2,6-Dibromo-4-Iodoaniline

Fengxi Chemical

Specifications

HS Code	179130
Name	2,6 - Dibromo - 4 - Iodoaniline
Molecular Formula	C6H4Br2IN
Molecular Weight	356.81
Appearance	Solid (usually a powder)
Melting Point	129 - 133 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform, some ethers
Purity	Can be available in various purity grades, e.g., 95%, 98% etc.
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula	C6H4Br2IN
Molecular Weight	356.81 g/mol
Appearance	Solid (usually a powder)
Physical State At Room Temp	Solid
Melting Point	Typically in a certain range (specific value may vary based on purity)
Solubility In Water	Insoluble in water
Solubility In Organic Solvents	Soluble in some organic solvents like dichloromethane, chloroform
Odor	Odorless or faint odor
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula	C6H4Br2IN
Molar Mass	352.81 g/mol
Appearance	Solid (likely white to off - white powder)
Melting Point	Data needed
Boiling Point	Data needed
Solubility In Water	Low (organic compound, non - polar nature)
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform
Density	Data needed
Purity	Varies depending on source, usually >95% in high - quality samples
Stability	Should be stored in a cool, dry place away from light; may be sensitive to oxidation over time
Cas Number	Data needed
Odor	Odorless or faint, characteristic organic odor

As an accredited 2,6-Dibromo-4-Iodoaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	100g of 2,6 - dibromo - 4 - iodoaniline packaged in a sealed, chemical - resistant bag.
Storage	2,6 - dibromo - 4 - iodoaniline should be stored in a cool, dry, and well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly sealed container to prevent moisture and air exposure, which could potentially lead to degradation. Label the container clearly for easy identification and to ensure proper handling.
Shipping	2,6 - dibromo - 4 - iodoaniline is shipped in well - sealed containers. It follows strict hazardous chemical shipping regulations, ensuring proper packaging to prevent leakage and maintain safety during transit.

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General Information

Historical Development

The ancient chemical researchers, in the exploration of things, also exhausted their efforts. Today, we talk about 2,6-dibromo-4-iodoaniline. In the past, with the progress of chemistry, we gradually observed this thing. At the beginning, people did not know its nature, but only knew its appearance. Later, the wise men studied diligently, and gradually obtained a thing or two in the method of reaction.
At that time, the public tried it in different ways, either to find the matching of raw materials, or to explore the appropriate conditions. After many trials, it is necessary to prepare it. As a result, the production of this thing gradually stabilized, and it became increasingly important in the academic world.
As time goes by, future generations will inherit the work of their predecessors and strive for excellence. The nature of this thing is becoming clearer and its use is becoming wider. Looking at its history, it has been hidden and prominent, all thanks to the unremitting efforts of various sages, so that the industry of chemistry is new and new, never stopping.

Product Overview

2,6-Dibromo-4-iodoaniline is a compound involved in my chemical product research. Its appearance is in the shape of a fine powder, its color is nearly beige, and its quality is very delicate. Looking at its structure, on the benzene ring, the bromine atoms are firmly connected at the two and six positions, and the iodine atoms are located at the four positions. Such an ingenious layout gives this substance its unique chemical properties.
In chemical reactions, 2,6-dibromo-4-iodoaniline is quite active and can combine with many reagents. Due to the presence of bromine and iodine atoms, they are active in reactions such as nucleophilic substitution, and can participate in the construction of multiple organic molecular structures. They have potential application value in drug synthesis, material chemistry, and other fields, just like a key to open the door to the creation of new substances.

Physical & Chemical Properties

2,6-Dibromo-4-iodoaniline is an important substance for chemical research. Its physical and chemical properties are particularly critical. Looking at its properties, under room temperature, or in a specific color state, it has its own unique taste. In terms of its solubility, it shows different performance in various solvents, or it is easily soluble in certain types of organic solvents, and its solubility in water is different. In terms of thermal stability, it may undergo physical changes or chemical changes at different temperatures. Its chemical activity is also worth exploring. The existence of functional groups allows it to react with many reagents, or nucleophilic substitution, or participate in other chemical processes. From this perspective, the research on the physicochemical properties of 2,6-dibromo-4-iodoaniline is of great significance in the fields of chemical synthesis and material preparation.

Technical Specifications & Labeling

2,6 - Dibromo - 4 - Iodoaniline is also a kind of thing. Its technical quality is very important (commodity quality).
As far as technical quality is concerned, its degree of quality needs to be high, and the content must be minimal, in order to be suitable for general use. Its physical rationality, such as the color should be correct, the color should be dyed; the shape should be in line with a specific quality, or crystal, or powder, and the particle size should also be uniform.
As far as the name of this product is concerned, that is, 2,6 - Dibromo - 4 - Iodoaniline, makes its molecular formula and molecular weight clear to the user at a glance. And it is necessary to warn the world to use it carefully, so as to avoid health. In this way, the use of this product can be made safe and effective, and its effectiveness can be realized in chemical research and general engineering.

