Chemical Name | 3-(1,5-Disulfo-naphthalene-2-ylazo)-5-[4-(3-ethenesulfonyl-phenylamino)-6-fluoro-[1,3,5]triazin-2-ylamino]-4-hydroxy-naphthalene-2,7-disulfonic acid as sodium salt |
Form | sodium salt |
Type | azo dye |
Solubility | soluble in water (as sodium salt) |
Color | Typically exhibits a distinct color related to azo dyes, often used for coloring applications |
Molecular Structure | Contains naphthalene, triazine, and ethenesulfonyl - phenylamino groups with multiple sulfonic acid groups as sodium salts |
Chromophore | The azo group (-N=N-) is the main chromophore |
Reactivity | Can participate in reactions related to its functional groups like the reactive triazine ring for dye - fiber bonding |
Stability | Stable under normal storage conditions, but may be affected by light, heat, and strong chemicals |
Application | Used in textile dyeing, paper coloring, and other coloring industries |
Chemical Name | 3-(1,5-Disulfo-naphthalene-2-ylazo)-5-[4-(3-ethenesulfonyl-phenylamino)-6-fluoro-[1,3,5]triazin-2-ylamino]-4-hydroxy-naphthalene-2,7-disulfonic acid as sodium salt |
Chemical Name | 3-(1,5-Disulfo-naphthalene-2-ylazo)-5-[4-(3-ethenesulfonyl-phenylamino)-6-fluoro-[1,3,5]triazin-2-ylamino]-4-hydroxy-naphthalene-2,7-disulfonic acid as sodium salt |
Appearance | Typically a colored powder (exact color depends on azo - dye nature) |
Molecular Formula | Complex, considering naphthalene, triazine rings and sulfonic acid groups with sodium counter - ions |
Solubility | Good solubility in water due to sulfonic acid groups as sodium salts |
Ph Behavior | May act as an acid - base indicator or have pH - dependent solubility |
Absorption Spectrum | Absorbs light in visible region characteristic of azo - dyes, peak wavelengths vary |
Thermal Stability | Stable up to a certain temperature, then may decompose due to bond - breaking in aromatic rings |
Reactivity | Can react with electrophiles or nucleophiles depending on the groups present |
Toxicity | Toxicity may vary, but some azo - dyes have potential toxicity concerns |
Application | Used in textile dyeing, ink - jet inks, and some biological staining applications |
Chemical Name | 3-(1,5-Disulfo-naphthalene-2-ylazo)-5-[4-(3-ethenesulfonyl-phenylamino)-6-fluoro-[1,3,5]triazin-2-ylamino]-4-hydroxy-naphthalene-2,7-disulfonic acid as sodium salt |
Form | sodium salt |
Type | azo dye derivative |
Molecular Structure | Contains naphthalene, triazine, and ethenesulfonyl phenyl moieties |
Chromophore | Azo group (-N=N-) for color |
Solubility | Good solubility in water due to sulfonic acid groups |
Ionic Nature | Anionic due to sulfonic acid groups as sodium salts |
Ph Stability | Stable within a certain pH range |
Color Properties | Exhibits color related to azo chromophore |
Reactivity | Can react with substances having reactive sites towards triazine or ethenesulfonyl groups |
What is the chemical structure of the sodium salt of 3- (1,5-disulfonaphthalene-2-ylazo) -5- [4- (3-vinylsulfonylanilinyl) -6-fluoro- [1,3,5] triazine-2-ylamino] -4-hydroxy naphthalene-2,7-disulfonic acid of this product?
The chemical structure of the cobalt complex of the substance 3- (1,5-dicarboxylnaphthalene-2-ylethylene) -5- [4- (3-isopropylcarboxylnaphthalene thiophenyl) -6-chloro-[ 1,3,5] triazine-2-amino] -4-fluoronaphthalene-2,7-dicarboxylic acid is quite complex. Allow me to elaborate.
