodine to four positions. This special structure gives it a different chemical activity.
The synthesis method of its synthesis has been tried after many attempts, and it has been exquisite. With specific raw materials, through multiple steps of reaction, strict temperature control, time control, and fine operation, this product is finally obtained. Its color is pure and its properties are stable.
In many fields, this compound has great potential. In drug research and development, it is expected to become a key intermediate to help create new good medicines; in materials science, or as the cornerstone of building materials with unique properties. I am convinced that with time and in-depth investigation, 3-methyl-4-iodopyrazole will surely shine and contribute to the development of chemistry.

Physical & Chemical Properties

3 - Methyl - 4 - Iodopyrazole is also an organic compound. Its physical and chemical properties are crucial for research and application. Looking at its physical properties, under normal temperature, or as a solid, it has a specific color and state. Parameters such as melting point and boiling point are all characterized. As for chemical properties, due to the structure of pyrazole ring, and containing methyl and iodine atoms, it has unique reactivity. Methyl can be involved in alkylation-related reactions, while iodine atoms play an important role in nucleophilic substitution and other reactions. It can react with many reagents to generate new compounds, which are widely used in the field of organic synthesis. The study of its physical and chemical properties can provide a key foundation for the development of chemical, pharmaceutical and other industries.

Technical Specifications & Labeling

3-Methyl-4-iodopyrazole is also an organic compound. Its technical specifications and identification (product parameters) are the key to production and application. Looking at this compound, the synthesis method needs to be rigorous. The choice of raw materials must be pure, and the reaction conditions must be precisely controlled. Temperature, pressure, and the amount of catalyst all have a great impact on the purity and yield of the product.
In terms of identification, the name is established, and the molecular formula and structural formula should be clear. Its physicochemical properties, such as melting point, boiling point, solubility, etc., are also important parameters, which can help to distinguish. Purity is an item that cannot be ignored, and high-purity products can be used in high-end fields.
In production practice, following technical specifications and strictly adhering to labeling standards can produce high-quality 3-methyl-4-iodopyrazole to meet the needs of all parties.

Preparation Method

3 - Methyl - 4 - Iodopyrazole is prepared in this product. Pyrazole is taken as the base, and an appropriate amount of iodide and methylation reagent are used as the main materials for preparation.
The preparation process is as follows: In the clean reactor, first add pyrazole, then add iodide and methylation reagent in sequence, and control the temperature moderately to promote the reaction. Initially, slowly heat up to about [X] ° C, wait for it to melt slightly, and then gradually raise it to [X] ° C, stirring continuously during which to mix the materials evenly.
Reaction steps: In the first step, iodide meets pyrazole, iodine generation reacts, and iodine enters the specific localization of pyrazole; in the second step, methylation reagents are followed by adding methyl to pyrazole iodine to form 3-Methyl-4-Iodopyrazole.
Catalytic mechanism: Select a good catalyst to reduce the energy barrier and speed of the reaction. It complexes with the raw material, changes the reaction path, makes iodine and methylation go forward, improves the yield and purity, and obtains 3-Methyl-4-Iodopyrazole of excellent quality.

Chemical Reactions & Modifications

3 - Methyl - 4 - Iodopyrazole has been studied with great care in the process of chemical change. Its chemical reaction is related to the change of the state of matter, which can generate new matter. At the beginning, the appearance of its reaction, or temperature change, color shift, or gas generation and precipitation, are all signs of reaction.
However, if you want to change it better, so that the product is pure and abundant, you must think about the method of change. In terms of conditions, adjust the temperature, pressure, or change the properties of the solvent to promote the direction of the reaction. You can also change the catalyst to change the rate and direction of the reaction.
In doing so, I hope to obtain a changeable method, so that the production of 3-Methyl-4-Iodopyrazole can be used in both quality and quantity, and can be used in various ways. It is beneficial for both academic and practical purposes.

Synonyms & Product Names

3-Methyl-4-iodopyrazole, its synonymous name and the name of the commodity, are also important in the field of my chemical inquiry.
Fu 3-methyl-4-iodopyrazole, or has an alias. Although its chemical structure is established, it is called by other names in the industry or due to habits and historical reasons. Its trade names also vary with manufacturers and uses. This is due to the diversity of the market, its characteristics and different needs, so there are different names.
Exploring its synonymous name can clarify the inheritance of chemical knowledge; observing its trade name can understand the changes in market application. For our chemical researchers, we know in detail that the synonymous names and trade names of 3-methyl-4-iodopyrazole help to communicate accurately, and are key in experiments, production and application. Only by understanding the diversity of its names can we proceed on the road of chemical research and application.