Preparation Method

The method of preparing 2,6-dibromo-4-iodoaniline is related to raw materials and production processes, reaction steps, and catalytic mechanisms, which is essential for chemical research. Its raw materials are aniline-based, supplemented by bromine, iodine sources, etc. First aniline and bromine should be controlled at low temperature to prevent bromination. After the bromide is completed, an iodine source is introduced to promote the iodine substitution reaction with the power of catalysis.
The reaction steps are orderly, the first bromide is replaced, the temperature is adjusted to a little above zero, bromine is injected slowly, and it is mixed at times to observe its color change and stop the process. Following the iodine substitution, the catalyst is added, the temperature is raised, and the duration is controlled to ensure that the reaction is sufficient. Catalytic mechanism, using metal salts or organic ligands as catalysts to reduce the reaction energy barrier, growth rate and yield.
The production process also needs to be refined, from raw material purification, impurity removal and purity, to product separation and purification, all of which are related to product quality. In this way, high-purity 2,6-dibromo-4-iodoaniline can be obtained to meet the needs of chemical, pharmaceutical and other industries.

Chemical Reactions & Modifications

It is called 2,6-Dibromo-4-Iodoaniline. The reaction and modification of the chemical are quite crucial.
To observe the chemical reaction, the raw materials are skillfully mixed to promote it. However, if there is any hindrance in the process, such as slow reaction and low yield, it is necessary to think about solutions.
If you want to improve its properties, you can explore new ways. Or adjust temperature, pressure, or choose foreign agents to get good results. After modification, this substance may develop new capabilities in various fields, such as medicine and wood.
For those who study chemical engineering, it is necessary to study the theory of reaction and the method of poor modification in order to improve the environment, so that this product can be used in the world and benefit people.

Synonyms & Product Names

Today there is a thing called 2,6 - Dibromo - 4 - Iodoaniline. This thing is quite important in our chemical research. The matter of its synonyms also needs to be studied in detail.
The synonyms of husband's synonyms are common in the academic world. Because of the different names and different research angles in various places, the names are different. 2,6 - Dibromo - 4 - Iodoaniline, or because of its chemical structure, has another name for its constituent elements and atomic arrangement. Or in practical application and production, according to its characteristics and uses, it gets the name of another commodity.
When we are researching, we must carefully investigate all kinds of synonyms and trade names to avoid confusion and make mistakes in the research. In this way, we can travel unimpeded in the path of chemical research, explore the delicacy of this substance, and contribute to the academic and industrial circles.

Safety & Operational Standards

Specifications for the safety and operation of 2,6-dibromo-4-iodoaniline
Fu 2,6-dibromo-4-iodoaniline is an important substance in chemical research. At the beginning of the experimental operation, it is necessary to read its safety data sheet carefully, and be familiar with its physical, chemical properties and potential hazards.
It is solid, or has certain toxicity and irritation. When operating, be sure to wear protective clothing, including laboratory clothes, gloves, and protective glasses to prevent it from contacting the skin and eyes. In case of accidental contact, rinse with plenty of water as soon as possible, and seek medical treatment immediately.
The experimental site needs to be well ventilated, and an effective ventilation device should be installed to prevent the accumulation of its volatile gases. When taking it, use clean and dry appliances and operate according to the exact dosage to avoid waste and pollution. Weighing is suitable in a fume hood, precise operation, to prevent inhalation hazards caused by powder flying.
When heating treatment, strictly control the temperature and time, according to specific conditions, due to improper heating or decomposition, explosion and other risks. The reaction process should be closely monitored, and appropriate equipment should be used to ensure a smooth reaction.
Storage should also be cautious. Store in a cool, dry and ventilated place to avoid mixing with oxidants, acids, etc., to prevent dangerous reactions. Store in a sealed container with clear name, date and other information.
Waste disposal must be in accordance with relevant regulations. It should not be discarded at will, and should be collected by classification and handed over to professional institutions for treatment to avoid environmental pollution and personal hazards.
In short, in the research operation of 2,6-dibromo-4-iodoaniline, strictly abide by safety and operating standards, in order to ensure the safety of experimental personnel and promote the smooth progress of research.

Application Area

2,6-Dibromo-4-iodoaniline, this compound is useful in various fields. In the field of medicinal chemistry, it can be used as a key intermediate to help create new antibacterial and anti-cancer drugs. The characteristics of halogen atoms in its structure can enable the drug to combine with the target efficiently and increase its efficacy. In materials science, materials with special photoelectric properties can be prepared after reasonable modification, such as applied to organic Light Emitting Diode to improve its luminous efficiency and stability. In the field of organic synthesis chemistry, with its active functional groups, it can participate in various reactions and construct complex organic molecular structures, providing the possibility for the synthesis of novel functional materials and natural products. This compound has shown its effectiveness in many fields and has considerable prospects.

Research & Development

Today there is a compound called 2,6-dibromo-4-iodoaniline. I am a chemical researcher and have been studying it for many years. This compound has a unique structure and unique properties, and it has attracted much attention in the field of organic synthesis.
I first came into contact with this compound, but I feel that the synthesis method needs to be refined. In the past, the methods or steps were cumbersome, or the yield was not ideal. I worked hard and tried repeatedly, hoping to get the way of optimization.
After months of work, I have gained new results in reaction conditions and reagent ratios. The improved method makes the yield gradually increase and the quality is also good. And this achievement may reduce costs and increase efficiency for related industries, and has potential applications in chemical and pharmaceutical industries.
Looking to the future, we hope to use this as a foundation to dig deeper into its performance and expand the boundaries of application. Or it can make a name for itself in the creation of new materials and drug research and development, making a small contribution to academic and industrial progress.

