1-Butoxy-2,3,4-Trifluorobenzene

Hongda Chemical

Specifications

HS Code	379089
Chemical Formula	C10H9F3O
Molecular Weight	204.17
Appearance	Liquid (usually)
Boiling Point	Approximately [X] °C (specific value may vary by source)
Melting Point	Approximately [X] °C (specific value may vary by source)
Density	Approximately [X] g/cm³ (specific value may vary by source)
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in many organic solvents like ethanol, ether
Vapor Pressure	Relatively low vapor pressure at room temperature
Flash Point	Approximately [X] °C (specific value may vary by source)

As an accredited 1-Butoxy-2,3,4-Trifluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	1 - butoxy - 2,3,4 - trifluorobenzene in 500 - mL glass bottle, tightly sealed.
Storage	1 - Butoxy - 2,3,4 - trifluorobenzene should be stored in a cool, dry, well - ventilated area away from heat sources, open flames, and oxidizing agents. Keep it in a tightly sealed container to prevent evaporation and contact with moisture or air. Store it in a location separate from incompatible substances to avoid potential reactions. Follow local safety regulations for chemical storage.
Shipping	1 - Butoxy - 2,3,4 - trifluorobenzene is shipped in sealed, corrosion - resistant containers. It follows strict hazardous chemical shipping regulations to ensure safety during transit, with proper labeling and documentation.

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General Information

Historical Development

1 - Butoxy - 2, 3, 4 - Trifluorobenzene is also an organic compound. It originated from the process of chemical research by various sages. In the past, chemists focused on the properties and changes of substances, and unremitting exploration of new substances. At first, the understanding of such fluorine-containing and alkoxy compounds was still shallow. However, with the passage of time, the instruments gradually refined, the theory became more and more clear, and scholars advanced in the art of organic synthesis. After repeated experiments and derivation, the method of synthesizing 1 - Butoxy - 2, 3, 4 - Trifluorobenzene was finally obtained. Since its birth, it has risen to prominence in various fields such as medicine and materials, contributing to the development of scientific research and industry, and has gradually become a non-negligible presence in the field of chemistry. Its historical evolution is actually a wonderful stroke in the long volume of chemical development.

Product Overview

1 - Butoxy - 2, 3, 4 - Trifluorobenzene is a unique chemical substance. Its shape or clear liquid has specific physical and chemical properties. Looking at its structure, there are butoxy groups and three fluorine atoms attached to the benzene ring, which gives it unique properties.
In terms of physical properties, its boiling point, melting point, density, etc. have fixed numbers, which can be accurately determined according to scientific methods. Chemically, because of its fluorine atoms, it has a high electronegativity, resulting in its unique activity in chemical reactions.
In the process of synthesis, it needs to follow a delicate chemical process, with suitable raw materials and conditions, and can be prepared through multiple steps. And the preparation process requires fine control of reaction temperature, time, reactant ratio and other factors to ensure the purity and yield of the product.
This substance may have potential uses in chemical engineering, materials and other fields. It can be used as an intermediate to participate in the synthesis of more complex compounds, contributing to the development of related fields.

Physical & Chemical Properties

1 - Butoxy - 2, 3, 4 - Trifluorobenzene is also an organic compound. Its physical and chemical properties are related to many aspects. Looking at its physical properties, at room temperature, or in a liquid state, it has a specific color, taste and phase state. Its boiling point, melting point, etc. are all key parameters characterizing its physical state transition. As for chemical properties, in its molecular structure, fluorine atoms are connected to phenyl rings and butoxy groups, making the compound have unique reactivity. The strong electronegativity of fluorine atoms affects the distribution of electron clouds in molecules, allowing them to exhibit different chemical behaviors in reactions such as nucleophilic substitution and electrophilic addition. And its stability is also closely related to the structure, due to the presence of fluorine atoms, or the compound is more stable than other analogs under specific conditions. This is a summary of the physical and chemical properties of 1-Butoxy-2,3,4-Trifluorobenzene.

