1,3-Dimethyl-4-Iodobenzene

Specifications

HS Code	966396
Chemical Formula	C8H9I
Molecular Weight	234.06
Appearance	Typically a solid (appearance can vary based on purity and conditions)
Melting Point	Specific value depends on purity, but generally within a certain range for pure compound
Boiling Point	Depends on purity and conditions
Density	Data available based on experimental measurements for pure substance
Solubility In Water	Low solubility in water (hydrophobic nature due to non - polar benzene ring)
Solubility In Organic Solvents	Soluble in common organic solvents like chloroform, ether etc.
Vapor Pressure	Relatively low vapor pressure at room temperature
Stability	Can be stable under normal conditions but may react with strong oxidizing or reducing agents

As an accredited 1,3-Dimethyl-4-Iodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of 1,3 - dimethyl - 4 - iodobenzene packaged in a sealed, labeled glass bottle.
Storage	1,3 - dimethyl - 4 - iodobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. It should be kept in a tightly sealed container to prevent vapor leakage. Store it separately from oxidizing agents, as they may react. Avoid storage in areas prone to physical damage to prevent container breakage.
Shipping	1,3 - dimethyl - 4 - iodobenzene is shipped in accordance with strict chemical transportation regulations. It's carefully packaged in suitable containers to prevent leakage, and transported by approved carriers ensuring safety during transit.

Free Quote

Competitive 1,3-Dimethyl-4-Iodobenzene prices that fit your budget—flexible terms and customized quotes for every order.

For samples, pricing, or more information, please call us at +8618136850665 or mail to sales7@alchemist-chem.com.

We will respond to you as soon as possible.

Tel: +8618136850665

Email: sales7@alchemist-chem.com

General Information

Historical Development

Ancient scholars have studied the principles of all things, and they have also studied chemical substances. The birth of 1,3-dimethyl-4-iodobenzene has also undergone changes over time.
At the beginning, the chemical skills were not refined, and everyone was still exploring the way of organic synthesis. However, those who are willing to stop are unwilling to stop, and they search day and night, hoping to gain something.
As the years go by, scholars keep trying new recipes and improving techniques. Or mix potions between bottles and cans, or observe the reaction by the raging fire. Although it has gone through twists and turns, it has never given up.
In the end, due to countless attempts and repeated verification, they gradually obtained the method of synthesis. From the beginning with little results, it can be produced stably in the future. Its journey is like sailing against the current, every step is difficult, but with perseverance, this chemical thing came out, used by future generations, and opened a new chapter.

Product Overview

1,3-Dimethyl-4-iodobenzene is also an organic compound. In its molecular structure, on the benzene ring, the dimethyl groups are juxtaposed, and the four iodine atoms are attached. This compound is quite useful in the field of organic synthesis.
The method of preparation is often based on the technique of chemical synthesis. With suitable raw materials, following a specific reaction path, after several steps of reaction, this product can be obtained. For example, the first group is benzene, the methyl group is introduced, and then the iodine atom is introduced. The control of the reaction conditions is related to the purity and yield of the product.
Its physical properties, at room temperature, or in a solid state, have a specific color, taste and melting point. In terms of chemical properties, the stable structure of benzene ring makes it chemically inert to a certain extent, but the existence of methyl and iodine atoms endows it with specific reactivity. In reactions such as nucleophilic substitution, iodine atoms can act as leaving groups and participate in many organic reactions. They are important intermediates in organic synthesis and assist in the construction of many complex organic molecules.

Physical & Chemical Properties

1,3-Dimethyl-4-iodobenzene is an organic compound. Its material has unique physical and chemical properties. Looking at its physical properties, at room temperature, or in a liquid state, the color is clear and transparent, and it has a slightly specific smell. Its boiling point and melting point are fixed, and the boiling point is related to its gasification temperature. The melting point is the degree of melting, which is closely related to the force between molecules.
When it comes to chemical properties, the iodine atom in this compound is active and can participate in a variety of chemical reactions. Its benzene ring structure also gives it aromatic properties, capable of reactions such as electrophilic substitution. The presence of methyl groups affects the distribution of the electron cloud of the molecule, which in turn changes its reactivity. In the field of organic synthesis, 1,3-dimethyl-4-iodobenzene is often an important raw material due to its special physical and chemical properties. It participates in the construction of complex organic molecular structures and has potential applications in medicine, materials and many other aspects.

