What are the main uses of 8-aminonaphthalene-1,6-disulfonic acid?
8-Hydroxyquine-1,6-diacid, this substance has a wide range of uses. In the field of medicine, it can be used as an antibacterial agent. Due to its unique structure, it can interact with key bacterial enzymes or proteins to interfere with the normal metabolism and reproduction of bacteria, thereby inhibiting bacterial growth, and has a healing effect on some bacterial infections.
In terms of materials science, 8-hydroxyquine-1,6-diacid can be used to prepare functional materials. Because of its special coordination ability, it can complex with metal ions to form complexes with unique structures and properties. These complexes are widely used in the field of luminescent materials, or can improve the luminescent efficiency and stability of materials, and play an important role in the fabrication of devices such as organic Light Emitting Diodes (OLEDs).
In the field of analytical chemistry, this substance can be used as an analytical reagent. With its properties of forming stable complexes with specific metal ions, spectrophotometry, fluorescence analysis and other means can be used to detect and selectively certain metal ions. For example, it can be used to detect the content of specific metal ions in environmental water samples or biological samples, which can assist environmental monitoring and biomedical research.
Furthermore, in the field of catalysis, 8-hydroxyquinone-1,6-diacid or its metal complexes can sometimes act as catalysts. In some organic synthesis reactions, through its unique electronic effect and spatial structure, it can effectively catalyze the reaction, improve the reaction rate and product selectivity, and is of great significance to the development of organic synthesis chemistry.
What are the physical properties of 8-aminonaphthalene-1,6-disulfonic acid?
8-Hydroxyquinoline-1,6-disulfonic acid is a special compound with multiple unique physical properties.
Its appearance is mostly crystalline, white and pure, and the crystal structure is regular. Viewed under a microscope, an orderly crystal lattice can be seen. This regular structure has a great impact on its properties.
In terms of solubility, it has a certain solubility in water. Due to the hydrophilicity of the hydroxyl and sulfonic acid groups in the molecule, it can form hydrogen bonds with water molecules. However, the solubility is also restricted by temperature. When the temperature increases, the solubility often increases. In organic solvents, such as ethanol and acetone, there is also a certain degree of solubility, but the degree of solubility varies depending on the properties of the solvent.
Melting point is a key indicator to measure its thermal stability. The melting point of 8-hydroxyquinoline-1,6-disulfonic acid is quite high, indicating that the intermolecular force is strong, the structure is stable, and a higher temperature is required to destroy the lattice and cause it to melt. During the heating process, below the melting point, its physical state is stable, and its chemical properties do not change significantly; when approaching the melting point, the molecular vibration intensifies, and the lattice gradually becomes disordered.
The compound has certain hygroscopicity. Because the hydrophilic groups in the molecule are easy to absorb water molecules in the air, it is necessary to pay attention to moisture-proof when storing, otherwise the purity and related properties may be affected after moisture absorption.
In addition, its aqueous solution or molten state can conduct electricity, although it is not a good conductor, because the sulfonic acid group in the molecule can ionize ions, and the ions can move in a directional manner under the action of an electric field to form an electric current. This conductivity has potential application value in some specific electrochemical systems or chemical reactions.
In summary, the physical properties of 8-hydroxyquinoline-1,6-disulfonic acid are unique, which is of great significance for its research and application.
Is the chemical properties of 8-aminonaphthalene-1,6-disulfonic acid stable?
The chemical properties of 8-hydroxyquinoline-1,6-disulfonic acid are quite stable. This is because 8-hydroxyquinoline has a certain stability. Its structure contains nitrogen heterocycles and hydroxyl groups, and nitrogen atoms and oxygen atoms in hydroxyl groups have lone pairs of electrons, which can participate in the formation of conjugated systems and make molecular structures more stable.
When the sulfonic acid group is introduced at the 1,6-position, the sulfonic acid group is a strong electron-absorbing group. Although it will affect the distribution of the original electron cloud of 8-hydroxyquinoline, the introduction of the sulfonic acid group makes the molecular charge distribution more uniform, and the sulfonic acid group itself is relatively stable, and can interact with surrounding groups, such as forming hydrogen bonds, which further enhances the molecular stability.
Furthermore, in the crystal structure formed by the substance, the intermolecular force also contributes to its stability. The intermolecular interaction can be closely combined through hydrogen bonds, van der Waals forces, etc., to build a stable crystal structure, making it difficult for external factors to destroy its structure and properties. In summary, 8-hydroxyquinoline-1,6-disulfonic acid is chemically stable under common conditions.
What is the preparation method of 8-aminonaphthalene-1,6-disulfonic acid?
To make 8-hydroxyquinoline-1,6-disulfonic acid, the method is as follows:
First take an appropriate amount of quinoline, put it in the reactor, and slowly add concentrated sulfuric acid. This step needs to be handled with caution. Because sulfuric acid is highly corrosive and oxidizing, the acid addition process should be constantly stirred to make the mixture uniform and dissipate heat well to prevent local overheating from triggering side reactions. The ratio of sulfuric acid to quinoline needs to be precisely controlled, usually in excess according to the stoichiometric ratio, in order to promote the reaction to the direction of generating the target product.
Add sulfuric acid and heat it up to a specific temperature range. This temperature is generally between 150 ° C and 180 ° C. Maintain this temperature and continue to stir the reaction for several hours. During the reaction, the reaction process is closely monitored, and the consumption of raw materials and the formation of products can be detected by thin-layer chromatography or other suitable analytical means.
When the reaction reaches the expected level and is slightly cold, the reaction mixture is slowly poured into ice water. This operation needs to be slow to prevent the solution from splashing due to severe exothermic heat. After that, neutralize with an appropriate amount of sodium hydroxide solution, adjust the pH value to neutral or weakly basic, so that the product can exist stably in the solution in the form of sodium salts.
After neutralization, the solution can be preliminarily separated by filtration, extraction, etc. If there are insoluble impurities in the product, it can be filtered off with filter paper; for further purification, the difference in solubility of the product in different solvents can be used, and a suitable organic solvent can be selected for extraction to remove unreacted raw materials and by-products
After extraction, the organic phase is collected, and the organic solvent is removed by distillation under reduced pressure to obtain crude 8-hydroxyquinoline-1,6-disulfonic acid. If a higher purity product is required, the crude product can be recrystallized, an appropriate solvent can be selected, the crude product is heated and dissolved, filtered while hot, the filtrate is cooled and crystallized, filtered and dried again to obtain refined 8-hydroxyquinoline-1,6-disulfonic acid.
What is the price of 8-aminonaphthalene-1,6-disulfonic acid in the market?
Today there are 8-hydroxyquinine-1,6-disulfonic acid, what is the price in the market? I will investigate it for you in detail.
The price of 8-hydroxyquinine-1,6-disulfonic acid is not constant and often varies due to various reasons. First, the supply and demand of the market, if there are many people who want it and there are few people who supply it, the price will rise; if the supply exceeds the demand, the price may drop. Second, the cost of making this product is also a major factor, and the price of raw materials, labor costs, energy consumption, etc. are all related to the cost. If the cost is high, the price is also high. Third, different merchants have different pricing, and they may have different prices due to their own strategies, brands, etc.
In terms of common market conditions, if 8-hydroxyquinine-1,6-disulfonic acid is used for industrial use, its quality and quantity are different, and the price is also poor. Usually, those with high purity and excellent quality must have a higher price than those with ordinary quality. If it is used for laboratory research, its price may be higher due to higher requirements for purity.
To know its exact price, it is necessary to check the chemical raw material trading platform, chemical reagent sales website, etc., or consult relevant merchants to obtain the actual price in the current market.