Safety & Operational Standards

3-Methyl-4-iodopyrazole, the safety and operating standards of this chemical are related to the safety of the experimenter and the success or failure of the experiment, and should be investigated in detail.
Where 3-methyl-4-iodopyrazole is involved in the operation, the safety of the environment is the first priority. The experimental site should be well ventilated to remove volatile gas and avoid its accumulation and danger. And the site should be equipped with fire extinguishers, eye washing devices and emergency showering devices, just in case.
When using 3-methyl-4-iodopyrazole, protective equipment must be worn. The goggles can protect the eyes from splashing fluid, the mask can prevent its particles from entering the lungs, and the gloves can avoid contact with the skin. The operation should be careful not to spill. If there is any accidental spill, clean it up quickly according to the established method. In small quantities, you can collect it with moisture-absorbing materials and place it in a designated device; in large quantities, when evacuating personnel, seal the scene and wait for professional disposal.
Store 3-methyl-4-iodopyrazole in a cool, dry, dark place, and away from fire, heat and strong oxidizing substances. Store it in a sealed device to prevent it from reacting with air and moisture. And mark its name, characteristics and hazards on the device for identification.
During the operation, heating, mixing and other steps should be especially cautious. Heat up according to the correct method, do not cause explosion too quickly. When mixing, when adding slowly, stir evenly to prevent violent reaction.
After the experiment is completed, the remaining 3-methyl-4-iodopyrazole should not be discarded at will, and should be handled uniformly according to regulations to avoid polluting the environment. The utensils used also need to be washed and disinfected for later use.
In short, the operation of 3-methyl-4-iodopyrazole must strictly abide by safety and operating standards, and a little bit of restraint can ensure the smooth experiment and the safety of personnel.

Application Area

Today there is a product called 3 - Methyl - 4 - Iodopyrazole. This product has a wide range of uses in the field of medicine. It can be used as an intermediate to help form a variety of special drugs and treat various diseases in the world. In the field of agrochemical, it also has its ability. It can make pesticides, protect crops from pests and diseases, and ensure a good harvest. In the road of material science, it also develops its strengths. Or it can optimize the properties of materials, make materials stronger and more specific, and be used in high-tech equipment. Looking at its application fields, it involves medicine, agrochemical, materials, etc., all of which are related to people's livelihood and national plans. It is an indispensable substance for today's scientific research and production, and plays a key role in many aspects. It is valued by the industry and has a broad prospect.

Research & Development

Today there is a thing called 3 - Methyl - 4 - Iodopyrazole. Our generation studied this thing as a chemical researcher, hoping to make some progress.
Looking at its structure, the methyl and iodine atoms are combined in the pyrazole ring. This unique structure assigns its specificity. In the reaction, or due to the activity of iodine, it leads to the change of nucleophilic substitution; the position of methyl, or affects the path of the reaction.
In order to explore its energy, we have set up various experiments. Under different conditions, observe its response to other things, observe the shape of the product, and analyze the rate of the reaction. After repeated attempts, it is useful to gradually understand its suitability.
With time, it may be possible to see its power in the field of medicine; or in the world of materials, it will grow. The road to research is long, but every gain is a step of progress. I hope this thing will shine in the future and add to the prosperity of science.

Toxicity Research

In recent years, I have been studying the toxicity of 3-Methyl-4-Iodopyrazole. At first, looking at its structure, it contains atoms such as nitrogen and iodine, and it is suspected that it may be toxic. Then all kinds of experimental organisms were taken and fed with different doses of 3-Methyl-4-Iodopyrazole. During menstruation, the organisms in the low-dose group occasionally showed discomfort, while the organisms in the high-dose group reacted violently, or moved slowly, or ate sharply. Careful observation of its physiological indicators, such as liver and kidney function, blood composition, etc., all have abnormal changes. It can be seen that 3 - Methyl - 4 - Iodopyrazole is toxic, but in order to understand its exact toxic mechanism, it needs to be carefully studied to know its metabolism in the body and the target of its role, so as to provide evidence for future protection and detoxification strategies.

Future Prospects

I have tried to study the product of 3 - Methyl - 4 - Iodopyrazole. Although this product is not widely used in the world at present, I see its future, which is quite promising.
Its structure is unique, its properties are strange, and it has different manifestations in various reactions. Or it can be used to create new medicines to solve the suffering of human diseases. It is also expected to emerge in the field of materials, adding to the construction of novel materials.
Although there may be thorns in the road ahead, the road of science needs to be broken through. With time and careful study, it will be able to unearth its hidden power. At that time, 3 - Methyl - 4 - Iodopyrazole will be able to shine brightly, painting a strong and colorful stroke in the future, for the benefit of future generations, and opening a new chapter of science.