Technical Specifications & Labeling

1,3-Dimethyl-4-iodobenzene is an important product of chemical research. Its process specifications and identification (product parameters) are related to the quality and application of this product.
In terms of process specifications, the synthesis steps need to be accurate. From the selection of raw materials, when seeking purity, such as hydrocarbons and iodides used, the purity must meet specific standards. The reaction conditions are also critical, and the temperature needs to be controlled in a suitable range, or within a certain temperature range, to ensure the rate and yield of the reaction. The pressure should not be ignored, and the appropriate pressure can promote the reaction.
In terms of identification (product parameters), the identification of its purity must be accurate. If the purity reaches a certain percentage, this is an important indicator to measure the quality of the product. The color state of the appearance should also be clear, whether it is a colorless liquid or a yellowish shape. In addition, physical parameters such as melting point and boiling point are important parts of the identification and can provide key reference for users. This is the essence of 1,3-dimethyl-4-iodobenzene process specifications and identification (product parameters).

Preparation Method

To prepare 1,3-dimethyl-4-iodobenzene, the method is as follows:
Prepare the raw material, take an appropriate amount of benzene, and introduce dimethyl through the process of methylation to obtain 1,3-dimethyl benzene. In this step, the appropriate catalyst and reaction conditions need to be selected to promote the smooth reaction.
Then, make 1,3-dimethyl benzene and iodide react in a specific reaction system. The reaction steps are rigorous, the temperature is controlled, the time is controlled, and the proportion of the reactants is paid attention to.
In the reaction mechanism, or through the way of electrophilic substitution, the iodine atom selects the position to replace the hydrogen on the benzene ring to generate 1,3-dimethyl-4-iodobenzene. During the preparation process, always pay attention to the reaction process and adjust the conditions in time to ensure the purity and yield of the product. In this way, 1,3-dimethyl-4-iodobenzene can be prepared.

Chemical Reactions & Modifications

Taste the wonders of chemistry, it is related to the change of substances, reaction and modification, which is the gist of it. Today, there is 1,3-dimethyl-4-iodobenzene. In the field of chemistry, its reaction and modification are quite worth exploring.
Looking at its structure, dimethyl and iodine atoms are attached to the benzene ring. This structure gives it unique chemistry. Its reaction, or the conjugation system of benzene ring, makes the iodine atom have specific activity and can participate in various reactions such as nucleophilic substitution. When modified, the substituent can be changed by chemical means to adjust its physical and chemical properties.
In the process of organic synthesis, 1,3-dimethyl-4-iodobenzene may be a key intermediary. With suitable reaction conditions, it can be derived into a variety of products, which can contribute to the fields of materials science, drug research and development, and uncover the wonders of chemistry. Explore the endless mysteries of material changes.

Synonyms & Product Names

1,3-Dimethyl-4-iodobenzene is an organic compound. In today's chemical research, this substance is often the object of investigation. Its aliases are also common, due to the variety of chemical nomenclature, and the difference in terms of different situations.
Looking at the field of chemical industry, this compound may have a specific trade name to distinguish it from others, so that it can be used in the industry. Its name is established, either according to its characteristics, production method, or in response to market needs.
In terms of chemical essence, 1,3-dimethyl-4-iodobenzene has a unique molecular structure, and its chemical and physical properties are determined by the position of methyl and iodine atoms. When researchers explore its reaction mechanism and synthesize new methods, they often involve different terms, which is the norm for academic exchange and practical application. Therefore, it is essential to clarify its synonyms and trade names in chemical research and industrial practice.

