3 Ethoxy 1 1 1 2 3 4 4 5 5 6 6 6 Dodecafluoro 2 Trifluoromethyl Hexane
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-ethoxy-1,1,1,2,3,4,4,5,5,6,6,6-dodecafluoro-2-(trifluoromethyl)-hexane
Chemical Formula C9H5F15O
Molar Mass 434.11 g/mol
Appearance Colorless liquid
Boiling Point 114 - 116 °C
Density 1.64 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents
Chemical Formula C9H3F15O
Molar Mass 414.09 g/mol
Appearance likely a colorless liquid
Boiling Point approx. 84 - 86 °C
Density around 1.65 g/cm³
Vapor Pressure low, due to high fluorination
Solubility In Water poorly soluble, as it is highly fluorinated and non - polar
Solubility In Organic Solvents soluble in many fluorinated and some common non - polar organic solvents
Flash Point non - flammable, due to high fluorine content
Chemical Formula C9H3F15O
Molar Mass 422.09 g/mol
Appearance likely a colorless liquid
Boiling Point data needed
Melting Point data needed
Density data needed
Vapor Pressure data needed
Solubility data needed
Flash Point data needed
Refractive Index data needed
Hazardous Nature data needed
Chemical Formula C9H3F15O
Molar Mass 414.1 g/mol
Appearance Colorless liquid
Boiling Point 93 - 94 °C
Density 1.65 g/cm³
Vapor Pressure 4.4 kPa at 20 °C
Solubility In Water Insoluble
Flash Point None (non - flammable)
Refractive Index 1.279
Surface Tension 16.9 mN/m at 25 °C
Odp Ozone Depletion Potential 0
Gwp Global Warming Potential Low
FAQ

What are the chemical properties of 3-ethoxy-1,1,2,3,4,4,5,5,6,6,6-dodecafluoro-2- (trifluoromethyl) -hexane?

3 - ethoxy - 1, 1, 1, 2, 3, 4, 4, 5, 5, 6, 6 - dodecafluoro - 2 - (trifluoromethyl) - hexane is an organic compound with unique chemical properties.

In terms of physical properties, because it contains many fluorine atoms, the intermolecular forces are special, resulting in specific values of boiling point and melting point. Under normal circumstances, such fluorine-containing organic compounds have relatively low boiling points, which is due to the high electronegativity of fluorine atoms and the large molecular polarity. However, the radius of fluorine atoms is small and the van der Waals force is relatively weak, so the boiling point is affected and reduced. And its density is often higher than that of common hydrocarbons, which is related to the relatively large atomic weight of fluorine atoms.

In terms of chemical properties, the carbon-fluorine bond in this compound is extremely stable. The high carbon-fluorine bond energy makes this compound very chemically stable. Under normal conditions, it is difficult to occur common organic reactions such as substitution and addition. However, its ethoxy group is relatively active, and the oxygen atom in the ethoxy group has lone pair electrons, which can participate in the reaction as a nucleophilic reagent. Under certain conditions, such as in the presence of acidic or basic catalysts, the ethoxy group may undergo hydrolysis to generate corresponding alcohols and fluorocarboxylic acids. At the same time, the electron cloud density around the carbon atom connected to the fluorine atom in the compound decreases. If there are suitable nucleophilic reagents, a nucleophilic substitution reaction may theoretically occur. However, due to the high stability of the carbon-fluorine bond, such reactions usually require more harsh conditions to proceed.

What are the physical properties of 3-ethoxy-1,1,2,3,4,4,5,5,6,6,6-dodecafluoro-2- (trifluoromethyl) -hexane?

3-Ethoxy-1,1,1,2,3,4,4,5,5,6,6,6-dodecafluoro-2- (trifluoromethyl) hexane is a fluorine-containing organic compound. Its unique physical properties are of great significance for its research in materials science, chemical industry and other fields.

Looking at its properties, at room temperature and pressure, it is mostly a colorless and transparent liquid with a pure texture and no visible impurities. Its odor is very small and almost imperceptible, which makes it popular in many application scenarios sensitive to odors.

When it comes to density, because it contains many fluorine atoms, the relative weight of fluorine atoms is relatively large, resulting in a higher density than that of common organic compounds, about [X] g/cm ³. Higher density may play an important role in specific chemical operations such as separation and extraction.

Besides the boiling point, due to the strong van der Waals force caused by the presence of fluorine atoms between molecules, its boiling point is also relatively high, about [X] ° C. This higher boiling point allows the compound to maintain a stable liquid state under high temperature environments, providing the possibility for high temperature process applications.

Its solubility also has characteristics. Because the molecule contains both hydrophobic parts of fluoroalkyl groups and hydrophilic parts of ethoxy groups, it exhibits good solubility in some organic solvents such as toluene and dichloromethane, but poor solubility in water. This solubility property makes it suitable for use as a solvent and surfactant in systems with different polarities.

In addition, the compound has a low surface tension, which means that it is easy to spread on solid surfaces, which can effectively reduce the interfacial tension between liquids and solids. In the fields of coatings, inks, etc., it can improve the wettability and adhesion of products to substrates, thereby improving product performance.

What are the main uses of 3-ethoxy-1,1,2,3,4,4,5,5,6,6-dodecafluoro-2- (trifluoromethyl) -hexane?

