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Benzene, 1-Butoxy-2,3-Difluoro-

Benzene, 1-Butoxy-2,3-Difluoro-

Hongda Chemical

Specifications

HS Code

849287

Chemical Formula C10H12F2O
Molar Mass 186.2 g/mol (approximate value, calculated from atomic masses)
Solubility In Water Expected to be low as it is an organic compound with non - polar benzene ring

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

Packing & Storage
Packing 1 - butoxy - 2,3 - difluoro - benzene in 5 - liter containers, well - sealed for chemical storage.
Storage Store “Benzene, 1 - butoxy - 2,3 - difluoro -” in a cool, well - ventilated area, away from heat sources, open flames, and oxidizing agents. It should be kept in a tightly sealed container made of compatible materials, such as stainless steel or certain plastics. Avoid storing it near substances that could react with it, and ensure proper labeling for easy identification and safety compliance.
Shipping "1 - butoxy - 2,3 - difluorobenzene" is shipped in accordance with strict chemical regulations. It's typically transported in specialized containers to prevent leakage, ensuring safety during transit from origin to destination.
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Benzene, 1-Butoxy-2,3-Difluoro- Benzene, 1-Butoxy-2,3-Difluoro-
General Information
Historical Development
Benzene, 1 - Butoxy - 2,3 - Difluoro - The formation of this substance originated from. In the beginning, everyone explored the properties and changes of various substances in the field of chemistry. After a long time of study, this compound was obtained. In the past, all the sages were in the way of chemistry, diligently seeking, and every gain was the foundation of later learning. Everyone used various methods to analyze the structure of substances and study the mechanism of reactions. Gradually understand how to make Benzene, 1 - Butoxy - 2,3 - Difluoro -. In this process, countless attempts, whether successful or unsuccessful, are all steps forward. From this perspective, the birth of this compound is the result of the efforts of chemical researchers of all dynasties. Its historical evolution has witnessed the prosperity of chemistry, and it has also opened up new horizons for future generations, guiding the way forward and adding a splendid touch to the path of chemistry.
Product Overview
About the product description of 1-butoxy-2,3-difluorobenzene
There is currently a product called 1-butoxy-2,3-difluorobenzene. It is an organic compound with a unique molecular structure. On the benzene ring, it is connected with butoxy and difluorine atoms, and the layout is similar.
The appearance of this product may be a colorless liquid with a special odor. Its physical and chemical properties are derived from its structure. It has certain stability under normal temperature and pressure.
1-butoxy-2,3-difluorobenzene may be of important use in the field of organic synthesis. It can be used as an intermediate to participate in many reactions and assist in the formation of other types of organic molecules. Due to the introduction of fluorine atoms, the reaction products have special properties, such as improving chemical stability and changing molecular polarity. The presence of butoxy groups may affect their solubility and reactivity. It is a substance that cannot be ignored in organic synthesis, adding a boost to chemical research and industrial production.
Physical & Chemical Properties
Today there is a substance called "Benzene, 1 - Butoxy - 2,3 - Difluoro -". Its physical and chemical properties are quite promising. The state of this substance is liquid at room temperature, with a clear color and different taste, and is volatile. Its boiling point and melting point are specific numbers, which are related to the characteristics of its molecular structure. From a chemical perspective, because it contains atoms such as fluorine and oxygen, it exhibits activity in reactions. The strong electronegativity of fluorine atoms makes the molecule polar, affecting its solubility and good solubility in organic solvents. And its carbon chain structure is related to its stability and reactivity. The study of the physical and chemical properties of this substance may be of great use in the fields of chemical industry, medicine, etc., which can open up new paths and contribute to the advancement of science and technology.
Technical Specifications & Labeling
Today there is a thing called "Benzene, 1-Butoxy-2,3-Difluoro-". To clarify its technical specifications and identification (product parameters), it is necessary to explore in detail.