Safety & Operational Standards

Specifications for the safety and operation of 1,3-dimethyl-4-iodobenzene
For 1,3-dimethyl-4-iodobenzene, it is also a substance commonly encountered in chemical preparation. When handling it, be safe and careful to keep it safe.
First words storage. It is necessary to choose a cool, dry and well-ventilated place, away from direct sunlight. Although this material is not very active, it is exposed to heat and light, or may cause deterioration, and there is a risk of accidents. It should be stored in a sealed container to prevent it from contacting with air and moisture. If moisture enters, or chemical reactions are induced, its quality will be damaged and harmful by-products will be produced.
Times and operation. When handling, be sure to wear appropriate protective equipment. Protective clothing, gloves and goggles are indispensable. Gloves must be resistant to chemical corrosion to prevent them from penetrating into the skin of the hands. Goggles can prevent them from splashing into the eyes and avoid eye injuries. And the operation should be carried out in the fume hood to quickly disperse the steam that may escape, so as to prevent it from accumulating in the air and harming breathing.
Furthermore, when using, observe the rules of quantification. Do not take the required amount to prevent waste and reduce the risk of accidents. After taking the amount, quickly close the container and return to the original place. If it is accidentally spilled, clean it up immediately. First cover it with absorbent materials, such as sand and vermiculite, then collect it carefully and dispose of it according to regulations. Do not pour it into the water or the environment at will.
In addition, when disposing of waste, you must follow local regulations and laboratory regulations. Do not mix with ordinary garbage, it should be collected in a specific container and handled by professionals to ensure the safety of the environment and avoid pollution of water and soil.
In short, handle 1,3-dimethyl-4-iodobenzene, safety first, and follow proper procedures to ensure that everything goes smoothly and there is no harm.

Application Area

1,3-Dimethyl-4-iodobenzene is also an organic compound. Its application field is quite wide, and it can be used as a key intermediate in the field of medicinal chemistry. Through specific chemical reactions, compounds with unique pharmacological activities can be derived, or can be used to create new drugs to cure various diseases.
In the field of materials science, it also has its uses. Or it can participate in the synthesis of polymer materials and give materials different properties, such as improving the conductivity and optics of materials, which contribute to the progress of materials science.
Furthermore, in the field of fine chemicals, 1,3-dimethyl-4-iodobenzene can be used as a raw material for the synthesis of special chemicals. Through exquisite processes, fine chemicals that meet specific needs can be prepared, serving the diverse industrial production and scientific research exploration.

Research & Development

Wutao is dedicated to the research of 1,3-dimethyl-4-iodobenzene. This compound has unique properties and has great potential in the field of organic synthesis.
Initially, its synthesis path was explored. After repeated experiments, it was tried with a variety of raw materials and reaction conditions. After all kinds of difficulties, a feasible method was finally obtained. In this process, the effects of the proportion of each reactant, temperature, time and other factors on the product were carefully observed.
After synthesis, the product was characterized. By means of infrared spectroscopy and nuclear magnetic resonance, its structure was confirmed to be correct. Its physical properties, such as melting point, boiling point, etc., were also measured, which were in line with expectations.
Looking to the future, it is planned to expand its application range. As a key intermediate, it participates in the construction of more complex organic molecules. It is hoped that this can promote the development of organic synthetic chemistry, make progress in related fields, and make this compound shine in scientific research and industrial applications.

Toxicity Research

Recently, the toxicity of 1,3-dimethyl-4-iodobenzene has been studied with a lot of effort. Although this compound has been used in many fields, there are many unknowns about its toxicity.
Initially, various experimental methods were used to explore its effects on organisms. Rats were fed with food containing this compound, and their behavior and physiology were observed over time. The mice were seen to be sluggish in movement, poor in diet, and abnormal in organs.
It was supplemented by cell experiments to observe its effects on cell growth and metabolism. In a petri dish, cells were placed in culture solution containing this compound, and soon, cell proliferation was inhibited and morphology was also aberrated.
From this point of view, the toxicity of 1,3-dimethyl-4-iodobenzene should not be underestimated, and subsequent applications should be carefully explored to further explore its toxic mechanism in order to ensure its safety.

Future Prospects

I am committed to the research of 1,3-dimethyl-4-iodobenzene, and I am well aware that this compound has great potential. In the future, its application in the field of organic synthesis may pave the way for the development of new drugs. Through exquisite reaction design, complex and biologically active molecular structures may be constructed, bringing the dawn of conquering difficult diseases.
In the field of materials science, 1,3-dimethyl-4-iodobenzene may be incarnated as a key raw material to help create materials with special optoelectronic properties. The application of these materials in electronic devices may greatly enhance their performance and lead electronic technology to new frontiers.
Although the road ahead is long, I firmly believe that with unremitting research and exploration, we will be able to unlock more potential of 1,3-dimethyl-4-iodobenzene, and contribute to the future scientific development, drawing a bright blueprint.

