Hongda Chemical
Products
Home  /  Products  / 

3-Fluorobenzene-1,2-Dicarboxylic Acid

3-Fluorobenzene-1,2-Dicarboxylic Acid

Hongda Chemical

Specifications

HS Code

101938

Chemical Formula C8H5FO4
Molar Mass 184.12 g/mol
Appearance Solid
Melting Point Typically in a certain range (data needed for exact value)
Boiling Point Typically in a certain range (data needed for exact value)
Solubility In Water Limited solubility (data needed for exact value)
Solubility In Organic Solvents Varies by solvent (data needed for specific solvents)
Acidity Acidic due to carboxylic acid groups
Density Data needed for exact value
Odor Odor characteristics data needed

As an accredited 3-Fluorobenzene-1,2-Dicarboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage
Packing 500g of 3 - fluorobenzene - 1,2 - dicarboxylic Acid in a sealed plastic bag.
Storage 3 - Fluorobenzene - 1,2 - dicarboxylic acid should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and incompatible substances such as strong oxidizing agents. Store it in a tightly - sealed container to prevent moisture absorption and potential degradation. This storage approach helps maintain its chemical integrity and safety.
Shipping 3 - Fluorobenzene - 1,2 - dicarboxylic acid should be shipped in well - sealed, corrosion - resistant containers. Ensure proper labeling with chemical details. Ship via approved carriers following hazardous chemical shipping regulations to prevent leakage and ensure safety.
Free Quote

Competitive 3-Fluorobenzene-1,2-Dicarboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

For samples, pricing, or more information, please call us at +8615365186327 or mail to info@alchemist-chem.com.

We will respond to you as soon as possible.

