2 5 Diiodobenzoic Acid
Iodobenzene

2,5-Diiodobenzoic Acid

Fengxi Chemical

Specifications

HS Code

600773

Chemical Formula C7H4I2O2
Molar Mass 377.915 g/mol
Appearance Solid
Solubility In Water Low
Melting Point 187 - 190 °C
Boiling Point Decomposes before boiling
Density N/A (no common value found in basic data)
Pka N/A (no common value found in basic data)
Odor Odorless (assumed as no odor information is commonly reported for this solid)

As an accredited 2,5-Diiodobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 250g of 2,5 - diiodobenzoic Acid packaged in a sealed, air - tight plastic bottle.
Storage 2,5 - Diiodobenzoic Acid should be stored in a cool, dry place, away from direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and contact with air, which could potentially lead to degradation. Store it separately from incompatible substances like strong oxidizing agents. Ensure the storage area has good ventilation to avoid the buildup of any potentially harmful fumes.
Shipping 2,5 - Diiodobenzoic Acid is shipped in sealed, corrosion - resistant containers. These are carefully packed to prevent breakage. Shipments follow strict hazardous material regulations due to its chemical nature, ensuring safe transit.
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2,5-Diiodobenzoic Acid
General Information
Historical Development
2,5-Diiodobenzoic acid, the evolution of its material, there is really something to be studied. In the past, the chemical technology was not refined, and it was difficult to make this material. At that time, all kinds of raw materials were scarce, and the methods were mostly simple.
However, the years pass, and science and technology are gradually improving. Chemists have worked hard and worked hard. Or find new raw materials, or create ingenious processes. After years of work, the method of making 2,5-diiodobenzoic acid is becoming more and more complete. From the initial difficult exploration, to the maturity of the process, the output is also increasing. This chemical material is widely used in many fields such as medicine and materials. Its historical evolution is a witness to the development of chemistry, and it also depends on the unremitting efforts of scholars of all dynasties.
Product Overview
2,5-Diiodobenzoic acid is an important raw material for organic synthesis. Its shape is white to light yellow crystalline powder with stable properties. In the field of organic synthesis, it has a wide range of uses.
In this compound, the introduction of iodine atoms gives it unique reactivity. With the characteristics of iodine atoms, it can participate in many coupling reactions, such as Suzuki reaction, Heck reaction, etc., to construct complex organic molecular structures.
It also has potential value in drug development. Some iodine-containing organic compounds have excellent pharmacological activity, and 2,5-diiodobenzoic acid may be used as a key intermediate to help create new drugs.
Preparation of 2,5-diiodobenzoic acid, usually obtained from benzoic acid through iodization reaction. The precise control of reaction conditions has a significant impact on the purity and yield of the product.
In summary, although 2,5-diiodobenzoic acid is not amazing in appearance, it is an indispensable and important existence in the fields of organic synthesis and drug development.
Physical & Chemical Properties
2,5-Diiodobenzoic acid is also a chemical substance. Its physical and chemical properties are quite important to scholars. Looking at its shape, under room temperature, it is often a solid state with a specific color and state, which is its physical characteristic. In terms of its chemistry, in its structure, iodine is connected to the benzene ring, resulting in its unique reactivity. It can interact with various reagents under specific conditions, such as nucleophilic substitution reactions, and iodine atoms can easily become other groups, which is due to its activity of iodine. And the existence of benzene rings makes it unique in aromatic reactions. Its solubility is soluble in specific solvents, such as some organic solvents, which is related to its intermolecular forces and solvation. Such physical and chemical properties are useful in fields such as organic synthesis, and scholars should investigate them in detail.
Technical Specifications & Labeling
In May 2024, the chemical substance 2,5-Diiodobenzoic acid (2,5-Diiodobenzoic Acid) was made in my laboratory. The process specifications are rigorous, and the raw materials are selected to be pure. After many reactions and purification steps. Starting with iodide and benzoic acid derivatives, the temperature is controlled in a specific range, and a catalyst is used to promote a smooth reaction. The reaction time is also accurately measured, and then by extraction and crystallization methods, a pure product is obtained.