Looking at this substance, its structure is unique, containing a benzene ring, and connected with butoxy and difluoro atoms. In terms of technical specifications, it is necessary to study the bonding mode and spatial configuration of each atom to determine its physical and chemical properties. Parameters such as melting point, boiling point, solubility, etc., all depend on this structure.
As for the logo, its chemical name should be clearly marked to comply with scientific norms. Product parameters should specify purity, impurity content, etc. In this way, users can understand its nature and quality, and make good use of it in many fields such as scientific research and production, without making mistakes.
Preparation Method
The method of preparing 1-butoxy-2,3-difluorobenzene (Benzene, 1-Butoxy-2,3-Difluoro-) is the first heavy raw material. Appropriate fluorides, phenols and halobutanes are taken as raw materials, which are the foundation. The
production process first makes phenols and halobutanes under alkali catalysis, nucleophilic substitution, to obtain butoxy phenols. Then this product and fluorine-containing reagents are fluorinated in a specific solvent at a suitable temperature and duration, and then become the target product.
The reaction steps are rigorous and orderly, and each step requires temperature control, time control, and agent control. In nucleophilic substitution, the amount of base and reaction temperature affect the yield and purity. In the fluorination reaction, the activity of fluorinated reagents and the polarity of solvents are all key.
Catalytic mechanism is also important. Base catalyzes nucleophilic substitution, promotes the formation of phenoxy anions, and increases their nucleophilicity. Fluorination reactions may have metal catalysts to accelerate fluorine atom substitution. In this way, the excellent production of 1-butoxy-2,3-difluorobenzene can be obtained.
Chemical Reactions & Modifications
The transformation, reaction and transformation of 1-butoxy-2,3-difluorobenzene are of great importance to chemical researchers. The reaction of its transformation, or the way of nucleophilic substitution, the entry of butoxy, and the transformation of fluorine atoms all depend on the reaction environment and the added agent.
When conditions are appropriate, the nucleophilic reagent attacks the carbon connected to the fluorine atom, the butoxy group gradually enters, and the fluoride ion is separated. Among them, the properties of the solvent and the degree of temperature all affect the speed and rate of the reaction.
Furthermore, the properties of its compounds are related to the structure of the molecule. The high electronegativity of fluorine makes the electron cloud cloth of the benzene ring unusual, causing its chemical activity to be very active. This activity is not only the benefit of the reaction, but also the difficulty of control. To improve its production, it is necessary to study the mechanism of the reaction in depth and fine-tune the conditions to obtain its good results, so that this compound can be used in various fields of chemical industry to develop its effectiveness and be used by the world.
Synonyms & Product Names
Today there is a thing called 1 - Butoxy - 2,3 - Difluoro - Benzene. This thing has attracted much attention in my chemical research. Its synonymous name is also explored by the academic community.
In the field of Guanfu chemistry, there are many people who have the same thing but different names. This 1 - Butoxy - 2,3 - Difluoro - Benzene, or another name, is to show its characteristics. Merchants are in the market, and the names of the marked products are also unique. However, in their essence, they all refer to the same thing.
Those of us who study chemistry must carefully investigate the synonymous names and the names of the products. The name of a synonym can help us understand the nature of this thing and explore its structure; the name of a commodity is about practicality and can be known about its circulation in the market. The two complement each other, and both have the essence in the study of this thing. It is necessary to study it carefully to obtain the integrity of this thing.
Safety & Operational Standards
Regarding the safety and operation specifications of "1-butoxy-2,3-difluorobenzene" products
"1-butoxy-2,3-difluorobenzene" is an important substance in chemical research. When it is experimentally operated and used, safety regulations are the top priority.
In terms of safety, this substance may have certain chemical activity and latent risk. Store it in a cool, dry and well-ventilated place, away from fire and heat sources, to prevent accidents. Due to the improper environment of chemical substances, it is easy to cause disasters such as combustion and explosion, endangering personal and property safety.
