Sodium 2 Methyl 2 3 3 3 4 4 5 5 6 6 7 7 8 8 8 Tridecafluorooctyl Thio Propanoyl Amino Propane 1 Sulfonate
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
sodium 2-methyl-2-({3-[(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)thio]propanoyl}amino)propane-1-sulfonate
Chemical Formula C16H19F13NNaO4S2
Molecular Weight 613.44 g/mol
Appearance Solid (usually white powder)
Solubility Soluble in water
Surface Activity Good surfactant properties
Critical Micelle Concentration Typically in a specific range depending on conditions
Ph Stability Stable within certain pH range
Thermal Stability Has a certain decomposition temperature
Fluorine Content High fluorine content contributing to unique properties
Application Used in areas like surfactants for specific industrial processes
Chemical Formula C18H20F13NNaO5S2
Molecular Weight 669.46 g/mol
Appearance Typically a white - colored solid or powder
Solubility Soluble in polar solvents like water
Surface Active Property Acts as a surfactant, reducing surface tension of liquids
Ionic Nature Anionic surfactant
Fluorinated Characteristic Contains a long - chain fluorinated group which imparts hydrophobic and lipophobic properties
Ph Stability Stable over a certain pH range, usually around neutral pH
Thermal Stability Has a certain level of thermal stability up to a specific temperature
Application Used in various industries such as cosmetics, detergents for its surfactant properties
Chemical Formula C16H19F13NNaO4S2
Molecular Weight 631.43
Appearance Typically a white - to - off - white powder
Solubility Soluble in water
Purity Varies by manufacturer, usually high - purity grades available
Surface Active Property Acts as a surfactant
Ionic Nature Anionic
Ph Stability Stable within a certain pH range, often around neutral
Thermal Stability Stable under normal storage and handling temperatures
Critical Micelle Concentration Characteristic value specific to this compound in relevant solvents
Chemical Formula C19H22F13NNaO4S2
Molecular Weight 671.59 g/mol
Appearance Typically a white to off - white powder
Solubility Soluble in water
Surface Active Property Acts as a surfactant
Ionic Nature Anionic surfactant
Critical Micelle Concentration Varies with conditions, typically in the range of low mM
Ph Stability Stable within a certain pH range (e.g., around pH 5 - 9)
Thermal Stability Decomposes at elevated temperatures
Fluorine Containing Property Contains fluorinated alkyl chain for unique surface and chemical properties
FAQ

What is the main use of sodium 2-methyl-2- ({3- [ (3,3,4,4,5,5,6,6,7,7,7,8,8, 8-tridecafluorooctyl) thio] propanoyl} amino) propane-1-sulfonate

Sodium 2 - methyl - 2 - {3 - [ (3, 3, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8 - tridecafluorooctyl) thio] propanoyl} amino] propane - 1 - sulfonate is a rather special compound. Its main uses are diverse, and it is often used as a surfactant in the industrial field. Because of its special chemical structure, it has excellent ability to reduce surface tension, which can make liquids easier to spread and penetrate.

In some fine chemical processes, it can help disperse materials evenly and improve product quality. In specific textile printing and dyeing processes, it can improve the adsorption and leveling effect of dyes, making dyeing more uniform and bright. In some water-based coating systems, it can improve the wettability of the coating to the substrate, making the coating flatter and better adhesion.

It is also useful in the field of scientific research and experiments. In the research of interface chemistry, it is used as a model surfactant to explore the laws of surface and interface phenomena, helping scientists to deeply understand the behavior of substances at the interface. In the research and development of drug delivery systems, it may be possible to use its unique amphiphilicity to assist in the construction of stable drug-loaded particles and improve the delivery efficiency and targeting of drugs.

What are the physicochemical properties of sodium 2-methyl-2- ({3- [ (3,3,4,4,5,5,6,6,7,7,7,8,8, 8-tridecafluorooctyl) thio] propanoyl} amino) propane-1-sulfonate

Sodium-2-methyl-2 - ({3- [ (3,3,4,4,5,5,6,6,7,7,8,8-trifluorooctyl) thiopropionyl} amino) propane-1-sulfonate, this is a special organic compound, its physical and chemical properties are particularly critical.

First of all, solubility, because of its sulfonate group, this is the hydrophilic part, so when it has good solubility in water, it can form a stable solution. This property makes the compound in aqueous systems, such as some specific surfactant application scenarios, can effectively disperse and act.

Subsequent to surface activity, its molecular structure contains long-chain fluoroalkyl groups, which are hydrophobic parts and coexist with hydrophilic sulfonate groups. This unique structure gives it excellent surface activity, which can significantly reduce the surface tension of the solution. In many industrial processes, such as the preparation of coatings, inks, etc., it can improve the wettability of liquids to solid surfaces and make the product coating more uniform.

Furthermore, the thermal stability of the compound is also worthy of attention. The fluoroalkyl structure usually imparts good thermal stability to substances. At higher temperatures, its molecular structure may remain relatively stable and not easily decomposed. This property can be used as a stable additive in processes requiring high temperature treatment, such as some polymerization reactions.

As for chemical stability, due to the high bond energy of fluorocarbons, the compound may be resistant to many chemical reagents and is not easy to participate in general chemical reactions. This allows it to maintain its own structure and properties in complex chemical environments, making it suitable for a variety of special chemical application scenarios.