Its product indicators are clear, the appearance is white to light yellow crystalline powder, the purity is more than 99%, and the melting point is within a certain range, which is the characterization of quality. The impurity content is minimal, which meets the standards of high-end chemical products. We take a strict attitude, follow the process specifications, and strive for the perfection of our products to meet the needs of all parties for scientific research and production.
Preparation Method
This product of 2,5 - Diiodobenzoic Acid is made today, and its raw material is crucial to the production process, reaction steps and catalytic mechanism.
To make this product, benzoic acid is selected as the initial raw material. First, an appropriate amount of iodine is used as a halogenating agent, and a catalyst such as iron powder or its salts is added to a specific reaction vessel. The temperature is controlled in a moderate range, about 60 to 80 degrees Celsius, to promote the substitution reaction of benzoic acid and iodine. This step needs to be protected by inert gas, such as nitrogen environment, to prevent impurity interference.
During the reaction, iodine atoms gradually replace hydrogen atoms on the benzene ring of benzoic acid. After several reactions, a mixed product containing 2,5 - diiodobenzoic acid can be obtained. After distillation and extraction, the unreacted raw materials and by-products are separated. Appropriate organic solvents, such as ether, are extracted and separated by the difference in solubility of the products in different solvents.
During distillation, the temperature and pressure conditions are controlled to obtain a pure 2,5-Diiodobenzoic Acid product. The catalytic mechanism lies in the iron catalyst promoting the heterocleavage of iodine molecules, producing iodine positive ions, enhancing its electrophilicity, accelerating the attack on benzene rings, and improving the reaction rate and yield.
Chemical Reactions & Modifications
Nowadays, there is a chemical substance called 2,5-Diiodobenzoic acid (2,5-Diiodobenzoic Acid). In the study of chemical reactions, the characteristics of its reaction and modification are worth exploring.
Looking at this compound, its structure is unique, and the substitution position of the iodine atom has a great impact on its chemical properties. In many reaction systems, 2,5-diiodobenzoic acid often exhibits different reactivity from ordinary benzoic acid. Its iodine atom can be used as an excellent check point for electrophilic substitution reactions. Due to the electronegativity and atomic radius of iodine, the check point is easy to accept nucleophilic reagents and initiate various chemical transformations.
To optimize its performance, modification is essential. You can try to change the reaction conditions, such as temperature, solvent, or introduce specific catalysts, to promote its structural modification, in order to obtain the desired chemical properties, such as enhancing its stability, adjusting acidity and alkalinity, and even endowing it with special optical and electrical properties. This is the direction of unremitting exploration by chemical researchers, hoping to develop new chemical application fields through in-depth understanding of the reaction and modification of 2,5-diiodobenzoic acid.
Synonyms & Product Names
In 2024, a chemical substance called 2,5-Diiodobenzoic acid (2,5-Diiodobenzoic Acid) emerged in the field of chemical research. This substance, also known as 2,5-Diiodobenzoic acid, is widely used in chemical products.
As a key intermediate in organic synthesis, it can help create new drugs in the field of pharmaceutical research and development, contributing to human health and well-being; in the field of materials science, it can optimize material properties and make materials have more excellent characteristics.
Chemists have successfully improved its preparation efficiency and purity through repeated experiments and research. This achievement is of great significance, enabling the wider application of 2,5-diiodobenzoic acid, driving the chemical industry to new heights, and laying a solid foundation for innovative development in many fields.
Safety & Operational Standards
Safety and Handling Specifications for 2,5-Diiodobenzoic Acid
2,5-Diiodobenzoic Acid is an important substance in chemical research. During its experimental operation, safety comes first, and many norms need to be strictly adhered to.
Where you come into contact with this object, protective gear is essential. First hand protection, wear chemically resistant gloves to prevent skin contact. Cover it or irritate and corrode the skin. Accidentally contaminated, it may cause skin redness, swelling, pain, and even ulceration. Face protection should not be taken lightly. Goggles must be worn properly to avoid this object splashing into the eyes, damaging eye tissue and causing visual impairment.
The operating environment must be well ventilated. 2,5-Diiodobenzoic acid under certain conditions, or volatilize harmful gases, accumulate in a confined space, inhaled into the human body, damage the respiratory organs, causing cough, asthma and other diseases. Ventilation equipment can disperse harmful gases in time to ensure the safety of the experimenter's breathing.