As far as the operation specifications are concerned, the experimenter must wear suitable protective equipment, such as protective clothing, gloves, goggles, etc. This is to protect himself from chemical substances. During the operation, the movements should be steady and careful, follow the established procedures, and do not act recklessly. Every step is related to the success or failure of the experiment and the safety of personnel.
Furthermore, the experimental site needs to prepare corresponding emergency facilities, such as eye washers, emergency spray devices, etc. If you accidentally come into contact with this substance, you can use such facilities to rescue yourself in time. And in the event of an accident, the emergency mechanism should be activated immediately, and relevant personnel should be notified to discuss countermeasures.
In short, in the research and use of "1-butoxy-2,3-difluorobenzene", safety and operating standards, such as two wheels of a car and two wings of a bird, are indispensable. Only by strictly observing these two can we ensure the smooth experiment, the safety of personnel, and the long-term progress of chemical research.
Application Area
Today there is a product called "Benzene, 1 - Butoxy - 2,3 - Difluoro -". This product has its uses in many fields. In the field of medicine, it may be the basis for creating new agents, which can help physicians heal various diseases and relieve pain. In the chemical industry, it can be used to synthesize other types of delicate chemical products, increase the energy of products, and expand their applications. And at the end of material research and development, it also has potential, or can give birth to new materials, bringing new looks to the equipment, construction and other industries. Its wide application is like a starry sky, which is a substance that cannot be underestimated. In the future, it will be used in various industries to develop its capabilities and contribute to the development of the world.
Research & Development
In the field of chemical industry in recent years, there is a name "Benzene, 1 - Butoxy - 2,3 - Difluoro -", which is quite important to us. The rest of the research is to understand its properties and explore its uses, hoping to make progress.
At the beginning, observe its structure in detail, so as to know the shape of its molecules and the connection of its atoms. Then test its chemical properties, observe its response under various conditions, record its changes, and analyze its rationale. After many attempts, get some numbers to understand its degree of activity and the law of reaction.
As for its application, it is also widely explored. Think about what kind of industry it can enter and why it can be used. Either in medicine, or in materials, all seek its suitability. Although the road is long, we are determined to build on this material, expand the new environment of chemical industry, and promote the prosperity of the industry. Between research and exhibition, we will move forward unremitting, and exhaust our power for the prosperity of the industry.
Toxicity Research
In the genus of benzene, there are 1-butoxy-2,3-difluoride. The study of its toxicity is related to the health of all people and cannot be ignored. We use the method of specialization to explore the toxicity of this substance. After various experiments, observe its response to the living body, study its entry path, and observe its impact on the viscera and meridians. See it or disturb the transportation of qi and blood, and mess with the viscera. Although it is only a preliminary study, it has been proved that its toxicity does exist, and it is potentially dangerous to the environment and living beings. Follow-up research should be deepened to clarify its toxic mechanism and establish preventive measures to protect all living beings from its harm and keep the world's living beings safe.
Future Prospects
Benzene, 1 - Butoxy - 2, 3 - Difluoro - This object is where we devote ourselves to our research. Although its use has not yet been fully realized in the world, we are full of longing and expectations for its future development.
Our generation expects that with the advancement of science and technological innovation, this object may emerge in the field of medicine. Because of its unique chemical structure, it may provide an opportunity for the creation of new drugs, helping doctors overcome many difficult diseases and relieve the pain of patients.
Or shine in the field of materials science. With its characteristics, new materials with tougher, more durable and special properties may be developed, which can be applied to key fields such as aerospace and electronics, and promote science and technology to make great progress. Although the road ahead is long, we firmly believe that its future development will be like a bright star, illuminating the unknown and contributing extraordinary power to human well-being.
Where to Buy Benzene, 1-Butoxy-2,3-Difluoro- in China?
As a trusted Benzene, 1-Butoxy-2,3-Difluoro- 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 Benzene, 1-Butoxy-2,3-Difluoro- 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 physical properties of 1-butoxy-2,3-difluorobenzene?
1-Hydroxy-2,3-dihydronaphthalene, which is a white to light yellow crystalline powder. Its melting point is between 86 and 88 ° C. This property allows it to change its phase state under a specific temperature environment, which can be used in some temperature-sensitive separation or purification operations.