Sodium 2-methyl-2- ({3- [ (3,3,4,4,5,5,6,6,7,7,8,8, 8-tridecafluorooctyl) thio] propanoyl} amino) propane-1-sulfonate What are the precautions during use

This is the substance named "sodium + 2 - methyl - 2 - {3 - [ (3,3,4,4,5,5,6,6,7,7,8,8,8 - tridecafluorooctyl) thio] propanoyl} amino] propane - 1 - sulfonate". When using, be sure to pay attention to many things.

Bear the brunt of it. This substance may have special chemical activity, mix with other substances, or cause chemical reactions. Before use, read the relevant information carefully to be familiar with its chemical properties and reaction characteristics to prevent reckless mixing and dangerous occurrence.

Furthermore, because it contains special atoms such as fluorine, or has potential effects on the environment. During use, be sure to follow environmental protection regulations, properly dispose of waste, and do not discharge it at will to avoid polluting the environment.

In addition, good protection is required during operation. This substance may be irritating to the human body, such as contact with the skin, eyes, or cause discomfort. Therefore, when preparing protective equipment, such as gloves and goggles, clean the contact parts in time after operation.

and when storing, also be cautious. According to its characteristics, choose a suitable environment to avoid high temperature, humidity and fire sources, ensure its stability, prevent deterioration or cause safety accidents. Only by paying attention at all times and operating carefully can this substance be used safely and properly.

What is the synthesis method of sodium 2-methyl-2- ({3- [ (3,3,4,4,5,5,6,6,7,7,7,8,8, 8-tridecafluorooctyl) thio] propanoyl} amino acid) propane-1-sulfonate

To prepare sodium + 2-methyl-2- ({3- [ (3,3,4,4,5,5,6,6,7,7,8,8, 8-tridecafluorooctyl) thio] propanoyl} amino) propane-1-sulfonate, you can follow the following ancient method.

First take 2 - methyl - 2 - amino propane - 1 - sulfonate, which is the basis of the reaction. Another 3 - [ (3,3,4,4,5,5,6,6,7,7,8,8 - tridecafluorooctyl) thio] propanoyl chloride, this halide activity is quite good. < Br >
In a clean reactor, dissolve 2-methyl-2-amino propane-1-sulfonate in an appropriate amount of organic solvent, commonly used as dichloromethane, N, N-dimethylformamide, etc., to ensure uniform dissolution. The reaction system is cooled to a low temperature, such as about 0 ° C, slowly add 3 - [ (3, 3, 4, 4, 5, 6, 7, 7, 8, 8 - tridecafluorooctyl) thio] propanoyl chloride solution, when added dropwise, keep stirring to make the reaction sufficient.

During this reaction, the amino group and the acyl chloride group undergo acylation to form an amide bond. After the dropwise addition is completed, the reaction system is gradually raised to room temperature and stirred continuously for a few hours to ensure the complete reaction. After the reaction is completed, an appropriate alkali solution, such as sodium carbonate solution, is used to neutralize the excess acid in the reaction system.

The product is extracted with an organic solvent, and the organic phase is collected after separation. The organic phase is dried with anhydrous sodium sulfate to remove moisture. Subsequently, the organic solvent is removed by distillation under reduced pressure to obtain a crude product.

The crude product is purified by column chromatography, a suitable silica gel column is selected, and a suitable eluent is eluted with a suitable eluent, such as the mixture of ethyl acetate and petroleum ether. After separation and purification, pure sodium + 2-methyl-2- ({3- [ (3,3,4,4,5,5,6,7,8,8, 8-tridecafluorooctyl) thio] propanoyl} amino) propane - 1 - sulfonate can be obtained. The whole process requires fine operation and attention to the control of reaction conditions to obtain the product with good quality.

What are the environmental effects of sodium 2-methyl-2- ({3- [ (3,3,4,4,5,5,6,6,7,7,7,8,8, 8-tridecafluorooctyl) thio] propanoyl} amino) propane-1-sulfonate

2-Methyl-2- ({3- [ (3,3,4,4,5,5,6,6,6,7,7,7,8,8,8-trifluorooctyl) thio] propionyl} amino) propane-1-sulfonate, the impact on the environment, it is necessary to investigate in detail. In this case, fluorine-containing organic compounds also have different structures and characteristics.

The introduction of fluorine atoms makes the molecule hydrophobic and chemically stable. In the environment, or difficult to degrade. It may persist in water, soil and other media for a long time, causing risk of accumulation. In aquatic ecosystems, or affect aquatic organisms. Because of its surface activity, or change the surface tension of water bodies, it affects material mass transfer and biological activities. Fish, plankton, etc., or due to exposure to this compound, physiological processes are disturbed, such as respiration, feeding, reproduction, etc., or even population changes.

In soil ecology, or changing the surface properties of soil particles, affecting nutrient adsorption and desorption, and then affecting the uptake of nutrients by plant roots. Plant growth and development may be hindered, and this substance may be transmitted and enriched through the food chain, and eventually human beings. Long-term exposure to humans may threaten health and cause potential diseases.

Furthermore, when this compound is produced and used, if it is not disposed of properly, a large amount of it will escape into the environment, which will exacerbate pollution. Therefore, its environmental impact should be carefully studied to ensure the safety of the ecological environment and prevent it from developing.