Chemical Name | Sodium 1,2-bis[4-[4-{4-(4-sulfophenylazo)-2-sulfophenylazo}-2-ureido-phenyl-amino]-6-fluoro-1,3,5-triazin-2-ylamino]propane, sodium salt |
Form | sodium salt |
Composition Elements | Sodium, carbon, hydrogen, nitrogen, sulfur, fluorine, oxygen |
Chromophore Type | Azo-based chromophore |
Solubility | Soluble in water (due to sodium salt nature) |
Color | Typically shows color related to azo chromophore, likely some shade of colored depending on pH |
Molecular Weight | Calculated based on its chemical structure |
Ph Sensitivity | Azo compounds may show color changes with pH |
Stability | Can be affected by light, heat, and oxidation |
Application | Potential use in dyeing, as a colorant in some industries |
Chemical Name | Sodium 1,2-bis[4-[4-{4-(4-sulfophenylazo)-2-sulfophenylazo}-2-ureido-phenyl-amino]-6-fluoro-1,3,5-triazin-2-ylamino]propane, sodium salt |
Chemical Name | Sodium 1,2-bis[4-[4-{4-(4-sulfophenylazo)-2-sulfophenylazo}-2-ureido-phenyl-amino]-6-fluoro-1,3,5-triazin-2-ylamino]propane, sodium salt |
Chemical Name | Sodium 1,2-bis[4-[4-{4-(4-sulfophenylazo)-2-sulfophenylazo}-2-ureido-phenyl-amino]-6-fluoro-1,3,5-triazin-2-ylamino]propane, sodium salt |
Molecular Formula | unknown |
Molecular Weight | unknown |
Appearance | unknown |
Solubility | unknown |
Melting Point | unknown |
Boiling Point | unknown |
Density | unknown |
Ph | unknown |
Stability | unknown |
What is the chemical structure of Sodium 1,2-bis [4- [4- {4- (4-sulfophenylazo) -2-sulfophenylazo} -2-ureido-phenyl-amino] -6-fluoro-1,3,5-triazin-2-ylamino] propane, sodium salt?
This is a rather complex organic compound, named "Sodium + 1,2-bis [4- [4- {4- (4-sulfophenylazo) -2-sulfophenylazo} -2 -urea-phenyl-amino] -6-fluoro-1,3,5-triazine-2-ylamino] propane, sodium salt".
Looking at its name, it can be seen that its structure must be cleverly spliced by many groups. Among them, "1,2-bis... propane" reveals that the main chain is propane, and there are complex substituents at the 1 and 2 positions. This substituent is centered on a triazine ring, namely "6-fluoro-1,3,5-triazine-2-ylamino". The triazine ring has a fluorine atom at the 6 position and a nitrogen-containing group at the 2 position.
Furthermore, this nitrogen-containing group is connected to the benzene ring, such as "4- [4- {4- (4-sulfobenzene azo) -2-sulfobenzene azo} -2 -urea-phenyl-amino]". There are sulfobenzene azo, urea and other groups on the benzene ring. Many benzene rings are connected by azo groups, and this azo group (-N = N-) adds color to the compound and may have important uses in the field of dyes. The "sodium salt" indicates that the compound is in the form of a salt, and the sodium atom may be combined with some acidic groups to maintain the structural stability through ionic bonds. This complex structure endows this compound with unique physical and chemical properties, which may play a key role in the fields of materials and chemical engineering.
What is the main use of Sodium 1,2-bis [4- [4- {4- (4-sulfophenylazo) -2-sulfophenylazo} -2-ureido-phenyl-amino] -6-fluoro-1,3,5-triazin-2-ylamino] propane, sodium salt?
This is an organic compound named 1,2-bis [4- [4- {4- (4-sulfobenzenazo) -2-sulfobenzenazo} -2 -urea-phenylamino] -6 -fluoro-1,3,5-triazine-2-ylamino] propane sodium salt. This compound has many applications in industrial and scientific research.
In the industrial field, it is often used as a dye. Because of its special molecular structure, it can exhibit good affinity and dyeing properties for specific fiber materials. It can be applied to the textile printing and dyeing industry to give fabrics rich colors, and the dyed fabrics have good color fastness and lasting bright color, meeting people's needs for the beauty and durability of fabrics.
In the field of scientific research, it can be used as a chemical analysis reagent. With its unique chemical structure and azo group characteristics, it can undergo color reaction or interaction with specific substances in some analytical tests, thereby realizing qualitative or quantitative analysis of related substances, helping researchers to further explore various chemical and biological systems.
In addition, due to the molecular structure containing multiple active groups and complex conjugated systems, in the field of materials science, it can be used to prepare new materials with special optical and electrical properties, providing a key foundation for the research and development of new functional materials. Overall, this compound has important uses and potential applications in a wide range of fields.
What are the physical properties of Sodium 1,2-bis [4- [4- {4- (4-sulfophenylazo) -2-sulfophenylazo} -2-ureido-phenyl-amino] -6-fluoro-1,3,5-triazin-2-ylamino] propane, sodium salt?
