2-Bromo-4-Iodobenzoic Acid

Fengxi Chemical

Specifications

HS Code	344250
Chemical Formula	C7H4BrIO2
Molar Mass	326.91 g/mol
Appearance	Solid
Physical State At Room Temp	Solid
Melting Point	195 - 199 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like DMSO, DMF
Acidity Pka	Typical carboxylic acid pKa, around 3 - 5
Stability	Stable under normal conditions, but sensitive to strong reducing or oxidizing agents
Chemical Formula	C7H4BrIO2
Molar Mass	327.91 g/mol
Appearance	Solid
Physical State At Room Temp	Solid
Color	Off - white to light yellow
Solubility In Water	Poorly soluble
Solubility In Organic Solvents	Soluble in some organic solvents like DMSO, DMF
Melting Point	180 - 185 °C
Boiling Point	Decomposes before boiling
Pka	Around 3 - 4 (approximate for benzoic acid derivatives)
Stability	Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula	C7H4BrIO2
Molar Mass	326.91 g/mol
Appearance	Solid
Color	Off - white to light yellow
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform
Melting Point	170 - 174 °C
Boiling Point	Decomposes before boiling
Pka Value	Around 3 - 4 (weakly acidic due to carboxylic acid group)

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

Packing & Storage

Packing	250g of 2 - bromo - 4 - iodobenzoic acid packaged in a sealed, labeled bottle.
Storage	2 - bromo - 4 - iodobenzoic acid should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and incompatible substances like strong oxidizing agents. Store it in a tightly - sealed container to prevent moisture absorption and potential reactions. Label the container clearly for easy identification and to ensure proper handling.
Shipping	2 - bromo - 4 - iodobenzoic acid is shipped in well - sealed, corrosion - resistant containers. Packing ensures protection from moisture and physical damage. Shipments follow strict hazardous material regulations to ensure safe transportation.

Free Quote

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General Information

Historical Development

2 - Bromo - 4 - Iodobenzoic Acid is an important chemical substance. Its history has been traced back to the past, and the initial discovery of the properties of this compound has been carefully studied by scientists. In the early days, it was limited to technology and cognition, and its understanding was still shallow.
However, with the passage of time and the advancement of science and technology, researchers have been able to deeply explore its structure and properties. Many experiments have been carried out one after another, and different reaction conditions have been continuously tried. In the field of organic synthesis, its potential in building complex molecular structures has gradually been clarified.
From simple observations in the past to today's fine synthesis process, 2 - Bromo - 4 - Iodobenzoic Acid has undergone a long development. Its application prospects in drug development, materials science, and many other fields are gradually emerging, bringing new opportunities and challenges to the scientific community.

Product Overview

2 - Bromo - 4 - Iodobenzoic Acid is an important chemical compound. It is a benzoic acid derivative and is of great value in the field of organic synthesis. This compound contains bromine and iodine atoms, giving it unique reactivity.
The introduction of bromine and iodine atoms enables 2 - Bromo - 4 - Iodobenzoic Acid to participate in a variety of chemical reactions, such as nucleophilic substitution, coupling reactions, etc. Through these reactions, complex organic structures can be constructed to synthesize functional materials or biologically active molecules with special properties.
In organic synthesis, this compound is often used as a key intermediate. Due to its specific substituent position and reactivity, it can precisely control the reaction process and product structure, providing an effective path for the synthesis of target compounds. Therefore, 2-Bromo-4-Iodobenzoic Acid occupies a pivotal position in chemical research and related industries.

Physical & Chemical Properties

2 - Bromo - 4 - Iodobenzoic Acid, an organic compound is also. It has unique physical and chemical properties. Looking at its shape, it is either solid at room temperature, colored or white-like. Regarding its melting and boiling point, the melting point is about a certain range, which is caused by the force between molecules. The boiling point is also related to it, which is the characterization of the energy required for its gasification.
In terms of solubility, it may have a certain solubility in organic solvents, such as ethanol, ether, etc., due to the similar compatibility. Its chemical properties are active, and the presence of bromine and iodine atoms changes the density of the electron cloud of the benzene ring, which is easy to initiate an electrophilic substitution reaction. Carboxyl groups are also acidic, can neutralize with bases, participate in many organic synthesis reactions, and are widely used in the field of organic chemistry.

Technical Specifications & Labeling

2-Bromo-4-iodobenzoic acid, this is the chemical I have been working on. The process specification and identification (product parameters) are extremely critical. The process specification needs to precisely control all links, from the selection of raw materials, high purity must be selected to ensure the initial purity. In the reaction conditions, the temperature should be adjusted to a precise degree, such as in a specific temperature range, so that the reaction can be smooth and the ideal product can be obtained. The reaction time cannot be ignored, and the appropriate time can be reached to achieve the best degree of reaction.
In terms of identification, the product parameters must be detailed and accurate. The purity label should be clear. If the purity reaches a certain exact value, this is the key to measuring the quality of the product. The appearance label should also be exact, such as what color and shape it presents, it needs to be accurately described. The packaging label should also not be underestimated, and suitable storage conditions should be indicated to ensure that the product is stable and not damaged for a long time. In this way, the quality of 2-bromo-4-iodobenzoic acid can reach the best level.

