Sodium 2 4 4 Fluoro 6 2 Sulfoethylamino 1 3 5 Triazin 2 Ylamino 2 Ureidophenylazo 5 4 Sulfophenylazo Benzene 1 Sulfonate
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
Sodium 2-(4-(4-fluoro-6-(2-sulfoethylamino)-[1,3,5]triazin-2-ylamino)-2-ureidophenylazo)-5-(4-sulfophenylazo)benzene-1-sulfonate
Chemical Formula C30H26F N11 Na3 O13 S4
Molecular Weight 939.81 g/mol
Appearance Typically a colored powder (exact color may vary based on purity and form)
Solubility Soluble in water due to multiple sulfonate groups
Ph Range In Solution Can be in the neutral to slightly basic range depending on concentration
Stability Stable under normal conditions, but may degrade upon exposure to strong acids, bases, or high heat
Absorption Spectrum Absorbs light in the visible region, responsible for its color
Ionic Nature Anionic due to sodium - sulfonate salt form
Crystal Structure Crystals may form under specific crystallization conditions, structure determined by X - ray diffraction
Surface Activity Can exhibit some surface - active properties in aqueous solutions
Chemical Formula Complex organic compound formula based on the given name
Molecular Weight Calculated from the formula
Appearance Color and form (e.g., powder, solid, liquid)
Solubility In water and common solvents
Ph Range Optimal or characteristic pH
Thermal Stability Temperature limits before decomposition
Absorption Spectrum Wavelengths of absorption
Fluorescence Properties If any, emission wavelengths etc.
Chemical Reactivity Reacts with certain substances
Storage Conditions Required storage environment
Chemical Formula C27H25F N10 Na3 O13 S3
Molecular Weight 886.75 g/mol
Appearance Usually a colored powder (due to azo groups)
Solubility Soluble in water (due to sulfonate groups)
Ph Range Stable in a certain pH range, likely around neutral
Absorption Spectrum Absorbs light in visible region, related to azo chromophores
Thermal Stability Decomposes at elevated temperatures
Stability In Air Can be stable in air under normal conditions
Ionic Nature Anionic (due to sodium sulfonate groups)
Dyeing Property Can be used as a dye for certain materials
Chemical Name Sodium 2-(4-(4-fluoro-6-(2-sulfoethylamino)-[1,3,5]triazin-2-ylamino)-2-ureidophenylazo)-5-(4-sulfophenylazo)benzene-1-sulfonate
Molecular Formula C30H27FN10Na3O12S3
Molar Mass 924.79 g/mol (approximate, considering average atomic masses)
Appearance Likely a colored solid (due to azo groups, color may vary but common azo dyes are often brightly colored)
Solubility Expected to be soluble in polar solvents like water, given the presence of multiple sulfonate (-SO3Na) groups which enhance water solubility
Ph Sensitivity May be affected by pH changes as the sulfonate groups can interact with acidic or basic environments
Stability Can be sensitive to light, heat, and oxidizing agents; azo groups are prone to decomposition under certain conditions
Absorption Maximum Typical azo dyes absorb in the visible region of the electromagnetic spectrum, likely with an absorption maximum in the range of 400 - 600 nm
Chemical Reactivity The triazine ring and azo groups can participate in various chemical reactions such as nucleophilic substitution reactions
Toxicity Some azo dyes may have potential toxicity; exact toxicity would depend on further studies, but concerns may include mutagenicity or carcinogenicity in some cases
FAQ

What is the chemical structure of Sodium 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazin-2-ylamino) -2-ureidophenylazo) -5- (4-sulfophenylazo) benzene-1-sulfonate

This is a rather complex organic compound, according to its name "Sodium + 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazin-2-ylamino) -2-ureidophenylazo) -5- (4-sulfophenylazo) benzene-1-sulfonate", its chemical structure can be gradually analyzed.

"benzene-1-sulfonate", it can be seen that this compound is based on the benzene sulfonate group, and the first position of the benzene ring is connected to the sulfonate negative ion, and it is combined with the sodium ion to form the state of benzene sulfonate sodium salt.