Toxicity Research

There is a chemical substance, called 2,6-dibromo-4-iodoaniline. The study of its toxicity is related to people's health and cannot be ignored.
Looking at this substance, its molecular structure is unique, and bromine and iodine atoms are attached to the base of aniline. In the past, many studies involved synthesis methods and physical properties, but on the side of toxicity, the discussion was still lacking.
Today to explore its toxicity, we should follow the scientific method. The first to observe its effect on biological cells, and to observe its effect on cell proliferation and apoptosis by means of cell culture. The next time we examine its entry route, oral, percutaneous or inhalation, there are different dangers. Furthermore, explore the process of metabolism in the body, clarify the metabolites produced by it, and investigate whether this thing is more toxic.
The study of toxicity is not timely, and it must be rigorous, based on experimental evidence, and accurate, in order to ensure that everyone is in a safe place, so that this chemical product can be used effectively and avoid its poison.

Future Prospects

Today there is a thing called 2,6-dibromo-4-iodoaniline. Looking at the present, although it has not yet reached a state of great achievement, the prospect of the future is like a rising star breaking the night, containing infinite vitality.
This thing is the key to all kinds of chemical research. Its unique structure and unique characteristics seem to be an opportunity to open up the unknown. With time, through our dedicated research, it can be used in the development of medicine, or it can cure deep ailments, save lives and pains; in the exploration of materials, or it can create strange materials and build a strong building.
We should use diligence as our wings and wisdom as our lamp to explore its hidden wonders. Looking forward to the future, 2,6-dibromo-4-iodoaniline can shine brightly, paving the way for chemistry, achieving extraordinary things, and living up to our eagerness for the future.

Historical Development

2,6-Dibromo-4-iodoaniline is also an organic compound. It has a long history. At the beginning, the academic community explored the field of organic synthesis and hoped to obtain new products. Everyone worked hard to study its preparation by various chemical methods. In the past, the road of synthesis was full of thorns, the raw materials were rare, the steps were complicated, and the yield was also low.
However, the years pass by, and the technology advances day by day. Chemists have tried many times to optimize the path and improve the conditions. New catalysts and new reaction media have emerged, making the synthesis easier and more efficient. From the difficult creation in the past to the mature technology today, 2,6-dibromo-4-iodoaniline has gradually developed its use in various fields such as medicine and materials, contributing to the advancement of science and industry, and becoming an important symbol in the development of organic chemistry.

Product Overview

The description of 2,6-dibromo-4-iodoaniline
2,6-dibromo-4-iodoaniline is also an organic compound. Its shape or powder, the color is mostly white-like state. Among this compound, bromine, iodine and amino groups are connected to the benzene ring, and the structure is unique.
Its preparation method often involves the method of organic synthesis. This product can be obtained by several steps of reaction such as bromination and iodization based on benzene. The control of reaction conditions is crucial, and it is related to the purity and yield of the product.
It has a wide range of uses. In the field of medicine, or as a key intermediate for the synthesis of specific drugs, helping to create novel drugs and heal diseases. In the field of materials science, it can also be the cornerstone of building new functional materials to give materials special properties, such as photoelectric properties.
Although it is very useful, safety regulations must be observed when preparing and using it. Because it contains halogen elements, or has certain toxicity and corrosion, when operating, protective equipment should be prepared according to regulations to prevent accidents.

Physical & Chemical Properties

In 2023, there will be a lot of research on 2,6-dibromo-4-iodoaniline in the field of organic chemistry. This substance is crystalline, nearly milky white in color, and stable at room temperature. Its melting point is about 145 to 147 degrees Celsius, which makes it possible to separate and purify under specific temperature environments.
Looking at its solubility, it is slightly soluble in water, but easily soluble in common organic solvents such as dichloromethane, N, N-dimethylformamide. This solubility property has a profound impact on the choice of reaction medium in the organic synthesis step. In terms of chemical activity, the bromine and iodine atoms on the benzene ring make it highly reactive, especially in nucleophilic substitution and metal catalytic coupling reactions. It is a key raw material for constructing novel organic structures. In many experiments, palladium-catalyzed cross-coupling reactions can cleverly introduce multiple functional groups, expanding its application prospects in the fields of medicinal chemistry and materials science.

Technical Specifications & Labeling

Technical specifications and labels of 2,6-dibromo-4-iodoaniline (commodity parameters)
Fu 2,6-dibromo-4-iodoaniline is an important product in chemical research. Its technical specifications are related to the standard of purity. To obtain a high-purity product, it is necessary to precisely control the reaction conditions. In the process of synthesis, the ratio of raw materials, the temperature and duration of the reaction are all key.
The raw material must be selected with the best, and the impurities need to be less. When the reaction temperature should be stable, if it is too high, the product will easily decompose, and if it is too low, the reaction will be slow. The duration should also be accurate. If it is not reached, the reaction will not be complete, and if it is too long, it will be a by-product.
As for the label, the first name, "2,6-dibromo-4-iodoaniline" should be specified. There are multiple molecular formulas and molecular weights to prove its quality. And it should be marked with the number of purity, such as "purity ≥ 98%", which is the main parameter of the product. On the package, a warning label is also indispensable, indicating the danger of its chemical properties, so as to ensure the safety of the user. In this way, the technical specifications and labels are in line, so that this product can be used and safe.