In this structure, the core part is cobalt ion, which is combined with many surrounding ligands. As can be seen from the name, the ligand contains groups containing naphthalene ring, tricyclic azine and other structures. 3- (1,5-dicarboxylnaphthalene-2-ylacetylene) moiety, the 1 and 5 positions on the naphthalene ring have carboxyl groups, and the 2 positions are connected to ethylene groups. This structure is connected to cobalt ions through coordination atoms, providing a specific spatial structure and electronic effect for the entire complex. 5- [4- (3-isopropylcarboxylnaphthalene thiophenyl) -6-chloro- [1,3,5] triazine-2-amino] This long chain ligand, the triazine ring has a chlorine atom at the 6 position, and an amino group is connected at the 2 position. The amino group is then connected to the structure containing thiophenyl and isopropylcarboxylnaphthalene, which is also coordinated with cobalt ions with suitable atoms, which affects the stability and electron distribution of the complex. The 4-fluoronaphthalene-2,7-dicarboxylic acid part has fluorine atoms at 4 positions and carboxyl groups at 2 and 7 positions on the naphthalene ring, which also participates in the coordination with cobalt ions.
These ligands surround cobalt ions and form a specific spatial configuration through coordination bonds. The interaction of each part gives the cobalt complex unique chemical and physical properties. The complexity of the coordination environment determines that it may have unique applications in catalysis, optics and other fields.
The product 3- (1,5-disulfonaphthalene-2-ylazo) -5- [4- (3-vinylsulfonylanilinyl) -6-fluoro- [1,3,5] triazine-2-ylamino] -4-hydroxy naphthalene-2,7-disulfonic acid sodium salt What are the main application fields?
This drug is 3- (1,5-disulfonic acid naphthalene-2-ylamino) -5- [4- (3-ethylsulfonylnaphthalamino) phenyl] -6-chloro- [1,3,5] triazine-2-ylamino-4-fluoronaphthalene-2,7-disulfonic acid sodium salt, its main application fields are as follows:
This compound is widely used in the field of dyes. Because of its specific sulfonic acid group, amino group and triazine groups in its structure, it has the ability to combine well with fibers, and is often used in the dyeing of various fiber fabrics. Natural fibers such as cotton and hemp can firmly adhere to the fibers by virtue of their sulfonic acid groups forming hydrogen bonds with the hydroxyl groups on the fibers, and the reactivity of the triazine ring, showing high color fastness and bright color. In silk dyeing, this substance can also play a full role, giving silk its unique color and luster.
In the paper industry, this sodium salt can be used as a paper dye. During the papermaking process, it can be combined with pulp fibers to achieve uniform dyeing of paper. It is widely used in the dyeing of paper products such as writing paper and wrapping paper to improve the aesthetics and commercial value of paper products.
In addition, it is also used in the preparation of some special functional materials. Because its structure contains multiple reactive groups, it can participate in material synthesis as a functional monomer. For example, in the preparation of some polymer materials with adsorption and separation properties, the sulfonic acid groups in their structures can undergo ion exchange or complexation with specific substances, endowing the materials with special properties and providing a new direction for the development of materials science.
This product 3- (1,5-disulfonaphthalene-2-ylazo) -5- [4- (3-vinylsulfonylanilino) -6-fluoro- [1,3,5] triazine-2-ylamino] -4-hydroxy naphthalene-2,7-disulfonic acid What is the production process of the sodium salt?
To prepare this 3- (1,5-dicarboxylnaphthalene-2-yloxy) -5- [4- (3-isopropylnaphthalenylphenoxy) -6-fluoro- [1,3,5] triazine-2-ylamino] -4-fluoronaphthalene-2,7-dicarboxylic acid immobilized salt, the process is as follows:
First take an appropriate amount of 1,5-dicarboxylnaphthalene, under specific reaction conditions, introduce 2-yloxy group to obtain an intermediate product containing this structure. This step requires precise temperature control and solvent selection to make the reaction smooth and obtain a higher yield.
Then, for the obtained intermediate product, through a series of reactions, the 5- [4- (3-isopropylnaphthyl phenoxy) -6-fluoro-[ 1,3,5] triazine-2-ylamino] structure is connected. In the meantime, multi-step reactions are involved, such as halogenation, condensation, etc. Each step needs to adjust the reaction parameters according to the characteristics of the reactants to ensure that the reaction in each step is complete and the product is pure.
Then the product with the above complex structure is further reacted with 4-fluoronaphthalene-2,7-dicarboxylic acid, and the structure of each part is integrated through a cleverly designed reaction path. In this process, the polarity of the solvent, reaction time and temperature are all key factors, and subtle deviations can cause impurity or low yield of the product.
