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1,3-Difluorobenzene

1,3-Difluorobenzene

Hongda Chemical

Specifications

HS Code

946721

Chemical Formula C6H4F2
Molar Mass 114.09 g/mol
Appearance Colorless liquid
Odor Aromatic odor
Density 1.159 g/cm³ at 20 °C
Boiling Point 126 - 128 °C
Melting Point -57.3 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in many organic solvents
Flash Point 21 °C
Vapor Pressure 3.4 kPa at 25 °C
Refractive Index 1.455 (20 °C)

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

Packing & Storage
Packing 1,3 - difluorobenzene packaged in 5 - liter drums for chemical use.
Storage 1,3 - Difluorobenzene should be stored in a cool, well - ventilated area away from heat, sparks, and open flames. Keep it in a tightly sealed container to prevent vapor leakage. Store it separately from oxidizing agents and incompatible materials. The storage location should be dry to avoid potential reactions with moisture, and it should be clearly labeled for easy identification.
Shipping 1,3 - difluorobenzene is shipped in sealed, corrosion - resistant containers. These are carefully packed to prevent leakage during transit. Shipments follow strict chemical transport regulations to ensure safety.
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1,3-Difluorobenzene 1,3-Difluorobenzene
General Information
Historical Development
The historical evolution of 1,3-difluorobenzene has been around for a long time. In the past, at the beginning of organic chemistry, all kinds of compounds needed to be explored. At that time, chemical craftsmen worked hard to study new things.
At the beginning, in the field of organic synthesis, only simple compounds could be obtained. However, everyone's heart for knowledge has not been exhausted, and they have been unremitting in their exploration. Later, organic synthesis techniques have gradually improved, and chemists have become more complex.
The synthesis of 1,3-difluorobenzene has also been honed many times. Chemists follow the principle, change the reaction conditions, change the raw materials, and finally get the method of synthesis. Its function in organic synthesis, medicine, materials and other fields is gradually showing. From unknown to the most important in the industry, the history of 1,3-difluorobenzene is a testament to the progress of chemical development.
Product Overview
1,3-Difluorobenzene is an organic compound. It is a colorless liquid with a special odor. This substance has a wide range of uses in the chemical industry and is often an important raw material for the synthesis of many fine chemicals.
Looking at its structure, the dicarbon above the benzene ring is connected to a fluorine atom, and the unique structure gives it its specific properties. Its physical properties, with a suitable boiling point, can be gasified into steam at a specific temperature, which is convenient for reaction operation.
In terms of chemical properties, due to the strong electronegativity of fluorine atoms, the electron cloud density of the benzene ring changes, making it exhibit different activities in reactions such as electrophilic substitution. It can react with a variety of reagents, and through ingenious synthesis paths, materials and drug intermediates with special functions can be prepared. Therefore, 1,3-difluorobenzene plays an indispensable role in the stage of chemical synthesis, promoting the progress and development of related industries.
Physical & Chemical Properties
1,3-Difluorobenzene is an organic compound. Its physical and chemical properties are quite specific. Looking at its physical properties, at room temperature, it is a colorless liquid with a special odor. Its boiling point is moderate, about 126 ° C, due to the intermolecular force. Its density is slightly smaller than that of water, and it can float on water.
As for its chemical properties, the benzene ring is connected to a difluorine atom, resulting in its chemical activity. The fluorine atom has strong electronegativity, which changes the electron cloud density of the benzene ring. In the electrophilic substitution reaction, it shows a different activity. It can react with many reagents, such as halogenating agents, it can form new halogenated compounds; in the case of nucleophiles, it may also have different changes. This is determined by the atomic properties and interactions in its molecular structure.
Technical Specifications & Labeling
Today there is a product named 1,3-difluorobenzene. The preparation of its technology is related to the process specification and identification (product parameters), which is really the focus of our research.