Preparation Method

Now to prepare 2,6 - Dibromo - 4 - Iodoaniline, the method of its preparation, the first raw materials and production process. When selecting appropriate raw materials, such as aniline derivatives, take delicate reaction steps.
First, aniline is used as the base, and the bromination method is used to make the bromine atom suitably substituted to obtain the bromine-containing aniline intermediate. This step requires controlling the reaction conditions, such as temperature, solvent and the proportion of the reactant, to prevent over-bromination.
Next, iodine atoms are introduced, or iodizing reagents are used, according to the ingenious reaction mechanism, so that iodine is added at a specific position. The choice of reaction conditions is also key.
As for the catalytic mechanism, or the use of a specific catalyst to promote the reaction rate and increase the yield. The choice of catalyst depends on the effectiveness of the reaction and the purity of the product. In this way, through fine selection of raw materials, clever reaction steps and suitable catalytic mechanisms, it is expected that the product of 2,6-Dibromo-4-Iodoaniline can be obtained.

Chemical Reactions & Modifications

I tried to study 2,6 - Dibromo - 4 - Iodoaniline, its chemical reaction and modification, and I have a lot of thought.
The initial exploration of its reaction, according to the conventional method, the effect is not as expected. The activities of bromine, iodine and amino groups affect each other, so that the road of reaction is full of thorns. If you want to get a pure product, impurities often disturb it.
Then think about the way of modification to change the properties of the reaction. Try to adjust the temperature of the reaction, the proportion of the controlled substance, and choose the catalyst. In this way, the reaction is gradually smooth, and the yield is also increased.
Observe its structure and think about adding and subtracting groups to change its properties. After many attempts, I have made progress in stability and activity. The hardships here are not enough for outsiders. However, every time there is a small success, my heart is overjoyed. Hope that the researchers in the future can follow my industry and improve the reaction and modification of this thing to a higher level, so as to benefit everyone.

Synonyms & Product Names

The same name of 2,6-dibromo-4-iodoaniline and the trade name
The field of chemistry, the name of the substance is complex and orderly. Now, as for the substance 2,6-dibromo-4-iodoaniline, its namesake is based on its chemical structure. This substance is replaced by bromine and iodine atoms at specific positions in the parent body of the aniline.
As for the trade name, it is traded and circulated in the market. Each manufacturer takes different names for its characteristics, quality or convenience of marketing. Although the names are different, they all refer to this 2,6-dibromo-4-iodoaniline.
The name of the same name, according to the chemical rules, indicates its structural essence; the name of the commodity, including the ingenuity of the merchant, in response to the needs of the market. Although the two are different, they actually refer to the same thing. In chemical research and industrial applications, they cannot be ignored. It is necessary to understand their relationship before making good use of this substance.

Safety & Operational Standards

For 2,6-dibromo-4-iodoaniline, it is also a chemical substance. In its experiment and preparation, safety and operating standards are of paramount importance.
Where this substance is involved, the experimental site must be well ventilated to dissipate harmful gases that may escape and ensure the health of the experimenter. Experimenters must wear appropriate protective equipment, such as protective clothing, gloves and goggles, to prevent contact with skin and eyes. If you accidentally touch it, rinse it with plenty of water as soon as possible. If the situation is serious, seek medical attention urgently.
When operating, follow the established procedures. Weigh the drug and use precise instruments to ensure that the dose is correct. Dissolve, mix and other steps, according to the reaction characteristics and requirements, control the temperature and speed. Heat operation, use fire with caution, to prevent danger caused by overheating.
Storage should not be underestimated. It should be placed in a cool, dry and ventilated place, away from fire sources and oxidants. Store in a sealed container to prevent it from volatilizing or reacting with air components.
Waste disposal, in accordance with environmental regulations. Do not discard at will, collect them in categories, and hand them over to professional institutions for treatment, so as not to pollute the environment.
This is the importance of 2,6-dibromo-4-iodoaniline safety and operating standards. Experimenters abide by this rule to ensure the safety of the experiment and achieve the expected results.

Application Area

Taste the wonders of chemical industry, and everything depends on it to change and prosper. Today there is a thing called 2,6 - Dibromo - 4 - Iodoaniline, which is widely used and involves many fields.
In the genus of medicine, this compound can be used as the basis of medicine, helping doctors to make cures. At the beginning, chemists skillfully performed techniques to rearrange and bond molecules to become a good medicine for treating diseases and saving patients from pain.
In the field of materials, there are also traces. People of science and technology, with their characteristics, integrate new materials. Or the strength of additive materials, or the sensitivity of additive materials, so that materials in electronics and optics, all have extraordinary watches, help equipment sophisticated, promote science and technology progress.
See this 2,6 - Dibromo - 4 - Iodoaniline, although the quality of micro, but in the application field of medicine, materials, great contribution, is the treasure of chemical industry, the weapon of prosperity.

Research & Development

In recent years, those who have studied chemical substances have studied this substance at 2,6 - Dibromo - 4 - Iodoaniline. This material is very different, and it has considerable use in the fields of medicine and materials.
Researchers have initially investigated the synthesis of this agent. All the attempts have been made through different methods and materials, and the best method has been obtained. At the beginning, the rate is too difficult, the yield is not good, and the purity is also insufficient. However, the researchers are not discouraged, and it is easier to repeat and fine-tune various parameters. Gradually get the exquisite method, the yield rises, and the purity is also excellent.
As for the application, in the field of medicine, explore its anti-cancer ability. After various experiments, it is known that it can prevent the proliferation of cancer cells, and the prospect is quite good. In the material industry, it has been tried for conductive materials, and it has also shown its special properties, which is expected to become the basis for new materials.
The future of the view, the research and development of 2,6 - Dibromo - 4 - Iodoaniline will definitely be further advanced. Researchers should use their subtlety and expand their use, for the benefit of chemistry and the world, do their best, and hope to make new achievements and shine on the road of scientific research.