Tel: +8615365186327

Email: info@alchemist-chem.com

3-Fluorobenzene-1,2-Dicarboxylic Acid 3-Fluorobenzene-1,2-Dicarboxylic Acid
General Information
Historical Development
3-Fluorobenzene-1,2-dicarboxylic acid, the history of its evolution has been a long time. At the beginning, the sages devoted themselves to studying the field of chemistry and gradually observed it. At that time, the scientific method was not as complete as it is today, and the exploration was hidden, and it was difficult step by step.
After the year, it was delayed, and the skills of the craftsmen advanced day by day, and the analysis of it became more and more detailed. Know that this thing has an exquisite structure and unique nature. Although there are thorns on the way, the masters are determined and unremitting. Or in the room of experiments, repeated trials; or between the classics, trace the roots and trace the source.
To this day, 3-fluorobenzene-1,2-dicarboxylic acid has emerged in various fields. The search of the past has become the cornerstone of today, and its future is also full of new opportunities. It all depends on the work of predecessors, paving the way for historical evolution step by step.
Product Overview
3 - Fluorobenzene - 1,2 - Dicarboxylic Acid is one of the important compounds involved in chemical research. Its molecular structure is unique. On the benzene ring, fluorine atoms and dicarboxylic groups are cleverly arranged, giving this compound unique chemical properties.
This compound has great potential in the field of organic synthesis. With its unique structure, it can be used as a key intermediate to participate in the construction of many complex organic molecules. During the reaction process, its carboxyl and fluorine atoms can play a key role, or participate in nucleophilic substitution, or participate in esterification and other reactions, helping to synthesize a variety of organic products.
And it is also emerging in the field of materials science. After proper modification and transformation, it is expected to prepare materials with special properties, such as new materials with excellent optical properties and good thermal stability, which will contribute to the development of the material field. Our chemical researchers should deeply explore its properties and applications in order to tap its greater potential value.
Physical & Chemical Properties
3-Fluorobenzene-1,2-dicarboxylic acid, its physical and chemical properties are particularly important. Looking at its physical properties, it is mostly solid at room temperature, with a white and pure color. Its melting point is a specific value, which is very critical for identifying and purifying the substance.
As for chemical properties, it contains carboxyl groups, which are acidic and can neutralize with alkali substances to form corresponding salts. And because of its fluorine atom, it exhibits unique activity in specific chemical reactions. It can participate in a variety of organic synthesis reactions and is an important raw material for the preparation of compounds with special structures. Its stability is good under certain conditions, but it will also undergo chemical changes under special circumstances such as high temperature and strong oxidizing agents. The various physical and chemical properties provide a solid foundation for its application in chemical, pharmaceutical and other fields.
Technical Specifications & Labeling
3-Fluorobenzene-1,2-dicarboxylic acid is also a chemical substance. Its process specifications and identification (product parameters) are crucial.
Looking at this 3-fluorobenzene-1,2-dicarboxylic acid, its purity needs to reach a very high level, and the impurity content must be minimal. Above the appearance, it should be a white crystal, free of variegation and foreign matter. Its melting point is also fixed, and it needs to be accurate. This is one of the keys to determine its quality.
In the label, the product name, chemical formula, molecular weight and other information should be clear. On the packaging, it should also be properly marked to prevent confusion. Only by strictly adhering to the process specifications and identification (product parameters) can high-quality 3-fluorobenzene-1,2-dicarboxylic acid be obtained to meet the needs of all parties.
Preparation Method
The raw materials of 3 - Fluorobenzene - 1,2 - Dicarboxylic Acid are the key to the production process, reaction steps and catalytic mechanism.
The selection of raw materials, when using fluorine-containing benzene compounds, supplemented by reagents with carboxylation potential. The delicate combination of the two forms the basis for the reaction.
The production process requires temperature control in a specific range, not too high or too low, causing the reaction to be unbalanced. And in a closed container, the raw materials are placed in a precise ratio to make them fully blend.
The reaction step, the first initiator is introduced, and the activity of the raw materials is surged, and they are close to each other and bonded. Then, the conditions are fine-tuned according to the reaction process to ensure the reaction goes as expected.
Catalytic mechanism, high-efficiency catalysts are selected, the reaction energy barrier is lowered, and the process is accelerated. The catalyst activity check point is in line with the raw material molecules, and the reaction is efficient and directional. In this way, 3 - Fluorobenzene - 1,2 - Dicarboxylic Acid can be prepared, which is what we need.
Chemical Reactions & Modifications
Yu Taste is dedicated to the chemical research of 3 - Fluorobenzene - 1,2 - Dicarboxylic Acid, and his chemical reaction and modification have been studied a lot.
To observe the reaction of this compound, it is often necessary to carefully observe the conditions. If the temperature is slightly different, it may lead to a different product. When catalyzed by a certain method, although the initial reaction is fast, the product is impure. After many adjustments, it is changed to a new catalyst, and the temperature control is precise, resulting in a high-purity product. This is a clear proof of the influence of chemical reaction conditions.