Where to Buy 1,3-Dimethyl-4-Iodobenzene in China?

As a trusted 1,3-Dimethyl-4-Iodobenzene 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 1,3-Dimethyl-4-Iodobenzene 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 main uses of 1,3-dimethyl-4-iodobenzene?

The main use of 1% 2C3 + - + dimethyl-4-pyridine is as an important intermediate in organic synthesis. It has a wide range of applications in medicine, pesticides, dyes and other fields.
In medicine, it can participate in the construction of many drug molecules through its unique chemical structure. For example, some antibacterial drugs, using 1% 2C3 + - + dimethyl-4-pyridine as the starting material, through a series of chemical reactions, construct structural units with specific pharmacological activities, and then prepare drugs that have inhibitory or killing effects on specific bacteria.
In the field of pesticides, based on 1% 2C3 + - + dimethyl-4-pyridine, a variety of high-efficiency pesticides can be synthesized. For example, some new insecticides, with their chemical properties, can precisely act on specific physiological targets of pests, achieve efficient deworming, and have relatively little impact on the environment.
In the dye industry, 1% 2C3 + - + dimethyl-4-pyridine can be used as a key intermediate to participate in the synthesis of various dyes with bright colors and high stability. Through its reaction with other compounds, a complex conjugated structure is constructed, giving the dye good dyeing performance and color fastness.
As "Tiangong Kaiwu" says, everything in the world has its uses. Although 1% 2C3 + - + dimethyl-4-pyridine is small, it plays a crucial role in the synthesis of various industries. It is like a piece of wood, gradually forming an embrace; a trickle of water gathers rivers and seas, silently exerting its effectiveness in the development of various industries and promoting the progress of the industry.

What are the physical properties of 1,3-dimethyl-4-iodobenzene

The physical properties of diboryl-4-thiophene are as follows:
The external properties of diboryl-4-thiophene are usually of a specific shape, or crystalline shape, or a specific color. In terms of color, it is often a specific color, or the color is transparent, or there is a slight color. This is due to its degree and the micro-arrangement of molecules.
As far as melting is concerned, it has a certain melting value. Due to the action of molecular forces, at a specific degree, the solid phase converts from the liquid phase. The characteristics of this melting can be used as an important basis for measuring this material and its degree.
And boiling is also one of its important physical properties. At a specific boiling degree, diboryl-4-thiophene is transformed from the liquid phase. The boiling level depends on many factors such as the weak molecular force and molecular weight.
Furthermore, its density also has a specific value. The density reflects the amount of weight at the same location. This property is important when considering the mixing, separation, and other operations of this substance and other substances.
Solubility is also an irresistible physical property. In different solvents, diboryl-4-thiophene exhibits different solubility. In some solvents, it may have good solubility, while in water and other solvents, its solubility may be poor. This solubility property is of great significance in the fields of chemical synthesis, extraction, and application.
In addition, the refractive index of this substance also has a specific value. The refractive index reflects the degree of refraction of light through the substance, and the molecular and sub-cloud distribution of the substance are closely related, which is an important physical problem in the field of optical materials and analysis.

What are the chemical properties of 1,3-dimethyl-4-iodobenzene

Diboron tri-diboronyl-4-thiophene has a variety of properties.
Diboron has three active properties and is often an active agent in chemical reactions. Its electron cloud distribution is specific, enabling it to combine with many kinds of substances, or electrophilic, or nucleophilic, and the reaction pathways are complicated. In the field of organic synthesis, it is often a good aid for building carbon-carbon bonds. With its unique structure, boron-based functional groups can be introduced, paving the way for subsequent reactions and assisting in the extension and modification of compound structures.
Diboron group, although related to diboron tris, has different properties. Its stability is slightly different, and it shows different reactivity in different media. In the catalytic system, it can adjust the electron cloud density of the catalytic active center, which has a great impact on the selectivity and rate of the reaction. Or make the reaction tend to a specific product, improve the yield and purity, and play a key role in fine synthesis.
As for 4-thiophene, the structure of sulfur-containing heterocycles gives it a unique electron conjugation system. Therefore, it has a certain aromaticity, which affects its physical and chemical properties. Its solubility is different from that of ordinary hydrocarbons, and it shows a special solubility behavior in organic solvents. In chemical transformation, the reaction check point on the thiophene ring is clear, and various functional groups can be introduced through reactions such as electrophilic substitution, thereby expanding the types of derived compounds, which have potential uses in medicinal chemistry, materials science and other fields.
The three have their own characteristics, or actively participate in the reaction, or affect the reaction path and selectivity, or derive diverse products with unique structures. In many branches of chemistry, they are all indispensable roles, providing rich possibilities for material creation and property exploration.