"5 - (4 - sulfophenylazo) " indicates that the 5th position of the benzene ring is connected to an azophenyl group, and the 4th position of the azophenyl group is connected to a sulfonic acid group. This structure adds the conjugate system of the compound, which affects its color and electronic properties.

"2 - (4 - fluoro - 6 - (2 - sulfoethylamino) - [1,3,5] triazin - 2 - ylamino) -2 - ureidophenylazo) " means that the 2nd position of the benzene ring is connected with a complex group. Among them, "4 - (4 - fluoro - 6 - (2 - sulfoethylamino) - [1,3,5] triazin - 2 - ylamino) " points to a triazine ring structure, the triazine ring has a fluorine atom at the 4th position, a 2 - sulfoethylamino at the 6th position, and a 2 - sulfoethylamino group is connected to another benzene ring. The 2 - sulfoethylamino group is connected to another benzene ring, and the 2-position urea group on this benzene ring is connected to the main benzene ring through an azo group.

Overall, this compound has a complex structure, including benzene ring, triazine ring, azo group, sulfonic acid group, urea group and other groups. The interaction of each group endows it with unique physical and chemical properties, or has potential applications in dyes, materials science and other fields.

What are the uses of Sodium 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazin-2-ylamino) -2-ureidophenylazo) -5- (4-sulfophenylazo) benzene-1-sulfonate

This is a rather complex organic compound called "Sodium + 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazin-2-ylamino) -2-ureidophenylazo) -5- (4-sulfophenylazo) benzene-1-sulfonate". Its uses are quite extensive, and depending on the complexity of its structure, it can be seen that it has important applications in many fields of industry and scientific research.

In the dyeing and weaving industry, this compound is often used as a reactive dye. Because its structure contains specific chromophore and reactive groups, it can be tightly bound to fiber molecules in covalent bonds, giving fabrics a bright color and good fastness to dyeing. This reactive dye can not only be used for dyeing natural fiber fabrics such as cotton and linen, but also has good performance in dyeing man-made fiber fabrics, which can meet the diverse needs of dyeing different fiber materials in the dyeing and weaving industry.

In the field of scientific research, due to its unique chemical structure and properties, this compound can be used as a model compound to study specific chemical reaction mechanisms. Through in-depth investigation of its participation in the reaction process, researchers can gain insight into the laws of chemical bond breaking and formation in organic reactions, providing an important theoretical basis for the development of organic synthetic chemistry. At the same time, it may also have potential uses in biomedical research. For example, with its special structure and properties, it is designed as a biological probe for labeling biomacromolecules to achieve accurate detection and localization of specific substances in organisms.

In addition, this compound may emerge in the field of materials science. Due to its special response properties to external factors such as light and heat, it is expected to be rationally designed and modified to prepare smart materials with special functions, such as photochromic materials and temperature-responsive materials, which will contribute to the innovative development of materials science.

What is the synthesis method of Sodium 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazin-2-ylamino) -2-ureidophenylazo) -5- (4-sulfophenylazo) benzene-1-sulfonate

This compound is a rather complex organic compound, and its synthesis method should follow the method of organic synthetic chemistry.

First, appropriate starting materials should be selected. Compounds containing fluorine, sulfonyl, amino, triazinyl and other functional groups can be the basis for constructing the target compound. To obtain the 4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazine-2-ylamino) -2-ureidophenyl azo moiety, the fluorine-containing triazine compound can first react with benzene derivatives containing urea groups and amino groups under suitable conditions. This reaction may need to be carried out in suitable solvents, such as dimethylformamide (DMF), dichloromethane, etc., and bases, such as potassium carbonate, triethylamine, etc., need to be added to promote the occurrence of the reaction, regulate the pH of the reaction system, make the reactants more prone to nucleophilic substitution reactions, and construct chemical bonds such as carbon-nitrogen.

For the formation of 5- (4-sulfophenylazo) benzene-1-sulfonate sodium part, it can be obtained by diazotization of a benzene derivative containing a sulfonyl group, and then coupling reaction with another benzene derivative containing active hydrogen. The diazotization reaction is usually at a low temperature, such as 0-5 ° C, in an acidic medium such as hydrochloric acid or sulfuric acid, so that the aryl primary amine reacts with sodium nitrite to form a diazo salt. Subsequently, the diazo salt is coupled with another suitable benzene derivative under weakly basic conditions to form an azo structure.