As for modification, it is also difficult to think. Try to introduce groups, hoping to change their characteristics. At first, the reaction is not as expected, and the groups are difficult to attach. Repeated research, changed the steps, activated the substrate first, and then connected, and finally succeeded. After modification, its stability is greatly increased, and the application path is also wide.
The way of chemical research, every time you need to study the subtlety of the reaction, and study the modification method carefully, you can make progress. In the exploration of 3 - Fluorobenzene - 1,2 - Dicarboxylic Acid, but it can also be seen from the tube.
Synonyms & Product Names
The name of this substance is 3-fluorobenzene-1,2-dicarboxylic acid. It is also an important quality in the research of chemical materials. Its names vary, depending on the industry and use.
Or this substance, another name is similar to that of others. It is the same as the title, which is based on its chemical nature and structure. Some are called aliases because of its chemical composition, for the convenience of research and communication.
Looking at the field of chemical industry, the name of this substance is also used for commercial purposes. Merchants recognize its characteristics, or give unique trade names, hoping to show its differences in the city. Although the names are different, they all refer to the quality of 3-fluorobenzene-1,2-dicarboxylic acid. As far as researchers are concerned, only by knowing the same name can they travel freely in academic and practical paths, avoid mistakes, and achieve the purpose of research and promote the progress of chemical industry.
Safety & Operational Standards
3-Fluorobenzene-1,2-dicarboxylic acid is also one of the chemical substances. In our research and development, safety and operating standards are the most important and must not be overlooked.
To make this 3-fluorobenzene-1,2-dicarboxylic acid, the place must be neat and orderly, and well ventilated. All kinds of utensils used must be clean and intact to avoid impurities from mixing in and damaging its quality. And when operating, temperature and humidity also need to be controlled in detail. There is a slight difference between the two, or the reaction is wrong, and the product is impure.
When using raw materials, when using accurate quantities, do not do it hastily. When weighing, the balance must be calibrated correctly. If the raw materials are collected, mixing and stirring also need to be done in a way to make the things blend evenly and the reaction is smooth.
Between reactions, people should not leave without permission. Pay close attention to its changes, such as color changes, temperature rises and falls. If there is any abnormality, quickly turn off the heat source and check the cause in detail to prevent accidents. After the reaction is completed, the product should be separated and purified, and it is also necessary to be cautious. Either use filtration or distillation, according to their own nature, choose the best.
There are also rules for product storage. It must be placed in a cool and dry place, away from fire sources and oxidants. The container used must be well sealed to prevent its volatilization and leakage.
As for the participants, they should be familiar with the rules of operation and wear protective equipment, such as protective clothing, gloves, goggles, etc., to ensure their own safety. Every operation must first study the process and clarify the steps before it can be done. In this way, only in the development of 3-fluorobenzene-1,2-dicarboxylic acid can we ensure safety, operation compliance, and obtain pure products, which will add to the road of chemical research and development.
Application Area
3-Fluorobenzene-1,2-dicarboxylic acid is a unique chemical substance. Its application field is quite wide. In the process of pharmaceutical research and development, this compound may become a key raw material for the creation of new pharmaceuticals. Due to the special properties of fluorine atoms, it may improve the lipophilicity, biological activity and metabolic stability of drug molecules, and help to develop drugs with better efficacy and less side effects.
In the field of materials science, it can participate in the preparation of high-performance functional materials. For example, it can be used to synthesize polymers with special optical and electrical properties, or can be used in optoelectronic devices, such as organic Light Emitting Diodes, solar cells, etc., to inject new energy into the improvement of material properties.
In the field of fine chemicals, it is also an important intermediate. With its unique structure, many high-value-added fine chemicals can be derived to meet diverse industrial needs and contribute to the development of related industries.
Research & Development
3 - Fluorobenzene - 1,2 - Dicarboxylic Acid is an important chemical product that I have been focusing on recently. This compound has a unique structure, and its substitution of fluorine atoms gives the molecule unique physicochemical properties.
I focused on the optimization of its synthesis path and tried a variety of novel reaction conditions and catalysts. After repeated experiments, it was found that under specific temperatures and pressures, a new type of metal complex as a catalyst can significantly improve the purity and yield of the product.
In terms of application expansion, this product has promising potential in the field of materials science. After testing, the materials containing this compound exhibit good optoelectronic properties in optoelectronic devices, which is expected to contribute to the development of this field. In the future, I will explore more potential applications in depth, with the goal of promoting the comprehensive development of this product.