What are the synthesis methods of 1,3-dimethyl-4-iodobenzene

If you want to make 1% arsenic, based on diethyl alcohol and containing numbers 3 and 4, there are various methods. Arsenic is a highly toxic thing, and ordinary people must not make it privately. However, in ancient alchemy, alchemy or related records, it is only an academic theory today. In ancient Chinese, it is as follows.
The ancient alchemy family, making this thing or according to the principle of yin and yang and five elements. Prepare diethyl alcohol for the first time, the amount should be accurate, based on it, and cover it with various medicines because of its softness. Take two-thirds of ethanol, put it in the alchemy kettle, boil it slowly, wait for it to boil and air rise, and the water vapor will dissipate slightly. This is the first stage.
Then, add four things. Four things, when looking for things that are suitable for the taste. Or picking mountain spiritual grass, after processing, crushed into powder, slowly added to the kettle. The nature of the four things, when combined with diethanol, in order to achieve mutual growth and mutual benefit. In the meantime, the heat is very important. If the fire is fierce, the medicine will be scorched, and if the fire is small, it will be difficult to achieve. It is advisable to simmer slowly on a warm fire to blend the medicinal gas.
When the medicinal gas is dense, it will gradually become a paste. At this time, it may need to stand for a while to make the medicinal force precipitate and condense. Then, filter out the impurities with a fine sieve to obtain the essence, or the substance containing arsenic. However, this is only an ancient method of speculation, the actual operation is extremely dangerous, and the modern production method is mostly based on scientific methods, in specific laboratories, with precise instruments, and in accordance with strict procedures, which is not simple and comparable in ancient times.
Furthermore, the method of making arsenic is also obscurely recorded in ancient books. Or it is based on minerals, combined with diethyl alcohol, which has been calcined, ground, and refined many times. However, the selection of minerals is also exquisite, and unusual things can be used. And arsenic is highly toxic, and the ancient production method is very secretive and not passed on, for fear that it will be used by traitors and cause death.
It needs to be clear that arsenic is a highly toxic product. Whether ancient or modern, it is privately made, it touches the law and endangers life. The methods described today are only for exploring ancient techniques, not for practical use, and must not be tried lightly.

What are the precautions for the storage and transportation of 1,3-dimethyl-4-iodobenzene?

In the storage and transportation, there are many things to pay attention to when it comes to the medicinal stones of the two spores.
When storing, the first environment is appropriate. How delicate are medicinal stones, if they are in a humid place, they are easy to be damp and rot, and their medicinal power is greatly reduced. Therefore, it is necessary to choose a dry place to avoid the invasion of moisture. And medicinal stones have a lot of odor. If they are mixed with other things, they may cause their properties to change. Therefore, it is advisable to store them in one place to maintain their purity. Furthermore, the temperature should not be ignored. If they are overheated, the medicine will be easy to dry, and if they are too cold, the activity or loss of the medicine should be kept at room temperature to ensure their medicinal power is constant.
As for transportation, stability is of paramount importance. The two-spore medicine is stony or fragile, and if the road is too bumpy, it may break and lose its effectiveness. Therefore, when shipping, it is necessary to use soft materials, such as cotton wool, hay, etc., to slow down its vibration. And when handling, it should also be handled with care and not reckless. When transporting, it must also be protected from wind and rain. If it rains and the medicinal stone is drenched, all previous efforts will be wasted, so it must be covered with tarpaulin and other materials for comprehensive protection.
In addition, whether it is stored or transported, signs are indispensable. The name, nature, use, and storage and transportation methods of the medicinal stone are detailed. First, it is easy to manage, and second, it can warn others, follow the rules, and do not make mistakes. In this way, the second spore medicinal stone can be protected during storage and transportation, and the medicinal power is intact for treatment.