When taking 2,5-diiodobenzoic acid, precise operation is essential. Measure with a clean and dry appliance, do not touch it directly with your hands. After use, properly seal it to avoid moisture and oxidation, and cause quality changes. If there is any spill during the experiment, clean it up immediately. Collect it with a clean appliance first, and then wipe the residue with a suitable solvent to ensure that there is no residue on the experimental table to prevent others from accidentally touching.
Furthermore, the storage of 2,5-diiodobenzoic acid is also regulated. It should be stored in a cool, dry place, away from fire and heat sources. Due to its active chemical properties, high temperature, open flame or dangerous reaction. And should be separated from oxidizing agents and reducing agents to prevent interaction and cause accidents.
Follow the above safety and operation specifications in order to ensure the safety of the experimenter in the research and use of 2,5-diiodobenzoic acid, maintain the smooth progress of the experiment, and achieve the purpose of scientific research.
Application Area
2,5-Diiodobenzoic acid (2,5-Diiodobenzoic Acid) is useful in many fields. In the field of pharmaceutical research and development, it may be used as a key intermediate to help create new drugs to cure various diseases and seek well-being for people with diseases. In the field of material science, it can also participate in the synthesis of specific materials, so that materials have specific properties, such as improving their optical and electrical properties, and applying them to optoelectronic devices. And in organic synthetic chemistry, it is an important reagent, helping to build complex organic molecular structures, expand the variety of organic compounds, and promote the progress of organic synthesis. It exhibits its unique effectiveness in many application fields, which is beneficial to the development of science and technology and the progress of society.
Research & Development
Today there is a chemical thing called 2,5 - Diiodobenzoic Acid, and I have devoted myself to studying it. Its nature and quality are all important for my research. At the beginning, I did not know its details, but with a diligent heart, I explored its mysteries.
After months of study, the method of its synthesis has gradually gained. What material was used first, and what method was used next, are all studied in detail. Every step is taken with care and caution, for fear of mistakes.
and the synthesis has been completed, re-examine its properties. In different environments, observe its changes and record its data. Hope to know its nature to the fullest, for future use.
Looking at this research today, although there are small achievements, the road ahead is still far. If you want to use this achievement widely and make it beneficial to the world, you still need to forge ahead and make unremitting exploration, hoping to make greater progress for the benefit of everyone.
Toxicity Research
The industry of chemical industry is related to people's livelihood, but the study of poisons in it should not be careless. Today there is 2,5 - Diiodobenzoic Acid, and the investigation of its toxicity is an important matter.
I will investigate the matter in detail. Observe its shape and quality, test its properties. After various experiments, observe its response to various things, and have also been tested in living things. When this substance is found in a small concentration, it will disturb the state of living things, or hinder its growth, or disrupt its metabolism.
And when it enters the environment, it also has the danger of persistence. It may accumulate in water and soil, or pass on to the chain of living things. Although it has not been seen that its serious harm is now, it must be prevented in the long run. It is necessary to deeply investigate the source of its toxicity and find ways to control it, so as to ensure the safety of people's livelihood and the environment, and not to cause disasters in future generations.
Future Prospects
The 2,5-Diiodobenzoic Acid (2,5-Diiodobenzoic Acid) is a good product of the chemical industry. There is nothing we can do about the prospect of its future.
This physical property is very special, and it is deeply hidden in the power of multiple domains. On the way of development, it may be possible to conduct new research and development, helping to cure diseases. In the field of materials, it may also give birth to new materials to meet the needs of science and technology.
Our researchers, we will explore its secrets and explore its depths. With intensive research and diligent understanding, we hope to be able to explore the power of 2,5-Diiodobenzoic Acid. In the future, I have high hopes to be able to make this thing, promote the transformation and even the progress of polyphasic families, and benefit the world.
Where to Buy 2,5-Diiodobenzoic Acid in China?
As a trusted 2,5-Diiodobenzoic Acid manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
Frequently Asked Questions

As a leading 2,5-Diiodobenzoic 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 main uses of 2,5-diiodobenzoic acid?