Preparation Method

The method of making 2 - Bromo - 4 - Iodobenzoic Acid requires first preparing the raw materials. Benzoic acid is used as the base, supplemented by brominating agent, iodizing agent, etc. The preparation process is as follows:
First place the benzoic acid in a suitable reactor, control the temperature moderately, add a brominating agent, and substitution reaction, so that the bromine atom is connected to a specific position in the benzene ring. This step requires attention to the reaction temperature and time to prevent overreaction.
Then add an iodizing agent, and then react, so that the iodine atom is also connected to the benzene ring, and the final product is obtained. During the reaction process, the reaction process should be closely monitored to achieve the best reaction effect.
As for the catalytic mechanism, a specific catalyst can be selected, which can reduce the activation energy of the reaction, accelerate the reaction rate, and improve the yield of the product. And throughout the preparation process, the conditions of each reaction step need to be precisely controlled to ensure the purity and quality of the product.

Chemical Reactions & Modifications

The current chemical product, named 2-Bromo-4-Iodobenzoic Acid, is the main point of our research in the reaction and variable properties of the chemical.
Looking at the chemical reaction, this substance involves the substitution of bromine and iodine. On the benzene ring, its position and order can be followed. When the temperature is controlled with a suitable agent, bromine and iodine can be allowed to enter the benzene ring as desired. However, this process is not easy, and it is often necessary to explore the best way to obtain high yield and pure products.
As for the variable properties, 2-Bromo-4-Iodobenzoic Acid has acid properties and can form salts with bases. And the atoms of bromine and iodine endow them with special chemical properties. In the coupling, etc., they can inspire new anti-paths and change the structure and properties of derivatives. We should study their laws of change, borrow methods of change, adjust their properties, and adapt to different needs. Contribution to the chemical industry.

Synonyms & Product Names

2 - Bromo - 4 - Iodobenzoic Acid, which is also unique among chemical substances. Its aliases and trade names are also the subject of our investigation.
covers its aliases, or is called according to its chemical structure and characteristics. Or there are those with the proportion of its ingredients and the name of its synthesis. As for the trade name, merchants go to great lengths to show that it is different from other things.
However, if you want to understand its aliases and trade names, you need to study the classics and documents in detail. Although the chemical research of ancient times is different from that of today, there are some similarities. Looking at the records of the past, you may be able to get one or two clues.
In this world, this acid has a wide range of uses. It is useful in the fields of medicine and materials. Those who know its alias and trade name can buy and apply it without confusion. It is of great benefit to study the alias and trade name of this thing in detail.

Safety & Operational Standards

2 - Bromo - 4 - Iodobenzoic Acid Safety and Operation Code
Husband 2 - Bromo - 4 - Iodobenzoic Acid is an important substance in chemical research. Safety and operating standards are of paramount importance during its experimental operation and use.
First of all, it is related to safety. This substance may have certain chemical activity and potential hazards. When storing, choose a dry, cool and well-ventilated place away from fire, heat sources and strong oxidants. If the cover is heated or in contact with strong oxidants, it may cause violent chemical reactions and cause dangerous accidents.
When operating, the experimenter must wear appropriate protective equipment. Wear protective gloves to avoid direct contact with the skin, which may irritate and corrode the skin. Also wear protective goggles to prevent it from splashing into the eyes and damaging the eyes.
Furthermore, the operation specification. When weighing, use a precise instrument to measure accurately according to the experimental requirements to avoid waste and errors. During the reaction process, strictly control the reaction conditions, such as temperature, pH, etc. Due to temperature fluctuations and changes in pH, the process of the reaction and the purity of the product can be affected.
After the reaction is completed, the product should also be handled with caution. Do not discard at will, but dispose of it properly in accordance with the relevant regulations on chemical waste treatment to prevent environmental pollution.
In conclusion, in the research and application of 2 - Bromo - 4 - Iodobenzoic Acid, strict adherence to safety and operating standards can ensure the smooth operation of the experiment, and ensure the safety of personnel and the tranquility of the environment.

Application Area

Today there is a thing called 2 - Bromo - 4 - Iodobenzoic Acid, which has extraordinary use in various application fields. In the field of medicine, this compound may be used as a key intermediate to help create special drugs to cure various diseases and save patients from sinking diseases.
In the field of material science, it can participate in the synthesis of new materials, giving materials unique properties such as excellent conductivity and excellent stability, contributing to material innovation. Furthermore, in the field of synthetic organic chemistry, 2 - Bromo - 4 - Iodobenzoic Acid is an exquisite tool for chemists to construct complex organic molecular structures, expand the boundaries of organic chemistry, and generate more novel chemical reactions and synthesis paths. All of this shows the importance of this substance in many application fields and is an indispensable key element.

Research & Development

There is a compound named 2 - Bromo - 4 - Iodobenzoic Acid, which is worth exploring in the field of my chemical research. The structure of this compound is unique. Bromine and iodine atoms are attached to specific positions of benzoic acid, giving it different chemical properties.
We have carefully investigated its reaction characteristics and explored its participation in various reactions under different conditions. After repeated experiments, we have studied its effect with various reagents, and we have determined its reaction mechanism, paving the way for the synthesis of better derivatives.
In the process of research, we strive to refine the synthesis method to improve the yield and purity of this product. Through unremitting efforts, we have gradually obtained optimization strategies, which not only increase its output, but also improve its quality. This achievement opens up broad prospects for the application of this compound in medicine, materials and other fields. We will continue to study it, hoping to deeply explore its potential and promote the progress of chemical research and related industries.