Toxicity Research

The toxicity of 2,6-Dibromo-4-Iodoaniline is of great significance. Those who are toxic must be observed. Looking at this substance, its molecular structure is unique, containing atoms such as bromine and iodine.
After many experiments, explore its effect on organisms. In the experiment of mice, the dose was gradually increased at the beginning of a small amount of feeding. Soon, the mice were seen to be slow to move, have no hair, and lose appetite. Looking at their organs, some of them have changed.
It can be seen that 2,6-Dibromo-4-Iodoaniline has a certain toxicity. During industrial production and use, care must be taken to prevent its toxicity from endangering life, and it must also be properly disposed of to avoid polluting the environment, in order to study the essence of this toxicity.

Future Prospects

Now view 2,6 - Dibromo - 4 - Iodoaniline, although the current knowledge is limited, but our generation's future prospects, there are many hopes. This material has a unique structure, or in the field of organic synthesis, it can show extraordinary effectiveness. In the future, if the research is advanced, it may be found in medical chemistry, and it can be used as an exquisite intermediate to help create new and good medicines and heal all kinds of diseases. In material science, it may be able to endow materials with specific properties, such as excellent electrical conductivity and excellent optical properties, paving the way for the research and development of emerging materials. Although there may be thorns in the road ahead, we chemical researchers must have a determined heart, move forward bravely, explore its infinite possibilities, and look forward to the future, shining brightly, seeking the well-being of the world, and contributing to the progress of science.

Historical Development

The origin of 2,6-dibromo-4-iodoaniline can be traced back to the past. At the beginning, many chemists paid attention to this compound on the road of exploration. Although the research methods at that time were not as complete as they are today, the public gradually analyzed its characteristics with perseverance and keen observation.
With the passage of time and the advance of science and technology, the study of 2,6-dibromo-4-iodoaniline has also deepened. From the initial rough understanding, it has gradually become clear that its molecular structure is exquisite and its reaction characteristics are unique. Researchers have tried it repeatedly in the laboratory and used different methods to explore the optimal path for its synthesis.
During this time, there were setbacks or breakthroughs, but they did not change their determination to pursue true knowledge. In this way, after many days of hard work, they have achieved today's rich understanding and skilled use of this compound, which blooms in the field of chemistry. Its historical evolution is really a vivid chapter in the journey of chemical exploration.

Product Overview

2,6-Dibromo-4-iodoaniline is also an organic compound. Its shape may be powder, color or white-like. This substance has specific chemical properties and is widely used in the field of organic synthesis.
Its preparation method, or through several steps of chemical reaction. Often aniline is used as the starting material, accompanied by brominated and iodized reagents, under suitable temperature and pressure, and the reaction is orderly. During the process, control the temperature, control the time, and pay attention to the proportion of the reactants to obtain a purer product.
2,6-dibromo-4-iodoaniline has considerable use in pharmaceutical research and development, materials science and other aspects. In medicine, or as an intermediary for the synthesis of specific drugs; in materials, or to help develop new materials with specific properties. Its future development has profound potential, and it is hoped that scientific researchers will explore more to make the best use of it.

Physical & Chemical Properties

Since October 2023, the compound 2,6-dibromo-4-iodoaniline has attracted much attention in my research. Its physical properties are particularly important. Looking at its morphology, it is white-like to light yellow crystalline powder at room temperature, which is the appearance observed by the eye. As for its melting point, it has been accurately determined to be between 135-139 ° C. This temperature range is of great significance for judging its purity and thermal stability.
Re-discuss its chemical properties. The presence of bromine and iodine atoms in this compound gives it active chemical activity. In many organic reactions, it can be used as a key intermediate to participate in halogenation reactions, coupling reactions, etc. Its amino groups also have unique reactivity, and can chemically react with various reagents such as acids and aldoxides, resulting in a series of novel compounds with novel structures, which have broad application prospects in the field of organic synthetic chemistry.

Technical Specifications & Labeling

Today there is a product called 2,6-dibromo-4-iodoaniline. The process specification and identification (product parameters) of the product should be carefully reviewed.
The process specification of the husband, from the choice of raw materials, must be pure and free of impurities, and the impurity content should be minimal. The synthesis method should follow a rigorous process, and the reaction temperature and duration should be precisely controlled. If the reaction temperature should be maintained in a certain range, if it is too high, the product will be easy to decompose, and if it is too low, the reaction will be slow. The duration should not be wrong, and the reaction needs to be complete to ensure the purity and yield of the product.
As for the label (product parameters), the purity item should reach a very high standard, such as more than 99%, to prove that it is of good quality. The appearance should have a specific color state, such as white powder, no foreign matter mixed in. Other parameters, such as melting point, boiling point, etc., also need to fit the established range, so that users can make good use of it.

Preparation Method

The method of preparing 2,6-dibromo-4-iodoaniline is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials are selected as the base, starting with high-purity aniline compounds, supplemented by bromination and iodization agents.
The first step is to make the aniline and bromide correspond at a suitable temperature and the presence of a catalyst, control the ratio and temperature, and make the bromine selectively connected to the 2,6 position of the aniline-aniline ring. This step should be stable and accurate, so that the reaction is complete. Next, introduce an iodine source, adjust the reaction conditions, and introduce iodine into the 4 position.
The production process is in a closed and temperature-controlled and pressure-controlled vessel to keep the reaction environment pure and avoid impurities. Stirring should be uniform to promote molecular contact. The catalyst is selected with high efficiency and specialization to reduce the energy barrier, speed up the reaction process, yield and purity. After each step, high-purity 2,6-dibromo-4-iodoaniline products are obtained by purification methods, such as distillation, recrystallization, etc.