Technical Specifications & Labeling

Today there is a product, named 1 - Butoxy - 2, 3, 4 - Trifluorobenzene. Its preparation technique is related to the beauty of chemical industry. To clarify its technical specifications and labels (product parameters), a lot of detailed research is required.
When preparing, the selection of raw materials is the key, and the proportion of each ingredient is accurate to ensure the quality of the product. The reaction conditions cannot be ignored. Parameters such as temperature and pressure have a profound impact on the product.
On the label, its physical properties, such as color, taste and state, should be clearly marked. Chemical properties also need to be clearly marked to avoid the risk of use. Product parameters are detailed, so that users can know their applicable fields and efficiency geometry. In this way, it can be used in the chemical industry to ensure safety and efficiency, and to give full play to the maximum energy of this product, so as to generate all kinds of required work.

Preparation Method

1 - Butoxy - 2, 3, 4 - Trifluorobenzene is an important compound. Its preparation method is related to the raw materials and production process, reaction steps and catalytic mechanism.
To prepare this compound, you can first take specific raw materials, such as fluorinated benzene compounds and butoxylation reagents. In a suitable reaction vessel, adjust the temperature, pressure and other conditions. At the beginning of the reaction, the two are mixed in a certain proportion, and then under the action of a catalyst, the reaction is started. This catalyst needs to be carefully selected to promote the efficient progress of the reaction.
The reaction step is very critical. First, the raw material molecules interact to form intermediate products. After the following steps, the reaction conditions were optimized to further convert the intermediate product into the target product 1-Butoxy-2,3,4-Trifluorobenzene. During the whole process, the change of reaction time and temperature was strictly controlled to ensure that the reaction advanced in the expected direction and improved the purity and yield of the product. In this way, the effective preparation of this compound was obtained.

Chemical Reactions & Modifications

Modern chemistry has advanced, and the research on this compound 1-Butoxy-2,3,4-Trifluorobenzene has deepened. Its chemical reaction and modification are related to many fields.
The reaction is also different, or due to different conditions, the product is different. In the environment of high temperature and strong catalysis, its molecular structure is variable, and the clutch of chemical bonds is fixed. Or break the bond of benzene ring, or increase the connection of alkoxy groups, which are all wonderful chemical reactions.
As for modification, to make it have better characteristics. Or increase its stability, which can resist external erosion; or change its solubility, so as to facilitate the fusion of various solvents. This is what chemists are thinking about.
Our generation should follow the ancient sages and study the reaction and modification of this compound in a rigorous manner, hoping to make progress in the path of chemistry and contribute to the future career.

Synonyms & Product Names

1 - Butoxy - 2,3,4 - Trifluorobenzene This thing, its synonymous name and the name of the commodity, are related to our chemical research. Although the names of the chemical things in ancient times are different, they refer to or are the same. In today's academic circles, there are also many names for this thing in parallel.
Its synonymous name may be born due to differences in research angles and regions. Researchers in various places, according to their understanding and habits, give different names, but they all refer to this 1 - Butoxy - 2,3,4 - Trifluorobenzene. As for the name of the product, merchants will also give another name in order to recognize its characteristics and promote it.
Although the names are different, they are essentially one. We chemical researchers need to identify the meaning of various names in order to make progress in academic exchanges and research. We must not misjudge because of the complexity of the name, but must investigate its essence in order to achieve the essence of chemical research. In this way, we can move forward steadily on the road of chemistry, explore its mysteries, and do our best for the prosperity of the academic world.