The preparation of this 1,3-difluorobenzene requires precise process specifications. The choice of raw materials must be pure, and the ratio must be consistent with a certain number. The temperature and pressure of the reaction are strictly regulated, and there should be no slight difference. The equipment used in the meantime should also be clean and intact to ensure a smooth reaction.
As for the logo (product parameters), 1,3-difluorobenzene has a colorless appearance and a special smell. Its purity must be up to standard, and the amount of impurities must be minimal. Physical parameters such as boiling point and melting point are all evidence of quality. In this way, according to strict process specifications and clear identification (product parameters), high-quality 1,3-difluorobenzene can be prepared to meet the needs of all parties.
Preparation Method
In order to make 1,3-difluorobenzene, the method of making it is to discuss the raw materials first. Those containing benzene ring and groups that can be substituted by fluorine can be selected as the starting material, such as a halogenated benzene, and the halogen atom can be chlorine, bromine and the like.
As for the production process, the raw materials are first taken and placed in a special reactor. Under the conditions of temperature control and pressure, a fluorine source, such as potassium fluoride, is introduced. After the substitution reaction, the halogen atom is replaced by a fluorine atom. The reaction step is to first mix the halogenated benzene with the fluorine source, stir well, and heat up to a suitable temperature to make the reaction proceed smoothly.
The catalytic mechanism is also critical, and a catalyst can be added to promote the reaction rate This catalyst can reduce the activation energy of the reaction, making the reaction easy to occur. In this way, through fine regulation of raw materials, processes and catalytic mechanisms, 1,3-difluorobenzene can be obtained to meet the needs of scientific research and production.
Chemical Reactions & Modifications
To taste the wonders of chemical industry, it is related to reaction and modification, and it is the important task of scholars. Today, we will discuss this substance with 1,3-Difluorobenzene. The way of reaction often depends on various reagents and conditions. In the past, to obtain this compound, many complicated methods were used, which were time-consuming and laborious, and the yield was not good.
After research by everyone, the reagent ratio and temperature control of the reaction have changed. With the newly prepared reagent, adjust the ratio, control the temperature at a precise degree, and optimize the reaction path. In this way, the yield of 1,3-Difluorobenzene gradually increased, and the quality was also good. This is all due to the work of modification, changing its reaction environment, changing its molecular properties, and making the chemical technology more and more exquisite. In the preparation of 1,3-Difluorobenzene, a good method was obtained, and it is also a reference for the research of other things.
Synonyms & Product Names
1,3-Difluorobenzene is also an organic compound. The name of its congener and the name of the product are also of concern to us.
This product is widely used in the field of chemical industry. Or it is a raw material for synthesizing other products. With its unique structure, it can form a variety of products. The name of the same product, or due to the difference in structure, has different names. The name of the product, or according to its performance and use, gets different names.
In today's world, chemical refinement, and the research on 1,3-difluorobenzene is deepening. Seek better production methods, increase its purity, and expand its application. The name of the same thing and the name of the commodity are also becoming clearer with the progress of research. Scholars should be careful about the reason and distinguish the name, so as to promote the good use of this thing in industry and scientific research, and add bricks and mortar to the rise of chemistry.
Safety & Operational Standards
In the case of 1,3-difluorobenzene, the product of chemical reaction is also the product. In this case, the product, safety and operation regulations are of paramount importance.
All matters involving the preparation, storage and use of 1,3-difluorobenzene should follow certain rules. At the beginning of preparation, all kinds of utensils must be clean and good, and the dosage used must be accurate and the quality must be pure. During the reaction, temperature, pressure and response time should be carefully monitored and controlled. If the temperature is improper, or the reaction may be too fast, there is a risk of explosion; or the reaction may be too slow, and the yield is low.