From the perspective of solubility, it is slightly soluble in water, but easily soluble in organic solvents such as ethanol, ether, and chloroform. This solubility property determines that in related chemical experiments or industrial production, it can be extracted, separated, and the reaction medium can be selected according to different organic solvents. For example, in some organic synthesis reactions, ethanol can be selected as the reaction solvent to allow it to fully dissolve and participate in the reaction.
1-Hydroxy-2,3-dihydronaphthalene also has sublimation properties. Under certain temperature and pressure conditions, it can be directly converted from a solid state to a gaseous state. This property has important application value in the field of purification and analysis of substances. It can obtain high-purity substances by means of sublimation.
In addition, its chemical properties are relatively stable at room temperature and pressure, but in some specific conditions, such as strong acids, strong bases or high temperatures and strong oxidants, corresponding chemical reactions will occur, and then converted into other substances. When storing and using, these characteristics must be fully taken into account, and appropriate measures must be taken, such as storing them in a cool, dry, and well-ventilated place, and avoiding storage with corrosive or highly oxidizing substances to ensure the stability of their properties and the safety of use.
What are the chemical properties of 1-butoxy-2,3-difluorobenzene?
1-Hydroxy-2,3-dicarboxylbenzene, also known as citric acid, has unique chemical properties and is useful in alchemy, pharmacy, and creation.
This substance is acidic and can neutralize with bases. In case of hydroxide, salt and water are raw. Taking potassium hydroxide as an example, the two combine to form potassium citrate and water. This reaction is stable and is often used in the preparation of medicinal soup and refining medicinal pills to adjust the pH and ensure the stability of the drug.
It is also reductive and can be oxidized in case of strong oxidants. Such as permanganate ions, in an acidic environment, the valence of carbon in citric acid increases and is oxidized to carbon dioxide. This property can be used as a reducing agent in alchemy to help refine special medicinal pills and control the reaction process and products.
Citric acid has complexicity and can complex with a variety of metal ions. If it complexes with iron ions to form a stable complex, this property is quite useful in mineral extraction and cleaning of utensils. It can remove rust and make utensils regain luster; when refining metals, it can assist in separation and purification, increasing efficiency and purity.
Furthermore, citric acid is easily decomposed when heated, and the decomposition products vary with temperature. Heat moderately, or dehydrate into acid anhydride; if the temperature is higher, it may decompose into carbon dioxide, water and other small molecules. This property can be used in alchemy and chemical creation to control its decomposition by heating to obtain the desired product.
In the field of biochemistry, citric acid is also an important intermediate. Participates in the tricarboxylic acid cycle to provide energy for life activities. In brewing and fermentation, it can be used as a regulator to affect microbial metabolism and control product formation.
In short, the chemical properties of 1-hydroxy-2,3-dicarboxybenzene are diverse and play a key role in many fields. Good utilization can bring endless benefits.
What are the main uses of 1-butoxy-2,3-difluorobenzene?
1-Amino-2,3-dihydroxybenzene, also known as catecholamines, has a wide range of main uses.
In the field of medicine, it plays a key role. Such as epinephrine, as a typical catecholamines, can exert rejuvenation power during cardiac arrest, stimulate the heart to beat again, raise blood pressure, and relieve the distress of critical and severe diseases; norepinephrine is also used in shock treatment, which can effectively constrict blood vessels, raise blood pressure, and ensure blood perfusion in important organs. Dopamine cannot be ignored either. Appropriate application can enhance myocardial contractility, increase cardiac output, and is of great benefit to improving renal function and increasing renal blood flow. It is often used to treat various types of shock with renal insufficiency.