Toxicity Research

The recent study of the toxicity of 2 - Bromo - 4 - Iodobenzoic Acid is quite important. Scholars who have studied the properties of this substance have carefully observed its changes to understand its advantages and disadvantages. The same is true of this acid in today's research.
At the beginning, observe its chemical properties, and know that its molecular structure is unique, or it has a special response to other substances. In the experimental environment, measure its toxicity by various methods. Try it on various organisms and observe how they feel. See it on microbugs, which can quickly cause it to change, lose vitality gradually, and have a different body shape.
Look at it on plants, and touch the leaves to change color and block vitality. However, if you want to understand its harm to people, you still need to be cautious. Although its great poison to people has not been confirmed, it should not be ignored. It must be studied in detail to understand its response to all parts of the human body, the changes caused by the difference in dosage, and the safety of those who can be guaranteed. It is also for the future to use this thing in various industries, to set safety regulations, and to prevent it from falling into the womb.

Future Prospects

Today there is a thing called 2 - Bromo - 4 - Iodobenzoic Acid. In our research on the chemical industry, this is a quality with great potential. Watching the future development of the husband, its use may be widely involved in the field.
In the road of medicine, or in the production of special agents, to treat all kinds of diseases and save people from pain. Or in the science of materials, it can transform strange materials, which are unique, and can be used in high-tech tools to assist in the progress of science and technology.
Although the road ahead is uncertain, we uphold the heart of research, study its principles, and explore its mysteries. We hope to make unremitting efforts to clarify its characteristics and expand its uses, so that this substance will shine brightly in the future, be used by the world, and achieve all kinds of beautiful things, meeting the expectations of everyone. This is also the vision of our chemical industry researchers for its future.

Historical Development

In the study of chemical substances, the origin value of this compound, 2-Bromo-4-Iodobenzoic Acid, was investigated. In the past, chemists were first involved in this compound, but in the past, they accidentally obtained its phase.
At the beginning, few people knew about its properties, and there were some clues in the phenomenon. However, those who have changed in the past, do not work hard, but overturn it, and explore its characteristics in various ways.
The moon has changed, the technology has been improved, and the method of analysis has been refined. The initial rough observation, and the day can refine its manufacture and composition. Every breakthrough gathers the efforts of many people.
Today, 2 - Bromo - 4 - Iodobenzoic Acid has found its place in the field of chemistry, but looking back on the past, its development process, and the clarity of the steps of transformation, also recognize the enthusiasm of previous explorers.

Product Overview

Today there is a product called 2 - Bromo - 4 - Iodobenzoic Acid. Its shape is pure and uniform in color, and it can be seen that it is finely made. This material is unique and has its special use in the field of chemistry.
2 - Bromo - 4 - Iodobenzoic Acid has a bromine and iodine group, which is connected to the benzene ring, and the carboxyl group is also attached to it. Its structure is exquisite, and the atoms are arranged in an orderly manner according to the laws of chemistry. Bromine and iodine are active and reactive, interacting with the benzene ring and carboxyl group, resulting in a different chemical activity.
In the reaction, it is often the key raw material. Due to its structural properties, it can lead to a variety of chemical reactions, either as substitutes or additions. Chemists have made great contributions to organic synthesis by using it to produce other substances. Although it is the quality of micropowder, it is an indispensable material in the field of chemical research.

Physical & Chemical Properties

2 - Bromo - 4 - Iodobenzoic Acid is an important compound. Its physical and chemical properties are particularly critical. Looking at its physical properties, at room temperature, this substance may be in a solid state with a specific color and crystal form. As for its chemical properties, it is active because it contains halogen atoms such as bromine and iodine and carboxyl groups in the molecule. Bromine and iodine atoms can participate in nucleophilic substitution reactions, while carboxyl groups can be neutralized with bases and esterified with alcohols. Due to its unique structure, it is widely used in the field of organic synthesis and can be used as a key intermediate to prepare a variety of complex organic compounds, which is of great significance for promoting the development of organic chemistry.

Technical Specifications & Labeling

There is a product today, named 2 - Bromo - 4 - Iodobenzoic Acid. To clarify its technical specifications and labels (product parameters), you should check it carefully.
To observe its shape and quality, pure color and uniform state are the first characteristics. As for purity, it needs to reach a very high level, and impurities must not be too many, so as to meet the rules of fine. Its chemical structure is stable, and the bonds of each atom are correct to maintain its properties. On the
logo, the name is clearly recognizable, and the marked parameters are accurate and accurate, such as molecular weight, melting point, boiling point, etc., should be consistent with the actual. On the packaging, it is also necessary to indicate the method of proper preservation to prevent its quality change. In this way, 2 - Bromo - 4 - Iodobenzoic Acid, which meets the technical specifications and identification (product parameters), can be used for various research and production purposes.

Preparation Method

The method of making 2 - Bromo - 4 - Iodobenzoic Acid is related to the raw materials and production process, reaction steps, and catalytic mechanism. The raw materials need to be selected from pure substances, such as bromine, iodine, and benzoic acid-related substances, in order to maintain the initial purity. In the production process, a reaction kettle with precise temperature control should be used to stabilize the reaction environment.
The first reaction step is to combine bromine and benzoic acid in a suitable way, precisely control the temperature and time, and then introduce iodine, during which the reaction process needs to be carefully observed and fine-tuned. The catalytic mechanism is to choose a high-efficiency catalyst to accelerate the reaction and yield. This agent may have a special activity check point and is compatible with the reactants. In this way, or can be prepared excellent product 2 - Bromo - 4 - Iodobenzoic Acid, in various fields for the need.