Toxicity Research
The nature of taste and smell is related to human use, and the study of poisons is particularly important. There is a substance today, called 3 - Fluorobenzene - 1,2 - Dicarboxylic Acid, which is the object of my research.
I observe its toxicity and examine its changes in detail. Use various methods to explore its response to things. Or enter the water and observe the state of water life; or apply it to plants and see its long state. After years of research, many images have been obtained. This substance has the effect of inhibiting its growth and messing with its growth in aquatic organisms; in plants, it can also change its physiological process.
However, the study of toxicity is not a day's work, and it still needs to be deeply researched to clarify its mechanism, explore its source, and hope to be able to fully understand its nature, so that future generations can use this product to avoid harm and profit, so as to ensure the safety of all things and the balance of ecology.
Future Prospects
Husband 3 - Fluorobenzene - 1,2 - Dicarboxylic Acid, it is also a matter of transformation. Now we can make great progress in the future. This object may be exposed in the way of research and development, and its characteristics may be improved, or it can be used to make special effects, so as to create diseases. And in the field of material science, it also has power. It can be the cornerstone of new materials, and the properties of new materials, such as corrosion resistance. Our scientific researchers, we will study the mind and explore its secrets, so that this compound can be used in the world, and it can be used for the benefit of the people, so as to recognize the power of science and promote the progress of the world. This is a great achievement that I have not yet made.
Where to Buy 3-Fluorobenzene-1,2-Dicarboxylic Acid in China?
As a trusted 3-Fluorobenzene-1,2-Dicarboxylic 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 3-Fluorobenzene-1,2-Dicarboxylic 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 3-fluorobenzene-1,2-dicarboxylic acid?
3-Hydroxyanthracene-1,2-dicarboxylic acid is an important member of anthraquinone compounds, which is widely used in medicine, chemical industry and other fields. Its chemical properties are unique and have a significant impact on the development of related fields.
This substance is acidic. Because its structure contains carboxyl groups, the oxygen atom in the carboxyl group has strong electronegativity, and the polarity of the hydrogen-oxygen bond increases, hydrogen is easily dissociated in the form of protons, so it is acidic. It can neutralize with bases to form corresponding carboxylate salts and water. Such as reacting with sodium hydroxide to form 3-hydroxyanthracene-1,2-dicarboxylate sodium and water. This property is commonly used in the separation, purification and preparation of derivatives.
It also has oxidizing and reducing properties. The conjugated system of anthraquinone structure makes 3-hydroxyanthracene-1,2-dicarboxylic acid have certain redox properties. Under specific conditions, it can be reduced to anthracenols or anthraconones. In case of strong oxidants, the quinone ring may be oxidized to open the ring and form oxidation products containing more functional groups such as carboxyl groups. In organic synthesis, its redox properties are often used to construct new compounds and transformation structures.
In addition, 3-hydroxyanthracene-1,2-dicarboxylic acids have substitution reactivity. Hydroxyl and carboxyl groups affect the distribution of electron clouds in the benzene ring, making the electron cloud density in some positions of the benzene ring change, and electrophilic substitution reactions are more likely to occur. Under appropriate catalysts and conditions, reactions such as halogenation, nitrification, and sulfonation can occur, and other functional groups can be introduced to expand their chemical properties and uses, providing the possibility for the synthesis of complex organic compounds.
What are the physical properties of 3-fluorobenzene-1,2-dicarboxylic acid?
3-Naphthalene-1,2-dicarboxylic acid is a rare and complex compound, and its physical properties are very specific.
Its external appearance is often crystalline, and the crystalline form is very complete, which is very beautiful. The color of this compound is often white or almost white, and it is very beautiful, just like snow.
As far as melting is concerned, it has a specific degree of melting. To a certain extent, the energy of the crystal lattice is sufficient to overcome the molecular force, so it is solid and liquid. This melting is an important basis for determining its degree and characteristics.
In terms of solubility, it varies in different solubility. In water, such as water, the solubility is limited, because of the molecular distribution, the interaction between water molecules is not low. However, for some soluble molecules, such as ethanol, acetone, etc., the solubility of the phase is high. Due to the soluble molecular force form, it is more suitable for the characteristics of 3-naphthalene-1,2-dicarboxylic acid, which can make its molecules disperse uniformly.
In addition, its density is also a fixed value, reflecting the amount of its position. The determination of density is important for studying its physical behavior in different environments, such as distribution and mixing in solutions. The characteristics of its density also depend on the arrangement density of molecules and the amount of molecules.
In addition, the physical properties of 3-naphthalene-1,2-dicarboxylic acids, including externality, melting, solubility, and density, are all important for in-depth understanding of the basis of this compound, and for its application in various fields.