When the target organic structure is synthesized, react with a suitable imprisoned reagent to form an imprisoned salt. In this step, the activity of the imprisoned reagent and the pH of the reaction system need to be considered. By optimizing the reaction conditions, the imprisoned ion can be fully combined with the organic ligand to generate a high-purity target product 3- (1,5-dicarboxylnaphthalene-2-yloxy) -5- [4- (3-isopropylnaphthalene-2-yloxy) -6-fluoro- [1,3,5] triazine-2-ylamino] -4-fluoronaphthalene-2,7-dicarboxylic acid imprisoned salt. Throughout the process, each step is closely interlocked, and precise control of reaction conditions is required to achieve efficient and high-quality production.
What are the physical and chemical properties of the sodium salt of this product 3- (1,5-disulfonaphthalene-2-ylazo) -5- [4- (3-vinylsulfonylanilinyl) -6-fluoro- [1,3,5] triazine-2-ylamino] -4-hydroxynaphthalene-2,7-disulfonic acid?
This is about the physical and chemical properties of the cobalt salt of 3- (1,5-disulfonaphthalene-2-yloxy) -5- [4- (3-isopropylsulfonylphenoxy) -6-bromo-[ 1,3,5] triazine-2-ylamino] -4-fluoronaphthalene-2,7-disulfonic acid. The physical and chemical properties of this compound are rich and diverse, let me tell you one by one.
Looking at its solubility, the solubility of this cobalt salt in water may be good due to the presence of sulfonic acid groups. The sulfonic acid group is hydrophilic, which can interact with water molecules and improve dissolution. In polar organic solvents, it may also have a certain solubility, because the polar part of the molecular structure is compatible with the polarity of the organic solvent.
When it comes to stability, various chemical bonds in its chemical structure interact, giving certain stability. However, under specific conditions, such as high temperature, strong acid or strong base environment, chemical bonds may be affected. At high temperature, some chemical bond energies increase, which may break and cause structural changes; under strong acid and strong base, groups such as sulfonic acid groups and amino groups may react, affecting the overall stability.
When it comes to acidity and alkalinity, sulfonic acid groups can ionize hydrogen ions in solution, making compounds acidic to a certain extent. And its acidity may interact with other groups in the solution environment and molecular structure.
Besides its optical properties, the conjugated system such as benzene ring and naphthalene ring in the structure gives special optical properties. There may be a certain absorption spectrum. Under the irradiation of light at a specific wavelength, electrons transition and produce absorption peaks. This property may have applications in the field of analysis and detection and optical materials.
In addition, the density, melting point, boiling point and other physical properties of this cobalt salt are also affected by molecular structure and intermolecular interactions. Molecular stacking mode, relative molecular mass and other factors determine the density; the type and strength of intermolecular forces affect the melting point and boiling point.
How competitive is the sodium salt of this product 3- (1,5-disulfonaphthalene-2-ylazo) -5- [4- (3-vinylsulfonylanilino) -6-fluoro- [1,3,5] triazine-2-ylamino] -4-hydroxy naphthalene-2,7-disulfonic acid in the market?
Looking at this product of 3- (1,5-disulfonic acid naphthalene-2-yloxy) -5- [4- (3-isopropylsulfonylphenoxy) benzoyl] -4-fluoronaphthalene-2,7-disulfonic acid, how is it competing in the market?
For this product, the sulfonic acid is cleverly connected to naphthalene, phenoxy and other groups, and the structure is exquisite. However, looking at its competitiveness, the first thing to look at is its use. If it is a raw material for fine chemicals and has precise needs in specific fields, its structure is unique or advantageous. If it is used in the preparation of special dyes and high-performance materials, it can give the product special properties, such as high color fastness and excellent mechanical properties, etc., it is quite competitive.
Furthermore, depending on the difficulty of production. If the synthesis steps are complicated, the raw materials are scarce and the price is high, the cost will be high, and the competitiveness will be weak in the price-sensitive market. On the contrary, if the synthesis process is gradually mature and the cost is controllable, it can compete for a place.
Also check the market supply and demand. If the relevant industry is booming, the demand for compounds containing such structures will increase sharply, and the supply is limited, its competitiveness will be obvious. However, if the market is saturated and there are many congeneric products, if you want to stand out, you need to make efforts in quality, price, service and other aspects.
In addition, policies and regulations and environmental protection requirements also have an impact. If it conforms to the orientation of green chemistry and the environmental compliance of the production process, it can conform to the general trend and enhance competitiveness; otherwise, it may be limited.
In summary, the competitiveness of this product needs to consider many factors such as use, cost, supply and demand, and policies to be clear.