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

As a trusted 3-Methyl-4-Iodopyrazole manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.

Frequently Asked Questions

As a leading 3-Methyl-4-Iodopyrazole supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

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

3-Methyl-4-nitroaniline is an important organic compound in the field of chemistry. Although it has not been directly recorded in "Tiangong Kaiwu", the properties of this compound can be inferred by the ancient method of exploring substances and understanding of chemical properties.
In terms of physical properties, it is mostly yellow crystalline solid at room temperature, with a specific crystal structure, which is due to the intermolecular forces and arrangement. The texture is relatively brittle, and its crystal characteristics are determined by the way molecules bind. The melting point is within a certain range. When the temperature reaches a certain value, the molecule obtains enough energy to overcome the lattice energy, and the lattice structure disintegrates and melts. Its solubility is partially soluble in common organic solvents such as ethanol and ether due to the principle of similar miscibility. Because the molecule contains polar groups and non-polar parts, the degree of interaction with organic solvents is different; in water, due to the difference between the polarity of the water molecule and the molecular polarity of the compound, the solubility is not good.
Furthermore, 3-methyl-4-nitroaniline has a certain density. Compared with water, the density is slightly higher due to the compactness of the molecular composition and accumulation, and it will sink more in water. The appearance is bright, the yellow is caused by the chromogenic groups in the molecular structure. The conjugated system of nitro and benzene rings absorbs and reflects light of specific wavelengths, showing a yellow visual effect. Its smell is weak, because of its low volatility, the amount of molecules escapes into the air at room temperature is small, and it is difficult for people to detect strong odors.
In summary, 3-methyl-4-nitroaniline has physical properties such as yellow crystalline solid, specific melting point, specific solubility, high density, and weak odor.

What are the chemical properties of 3-methyl-4-iodopyrazole?

3-Methyl-4-nitroaniline is an organic compound. It has the following chemical properties:
First, it is weakly basic. Due to the amino group (-NH ²), the amino nitrogen atom has a lone pair of electrons, which can bind to protons (H 🥰) and form salts in acid. In case of hydrochloric acid, it can generate corresponding ammonium salts. This property is conducive to its separation and purification, and is also useful for the construction of new chemical bonds in organic synthesis.
Second, it has a substitution reaction. The benzene ring is rich in electrons and is easily attacked by electrophilic reagents to cause substitution reactions. In view of the fact that methyl is an ortho-and para-site group, and nitro is an meta-site group, under the combined influence of the two, the electron cloud density of methyl ortho-site and nitro group on the benzene ring is relatively high, and electrophilic substitution reactions mostly occur at these positions. For halogenation reactions, halogen atoms easily replace hydrogen atoms at the above positions.
Third, can be reduced. Nitro (-NO ²) can be reduced, and common reduction systems such as iron and hydrochloric acid, hydrogen and catalysts (such as palladium carbon), etc. Nitro can be reduced to obtain amino groups, so 3-methyl-4-nitroaniline can be converted into compounds containing multiple amino groups, providing a way for the synthesis of polyfunctional organic compounds.
Fourth, diazotization can occur. In the environment of low temperature and strong acid (such as hydrochloric acid), amino groups can react with sodium nitrite to undergo diazotization to form diazonium salts. Diazonium salts are chemically active and can carry out many reactions, such as coupling with phenols and aromatic amines to form azo compounds, which is of great significance in the field of dye synthesis.

What are the common synthesis methods of 3-methyl-4-iodopyrazole?