3-Ethoxy-1, 1, 1, 2, 3, 4, 4, 5, 5, 6, 6-dodecafluoro-2 - (trifluoromethyl) hexane, which is widely used. In the chemical industry, it is often used as a special solvent. Because of its unique physical and chemical properties, it has good solubility to many organic compounds, and high chemical stability. It can also remain stable under harsh conditions such as high temperature and strong acid and alkali. Therefore, it acts as a reaction medium in some special chemical reactions to help the reaction proceed smoothly.

In the field of electronics industry, it plays an important role. As an electronic cleaning agent, it can effectively remove impurities such as oil, dust and flux residues on the surface of electronic components. Due to its good volatility, no traces are left after cleaning, and no corrosive effect on electronic components, it can ensure the stability and reliability of electronic equipment performance.

In the refrigeration industry, it has also attracted much attention as a new type of refrigerant. With suitable boiling point and condensation pressure, good heat transfer performance, low ozone layer destruction coefficient, in line with environmental protection requirements, it is expected to become an ideal substitute for traditional refrigerants, and promote the development of the refrigeration industry towards green environmental protection.

In the field of fire protection, this substance can be used to prepare high-efficiency fire extinguishing agents. With its chemical stability and low flammability, it can effectively inhibit the spread of flames, quickly reduce the temperature of the fire scene, provide strong support for fire fighting work, and protect the safety of life and property.

What is the synthesis of 3-ethoxy-1,1,2,3,4,4,5,5,6,6,6-dodecafluoro-2- (trifluoromethyl) -hexane?

To prepare 3 - ethoxy - 1, 1, 1, 2, 3, 4, 4, 5, 5, 6, 6 - dodecafluoro - 2 - (trifluoromethyl) - hexane, the following ancient method can be followed:
First take fluorine-containing alkenes, such as hexafluoropropylene, and ethoxy-containing reagents, such as sodium ethanol, in a suitable temperature and inert solvent, perform nucleophilic addition. The ethoxy negative ion of sodium ethanol is nucleophilic and can attack the double bond of hexafluoropropylene to form an ethoxy-containing intermediate. This step needs to be controlled at a moderate temperature range, and the solvent should have good solubility and stability, such as anhydrous ether or tetrahydrofuran, to promote the smooth reaction.
Then, the intermediate and trifluoromethylation reagent, such as trifluoromethyl magnesium halide, undergo nucleophilic substitution reaction in the presence of metal catalysts. Metal catalysts, such as copper salts or palladium salts, can activate the reaction check point, so that trifluoromethyl can smoothly replace the specific position of the intermediate to obtain the target product. The reaction conditions in this step also need to be precisely controlled, and the temperature and catalyst dosage will affect the yield and selectivity.
After the reaction is completed, the product is separated from the reaction system by conventional separation and purification methods, such as extraction, distillation, column chromatography, etc., to obtain pure 3-ethoxy - 1, 1, 2, 3, 4, 4, 5, 5, 6, 6 - dodecafluoro - 2 - (trifluoromethyl) - hexane. Each step of the reaction requires careful operation, detailed measurement of the reaction process and product purity, and fine-tuning of the reaction conditions according to the actual situation in order to obtain ideal results.

What are the precautions for the use of 3-ethoxy-1,1,2,3,4,4,5,5,6,6,6-dodecafluoro-2- (trifluoromethyl) -hexane?

3-Ethoxy-1, 1, 1, 2, 3, 4, 4, 5, 5, 6, 6-dodecafluoro-2 - (trifluoromethyl) hexane, this is a fluorine-containing organic compound, in the use process, many matters need to be paid attention to.

The first thing to bear the brunt is safety. Fluorinated organic compounds, or with special chemical properties, such as partial fluorides, although chemically stable, can be heated, exposed to open flames or mixed with specific substances, or potentially dangerous. Therefore, in the place of use, it is necessary to strictly prohibit open flames and hot topics, and keep away from strong oxidants, reducing agents, etc., to prevent violent chemical reactions, resulting in fire and explosion. Operators should also wear appropriate protective equipment, such as protective gloves, goggles, gas masks, etc., to avoid contact with the skin, eyes, or inhalation into the body. In case of inadvertent contact, rinse immediately with a large amount of water and seek medical treatment in time.

Furthermore, its environmental impact should not be underestimated. Fluorinated compounds are difficult to degrade in the environment or will remain for a long time. During use, strict control should be taken to prevent them from leaking into the environment. If there is a leak, immediate and effective measures should be taken to collect and clean it up to avoid its spread and pollution to soil and water sources. In addition, the disposal of its waste should also follow relevant environmental regulations and cannot be discarded at will. It should be handed over to a professional organization for disposal.

Repeat, the standard of use is also crucial. Before use, it is necessary to understand its physical and chemical properties, such as boiling point, melting point, solubility, etc., in order to facilitate the operation process and select suitable conditions and methods. When configuring the solution, according to its solubility, choose the right solvent to precisely control the concentration. When using equipment, regular maintenance and inspection are also required to ensure its normal operation and prevent its leakage due to equipment failure.

Finally, storage conditions cannot be ignored. It should be placed in a cool, dry and well-ventilated place, away from heat and fire sources. Storage containers should be made of corrosion-resistant materials and tightly sealed to prevent them from evaporating or reacting with air components. At the same time, their names, properties, hazards and other information should be clearly marked for easy access and management. In this way, the use process is guaranteed to be safe and secure, minimizing harm to the environment and human health.