2% 2C5-dichlorobenzoic acid is a crucial raw material in organic synthesis and has a wide range of uses in many fields. First, in the field of pharmaceutical synthesis, this compound can be used as a key intermediate. For example, when synthesizing specific antibacterial drugs, 2% 2C5-dichlorobenzoic acid can be converted into structural units with antibacterial activity through a series of chemical reactions, thereby constructing antibacterial drugs with excellent efficacy and making great contributions to human health. Second, it is also indispensable in the creation of pesticides. With its unique chemical structure, pesticide products with high insecticidal, bactericidal or herbicidal properties can be derived. These pesticides can effectively prevent and control crop diseases and pests, improve crop yield and quality, and are of great significance to ensuring food security. Third, in the field of materials science, 2% 2C5-dichlorobenzoic acid can participate in the synthesis of polymer materials. By polymerizing with other monomers, polymer materials can be endowed with unique properties, such as better heat resistance and corrosion resistance, thereby expanding the application range of polymer materials, showing broad application prospects in high-end fields such as aerospace and automobile manufacturing. In addition, in the dye industry, 2% 2C5-dichlorobenzoic acid can be used as an important raw material for the synthesis of new dyes. Due to the introduction of 2% 2C5-dichlorobenzoic acid, new dyes may have better dyeing properties and color fastness, meeting the demand for high-quality dyes in textile, printing and dyeing industries. Therefore, 2% 2C5-dichlorobenzoic acid plays a pivotal role in many fields such as medicine, pesticides, materials and dyes, and has made great contributions to the development of related industries.
What are the physical properties of 2,5-diiodobenzoic acid?
2% 2C5 -dithiophenylacetic acid is a class of organic compounds. Its physical properties are quite unique. At room temperature, it is mostly in a solid state. Due to the existence of a certain interaction force between molecules, it has a relatively stable structure. Looking at its color, it is often white or almost white powder, which makes its appearance relatively pure and easy to distinguish. When it comes to melting point, it is usually within a certain range. This value is of great significance for determining the purity of the compound and the phase change under specific conditions. Generally speaking, the melting point is relatively clear. If impurities are mixed in, the melting point may be reduced and the melting range widened. As for solubility, 2% 2C5-dithiophenylacetic acid exhibits different solubility characteristics in organic solvents. In common organic solvents, such as ethanol, dichloromethane, etc., it has a certain solubility. This is because some groups in the molecular structure can form interactions with organic solvent molecules, such as van der Waals force, hydrogen bond, etc., which can promote its dissolution. However, the solubility in water is low, because the hydrophobic groups of the compound account for a large proportion, and the interaction with water molecules is weak, making it difficult to dissolve in aqueous systems with strong polarity. Its density is also an important physical property. The specific density value reflects the compactness of its molecular packing. Compared with similar compounds, this density characteristic may affect its distribution and behavior in the mixed system. In addition, the compound may have a certain odor, but its odor is usually not strong and pungent, but mostly a relatively weak special odor. This odor characteristic is also an auxiliary basis for identifying the substance. Overall, the physical properties of 2% 2C5-dithiophenylacetic acid lay the foundation for its application in chemical synthesis, materials science and other fields. Scientists can separate, purify and use it rationally according to these properties.
What are the chemical properties of 2,5-diiodobenzoic acid?
2% 2C5-dichlorobenzoic acid is an organic compound, and its shape is white to light yellow crystalline powder. It has many chemical properties and is widely used in organic synthesis and other fields. Its acidity is quite significant, because the carboxyl group can ionize hydrogen ions, it can show a certain acidity in water, and can neutralize with bases to form corresponding carboxylic salts and water. For example, when reacted with sodium hydroxide, 2% 2C5-dichlorobenzoic acid is formed with water. The chlorine atom in 2% 2C5-dichlorobenzoic acid is extremely active and can participate in nucleophilic substitution reactions. Under appropriate conditions, nucleophiles such as alcohols and amines can attack the carbon atoms attached to chlorine atoms and replace chlorine atoms to form new compounds. For example, when reacted with ethanol under alkali catalysis, chlorine atoms will be replaced by ethoxy groups to form new ester compounds. This compound can also participate in esterification reactions. Under the action of catalysts such as concentrated sulfuric acid, it reacts with alcohols to form esters. This reaction is often used in organic synthesis to prepare ester compounds with specific structures and properties, and is of great significance in fragrance and drug synthesis. In addition, the benzene ring of 2% 2C5-dichlorobenzoic acid can undergo electrophilic substitution reactions. Due to the influence of the electron effect between the carboxyl group and the chlorine atom, the electron cloud density at different positions on the benzene ring is different, which makes the electrophilic reagents more inclined to attack specific positions, and then synthesize a series of derivatives to meet the needs of different fields.