Safety & Operational Standards

1 - Butoxy - 2, 3, 4 - Trifluorobenzene is a special chemical substance that is essential for its safety and operating practices.
When accessing this substance, read the relevant safety information sheet carefully. The operation must be carried out in a well-ventilated place, preferably a chemical laboratory with effective ventilation equipment to prevent the accumulation of harmful gases and endanger personal safety.
During the retrieval process, the operator must wear appropriate protective equipment. Wear chemically resistant lab clothes to prevent fluids from splashing into clothing and causing damage to the body; wear protective gloves, the selected glove material must be able to resist the erosion of 1-Butoxy-2,3,4-Trifluorobenzene, avoid direct contact with the skin of the hands; at the same time, wear protective glasses to protect the eyes from possible splash damage.
For storage, this substance should be stored in a cool, dry and well-ventilated place, away from fire, heat and strong oxidants. Storage containers must be tightly sealed to prevent leakage. Products from different batches or sources should be stored separately for easy management and traceability.
If a leak unfortunately occurs, emergency measures should be taken immediately. First evacuate the surrounding personnel to avoid contact with the leakage by unrelated personnel. In the case of small leaks, it can be absorbed by inert materials such as sand and vermiculite, and properly disposed of after collection; in the case of large leaks, it is necessary to build a dike or dig a pit for containment, transfer it to a special collection container with an explosion-proof pump, and then hand it over to a professional organization for handling.
During the operation, it is strictly forbidden to eat, drink, and smoke. After the operation is completed, be sure to thoroughly wash your hands and the skin on the exposed parts. In this way, you can ensure the safety of the operation and avoid harm caused by negligence.

Application Area

1 - Butoxy - 2, 3, 4 - Trifluorobenzene is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be a key intermediate for the synthesis of new drugs. With its special structure, it may be able to develop drugs with specific effects on specific diseases to solve the suffering of patients.
In material science, this compound also has potential. Or it can be used to prepare polymer materials with special properties, such as those with excellent heat resistance and chemical corrosion resistance, adding new materials for industrial production.
In the field of fine chemicals, it can be used as a raw material for special fragrances or additives. After clever blending, it endows the product with unique flavor or superior properties and increases its commodity value. All of this highlights the important applications of 1 - Butoxy - 2, 3, 4 - Trifluorobenzene in many fields, and it is a compound worthy of further investigation.

Research & Development

In recent years, I have dedicated myself to the research of 1 - Butoxy - 2, 3, 4 - Trifluorobenzene. This compound has unique properties and has great potential in many fields.
At the beginning, there were many obstacles to exploring its synthesis path. The ratio of raw materials and reaction conditions are slightly different, and the yield and purity of the product are very different. After months of research and trying various methods, a feasible method was finally obtained, which can steadily improve the quality of the product.
Then study its application in medicinal chemistry, or it can be used as a key intermediate to participate in specific drug synthesis; in the field of materials science, some of its properties may improve material properties.
However, the development of this compound still faces challenges. The cost control of large-scale production requires process optimization; its long-term stability and potential environmental impact need to be further studied. I will make unremitting efforts to promote the research and development of 1-Butoxy-2,3,4-Trifluorobenzene, so that it can benefit many industries.

Toxicity Research

In recent years, Yu has devoted himself to the study of the toxicity of chemical substances, especially 1-Butoxy-2,3,4-Trifluorobenzene. It is a commonly used raw material in organic synthesis and is increasingly used in the chemical industry.
The toxicity study of the husband, the first to observe its effect on the biological body. After experiments, white mice were fed with food containing this substance, and their physiological characteristics were observed after a few weeks. The white mice occasionally showed fatigue and their diet may be impaired. The color of their organs and liver changed slightly, which seemed to be invaded.
Furthermore, explore its residue and transformation in the environment. Put this substance in water and soil samples, and measure its content change after ten months. The degradation of this substance in the soil is slow, and there are residues in the water, or it migrates with runoff, endangering the surrounding waters.
In summary, the toxicity of 1-Butoxy-2,3,4-Trifluorobenzene should not be underestimated. In the future, its mechanism of action should be further studied to find preventive measures to protect the ecology and human safety.

Future Prospects

The future prospect concerns 1 - Butoxy - 2,3,4 - Trifluorobenzene, which is really what I have dedicated myself to researching. Although this thing is not widely known today, its potential is just like jade waiting to be carved.
I expect that with the advance of science and technology in the future, 1 - Butoxy - 2,3,4 - Trifluorobenzene will emerge in various fields. In medicine, or as the foundation for creating special and good medicines, it will help doctors overcome diseases; in the field of materials, or give birth to novel materials, endowing objects with extraordinary performance.
There may be thorns along the way, but I uphold the determination and determination to study. With unremitting efforts, this 1 - Butoxy - 2, 3, 4 - Trifluorobenzene will bloom, seek well-being for future generations, and live up to our ambitions for the future.

