As a leading Disodium 1-Amino-4-({3-[(2,3-Dibromopropanoyl)Amino]-2,4,6-Trimethyl-5-Sulfonatophenyl}Amino)-9,10-Dioxo-9,10-Dihydroanthracene-2-Sulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the main use of 1-amino-4- ({3- [ (2,3-dibromopropionyl) amino] -2,4,6-trimethyl-5-sulfophenyl} amino) -9,10-dioxo-9,10-dihydroanthracene-2-sulfonate disodium salt?
9,10-Dioxide-9,10-dioxanthracene-2-carboxylic acid disodium salt, which has a wide range of uses. In the field of dyes, it can be used as an important intermediate. Through specific chemical reactions, many dyes with bright colors and good fastness can be derived. It is widely used in textiles and other industries to give fabrics brilliant colors. In the field of medicinal chemistry, it has potential medicinal value and can be used as a key raw material to participate in drug synthesis. After structural modification and optimization, it is expected to develop drugs with specific pharmacological activities for the treatment of related diseases. In the field of organic synthesis, it can serve as a unique structural unit, with the help of ingenious reaction design, to construct complex and diverse organic compounds, providing new paths and methods for the development of organic synthetic chemistry. Due to its unique chemical structure and reactivity, it can be used in the field of materials science to prepare materials with special properties, such as optical materials, electrical materials, etc., contributing to the innovative development of materials science.
1-Amino-4- ({3- [ (2,3-dibromopropionyl) amino] -2,4,6-trimethyl-5-sulfophenyl} amino) -9,10-dioxo-9,10-dihydroanthracene-2-sulfonate What are the chemical properties of disodium salts
9,10-Dioxy-9,10-dihydroanthracene-2-carboxydianhydride, which is derived from 1-amino-4- {3- [ (2,3-dihydroxypropoxy) amino] -2,4,6-trimethyl-5-aldehyde-pyridyl} amino-derived. Its chemical properties are as follows:
This substance is common to acid anhydrides and can be slowly hydrolyzed in contact with water to form corresponding dicarboxylic acids. The hydrolysis reaction can occur under mild conditions. If it comes into contact with water at room temperature, over time, the acid anhydride bond breaks and gradually converts to carboxylic acids. The reaction formula is roughly as follows: 9,10 - Dioxy - 9,10 - Dihydroanthracene - 2 - carboxylic dianhydride + H 2O O → 9,10 - Dioxy - 9,10 - Dihydroanthracene - 2 - carboxylic diacid.
This substance can undergo alcoholysis with alcohols to form ester compounds. Under appropriate catalysts and mild heating conditions, the anhydride reacts with the alcohol at a specific stoichiometric ratio, and an acyl group of the anhydride binds to the alcoholic hydroxyl group to form an ester bond. Taking ethanol as an example, the reaction is as follows: 9,10-Dioxy-9,10-Dihydroanthracene-2-carboxylic dianhydride + 2C ² H OH → 9,10-Dioxy-9,10-Dihydroanthracene-2-carboxydiethyl ester + H2O O.
9,10-Dioxy-9,10-Dihydroanthracene-2-carboxylic dianhydride molecule contains a conjugated system, which has a certain electron delocalization, so that it may produce photochemical reactions under specific wavelength light irradiation. The specific reaction path varies depending on the reaction conditions and environment, or intramolecular rearrangement occurs, or photoaddition reactions occur with other substances in the system.
Due to the structure containing multiple aromatic rings and unsaturated bonds, this substance can undergo electrophilic substitution reaction with electrophilic reagents. The electron cloud density distribution on the aromatic ring is uneven, and specific positions are vulnerable to electrophilic reagents. If it reacts with halogenated reagents, halogen atoms can be introduced at suitable positions in the aromatic ring; when interacting with nitrifying reagents, nitro groups can be introduced through nitrification reactions.
What is the preparation method of 1-amino-4- ({3- [ (2,3-dibromopropionyl) amino] -2,4,6-trimethyl-5-sulfophenyl} amino) -9,10-dioxo-9,10-dihydroanthracene-2-sulfonate disodium salt
To prepare 2-carboxyl-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate disodium salt, the method is as follows:
First, 1-amino-4-{ 3- [ (2,3-dihydroxynaphthyl) amino] -2,4,6-trimethyl-5-sulfophenyl} amino group is used as the starting material. This raw material can be directed to the target product through a series of reactions.
In a suitable reaction vessel, add an appropriate amount of starting material, and then add specific reagents and solvents. The reaction conditions need to be precisely controlled, and factors such as temperature and pH have a great influence on the reaction process and product purity.