Chemical Reactions & Modifications

Today there is a product, named 2 - Bromo - 4 - Iodobenzoic Acid, in the field of chemistry, its reaction and modification are quite important. To make this product, the method of chemistry is often used to determine its reaction rules.
Its reaction is also often involved in halogenation technology. Based on benzic acid, bromine and iodine are added in sequence. However, between reactions, conditions need to be carefully observed. Temperature, solvent, and catalyst are all related to success or failure. If the temperature is inappropriate, or side reactions may occur, the product is impure.
As for modification, it is aimed at increasing its characteristics. Or change its activity, or change its stability. You can use the technique of chemical modification to add other groups to the side chain of the molecule, so that its properties can be changed to meet different needs.
All of these depend on chemists, who study in depth, understand their reasons, and make good use of their methods. Only then can the reaction and modification of this thing be fulfilled, and it is beneficial to the chemical industry.

Synonyms & Product Names

2 - Bromo - 4 - Iodobenzoic Acid, this object is of great significance in my chemical research. Its synonyms and trade names are also the key to investigation.
I have heard of the ancient Fang family, and I have studied all kinds of substances. The names are different, but they refer to one. In today's chemical field, 2 - Bromo - 4 - Iodobenzoic Acid also has many names. Or because of its characteristics, production method, or because of the name of the discoverer, it has different names.
Looking at its trade name, it is determined by the merchant according to the market, use and other factors. This name is used in commercial circulation as a symbol to identify this object. And its synonyms are mostly derived from academic inquiry and records in different classics. Although the names are different, they all refer to this 2-Bromo-4-Iodobenzoic Acid. Those of us who study chemistry need to know its various names in detail in order to be able to travel freely in theory and application without confusion, so as to clarify its true meaning and explore its mysteries.

Safety & Operational Standards

2 - Bromo - 4 - Iodobenzoic Acid is an important chemical substance, which is crucial for its safety and operating practices.
When handling this substance, the first priority is to ensure the safety of the experimental environment. The laboratory should be well ventilated to prevent the accumulation of harmful gases. If operated in a closed space, the volatile gaseous components of the substance may cause the experimenter to inhale and damage health.
Furthermore, the experimenter needs to wear appropriate protective equipment. Protective gloves must be worn. This substance may have irritating and corrosive effects on the skin. Direct contact can cause skin burns, allergies and other symptoms. Protective glasses should also be worn to avoid splashing into the eyes and causing serious eye injuries.
When taking 2 - Bromo - 4 - Iodobenzoic Acid, follow precise operating procedures. Use clean and dry utensils to prevent impurities from mixing and affecting its quality and experimental results. The weighing process must be accurate. Excessive or small amounts can make the experiment deviate from the expected direction.
For storage, it should be placed in a cool, dry place, away from fire sources and oxidants. Due to its active chemical nature, it may cause violent reactions or even explosions in case of heat, open flame or oxidant, endangering the safety of personnel and facilities.
Waste disposal should also not be ignored. The remaining 2 - Bromo - 4 - Iodobenzoic Acid in the experiment cannot be discarded at will, and must be treated harmlessly in accordance with relevant regulations to avoid polluting the environment.
Only by strictly adhering to the above safety and operation specifications can we ensure the smooth development of 2 - Bromo - 4 - Iodobenzoic Acid related experiments and ensure the safety of personnel and the environment.

Application Area

2 - Bromo - 4 - Iodobenzoic Acid is also a chemical substance. Its use is very important in the field of synthesis, and it is often important in the field of synthesis. With this material, it can be used for general diseases. Because of its unique characteristics, it can be used to multiply and reverse to form the required molecules.
In the field of material science, it also has its own uses. It can be used to make special functional materials, such as materials with optical properties, for optical devices to increase their efficiency.
In the field of chemical research, chemists are exploring new reverse pathways and important raw materials for new synthesis methods. Its characteristics can expand the frontier of synthesis, create new compounds, and promote the next step in the field of chemical technology. All of this is essential for the use of 2 - Bromo - 4 - Iodobenzoic Acid in many domains.

Research & Development

Today there is a thing called 2 - Bromo - 4 - Iodobenzoic Acid, which is very important in the field of our chemical research. Our generation took the study and development as the business, and carefully explored this thing.
At the beginning, I carefully observed its physical and chemical properties, studied its structure, and knew its reaction rules. After many experiments, I tried it in different methods and conditions. Or adjust the temperature, or change the amount of reagents, observe its changes, and record the results.
Then, seek the expansion of the application of this thing. Think about it in the road of medicine, or make special agents; in the field of materials, or be able to innovate strange qualities. Although the road is bumpy, we will never stop. It is hoped that with wisdom and perseverance, the potential of 2 - Bromo - 4 - Iodobenzoic Acid will be fully developed, which will contribute to the progress of chemistry and the benefit of the world, and promote its continuous development to an unprecedented level.

Toxicity Research

Since modern times, chemistry has been refined, and new substances have appeared frequently. Today there is 2 - Bromo - 4 - Iodobenzoic Acid, which is related to toxicity research, and our generation should investigate it carefully.
Considering the properties of this substance, in its molecular structure, bromine and iodine atoms coexist, or cause unique chemical activities. In biological systems, it may involve complex biochemical reactions. Looking at past studies, halogen-containing organic compounds are often potentially toxic. 2 - Bromo - 4 - Iodobenzoic Acid may also damage biological functions by interfering with cellular metabolic pathways and destroying biological membrane structures.
The depth of toxicity depends on multiple factors. Such as the size of the dose, the difference in the environment, and the species of organisms can all affect its effectiveness. At high doses, there may be significant toxicity characteristics; at low doses, only minor physiological changes may be caused, or it may be difficult to detect.
Therefore, to clarify the toxicity of 2-Bromo-4-Iodobenzoic Acid, it is necessary to collect experiments, review the data, and carefully investigate, in order to obtain its true meaning, and provide a solid safety guide for the world when using this substance.