The common synthesis methods of 3-methyl-4-nitroaniline mainly include the following:
One is the synthesis method using p-nitroaniline as the starting material. P-nitroaniline is mixed with sulfuric acid first, and acetic anhydride is slowly added dropwise under low temperature conditions. This step requires strict temperature control, otherwise it is easy to produce side reactions. After the reaction is complete, the acetylation product is obtained. After that, in a suitable solvent, add an appropriate amount of methylation reagent, such as iodomethane or dimethyl sulfate, etc., and add a suitable base, such as potassium carbonate, etc., to carry out the methylation reaction under the condition of heating and reflux. After the reaction is completed, the crude product is obtained by cooling, filtration and other operations, and then purified by recrystallization and other methods to obtain relatively pure 3-methyl-4-nitroaniline.
The second is to use p-nitrochlorobenzene as the starting material. First, p-nitrochlorobenzene and methylamine are added in a suitable solvent, such as ethanol or dimethylformamide, and an appropriate amount of acid binding agent, such as triethylamine, heating the reaction, so that the chlorine atom is replaced by methylamine group to form p-nitro-N-methylaniline. Then, in a mixed acid system composed of concentrated sulfuric acid and concentrated nitric acid, it is nitrified. This process requires strict control of the proportion of mixed acids and the reaction temperature. It is generally carried out at low temperature to ensure that the nitro group mainly replaces the ortho-position of the amino group, that is, generates 3-methyl-4-nitroaniline. After the reaction is completed, the target product is obtained through a series of post-processing operations, such as liquid separation, neutralization, crystallization, etc.
The third is to use o-methylaniline as the starting material. O-methylaniline is first nitrified with a mixed acid composed of nitric acid and sulfuric acid. Due to the ortho-positioning effect of the amino group, the nitro group mainly enters the ortho-position and para-position of the amino group to form a mixture of 2-methyl-5-nitroaniline and 2-methyl-3-nitroaniline Afterwards, 2-methyl-5-nitroaniline was separated by recrystallization using the difference in physical properties of the two, such as the difference in solubility, and then carried out intramolecular rearrangement reaction under suitable conditions, and finally obtained 3-methyl-4-nitroaniline.

What fields is 3-methyl-4-iodopyrazole used in?

3-Methyl-4-nitropyridine-N-oxide is used in many fields such as medicine, pesticides, and materials.
In the field of medicine, this compound can be used as a key intermediate. Due to its specific chemical structure, it can participate in many drug synthesis processes. For example, in the preparation of some drugs with antibacterial and anti-inflammatory properties, 3-methyl-4-nitropyridine-N-oxide can be converted into biologically active drug molecules through a series of chemical reactions, which can achieve the purpose of treating diseases by acting on specific targets.
In the field of pesticides, it also occupies an important position. It can be used as a raw material for the synthesis of new pesticides, which may have efficient poisoning properties against pests or significant inhibitory effects on plant diseases. With precise molecular design, pesticides derived from 3-methyl-4-nitropyridine-N-oxide may achieve low toxicity, high efficiency and environmental friendliness, providing strong support for pest control in agricultural production.
In the field of materials, 3-methyl-4-nitropyridine-N-oxide can be used to prepare materials with special properties. For example, in the synthesis of some functional polymer materials, introducing them into the polymer chain may endow the material with unique properties such as electrical conductivity and optical activity. These special materials show potential application value in electronic devices, optical devices and other fields, such as application in new display materials, or bring new opportunities for the improvement of screen performance of electronic devices.
In summary, 3-methyl-4-nitropyridine-N-oxide has shown a wide and important application prospect in the fields of medicine, pesticides and materials due to its unique chemical structure. With the development of science and technology, its application may continue to expand and deepen.

What are the market prospects for 3-methyl-4-iodopyrazole?

The market prospect of 3-methyl-4-nitroanisole is really promising. It is widely used in chemical fields.
From the field of medicine, this is a key intermediate for the preparation of various drugs. For example, the synthesis of some antibacterial drugs and cardiovascular drugs often relies on its participation to provide a solid foundation for pharmaceutical research and development. At present, the pharmaceutical industry is booming, and the demand for various specific drugs is increasing. As an important raw material, the demand for this compound is also rising.
In terms of pesticides, 3-methyl-4-nitroanisole can be used to create new and efficient pesticides. Nowadays, agriculture pursues green and efficient, and the research and development of new pesticides has become a hot spot. The pesticides that participate in the synthesis may have stronger insecticidal and weeding properties, and are less harmful to the environment, which is in line with the current agricultural development needs, so there is also a wide world in the pesticide market.
Furthermore, the dye industry also regards it as an important component. It can help dye bright colors and good fastness, and meet the demand for high-quality dyes in textile and other industries. With the improvement of people's quality of life, the color and quality requirements of textiles are becoming more and more strict, and the demand for high-quality dyes is increasing. The demand for this compound in the field of dyes should not be underestimated.
In terms of market supply and demand situation, although there is currently a certain output, with the development of the above industries, the demand growth is more rapid. Many companies have expanded their production capacity, but it is still difficult to fully meet the needs of the market. And its production process is continuously optimized, the cost is expected to be reduced, and the market competitiveness can be enhanced.
From this perspective, the 3-methyl-4-nitroanisole market has a bright future. In the next few years, demand may continue to rise, and it will occupy an increasingly important position in the chemical industry chain.