This compound is named: Sodium + 1,2-bis [4- [4- {4- (4-sulfobenzenazo) -2-sulfobenzenazo} -2-ureyl-phenylamino] -6-fluoro-1,3,5-triazine-2-ylamino] propane, sodium salt. Its physical properties are as follows:
1. ** Appearance **: Generally speaking, such compounds containing complex structures and sodium salt forms are often presented in solid form, mostly in powder or crystalline form, with specific colors or due to the presence of many nitrogen-containing conjugate systems in the molecular structure, especially azo groups, showing a specific color, or yellow to orange, etc.
2. ** Solubility **: In view of the presence of multiple sulfonyl groups in the molecule, these groups have good hydrophilicity, so the compound should be easily soluble in water to form a homogeneous solution. The solubility in organic solvents depends on the polarity of the organic solvent. Polar organic solvents such as methanol and ethanol may have a certain solubility, while in non-polar organic solvents such as n-hexane and benzene, the solubility may be extremely low.
3. ** Melting point **: Due to the complex molecular structure, containing many hydrogen bonds, van der Waals forces and other interactions, its melting point is relatively high. The exact melting point needs to be determined experimentally, but usually the melting point of complex organic salts will be around a few hundred degrees Celsius.
4. ** Stability **: The azo group in the molecule -N = N- is sensitive to light and heat. Under light or high temperature, it may decompose or rearrange the structure, resulting in a decrease in the stability of the compound. At the same time, in a strong acid and strong base environment, functional groups such as urea groups and amino groups in the molecule may react with acid and base, which affects their stability.
What is the synthesis method of Sodium 1,2-bis [4- [4- {4- (4-sulfophenylazo) -2-sulfophenylazo} -2-ureido-phenyl-amino] -6-fluoro-1,3,5-triazin-2-ylamino] propane, sodium salt?
The name of this compound is long and complex, and its synthesis method involves multi-step organic synthesis reactions. In the first step, 4- (4-nitrophenylazo) -2-sulfonated benzene is used as the starting material, and the condensation reaction is carried out with urea under appropriate conditions to form a specific compound containing urea group structure. This step requires strict control of the reaction temperature, the proportion of reactants and the reaction time. If the temperature is too high or the reaction time is too long, it may initiate side reactions and form impurities.
Subsequently, the obtained product is nucleophilic substitution with 2,4,6-trifluoro-1,3,5-triazine to introduce the triazine ring structure. During the reaction process, a suitable base should be selected as a catalyst to precisely regulate the pH of the reaction system, otherwise it will affect the reaction rate and product purity.
Next, using diazotization and coupling reaction, 4 - (4 - (4 - (4 - sulfophenylazo) - 2 - sulfophenylazo) - 2 - urea - phenylamino) - 6 - fluoro - 1,3,5 - triazine - 2 - amino structure reacts with 1,2 - bis (halogenated) propane to achieve 1,2 - bis [4 - [4 - {4 - (4 - sulfophenylazo) - 2 - sulfophenylazo} - 2 - The construction of the structure of urea-phenylamino] -6-fluoro-1,3,5-triazine-2-amino] propane requires harsh reaction conditions, and factors such as the activity of halopropane and the polarity of the reaction solvent will affect the reaction process and product yield.
Finally, by reacting with basic substances such as sodium hydroxide, the compound is converted into sodium salt form, which is the target product Sodium 1,2 - bis [4 - [4 - {4 - (4 - sulfophenylazo) - 2 - sulfophenylazo} - 2 - ureido - phenyl - amino] - 6 - fluoro - 1,3,5 - triazin - 2 - ylamino] propane, sodium salt. The whole synthesis process requires fine operation, and each step requires strict separation, purification and structural identification of the reaction product to ensure the purity and structural correctness of the final product.
Sodium 1,2-bis [4- [4- {4- (4-sulfophenylazo) -2-sulfophenylazo} -2-ureido-phenyl-amino] -6-fluoro-1,3,5-triazin-2-ylamino] propane, sodium salt What are the precautions during use?
This is 1,2-bis [4- [4- {4- (4-sulfophenylazo) -2-sulfophenylazo} -2 -ureyl-phenylamino] -6-fluoro-1,3,5-triazine-2-ylamino] propane sodium salt. When using, there are many things to pay attention to.
First, this substance may have potential chemical activity and reactivity. When using and handling, adhere to established procedures and safety guidelines. Make sure the operating environment is well ventilated to prevent the accumulation of harmful gases.
Second, in view of its sodium salt form, it is easily soluble in water or moisture, so when storing, it must be placed in a dry place and well sealed to prevent moisture and deterioration.
Third, during operation, take good personal protection. It is advisable to wear suitable protective gloves, protective glasses and masks to avoid direct contact with the skin, eyes and respiratory tract. If inadvertently exposed, rinse with plenty of water immediately and seek medical treatment according to specific conditions.
Fourth, during use, if mixing or chemical reactions are involved, the nature of the reaction, conditions and possible products must be fully understood and evaluated in advance. Do not mix with unknown chemicals at will to prevent dangerous reactions.
Fifth, after use, the remaining items and waste should be properly disposed of according to regulations. Do not discard at will to avoid pollution to the environment. Follow local environmental regulations and laboratory-related waste disposal procedures.