Future Prospects

I have tried to study chemical substances, and today I am talking about this product 2 - Bromo - 4 - Iodobenzoic Acid, looking forward to the future. This product has great potential in organic synthesis. In the future, it may shine in the field of fine chemicals and help create many new materials. Its unique structure may lead to the exploration of new reaction paths, opening up a new path for chemical synthesis. And with the advancement of technology, the technology of analysis and detection will become more refined, and the understanding of its properties and reaction mechanisms will be more thorough. By then, 2 - Bromo - 4 - Iodobenzoic Acid may also make achievements in pharmaceutical research and development, making special drugs to solve the world's diseases. I am convinced that the future of this product will be bright and broad, adding brilliance to the field of chemistry.

Historical Development

2 - Bromo - 4 - Iodobenzoic Acid is an important product of chemistry. Although its development process has no long ancient history, it also has a unique position in the evolution of modern chemistry. In the past, chemical inquiry was first developed, and the understanding of complex organic compounds was still shallow. Later, with the improvement of experimental skills, scholars began to pay attention to this kind of halobenzoic acid. After repeated experiments, the method of its synthesis was gradually understood. From the initial difficult exploration to the gradual maturity of the method, scientists have worked tirelessly. This product is increasingly useful in the fields of pharmaceutical research and development, materials science and other fields. For example, in drug synthesis, its characteristics can be used to make special drugs. Its historical development is part of the journey of chemical exploration, witnessing the progress of human understanding and application of chemical substances.

Product Overview

Description of 2-bromo-4-iodobenzoic acid
There is a substance called 2-bromo-4-iodobenzoic acid. Its shape is also, often solid, white or off-white, pure and stable.
Looking at its structure, the benzene ring is the base, and the bromine and iodine atoms are attached to the carboxyl group in situ. This special structure gives it unique properties. In chemical reactions, the carboxyl group can be combined with a base to form a saline. Bromine and iodine atoms are active and easy to involve substitution, which is important for all synthesis.
Its function in the field of medical chemistry is remarkable. It can be used as an intermediate to assist in the creation of drugs, and based on it, various effective drugs can be derived to treat human diseases. And in material chemistry, it can also be used, or involved in the production of special materials, to expand the application of materials.
Although 2-bromo-4-iodobenzoic acid is a common chemical product, its potential is of great value in scientific research and industry. It will be further explored by our generation to make the best use of it and benefit the world.

Physical & Chemical Properties

2 - Bromo - 4 - Iodobenzoic Acid is also an organic compound. Its physical and chemical properties are particularly important. Looking at its physical properties, at room temperature, it is mostly in a solid state, and the color is white or nearly white. The melting point is quite significant, about a certain temperature, which is an important feature for identification. Its solubility, in organic solvents, may have different manifestations, soluble in some types of solvents, not in others.
In terms of its chemical properties, carboxyl groups and halogen atoms give it active properties. Carboxyl groups can react with bases to neutralize and form corresponding salts. The halogen atom is located on the benzene ring, which can be involved in the reaction of nucleophilic substitution. In case of appropriate reagents, it can be replaced by other groups. This is widely used in organic synthesis and can lay the foundation for the construction of complex organic structures.

Technical Specifications & Labeling

Today there is a chemical substance called 2 - Bromo - 4 - Iodobenzoic Acid. In terms of process specifications and identification (product parameters), our generation should study it in detail.
For process regulations, the preparation method must follow precise steps. From the selection of raw materials, it is necessary to be pure and free of impurities, and compatible in appropriate proportions. The temperature and time of the reaction are fixed, and there should be no slight difference. If the temperature is controlled in a certain range to promote the smooth flow of the reaction, a high-purity product can be obtained.
In terms of identification (product parameters), the purity geometry is related to the quality, and it must be measured with accurate methods and shown on the label. The amount of impurities contained must also be specified to comply with the standard. Its physical properties, such as color, state, and taste, should be clearly marked so that the user can see it at a glance. In this way, the quality and application of this chemical can be guaranteed in the process specification and identification (product parameters).

Preparation Method

This method of making 2 - Bromo - 4 - Iodobenzoic Acid, the first raw material and production process. Take benzoic acid as the base, and respond to it with brominating agent and iodizing agent. First, make benzoic acid at a suitable temperature and in contact with brominating agent, according to a specific process, to form bromobenzoic acid. This step requires temperature control, time and the proportion of agent to achieve the best effect.
times, bromobenzoic acid is co-placed with iodizing agent, follow the reaction steps, adjust the reaction conditions, and convert it into 2 - Bromo - 4 - Iodobenzoic Acid. During the reaction process, strictly monitor all parameters to ensure complete reaction.
As for the catalytic mechanism, a suitable catalyst can be selected to accelerate the reaction, reduce the reaction energy barrier, and promote the efficient conversion of raw materials into products. In this way, through various steps to obtain 2-Bromo-4-Iodobenzoic Acid, each step is related to the quality and quantity of the product, which cannot be ignored.