Store 1,3-difluorobenzene in a cool, dry and well-ventilated place. Avoid contact with fire, heat and strong oxygen agents to prevent ignition and explosion. The receptacle must also be tight to prevent it from leaking outside, polluting the environment, and endangering the human body.
As for the use of 1,3-difluorobenzene, the operator must take appropriate protection. Wear anti-corrosion gloves to prevent touching the skin; wear a gas mask to prevent inhalation of its gas and damage to the lungs. Operate in the fume hood to make the gas dissipate quickly and reduce the damage to the invisible.
If 1,3-difluorobenzene accidentally leaks, leave the scene quickly and prohibit fireworks. For small leaks, cover it with sand, soil, etc., and collect it in a secret container; for large leaks, block it with an embankment, and invite professionals to deal with it.
In short, in all kinds of things with 1,3-difluorobenzene, we should be cautious, keep safe and operate rules, in order to ensure the smooth, people's safety, and the cleanliness of the environment.
Application Area
1,3-Difluorobenzene is also a chemical product. It is widely used in the field of medicine and can be used as a material for making good medicines. With its unique properties, it can participate in the structure of drugs, increase the effect of drugs and reduce their side effects.
In the domain of agriculture, it can be used as a raw material for agricultural agents. It can help farmers eliminate pests and protect crops from insect diseases.
In the industry of materials, it also has its uses. It can involve the research and creation of new materials, and endow materials with special properties, such as the stability and corrosion resistance of additives.
All these uses rely on the characteristics of 1,3-difluorobenzene. Researchers should delve deeper into its nature and expand the boundaries of its use to benefit the world.
Research & Development
Today there is a product named 1,3-difluorobenzene. I am a chemical researcher and have been studying it for many years. This material is unique in nature, has a wide range of uses, and has outstanding performance in the fields of medicine and materials.
My research focuses on the synthesis method. After repeated attempts to explore different reaction conditions and raw material ratios, I strive to find an efficient and environmentally friendly preparation path. There are many setbacks in the process, but I have not slack off.
Looking forward to its development, 1,3-difluorobenzene has broad prospects. With the advance of science and technology, its application in emerging fields may have new breakthroughs. I should make unremitting research, hoping to contribute to its promotion and expansion, so that this material can better benefit the world.
Toxicity Research
Since modern times, chemical refinement has made all kinds of substances appear in the world. Now it is very important to study the toxicity of 1,3-Difluorobenzene.
Detailed observation of its properties, 1,3-Difluorobenzene may have certain toxicity. In experiments, looking at its impact on organisms, it can be seen that some biological physiological functions have changed. Its molecular structure contains fluorine atoms, and the activity of fluorine may make the substance interfere with biochemical reactions in organisms.
However, toxicity research still needs to be further explored. Or consider its stability in different environments and its metabolic pathways in organisms. This is the key to knowing the toxicity of 1,3-Difluorobenzene. Only through thorough research can we know its advantages and disadvantages, use it wisely, avoid its harm and pursue its benefits, ensure the safety of all beings, and promote the steady progress of the chemical industry.
Future Prospects
The future development concerns 1,3-difluorobenzene. Looking at it today, 1,3-difluorobenzene has emerged in various fields of chemical industry. It is a key raw material in the synthesis of medicine, helping to create new drugs, solving people's diseases, and has promising prospects. In the process of material research and development, it also has extraordinary potential, or can give birth to new materials, which should meet the diverse needs of the times.
Our generation of chemical researchers should be diligent. With scientific methods, explore its optimal preparation techniques, reduce its cost, and improve its quality. With time, 1,3-difluorobenzene will surely shine. In the forest of medicine, it has become a sharp blade to remove diseases and diseases; in the world of materials, it is the cornerstone of innovation and development. We are eagerly looking forward to its future expansion, adding brilliance to the world, and benefiting everyone.
Where to Buy 1,3-Difluorobenzene in China?
As a trusted 1,3-Difluorobenzene manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
Frequently Asked Questions