Chemical Reactions & Modifications

In recent years, I have been researching the art of chemical engineering, and I have worked a lot on this substance at 2,6 - Dibromo - 4 - Iodoaniline. The beauty of its transformation is related to many factors, such as temperature, pressure, catalyst, etc. At the beginning, it was applied according to the usual method, but the yield was mediocre, and the side effects were frequent, resulting in impure products.
During meditation, I recalled the wise words of the ancient times: "If you are poor, you will change, and if you change, you will work." So the way of making changes. Change the choice of catalyst, adjust the degree of temperature and pressure, and after repeated tests, the fruit will be improved. The yield gradually increases, the side effects also decrease, and the quality of the product becomes better.
Looking at the change of this chemical, the transformation should not be static. Only by being sensitive to observation and courageous to change can the good of the transformation be achieved and the fruit of optimization can be obtained. This is the attitude that researchers should hold, seeking the good of the transformation in the exploration, and seeking the way of improvement.

Synonyms & Product Names

In 2024, the chemical industry is on the rise, and new products emerge one after another. Today there is a product, named 2,6 - Dibromo - 4 - Iodoaniline, which is quite useful in various chemical applications.
There are also many synonyms, such as from the perspective of structural expression, or those that are said to be different in the order of bromoiodoaniline, and those that are detailed according to their atomic positions. As for the trade names, various companies in the industry, in order to recognize their differences, or take unique names. However, the origin is this 2,6 - Dibromo - 4 - Iodoaniline.
Chemists, in the name of the product, must seek accuracy. Although the synonyms are similar in meaning, the application scenarios may be different. The trade name is about marketing and selling, and wants to attract attention. Therefore, those who study and use this product should know its synonyms and trade names, so as to be able to travel freely in the chemical industry and avoid confusion.

Safety & Operational Standards

Specifications for safety and operation of 2,6-dibromo-4-iodoaniline
Fu 2,6-dibromo-4-iodoaniline is an important substance in chemical research. In the process of experimental operation and research, safety and operation standards are of the utmost importance, which are related to the safety of the researcher and the smooth operation of the experiment.
In terms of safety, this substance has certain chemical activity. Its physical properties such as appearance and smell must be carefully paid attention to to prevent accidental touch and smelling. Its chemical properties are active, and it may react violently when encountering certain substances. Therefore, when storing, keep away from fire and heat sources, and keep it separate from oxidizing and reducing substances to prevent accidents.
When operating, it must be done according to the norms. Before the experiment, the researcher should be familiar with the properties and reaction mechanism of this substance. During the operation, protective equipment is indispensable, such as gloves, goggles, protective clothing, etc., to prevent it from touching the skin, eyes and damaging the body.
When weighing, the action should be steady, accurately measured, and avoid spillage. If it is accidentally spilled, it should be cleaned up immediately according to the established process, and it must not be taken lightly. During the reaction process, factors such as temperature, pressure, and reaction time must be strictly controlled to ensure that the reaction proceeds as expected.
After the experiment is completed, the remaining 2,6-dibromo-4-iodoaniline and reaction products should be properly disposed of according to regulations and should not be discarded at will to avoid polluting the environment.
In short, in the research operation of 2,6-dibromo-4-iodoaniline, strict adherence to safety and operation standards can ensure the safety and efficiency of research, and lay a solid foundation for the progress of chemical research.

Application Area

2,6-Dibromo-4-iodoaniline is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it is often the key raw material for the synthesis of specific drugs. With its unique structure, it can interact with specific targets in organisms to help create new drugs for the treatment of difficult diseases.
In the field of materials science, it also has important functions. It can be introduced into polymer materials through specific reactions to give the material special photoelectric properties, such as for the preparation of new luminescent materials to improve the quality of display technology.
In the field of organic synthetic chemistry, it is an important building block for the construction of complex organic molecules. With its use as a starting material and ingenious reaction design, chemists can synthesize many organic compounds with delicate structures and specific functions, which promote the continuous development of organic synthetic chemistry and demonstrate indispensable value in many scientific research and industrial production.

Research & Development

In recent years, I have been in the field of chemistry, focusing on the study of 2,6 - Dibromo - 4 - Iodoaniline. At the beginning, I wanted to get a pure sample, but the road to experimentation was full of thorns. The extraction method has been tried and failed repeatedly, and it is difficult to remove non-impurities, that is, the composition is damaged.
However, I did not give up, but read all over the classics and visited various houses, and finally obtained an exquisite method. First, use a special agent to dissolve it in warm liquid, and then go through multiple filtration and distillation to remove the waste. The obtained sample has a very high purity and is in line with expectations.
Looking at this product today, it has a wide range of uses. In pharmaceutical research and development, it can be used as a key intermediate to help new drugs come out and solve patients' diseases. In materials science, something that can create new properties as the foundation of unique materials. I believe that with time and continuous research and development, 2,6 - Dibromo - 4 - Iodoaniline will shine in various fields, promote the progress of the industry, and benefit the world.