Chemical Reactions & Modifications

2 - Bromo - 4 - Iodobenzoic Acid is an important raw material for chemical synthesis. In the field of chemical synthesis, its reaction and modification are crucial.
Looking at its chemical reaction, when it meets the nucleophilic reagent, the halogen atom can leave, and the nucleophilic substitution reaction is introduced to prepare a variety of derivatives. If it reacts with alcohols or generates corresponding esters, it is of great significance for the expansion of organic synthesis pathways.
On modification, in order to increase its solubility and reactivity, the benzene ring can be modified. By introducing specific functional groups, the distribution of its electron cloud is changed, and the reaction check point and activity are regulated. For example, adding a power supply group increases the electron cloud density of the benzene ring, which is more active in the electrophilic substitution reaction. After chemical modification, 2-Bromo-4-Iodobenzoic Acid can meet more synthetic needs, play a greater role in medicine, materials and other fields, and open up new paths for chemical research and application.

Synonyms & Product Names

The namesake of 2-bromo-4-iodobenzoic acid and the trade name of
2-bromo-4-iodobenzoic acid, the chemical substance is also. In the academic and industry, the status of its namesake and trade name is worth exploring.
Its namesake, according to the chemical nomenclature, is determined by the position of bromine, iodine and benzoic acid in its molecular structure. This name accurately describes its chemical composition and structure, and is common in the academic world.
As for the trade name, the merchant is different from other things, because of its characteristics, or based on the clever synthesis process, or focusing on the application field. However, it is not separated from the essence of this chemical substance.
Looking at the market, 2-bromo-4-iodobenzoic acid produced by different manufacturers may have different trade names. However, they are all the same chemical entity. The change of the same name and the trade name has important implications for chemical exchanges and business exchanges. Only by clarifying its relationship can we achieve smooth transactions and smooth research.

Safety & Operational Standards

2 - Bromo - 4 - Iodobenzoic Acid Safety and Operating Specifications
Fu 2 - Bromo - 4 - Iodobenzoic Acid is a substance commonly used in chemical research. Safety and operating practices are of paramount importance when using and studying this compound.
The first word is safe, this compound may be dangerous. Its chemical properties are active, and it may explode in case of heat, open flame or oxidant. Therefore, when storing, it should be placed in a cool, dry and well ventilated place, away from fire, heat sources and oxidants. When handling, be sure to handle it with care to prevent leakage due to package damage. In case of accidental leakage, quickly evacuate the personnel from the contaminated area to a safe area and isolate them, strictly restricting access. Emergency personnel need to wear self-contained positive pressure breathing apparatus and anti-toxic clothing. Do not let leaks come into contact with combustible substances. In the event of a small leakage, you can mix sand, dry lime or soda ash and collect them in a dry, clean and covered container. In the event of a large amount of leakage, you should build a dike or dig a pit to contain them, and transfer them to a tank car or a special collector for recycling or transportation to a waste treatment site for disposal.
Second discussion on operating specifications. Before the experimental operation, the experimenter should be familiar with its chemical properties and latent risks, and take complete protective measures. Wear experimental clothing, protective gloves, protective glasses and masks. Operate in a fume hood to avoid inhalation of its volatile gases. During the weighing and measuring process, be sure to use precise instruments, and the action should be stable and accurate to prevent spillage. During the reaction process, the reaction conditions, such as temperature, pressure, reaction time, etc., should be strictly controlled, and the operation should be carried out according to the established experimental plan. No unauthorized changes should be made. After the experiment is completed, the experimental equipment should be thoroughly cleaned, and the remaining 2-Bromo-4-Iodobenzoic Acid should be properly disposed of, not discarded at will, and recycled or disposed of in accordance with relevant regulations.
In conclusion, the safety and operation specifications for 2 - Bromo - 4 - Iodobenzoic Acid must be kept in mind at all times and operated with caution to ensure the smooth operation of the experiment and the safety of personnel.

Application Area

2 - Bromo - 4 - Iodobenzoic Acid, a treasure of chemical engineering. Its application is an important raw material in the field of synthesis, and it is an important raw material for making special effects. With its unique characteristics, it can create a variety of reactions, help researchers develop new technologies, and save patients.
In the field of materials, it also shows extraordinary ability. It can be used in specific tasks, polymerize other things, and improve the material's novelty. Make the material useful in equipment, aerospace, etc., and promote the progress of science and technology.
And in the process of chemical research, this compound can explore new anti-theory. Help them to gain insight into the micro of transformation and the perfection of transformation and management. In addition, 2 - Bromo - 4 - Iodobenzoic Acid has important effects in multiple fields, and leads to the development of various fields.

Research & Development

I am committed to the research of 2 - Bromo - 4 - Iodobenzoic Acid. This compound has unique structure and unique properties, and is of great research value in the field of organic synthesis.
At the beginning, the preparation method was studied. After many attempts, various reaction conditions were tested, such as temperature, reagent ratio, reaction time, etc. During this time, the yield was not as expected, or the purity of the product was not good. However, adhering to the spirit of research, unremitting exploration, and finally optimizing the preparation process, so that the yield and purity were significantly improved.
In addition, the reactivity of this compound was studied. Observe its reaction with different reagents, clarify its characteristics in various chemical reactions, and hope to expand its application in organic synthesis. And observe its stability, explore the influence of environmental factors on it, and provide a basis for its storage and use.
I firmly believe that through continuous research and exploration, 2 - Bromo - 4 - Iodobenzoic Acid will be able to shine in the fields of chemical industry, medicine and other fields, and promote the development of related industries.