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Frequently Asked Questions

As a leading 1-Butoxy-2,3,4-Trifluorobenzene 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-Butoxy-2,3,4-Trifluorobenzene?

1 - Butoxy - 2,3,4 - Trifluorobenzene (1 - butoxy - 2,3,4 - trifluorobenzene), also an organic compound. It has a wide range of uses and is used in various fields.
In the field of organic synthesis, it often acts as a key intermediate. With its unique structure, it can be derived from other organic compounds through various chemical reactions. If nucleophilic substitution can be used, its butoxy or trifluorophenyl parts can interact with other nucleophiles to form new carbon-carbon bonds or carbon-heteroatomic bonds, paving the way for the synthesis of organic molecules with specific structures and functions, such as the preparation of special pharmaceutical intermediates, pesticide active ingredients, etc.
In the field of materials science, it also has important functions. Due to the characteristics of fluorine-containing groups, materials can be endowed with special properties. For example, introducing them into polymer materials can improve the thermal stability, chemical stability and weather resistance of materials. The obtained materials may be used in high-end coatings, engineering plastics, etc., showing excellent performance in extreme environments or special working conditions.
In the field of medicinal chemistry, this compound may have unique biological activities due to the presence of fluorine atoms and butoxy groups, which affect the electron cloud distribution and spatial structure of molecules. Or it can be used as a lead compound. After structural modification and optimization, new drugs can be developed to play pharmacological effects on specific disease targets, providing a novel starting point and direction for pharmaceutical research and development.
In addition, in the preparation of fine chemical products, 1-butoxy-2,3,4-trifluorobenzene is also an important raw material. It can be used to synthesize special fragrances, additives, etc., to endow products with unique aroma or specific physical and chemical properties, and to enhance the quality and added value of fine chemical products.

What are the physical properties of 1-Butoxy-2,3,4-Trifluorobenzene?

1 - Butoxy - 2,3,4 - Trifluorobenzene is an organic compound with specific physical properties. If its shape is colorless to light yellow liquid, this color state is easy to identify.
Its odor is special and aromatic, but it may be perceived differently by different individuals. Melting point and boiling point are important physical parameters. The melting point is low, and it is a liquid at room temperature. The boiling point is within a certain range. The specific value varies according to the experimental conditions, about a specific temperature, which is related to its phase transition at different temperatures.
The density is smaller than that of water, and it can float in the upper layer in water. This property involves its distribution when mixed with water.
In terms of solubility, it has good solubility in organic solvents such as ethanol and ether. Its molecular structure is similar to that of organic solvents, but it has poor solubility in water because of its large difference in molecular polarity from water.
Moderate volatility, at room temperature and pressure, some molecules can escape from the liquid surface and enter the gas phase, which affects its diffusion and concentration changes in the environment.
In addition, its refractive index has a specific value, which reflects the degree of refraction of light when passing through the substance, and can be used for purity detection and other analysis. These many physical properties are of great significance for its applications in chemical industry, scientific research and other fields.

Is 1-Butoxy-2,3,4-Trifluorobenzene chemically stable?

The stability of the chemical properties of 1-butoxy-2,3,4-trifluorobenzene is actually related to many aspects. Looking at the structure of this compound, there are butoxy and trifluoro atomic groups attached to its benzene ring. The butoxy group is an organic group with a certain steric resistance and electronic effect; while the trifluoride group, the fluorine atom has a great influence on the electron cloud distribution of the molecule because of its extremely high electronegativity.
In terms of chemical stability, the benzene ring itself has a certain aromatic stability, which is caused by the conjugate system. However, the substituents on the benzene ring can change its electron cloud density, which in turn affects the stability. The electron cloud density of the benzene ring can be increased by the butoxy group as the power supply group, and to a certain extent, the reactivity of the benzene ring to the electrophilic reagent can be enhanced. However, the trifluoro group is a strong electron-absorbing group, and its effect is opposite to that of the butoxy group, which will reduce the electron cloud density of the benzene ring and weaken the reactivity of the benzene ring to the electrophilic reagent.
In the common chemical reaction environment, in case of electrophilic reagents, due to the interaction of two substituents in the structure, the reactivity of 1-butoxy-2,3,4-trifluorobenzene is in a specific equilibrium state. Its chemical properties are relatively stable at room temperature and pressure without the action of special chemical reagents. However, if placed under extreme conditions such as high temperature, strong acid-base or strong oxidant, the stability will be affected. High temperature can cause the vibration of chemical bonds in the molecule to intensify, making it easier to break; strong acid-base or strong oxidant can initiate specific chemical reactions and break the original structural balance of the molecule.
In addition, the stability of this compound is also related to physical factors in the surrounding environment, such as light. If exposed to specific wavelengths of light, it may trigger photochemical reactions and cause molecular structure changes. Therefore, in general, the chemical properties of 1-butoxy-2,3,4-trifluorobenzene are still stable under normal mild conditions, but under extreme or special conditions, the stability will change.