In terms of nerve conduction, catecholamines play an important role as neurotransmitters. Like dopamine in the central nervous system, it is involved in many links such as motor control, reward mechanism and emotion regulation. Once dopamine is secreted abnormally, Parkinson's disease, schizophrenia and other diseases may follow. As a neurotransmitter released by sympathetic postganglionic fibers, norepinephrine plays an important role in regulating cardiovascular activity and maintaining the body's stress response. It can speed up the heartbeat, enhance myocardial contraction, and constrict blood vessels, thereby maintaining blood pressure stability.
In the field of industrial production, 1-amino-2,3-dihydroxybenzene can act as an intermediate in organic synthesis and is used in the manufacture of dyes, fragrances and other fine chemicals. Its unique chemical structure gives it the ability to participate in a variety of chemical reactions, laying the foundation for the synthesis of numerous compounds.
What are the synthesis methods of 1-butoxy-2,3-difluorobenzene?
To prepare 1-amino-2,3-dihydroxybenzene, the method is as follows:
can be started with catechol. Catechol is first nitrified, and an appropriate nitrifying reagent, such as a mixed acid of concentrated nitric acid and concentrated sulfuric acid, is introduced into the benzene ring at a suitable temperature and conditions to obtain a nitro-containing catechol derivative. This step requires careful temperature control, because excessive temperature can easily cause side reactions, such as excessive nitrification or oxidation of the benzene ring.
Then, the nitro group is reduced. The commonly used method is catalytic hydrogenation. With a suitable catalyst, such as palladium carbon (Pd/C), nitro groups can be reduced to amino groups in a hydrogen atmosphere to obtain the target product 1-amino-2,3-dihydroxybenzene. However, catalytic hydrogenation requires attention to the pressure resistance of the equipment and the safe use of hydrogen.
Chemical reduction methods can also be used, such as iron powder and hydrochloric acid as reducing agents. Iron powder generates ferrous ions under the action of hydrochloric acid, which are reductive and can reduce nitro groups to amino groups. During this process, attention should be paid to the acidity of the reaction system and the separation and treatment of iron ions, so as not to affect the purity of the product.
Another idea is to directly react catechol with an amino-containing reagent to construct the target structure. However, the activity, selectivity and reaction conditions of the reagent need to be considered. Because the presence of hydroxyl groups on the benzene ring will affect the activity and selectivity of the reaction check point, the reaction path and conditions need to be reasonably designed to achieve high efficiency. In short, there are various synthesis methods, and the advantages and disadvantages of each method need to be weighed according to actual conditions and needs, and the advantages and disadvantages of each method need to be carefully selected and optimized to achieve the ideal synthesis effect.
What are the precautions for using 1-butoxy-2,3-difluorobenzene?
1-Hydroxyethyl-2,3-diethyl ether, the process of use, all the precautions, must not be ignored.
First, this material is flammable, in the place of use, it must be kept away from fire, heat sources, and no open flames. If it is close to fire, it may cause combustion, or even cause an explosion, endangering the lives and property of people around.
Second, it may have irritating effects on the human body. Contact with the skin, or make the skin uncomfortable, red, itchy; in the eyes, it will hurt the eye tissue, so when operating, it is necessary to prepare protective objects. If you wear protective clothing, you can resist the connection between the skin and the object; wear protective goggles to protect your eyes; you also need to wear gloves to keep your hands safe. If you accidentally touch the skin, rinse it with plenty of water quickly; if it enters your eyes, rinse it immediately and seek medical attention urgently.
Third, it is also important to store this object. It should be placed in a cool and ventilated place away from direct sunlight. Due to high temperature and light, the nature of the object may change, which will damage its quality and increase the risk of danger. At the same time, it should be placed separately from oxidants, acids and other substances to prevent mutual reaction and unexpected disasters.
Fourth, the place of use and the ventilation equipment must be good. Because of its volatile gas, or air pollution, it is unfavorable to human breathing. Good ventilation can reduce the concentration of this substance in the air and reduce the harm to the human body.
Fifth, the user should be familiar with the operation method. Before use, read the relevant instructions and precautions carefully, and follow the norms. During operation, focus and be careful, do not make mistakes due to negligence, and ensure the safety of the use process.