As a leading 1,3-Difluorobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the main uses of 1,3-difluorobenzene?
1,3-Divinylbenzene is an important organic compound with a wide range of uses.
In the field of polymerization, this compound plays a significant role. 1,3-Divinylbenzene contains two vinyl groups and has high chemical activity, which can be used as a crosslinking agent to participate in the polymerization reaction. When preparing an ion exchange resin, an appropriate amount of 1,3-divinylbenzene is added, which can copolymerize with monomers such as styrene. In this way, the formed polymer chains are cross-linked with 1,3-divinylbenzene, which greatly enhances the mechanical strength and chemical stability of the ion exchange resin, allowing it to operate stably for a long time in many processes such as water treatment, purification and catalysis.
In the synthesis of polymer materials, 1,3-divinylbenzene also plays a key role. For example, when preparing some engineering plastics or elastomers with special properties, the introduction of 1,3-divinylbenzene can adjust the degree of crosslinking and network structure of polymer materials. With the precise regulation of the number and distribution of cross-linking points, the physical and mechanical properties of materials can be effectively improved, such as improving the hardness, wear resistance and heat resistance of materials, and then expanding the application range of polymer materials in high-end fields such as aerospace and automobile manufacturing.
In the coating industry, 1,3-divinylbenzene also shows unique value. It can be added to the coating system as a modifier to improve the performance of the paint film by participating in the cross-linking reaction during the coating film formation process. For example, by enhancing the adhesion, corrosion resistance, and weather resistance of the paint film, the coating can better protect the surface of the coated object and extend its service life. It is widely used in the coating process of construction, marine, machinery, and other industries.
What are the physical properties of 1,3-difluorobenzene?
1% 2C3-divinylbenzene is an organic compound with the following physical properties:
First, looking at its properties, it is a colorless to slightly yellow transparent liquid under normal conditions, and its color will gradually darken due to polymerization under sunlight. Its odor is unique, with an irritating smell similar to styrene, and it is pungent.
Second, when it comes to boiling point, it is between 195 ° C and 207 ° C. This boiling point characteristic makes it change from liquid to gaseous state under specific temperature conditions, which is of great significance in chemical separation and purification processes.
Third, its melting point is low, roughly around -87 ° C. This characteristic allows 1% 2C3-divinylbenzene to maintain a liquid state at room temperature, providing convenience for practical operation and use.
Fourth, in terms of density, it is about 0.918 - 0.925g/cm ³, which is slightly lighter than water. In the process of liquid-liquid mixing or separation, this density difference can be used for the stratification and separation of substances.
Fifth, in terms of solubility, 1% 2C3-divinylbenzene is insoluble in water, but can be miscible with many organic solvents, such as ethanol, ether, acetone, etc. This solubility property is widely used in organic synthesis, coating preparation and other fields, and is often used as a solvent or a raw material to participate in the reaction.
Sixth, at the volatile level, 1% 2C3-divinylbenzene is volatile and can be easily volatilized into the air in an open environment. Due to its irritation, it will affect the environment and human health after evaporation. When using, it is necessary to pay attention to the ventilation of the operating environment.
Is the chemical properties of 1,3-difluorobenzene stable?
The chemical properties of 1,3-diene benzene are quite stable. This substance has a conjugated double bond structure, and the conjugated system can cause electron cloud delocalization, reduce molecular energy, and stabilize the structure.
Looking at its chemical behavior, it can resist the action of many common chemical reagents at room temperature and pressure. In case of mild oxidants, such as dilute potassium permanganate solution, it is difficult to oxidize without special conditions. In general acid-base environment, it can also maintain its own structure intact, and it is not easy to hydrolyze or neutralize acid-base reactions.
Investigate its reactivity. Although it contains double bonds, the conjugation effect changes the density distribution of the double bond electron cloud, and the electrophilic addition reactivity is slightly lower than that of isolated double bonds. In order for an addition reaction to occur, relatively severe reaction conditions are often required, such as the presence of specific catalysts, higher temperatures or pressures, etc.