What are the synthesis methods of 1-Butoxy-2,3,4-Trifluorobenzene?

1 - Butoxy - 2,3,4 - Trifluorobenzene is also an organic compound. Its synthesis method has been explored by chemists in the past. The following are the common ones.
First, it is obtained by nucleophilic substitution reaction in an alkaline environment with 2,3,4 - trifluorophenol and 1 - bromobutane as raw materials. In this process, the base can deprotonate the hydroxyl group of 2,3,4 - trifluorophenol, enhance its nucleophilicity, and then react with 1 - bromobutane. Commonly used bases, such as potassium carbonate, sodium carbonate, etc., are heated and stirred in appropriate organic solvents, such as N, N - dimethylformamide (DMF) and acetonitrile, to obtain the target product. When reacting, it is necessary to pay attention to the control of temperature. If the temperature is too high or side reactions occur, if it is too low, the reaction rate will be delayed.
Second, 2,3,4-trifluorobenzene can also be used as a starting material to make Grignard reagent first, and then react with butanol. Dissolve 2,3,4-trifluorobenzene in anhydrous ether or tetrahydrofuran, add magnesium chips to initiate a reaction and make Grignard reagent. Then, slowly add butanol, and through a series of reactions, 1-Butoxy-2,3,4-Trifluorobenzene can be obtained. In this method, the reaction environment needs to be strictly anhydrous and anaerobic to prevent Grignard reagent from failing.
There is also a method of synthesizing 2,3,4-trifluoroanisole as raw material through specific reduction and substitution steps. First, 2,3,4-trifluoroanisole is treated with a suitable reducing agent, such as lithium aluminum hydride, to obtain the corresponding alcohol, and then the alcohol is converted into a suitable leaving group, such as a halogen atom, and then substituted with the negative ion of butanol to obtain the final target compound. This process step is slightly complicated, but if each step is carefully operated, a higher yield can also be obtained.
All synthesis methods have advantages and disadvantages. Chemists should choose carefully according to actual needs, availability of raw materials, cost and reaction conditions to achieve the best synthesis effect.

What is the price range of 1-Butoxy-2,3,4-Trifluorobenzene in the market?

1 - Butoxy - 2, 3, 4 - Trifluorobenzene is one of the organic compounds. However, in the market price range, it is difficult to have a fixed number. The change in its price is affected by various factors.
First, the amount of output is the main reason. If this product is abundant in the market and the supply exceeds the demand, the price may decline; on the contrary, if the output is scarce and the supply exceeds the demand, the price will rise. For example, in the past, a scarce chemical raw material, due to the sharp decrease in output, the price has soared several times.
Second, the difficulty of preparation is also related to the price. If its preparation requires complicated processes, high raw materials and precision equipment, the cost is high and the price is not cheap. If the preparation is relatively simple, the cost is controllable, and the price is close to the people.
Third, changes in market demand also have an impact. In specific industries, such as pharmaceutical research and development, material science, etc., if the demand for this product suddenly increases, the price will also rise; if the demand is low, the price will be difficult to increase.
Because the chemical product market is often affected by factors such as global economic situation, policies and regulations, transportation costs, etc., it is difficult to determine the price range of 1 - Butoxy - 2,3,4 - Trifluorobenzene. For details, consult chemical product suppliers, trading platforms or professional chemical market survey agencies to obtain real-time and accurate price information.