Toxicity Research

Since modern times, chemistry has been refined, and new substances have appeared frequently. I have focused on the study of poisons, and today I will discuss it with 2,6 - Dibromo - 4 - Iodoaniline.
This substance is new, its toxicity is unknown, and it is related to the safety of everyone, so it must be observed. I am a disciple of the crowd, and I study it carefully. First observe its properties, and then explore its dissolution in various solvents. Then try it with all kinds of living beings, observe its symptoms of poisoning, and record the changes in detail.
After months of work, I gradually gain something. This substance has a certain toxicity, and in the body of living beings, it can disrupt its physiological order and damage its internal organs. However, if you want to understand its details, you still need to cultivate it deeply, explore the mystery of its toxicology, and seek solutions to cure it.

Future Prospects

In today's world, new chemical products have emerged one after another, and 2,6 - Dibromo - 4 - Iodoaniline is also the object of our dedicated research. Although its application may not be fully realized in the current situation, we look to the future, and its prospects are shining.
We speculate that in the field of materials science, 2,6 - Dibromo - 4 - Iodoaniline may be ingeniously integrated into new polymeric materials, giving it unique properties, such as excellent electrical conductivity or extraordinary heat resistance, for electronic equipment, aerospace equipment, etc., to improve its performance.
In the field of pharmaceutical chemistry, its unique structure may inspire new drug development. Based on it, with fine modification, new drugs with significant curative effect and minimal side effects may be prepared, which will contribute to saving the world and blessing the common people.
Although there may be thorns in the road ahead, we and other scientific researchers should have perseverance and unremitting exploration. In time, 2,6 - Dibromo - 4 - Iodoaniline will surely shine, write a brilliant chapter on the scientific stage of the future, and cast immortal deeds for the progress of mankind.

Where to Buy 2,6-Dibromo-4-Iodoaniline in China?

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Frequently Asked Questions

As a leading 2,6-Dibromo-4-Iodoaniline supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the chemical properties of 2,6-dibromo-4-iodoaniline?

2% 2C6-dibromo-4-chloroaniline is an organic compound with a wide range of uses in many fields. The following is a brief description of its chemical properties:
This compound contains halogen atoms such as bromine and chlorine. Halogen atoms have unique characteristics, which greatly affect the chemical properties of the substance. First, due to the high electronegativity of halogen atoms, the electron cloud density of the benzene ring will be reduced, resulting in changes in the electrophilic substitution activity of the benzene ring. Generally speaking, compared with benzene, its electrophilic substitution reaction is more difficult to occur, and the reaction check point will also be affected by the positioning effect of halogen atoms. Bromine and chlorine are ortho and para-localizers, which reduce the activity of the benzene ring, but guide the electrophilic reagents to mainly attack the ortho or para-position of the halogen atom on the benzene ring.
Second, the amino group in 2% 2C6-dibromo-4-chloroaniline is also a key functional group. The amino group has a certain basic nature and can react with acids to form salts. At the same time, the amino group can participate in many nucleophilic reactions. Due to the existence of lone pair electrons on the nitrogen atom, it has nucleophilic properties and can attack suitable electrophilic reagents.
Furthermore, the carbon-halogen bond in this compound has a certain polarity, and the carbon-halogen bond can be broken under specific conditions, participating in the substitution reaction or elimination reaction. For example, in nucleophilic substitution reactions, halogen atoms can be replaced by other nucleophilic reagents.
In addition, 2% 2C6-dibromo-4-chloroaniline may undergo some free radical reactions under conditions such as light or heating, and halogen atoms can generate free radicals due to homogenization, which in turn triggers a series of free radical chain reactions.
In short, the chemical properties of 2% 2C6-dibromo-4-chloroaniline are determined by the coordination of its functional groups. These properties make it play an important role in organic synthesis, medicinal chemistry, etc. Chemists can use its properties to carry out various organic reactions and prepare desired organic compounds.

What are the synthesis methods of 2,6-dibromo-4-iodoaniline?

The synthesis method of 2% 2C6-dibromo-4-chloroaniline, usually using aniline as the starting material, is prepared by bromination, chlorination and other steps. The following methods are described in detail:
First, starting with aniline, bromine is first brominated. In a suitable solvent, such as glacial acetic acid, aniline reacts with bromine in a specific ratio and reacts at a temperature control to obtain 2,6-dibromoaniline. This step requires attention to the dropwise addition rate of bromine and the reaction temperature to avoid excessive bromination. Afterwards, 2,6-dibromoaniline is reacted with a chlorination reagent, such as N-chlorosuccinimide (NCS), under suitable reaction conditions, 4-position chlorination is achieved, and 2,6-dibromo-4-chloroaniline is finally obtained.
Second, the aniline can be protected first, and the amino group can be protected with an acetyl group to obtain acetaniline. After that, the acetaniline reacts with bromine, and the bromine atom can be introduced at the 2,6-position due to the positioning effect of the acetamide group. Then hydrolysis removes the acetyl group to obtain 2,6-dibromoaniline. Finally, 2,6-dibromoaniline is obtained by chlorination step, such as chlorine gas or other chlorination reagents, under suitable conditions.
Third, other benzene-containing compounds are also used as starting materials to construct amino groups, bromine atoms and chlorine atoms in suitable positions through multi-step reactions. If o-dibromobenzene is used as raw material, through a series of reactions such as nitrification, reduction, diazotization and chlorination, 2,6-dibromo-4-chloroaniline can also be synthesized. However, this route has many steps, and the reaction conditions of each step need to be carefully controlled to ensure higher yield and purity.
Each method has its own advantages and disadvantages. In actual synthesis, the optimal synthesis path should be selected according to factors such as raw material availability, cost, reaction conditions and yield.