What is the synthesis method of 2,5-diiodobenzoic acid?
The synthesis of 2% 2C5-dibromobenzoic acid is an important issue in the field of organic synthesis. There are many methods, each with its advantages and disadvantages, and the choice of the best depends on the actual situation. One method is to use benzoic acid as the starting material and prepare the target product through bromination reaction. First, benzoic acid and bromine are reacted under the action of a suitable catalyst. Common catalysts such as iron powder, iron tribromide, etc. In the reactor, put benzoic acid and bromine in a certain proportion, add an appropriate amount of catalyst, and heat up to a suitable temperature. This reaction needs to be carried out in good ventilation, because bromine is corrosive and volatile. During the reaction, bromine atoms replace hydrogen atoms at specific positions on the benzene ring of benzoic acid. After controlling the reaction conditions, bromine atoms can mainly replace 2,5-positions. After the reaction is completed, pure 2,5-dibromobenzoic acid can be obtained through separation and purification steps, such as distillation, recrystallization, etc. Another method is to use the corresponding halogenated aromatics as raw materials and prepare them by carboxylation reaction. First take a suitable halogenated aromatic hydrocarbon, such as 2,5-dibromotoluene. React it with magnesium metal to make a Grignard reagent, and then react with carbon dioxide to introduce carboxyl groups. In this process, anhydrous and oxygen-free conditions are crucial to prevent the Grignard reagent from failing. After the reaction is completed, the carboxylate is converted into 2,5-dibromobenzoic acid by acidification treatment, and then the product is separated and purified. In addition, 2,5-dibromobenzoic acid is also synthesized by multi-step reaction with other benzene-containing compounds as starting materials. These methods may involve complex steps such as functional group conversion, protection and deprotection. Although the process is cumbersome, the route can be flexibly designed according to different raw materials and needs. All synthesis methods have their own advantages. In practical application, it is necessary to consider factors such as the availability of raw materials, cost, difficulty in controlling reaction conditions, and product purity requirements. Only prudent choices can be made to produce 2,5-dibromobenzoic acid efficiently.
What are the precautions for storing and transporting 2,5-diiodobenzoic acid?
2% 2C5-dithiophenecarboxylic acid is a very important chemical substance. When storing and transporting, many key precautions must not be ignored. The first to bear the brunt is the storage environment. This substance should be stored in a cool, dry and well-ventilated place. Because the humid environment is prone to moisture and deterioration, and high temperature will accelerate its chemical reaction, causing its chemical properties to change, affecting quality and utility. Be sure to keep away from fire and heat sources to prevent open flames. Because it may be flammable, open flames and hot topics may cause serious consequences of combustion or even explosion. Furthermore, pay attention to the integrity of the packaging when storing. The packaging should be tight to prevent dithiophenecarboxylic acid from leaking. If the package is damaged, not only will material loss be caused, but the leaked chemicals may cause harm to the surrounding environment and personnel. In the event of a leak, appropriate measures should be taken immediately to avoid its spread. The transportation process also requires caution. Transportation vehicles must ensure good fire protection, explosion protection and leak prevention devices. During transportation, severe vibrations and collisions should be avoided to prevent package rupture. At the same time, transportation personnel must be professionally trained and familiar with the characteristics of dithiophenecarboxylic acid and emergency treatment methods. In the event of an accident during transportation, prompt and correct measures can be taken to reduce losses and hazards. In addition, whether it is storage or transportation, relevant regulations and standards should be strictly followed. Make appropriate labels, clarify the name, nature, hazard and emergency treatment information of the chemical, so that relevant personnel can accurately identify and properly dispose of it. In this way, the safety and stability of 2% 2C5-dithiophenecarboxylic acid during storage and transportation can be ensured.