After the synthesis of each key part is completed, each part is connected through an appropriate reaction. This linking reaction may require specific conditions such as catalyst, reaction temperature and time. For example, by amidation reaction, nucleophilic substitution reaction, etc., each fragment is spliced into a complete target compound. During this period, it is necessary to carefully control the reaction conditions and monitor the reaction process. Thin-layer chromatography (TLC), high-performance liquid chromatography (HPLC) and other means can be used to ensure that the reaction proceeds in the expected direction and the purity and yield of the product are guaranteed. During the synthesis process, safety should also be paid attention to. Due to the toxicity and corrosiveness of some reaction reagents, relevant safety procedures must be followed.

What are the physical properties of Sodium 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazin-2-ylamino) -2-ureidophenylazo) -5- (4-sulfophenylazo) benzene-1-sulfonate

This is a rather complex organic compound named "Sodium + 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazine-2-ylamino) - 2-urea-benzenazo) - 5- (4-sulfobenzenazo) benzene-1-sulfonate". In terms of its physical properties, it has good water solubility due to the existence of many polar groups in its structure, such as sulfonic acid group (-SO 🥰), amino group (-NH2O), urea group (-NHCONH-), etc. This is because polar groups can form hydrogen bonds with water molecules, which makes the compound easily soluble in water.

Looking at its color characteristics, since there are multiple azo groups (-N = N-) in the molecule, this is a chromophore, so the compound should exhibit a specific color, or a bright color, which can often be used as a dye.

Furthermore, considering physical constants such as melting point, due to the complex structure of the molecule and its relatively large molecular mass, the intermolecular force is strong, and its melting point is estimated to be high. However, the exact melting point value needs to be accurately determined by experiments. In addition, its density will also vary depending on the compactness of the molecular structure, but until the experimental data are available, it can only be speculated that its density may be higher than that of common small molecule organics. Its solubility in organic solvents is better in polar organic solvents due to many polar groups, but poor in non-polar organic solvents.

What is the safety of Sodium 2- (4- (4-fluoro-6- (2-sulfoethylamino) - [1,3,5] triazin-2-ylamino) -2-ureidophenylazo) -5- (4-sulfophenylazo) benzene-1-sulfonate

This substance is a complex organic compound synthesized chemically. According to its name "Sodium+2-%284-%284-fluoro-6-%282-sulfoethylamino%29-%5B1%2C3%2C5%5Dtriazin-2-ylamino%29-2-ureidophenylazo%29-5-%284-sulfophenylazo%29benzene-1-sulfonate", it is known that the structure is extremely complicated.

Talking about safety, the safety of this compound depends on many factors. First, from the chemical structure analysis, it contains many groups such as fluorine, sulfur and nitrogen heterocycles. The introduction of fluorine atoms may change the physical and chemical properties of the compound. Some fluorine-containing compounds may be bioaccumulative or potentially toxic under specific conditions. However, it is difficult to determine its exact toxicity based on the structure.

Second, if this substance is used in industrial production, in the production process, the use of raw materials, the control of reaction conditions and the generation of by-products are all related to safety. Such as raw materials or those that are flammable, explosive, toxic and harmful, if they are not handled properly, there will be potential safety hazards. And if harmful by-products are produced during production and discharged into the environment without proper treatment, it will also endanger ecology and human health.

Third, in terms of its application scenarios, if it is used in consumer products, such as textile, paper dyeing, etc., its residue and migration need to be strictly considered. If it degrades slowly in the environment after use, or releases toxic and harmful substances, it will cause long-term harm to the environment and organisms.

Fourth, toxicological research is also indispensable. It is necessary to test its acute toxicity, chronic toxicity, mutagenicity, teratogenicity and other indicators before fully assessing its potential harm to organisms. Without sufficient toxicological data support, it is difficult to accurately determine its safety.

In summary, in order to clarify the safety of this compound, it is necessary to integrate chemical structure analysis, production process evaluation, application scenario consideration and toxicological research and other information to reach a more reliable conclusion.