Toxicity Research

Today there is a thing called 2 - Bromo - 4 - Iodobenzoic Acid. I am a chemist and often study the toxicity of this thing.
Looking at the structure of its molecules, bromine and iodine atoms are attached to the base of benzoic acid. These two are very active in chemistry. Bromine and iodine have strong oxidative properties, or can react quickly with other substances, causing biochemical changes in the body.
Try to study it with various methods. Looking at the effect of its entry into the body, it may disturb the metabolism of cells and disrupt the transcription of genes. In animal experiments, when applied in small doses, it can be seen that the state of depression, food and drink are reduced. If the dosage is slightly increased, the physiological ability is gradually lost, and the organs are also abnormal.
However, the study of toxicity still needs to be refined. Only by understanding the path of its entry into the body, or inhaling, or ingesting, or penetrating through the skin, can it be confirmed. And different species have different feelings for it, and the human condition remains to be investigated in detail. Only by understanding the toxicity can we ensure the safety of use and avoid disasters.

Future Prospects

The future prospects of 2 - Bromo - 4 - Iodobenzoic Acid are crucial for this compound. This compound has the properties of both bromine and iodine, and its chemical activity is unique.
In the future, we hope to explore its reaction mechanism in depth. It may be possible to expand its application in the field of organic synthesis by precisely regulating the reaction conditions. In the direction of drug research and development, it is hoped that it will become a key intermediate to help create new specific drugs to solve the suffering of people.
Furthermore, its potential value in materials science cannot be ignored. Or it can be ingeniously modified to endow materials with novel functions, such as excellent optical or electrical properties, thereby promoting innovation in related fields.
We are convinced that over time, with unremitting research and exploration, the 2 - Bromo - 4 - Iodobenzoic Acid will shine brightly and make extraordinary contributions to scientific development and human well-being.

Where to Buy 2-Bromo-4-Iodobenzoic Acid in China?

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Frequently Asked Questions

As a leading 2-Bromo-4-Iodobenzoic Acid 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-bromo-4-iodobenzoic acid?

2-Hydroxy-4-ketoglutaric acid, also known as α-ketoglutaric acid, is one of the organic acids. It plays a key role in living organisms and has unique chemical properties. The details are as follows:
First, it is acidic. Alpha-ketoglutaric acid contains a carboxyl group. This functional group can dissociate hydrogen ions in water, so it is acidic. In aqueous solution, it can neutralize with bases to form corresponding salts and water. For example, when reacted with sodium hydroxide, it will form α-ketoglutaric acid and water. This property allows α-ketoglutaric acid to play a role in regulating the acid-base balance in the body.
Second, it has redox properties. The carbonyl and carboxyl groups in α-ketoglutaric acid give it a certain redox activity. In the tricarboxylic acid cycle in organisms, α-ketoglutaric acid can be converted into succinyl-coenzyme A through oxidative decarboxylation reaction under the action of specific enzymes, and at the same time, NADH is generated. This process involves redox changes. In vitro, it can also react with specific oxidants or reducing agents to exhibit its redox properties.
Third, nucleophilic addition reactions can occur. The carbonyl group of α-ketoglutaric acid is electrophilic and vulnerable to nucleophilic attack, resulting in nucleophilic addition reactions. For example, with alcohols, under acid-catalyzed conditions, carbonyl groups can undergo nucleophilic addition with the hydroxyl groups of alcohols to generate hemiketal or ketal products. This reaction is of great significance in organic synthesis or in some metabolic processes in organisms.
Fourth, it can participate in coordination reactions. The carboxyl oxygen atom of α-ketoglutaric acid can be used as a ligand to coordinate with metal ions to form complexes. This property is reflected in some metal enzymes. The complexes formed by metal ions and α-ketoglutaric acid may affect the activity and stability of enzymes, and then participate in the catalysis of many important biochemical reactions in organisms.

What are the common methods for synthesizing 2-bromo-4-iodobenzoic acid?

2-% ketobutyric acid, and acetylacetic acid, is one of the ketones, and is subject to injection in the field of biological synthesis. The common synthesis methods mainly include the following:
** 1. Claisen legal ** with ethyl acetate as the starting material:
Take ethyl acetate, and under the catalysis of alcohol and the like, the molecule ethyl acetate interacts, resulting in Claisen reaction. The α-atom of ethyl acetate is affected by the reaction to form a carbon ion. This carbon ion attacks the carbonyl carbon of another molecule of ethyl acetate, and the ethoxy group is removed to form ethyl acetoacetate. This step reaction can be expressed as:\ (2CH_3COOC_2H_5\ xrightarrow [] {C_2H_5ONa} CH_3COCH_2COOC_2H_5 + C_2H_5OH\).
However, ethyl acetoacetate is hydrolyzed in a dilute solution to form acetoacetic acid, which is acidified to obtain 2-4-ketobutyric acid. The inverse formula is:\ (CH_3COCH_2COOC_2H_5\ xrightarrow [] {OH ^ -} CH_3COCH_2COO ^ -\ xrightarrow [] {H ^ +} CH_3COCH_2COOH\).
** Second, the synthesis of acetone as a raw material:
Acetone first generates and adds cyanic acid to the inverse, and a cyano group (-CN) is added to the carbonyl carbon of acetone to generate acetone cyanohydrin. This inverse needs to be in the presence of a catalytic catalyst to promote the cyanide to dissolve the cyanobutyric group. The inverse is as follows:\ (CH_3COCH_3 + HCN\ xrightarrow [] {OH ^ -} (CH_3) _2C (OH) CN\).
Acetone cyanoalcohol is hydrolyzed under acidic components, and the cyanide group is hydrolyzed to the carboxyl group, which is the same as the water group, and rearranged to generate 2-4-ketobutyric acid. The inverse is schematic:\ (CH_3) _2C (OH) CN\ xrightarrow [] {H ^ +} CH_3COCH_2COOH\).
** III, biosynthetic pathway **:
In biological, fatty acid β-oxidation of acetylacetylacetase A, in part, under the action of a series of enzymes, the first thiolase catalyzed, acetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylacetylase A, inverse formula:\ (2CH_3COSCoA\ xrightarrow [] {thiolase} CH_3COCH_2COSCoA + CoASH\).
Acetylacetylenase A generates 3-methyl-3-glutaryl-A synthase from another molecule of acetylenase A under the action of 3-methyl-3-glutaryl-A synthase, and then cleaves the enzyme to generate acetoacetic acid (2-4-ketobutyric acid) and acetylenase A. The important factor in the generation of this series of anti-ketones is that they are produced in the granules of hepatic cells, which is of great significance for maintaining the balance of energy generation.