What are the main uses of 2,6-dibromo-4-iodoaniline?

2% 2C6-dibromo-4-nitrobenzaldehyde is a crucial intermediate in organic synthesis. It is widely used in the field of medicinal chemistry to synthesize a variety of biologically active compounds. For example, in the development of antibacterial drugs, it can be used as a starting material to build molecular structures with specific antibacterial effects through a series of chemical reactions. In the field of materials science, materials with unique photoelectric properties can be prepared by reacting with other reagents for the fabrication of organic Light Emitting Diodes, solar cells and other devices. In the total synthesis of natural products, it is often used as a key building block to help build the carbon skeleton structure of complex natural products, providing a material basis for in-depth exploration of the biological activities and pharmacological effects of natural products.
Although there is no direct record of 2% 2C6-dibromo-4-nitrobenzaldehyde in Tiangong Kaiwu, the principles of chemical synthesis are actually the same in terms of ancient chemical processes. Ancient alchemy pursued the use of minerals as raw materials, through roasting, sublimation and other means to refine medicinal pills, which involved the control of many chemical reactions and material transformation. Similarly, the synthesis of 2% 2C6-dibromo-4-nitrobenzaldehyde also requires precise control of reaction conditions such as temperature, reactant ratio, and reaction time. In ancient technology, pottery production required controlling the kiln temperature to achieve the ideal texture and color; smelting iron required adjusting the ratio of heat and raw materials to obtain high-quality iron. This is similar to the strict requirements for the synthesis of 2% 2C6-dibromo-4-nitrobenzaldehyde. And the inheritance of ancient processes depends on the teaching of teachers and apprentices and the accumulation of experience. In the field of organic synthesis today, researchers also need to explore and summarize in practice to optimize the synthesis route and improve the yield and purity of 2% 2C6-dibromo-4-nitrobenzaldehyde.

What is the market price of 2,6-dibromo-4-iodoaniline?

Wen Jun inquired about the market price of dichlorobromo-4-nitrobenzaldehyde. This is an important compound in the field of fine chemicals, and its price often fluctuates due to many factors, making it difficult to hide it.
Let's talk about the raw materials first. The synthesis of dichlorobromo-4-nitrobenzaldehyde requires specific halides, nitro compounds, etc. as raw materials. If the origin of the raw material is damaged, or the international situation causes poor transportation, the supply of raw materials is tight, and the price rises, the cost of this compound will increase, and the market price will also rise.
Second discussion on the process. Synthesizing this compound, the complexity of the process and the advanced technology have a great impact. If a factory develops an efficient new process, which can reduce energy consumption, yield, and cost, it will be priced more flexibly in the market, and the price will have an advantage compared to those who are laggards in the process.
Further market demand. In the pharmaceutical, pesticide and other industries, if the research and development of new drugs and new pesticides requires this compound as a key intermediate, the demand will increase sharply. Supply is less than demand, and prices will rise; on the contrary, if demand is low, manufacturers will sell it for promotion, or reduce prices.
There are policies and regulations. Environmental protection policies are becoming stricter, manufacturers need to invest more money in environmental protection equipment to ensure production compliance, and costs will rise, affecting product prices.
Overall, the market price of dichlorobromo-4-nitrobenzaldehyde may fluctuate between hundreds of yuan per kilogram and thousands of yuan per kilogram. For accurate prices, you can consult chemical product suppliers, traders in the industry, or refer to real-time quotations on chemical product trading platforms to get the current market.

What are the precautions for storing and transporting 2,6-dibromo-4-iodoaniline?

2% 2C6-dichloro-4-nitroacetophenone requires attention to many matters during storage and transportation.
First, it concerns packaging. It must be tightly sealed with suitable packaging materials to prevent material leakage. This is because the substance has a certain chemical activity. If it leaks or reacts chemically with the surrounding environment, it will cause danger. If it is stored in a special corrosion-resistant container, it must be tightly sealed to prevent it from contacting with outside air, moisture, etc.
Second, temperature and humidity control. It should be stored in a cool, dry and well-ventilated place. If the temperature is too high, it may cause the chemical properties of the substance to be unstable, accelerate decomposition or cause other reactions; if the humidity is too high, it may also promote reactions such as hydrolysis. Therefore, a temperature and humidity control device should be installed in the storage place to keep the temperature within a reasonable range, and the humidity should not exceed a specific value.
Third, avoid mixed storage. Do not co-store and transport with oxidants, reducing agents, strong acids, strong bases, etc. Because its chemical structure contains chlorine and nitro groups, it has specific redox properties and reactivity. If it comes into contact with the above substances, it may trigger a violent chemical reaction, or even cause combustion and explosion.
Fourth, handle it with care when handling. This substance may be sensitive to a certain extent. If it is violently hit, vibrated, or damaged during handling, it will cause leakage, or cause a chemical reaction due to impact, endangering the safety of personnel and the environment.
Fifth, the label should be clear. On the package, the name of the substance, characteristics, hazard warnings and other information should be clearly marked. In this way, in all aspects of storage and transportation, personnel can know the characteristics of the substance according to the label, and take corresponding protection and operation measures.