What are the main uses of 3-fluorobenzene-1,2-dicarboxylic acid?
3-Hydroxyanthracene-1,2-dicarboxylic acid, which is an important member of anthraquinone compounds. Its main uses are quite wide and it has key value in many fields.
First, in the field of medicine, this compound shows unique medicinal potential. Some anthraquinone derivatives have pharmacological activities such as antibacterial, anti-inflammatory and anti-tumor. 3-Hydroxyanthracene-1,2-dicarboxylic acid or chemically modified to prepare drugs with specific therapeutic effects is expected to provide new ways for disease treatment. For example, for some inflammatory diseases, its anti-inflammatory properties may play a positive role, helping to relieve inflammatory symptoms and relieve patient pain.
Second, in the dye industry, this compound also plays an important role. Anthraquinone structure is often the basis for the synthesis of high-quality dyes. 3-hydroxyanthracene-1,2-dicarboxylic acid can impart excellent color and stability to dyes due to its own special structure. Taking textile printing and dyeing as an example, the dyes synthesized based on this compound can make fabrics bright and long-lasting, and are not easy to fade after multiple washes, greatly improving the quality and aesthetics of fabrics.
Third, in the field of organic synthesis, 3-hydroxyanthracene-1,2-dicarboxylic acid is a key intermediate and has a wide range of uses. Organic chemists can use it to perform various chemical reactions to construct more complex organic molecular structures. By ingeniously designing reaction pathways, using their active groups, condensation and substitution reactions occur with other compounds, and organic materials with specific functions, such as new photoelectric materials, are synthesized to promote the development of materials science.
What are the synthesis methods of 3-fluorobenzene-1,2-dicarboxylic acid?
To prepare 3-propargyl-1,2-dicarboxylic acid, the methods are as follows:
First, the propargyl halide and diethyl malonate are used as the starting point. First, the propargyl halide and diethyl malonate are nucleophilically substituted under the action of alkalis such as sodium alcohol to obtain diethyl propargyl malonate. Then it is co-heated with the alkali solution, the ester group is hydrolyzed to a carboxyl group, and the decarboxylation reaction occurs, and the target 3-propargyl-1,2-dicarboxylic acid is obtained. The raw materials of this path are easy to obtain, and the reaction steps are clear. However, the reaction conditions need to be precisely controlled to prevent side reactions.
Second, it is initiated through acetylene and acrylate. Under the action of a suitable catalyst, acetylene and acrylate undergo an addition reaction to obtain products containing alkynyl groups and ester groups. Subsequently, the ester group is hydrolyzed and converted to a carboxyl group, which can also be converted into 3-propargyl-1,2-dicarboxylic acid. The atomic economy of this method is quite good, but the choice of catalyst and the optimization of reaction conditions are crucial to increase the yield and selectivity of the reaction.
Third, propargyl alcohol is used as the starting material. First, propargyl alcohol is oxidized to obtain a carbonyl-containing intermediate, and then through a series of reactions, such as addition with cyanide, followed by hydrolysis, the carboxyl group is introduced, and the final product is obtained. This approach can adjust the reaction process according to different oxidation reagents and reaction conditions, but the steps are slightly complicated and require fine operation to achieve the desired results.
All these methods have their own advantages and disadvantages. In the actual synthesis, when considering the availability of raw materials, cost, reaction conditions and yield and other factors, the optimal method is selected to efficiently prepare 3-propargyl-1,2-dicarboxylic acid.
What are the precautions for storing and transporting 3-fluorobenzene-1,2-dicarboxylic acid?
For 3-hydroxyl-1,2-dicarboxylic acids, pay attention to many matters during storage and transportation.
The stability of this substance is the first priority. The properties of this substance may vary due to changes in temperature and humidity. If the temperature is high, it is easy to decompose, and if it is wet, it may cause deliquescence. Therefore, when storing, it is advisable to choose a cool and dry place. If conditions permit, the temperature should be controlled in a specific range, such as 15 to 25 degrees Celsius, and the humidity should be maintained at 40% to 60%. This can ensure the stability of its chemical properties and will not deteriorate during storage.
Times and packaging. The packaging must be tight to prevent contact with the air. It may react chemically with oxygen, water vapor, etc. in the air. Use a container with good airtightness, such as glass bottles and plastic bottles, and the bottle mouth must be tightly sealed. During transportation, it is also necessary to ensure that the packaging is not damaged. If the packaging is damaged, the substance will be exposed and prone to changes.
Furthermore, it is necessary to prevent it from being mixed with other substances. 3-Hydroxy-1,2-dicarboxylic acid has strong chemical activity or meets with certain substances or reacts violently. Therefore, when storing and transporting, it should not be stored and transported with alkalis and strong oxidants, and it must be isolated to avoid accidents.
In addition, the handling process should be cautious. Because it may be corrosive to a certain extent, if it is accidentally exposed to the human body, it can cause injury. Handlers should wear appropriate protective equipment, such as gloves, protective clothing, protective glasses, etc., and handle it with care to avoid container collision and dumping to prevent leakage. If there is any leakage, it should be properly handled according to corresponding emergency measures.