In addition, 1,3-diene benzene molecules can interact with each other by van der Waals forces, and its physical state and stability are also affected by this. In the solid state, the molecules are arranged in an orderly manner and have a certain lattice energy, resulting in relatively stable melting points and boiling points, and are not easy to volatilize or decompose.
In summary, 1,3-diene benzene is chemically stable due to its conjugate structure. It can maintain its own structure in common chemical environments. The reactivity is subject to the conjugation effect, and specific conditions are required to initiate chemical reactions.
What are the production methods of 1,3-difluorobenzene?
1% 2C3-divinylbenzene can be prepared by various methods. It can be obtained through chemical synthesis.
First, vinyl benzene is used as a base, and the vinyl groups are interacted and polymerized under specific reaction conditions to obtain 1% 2C3-divinylbenzene. Among them, a suitable catalyst needs to be selected to make the reaction proceed towards the formation of the target product. The catalyst can promote the reaction rate, but its type and dosage are all related to the purity and yield of the product. If a specific metal salt catalyst is selected, the reaction between vinylbenzene can occur in an orderly manner at a specific temperature and pressure, resulting in the formation of 1% 2C3-divinylbenzene.
Second, or from other vinyl-containing compounds, converted through a series of chemical reactions. First, these compounds are pretreated to expose or activate their activity check points, and then they interact to gradually build the molecular structure of 1% 2C3-divinylbenzene. In this process, it is extremely important to control the reaction environment, such as the pH of the reaction system, the type of solvent, etc., which will affect the process of the reaction and the quality of the product.
Third, there are also methods of chemical modification and transformation of natural products as starting materials. Natural products may contain available structural units, which can be transformed into 1% 2C3-divinylbenzene through ingenious chemical means. Although this approach is innovative to a certain extent, it often faces difficulties such as difficulty in obtaining raw materials and cumbersome reaction steps. Researchers need to carefully design reaction routes for the purpose of efficient preparation.
All these preparation methods have advantages and disadvantages. Researchers need to weigh and choose according to actual needs, availability of raw materials, cost considerations and many other factors in order to achieve the best preparation effect.
What are the precautions for storing and transporting 1,3-difluorobenzene?
1% 2C3-divinylbenzene is commonly used in chemical industry. During storage and transportation, many matters need to be paid attention to.
It is flammable. When storing, it must be kept away from fire and heat sources, and placed in a well-ventilated place. The temperature of the warehouse should be controlled to prevent its volatilization from intensifying due to excessive temperature and increasing the risk of fire. And it should be stored separately from oxidants, acids, and alkalis. It must not be mixed. The cover is easy to react with various chemicals and cause danger.
When transporting, the transportation vehicle should be equipped with the corresponding variety and quantity of fire equipment and leakage emergency treatment equipment. Summer transportation should be selected in the morning and evening to avoid high temperature, in case the temperature rises, the material evaporates and increases the danger. During transportation, make sure that the container does not leak, collapse, fall or damage. Before and after loading and unloading, the transportation tools should be thoroughly cleaned and washed, and it is strictly forbidden to mix with organic matter, flammable substances and other impurities.
Furthermore, 1% 2C3-divinylbenzene also has certain hazards to the human body. Contact can cause skin and eye irritation, and inhalation of its vapor can cause respiratory tract irritation. Therefore, storage and transportation personnel need to be professionally trained. When operating, they should wear protective clothing, protective gloves and goggles, etc., and take protective measures. If a leak occurs accidentally, quickly evacuate the personnel from the leaked contaminated area to the safe area and isolate them, strictly restricting access. Emergency responders need to wear protective gear to avoid contacting leaks with combustible substances (such as wood, paper, oil, etc.). Small leaks can be absorbed by inert materials such as sand and vermiculite. Large leaks need to be contained by building embankments or digging holes, covered with foam to reduce vapor disasters, and then transferred to a tanker or special collector with an explosion-proof pump for recycling or transportation to a waste treatment site for disposal.