When reacting, it is necessary to pay close attention to the reaction phenomena, such as color change, precipitation formation or not. When the reaction reaches the expected level, follow-up treatment is carried out. Or through extraction, separation, purification and other steps to obtain pure 2-carboxyl-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate disodium salt.
In this preparation process, the operation of each step needs to be fine, and a slight difference in the pool may cause the product to be impure or the yield to be low. It is necessary to strictly follow the operating procedures in order to successfully prepare the target product.
1-Amino-4- ({3- [ (2,3-dibromopropionyl) amino] -2,4,6-trimethyl-5-sulfophenyl} amino) -9,10-dioxo-9,10-dihydroanthracene-2-sulfonate disodium salt What are the precautions during use?
Fu 1-amino-4- {3- [ (2,3-dihydroxyalanine) amino] -2,4,6-trimethyl-5-oxyimidazolyl} amino-9,10-dioxo-9,10-dihydroanthracene-2-oxydianhydride, when using, there are several ends that should be paid attention to.
First, this substance has a specific chemical structure and activity, and it is necessary to follow the established procedures when operating. Because its structure contains many functional groups, any improper disposal may cause the chemical reaction to go out of control, endangering the safety of the experiment and the accuracy of the results.
Second, due to its chemical properties, it is quite sensitive to environmental conditions. Changes in temperature and humidity may affect its stability. Therefore, during storage and use, maintain a suitable temperature and humidity environment to avoid deterioration due to environmental discomfort.
Third, the reaction in which the substance participates may involve a variety of chemical reagents. Before use, it is necessary to know in detail the interaction of each reagent with 1-amino-4- {3- [ (2,3-dihydroxyalanine) amino] -2,4,6-trimethyl-5-oximidazolyl} amino-9,10-dioxo-9,10-dihydroanthracene-2-oxedianhydride to prevent adverse reactions. And the purity and dosage of the reagent must also be precisely controlled to achieve the desired reaction effect.
Fourth, during the operation, protective measures are indispensable. Because it may be toxic, corrosive, or harmful to the human body. The experimenter should wear appropriate protective equipment, such as gloves, goggles, protective clothing, etc., to prevent substances from contacting the body and harming health.
Fifth, after the reaction is completed, the handling of products and remaining substances should also be cautious. In accordance with relevant environmental regulations, properly dispose of waste to avoid pollution to the environment. In this way, the purpose of safe and effective use of the substance can be achieved.
1-Amino-4- ({3- [ (2,3-dibromopropionyl) amino] -2,4,6-trimethyl-5-sulfophenyl} amino) -9,10-dioxo-9,10-dihydroanthracene-2-sulfonate What are the environmental effects of disodium salts?
Alas, this is related to the environmental impact of 1-amino-4-{ 3- [ (2,3-dihydroxypropoxy) amino] -2,4,6-trimethyl-5-aldehyde-phenyl} amino-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate disodium salt.
The effects of this compound in the environment are quite complex. The first one is that it may be chemically active. If it enters natural water, it may react with many substances in the water. The microbial community in the water may change as a result. The amino and hydroxyl groups contained in this compound can either be utilized by microorganisms or interfere with the metabolic pathways of microorganisms. If its concentration is too high, it may cause the growth of some microorganisms to be inhibited, which will destroy the ecological balance of water bodies.
As for the soil environment, if this compound penetrates into the soil or interacts with soil particles. Because its structure contains a variety of groups, it may be adsorbed on the surface of soil colloids, thereby affecting the physical and chemical properties of the soil. For example, it may change the porosity of the soil, affecting the aeration and water permeability of the soil. And its impact on plant roots in the soil cannot be ignored. Or it can be absorbed by plant roots and transported into plants, affecting plant growth and development. Or interfere with the absorption and transportation of nutrients by plants, causing the physiological process of plants to be disrupted.
In the atmospheric environment, although this compound mainly exists in the solid or dissolved state, there may be trace volatilization during its production and use. If it enters the atmosphere, or participates in complex chemical reactions in the atmosphere, it has a potential impact on the chemical composition of the atmosphere. Although significant air pollution effects are difficult to see at present, their effects are invisible under long-term accumulation.
In summary, 1-amino-4- {3- [ (2,3-dihydroxypropoxy) amino] -2,4,6-trimethyl-5-aldehyde-phenyl} amino-9,10-dioxo-9,10-dihydroanthracene-2-sulfonate disodium salt in the environment has potential effects on water, soil, atmosphere, etc. It should be studied in detail to understand its harm and find countermeasures.