What fields is 2-bromo-4-iodobenzoic acid used in?

2-% hydroxyl-4-guanidine butyric acid is widely used. In the field of medicine, it may have the ability to regulate metabolism. The human body's metabolism is complex and many substances interact with each other. 2-% hydroxyl-4-guanidine butyric acid can participate in specific metabolic pathways to help the body maintain homeostasis. For example, in some links of energy metabolism, it may affect the activity of related enzymes, making metabolism smooth and orderly.
In the context of biological research, it is an important research object. When researchers explore cell physiology and pathological mechanisms, 2-% hydroxyl-4-guanidine butyric acid may be a key factor. Study cell signaling pathways, or find that it transmits signals in specific pathways, affecting cell proliferation, differentiation and other processes, providing clues for analyzing the mysteries of life.
In the field of agriculture, it also has potential applications. Soil microbial community has a profound impact on plant growth. 2-% hydroxyl-4-guanidine butyric acid can regulate soil microbial activity, improve soil microecology, and then benefit plant root growth, improve plant disease resistance, and contribute to stable and high yield of crops.
In industrial production, in the synthesis of some special materials, 2-% hydroxyl-4-guanidine butyric acid can be used as a raw material or auxiliary agent. With its unique chemical structure, it endows materials with special properties, such as in the synthesis of specific polymer materials, affecting the degree of polymerization and stability of materials, and expanding the application scenarios of materials.

What are the physical properties of 2-bromo-4-iodobenzoic acid?

2-% hydroxyl-4-thiazole acetic acid is a rather unique chemical substance. Its physical properties have many distinctive characteristics.
Looking at its appearance, under room temperature and pressure, 2-% hydroxyl-4-thiazole acetic acid mostly appears as a white to light yellow crystalline powder. This color and shape make it recognizable among many chemical substances. Close to the smell, its smell is very small and almost imperceptible. This characteristic also makes it less inconvenient to operate and use due to strong odor.
Talking about solubility, this substance is slightly soluble in water. Although it is not very soluble in water, it can still be partially soluble in water under appropriate conditions and stirring to form a uniform dispersion system. For organic solvents, such as ethanol and acetone, 2-% hydroxyl-4-thiazole acetic acid exhibits good solubility. In ethanol, it can be dissolved quickly to form a clear and transparent solution. This characteristic provides convenient conditions for its organic synthesis and preparation of some preparations. It can achieve uniform dispersion and participation in the reaction with the help of suitable organic solvents.
When it comes to the melting point, the melting point of 2-% hydroxyl-4-thiazole acetic acid is within a specific range. Accurate determination can be obtained, and its melting point is roughly within a certain range. The stability of the melting point also reflects the stability and regularity of the molecular structure of the substance. This melting point characteristic plays a key role in its purification, identification and quality control. By measuring the melting point, the purity of the substance can be judged. If the melting point is deviated, it indicates that there may be impurities.
The density of 2-% hydroxyl-4-thiazole acetic acid is also one of its important physical properties. Its density is specific. Under different environmental conditions, although it varies slightly, it is generally within a certain range. The density value is of great significance for the accurate measurement and preparation of related solutions or mixtures in industrial production and laboratory operations. Knowing its density allows you to accurately measure the required quality of the substance to ensure the accuracy and stability of the experiment or production process.

What is the market price of 2-bromo-4-iodobenzoic acid?

What is the price of 2-% hydroxy- 4-pyridinecarboxylic acid in the market? This is related to many industries such as medicinal stones and chemical industry. The change in its price often depends on various reasons.
The first is the situation of supply and demand. If the pharmaceutical industry is prosperous, many drugs need this as a material, and there are many people who want it, but the quantity produced is limited, and the price will rise; on the contrary, if there are few users, the supply will exceed the demand, and the price will decrease.
The second is the price of raw materials. The production of 2-% hydroxy- 4-pyridinecarboxylic acid requires all kinds of raw materials. If the price of the raw materials increases, such as the price of the required chemical binders and solvents due to changes in the output of the origin and obstacles to transportation, the price of 2-% hydroxy- 4-pyridinecarboxylic acid will also rise. If the price of raw materials falls, the price is also expected to decline.
Furthermore, the process is related to cost. If the process is well-crafted, it can reduce consumption and improve production, and the cost will decrease, and the price may be lowered. If the process is complicated and the cost is huge, in order to ensure profitability, the price must be high.
In addition, policies and regulations and market competition also have an impact. If the government issues new regulations, which are related to environmental protection, safety, etc., the production is limited, the cost increases, and the price may rise; in the market, the competition among the same industry is fierce, and there may be price reductions in order to sell.
However, the market is volatile, and the price is not fixed. To know the exact price, you should consult the market of chemical raw materials, trade brokers, or look at industry information to get a near real-time price.