Competitive Tetrasodium 3-[(E)-{4-[(E)-{4-[(2E)-2-(6-Amino-1-Oxo-3-Sulfonatonaphthalen-2(1H)-Ylidene)Hydrazinyl]-6-Sulfonatonaphthalen-1-Yl}Diazenyl]Naphthalen-1-Yl}Diazenyl]Naphthalene-1,5-Disulfonate prices that fit your budget—flexible terms and customized quotes for every order.
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Tetrasodium 3- [ (E) - {4- [ (E) - {4- [ (2E) -2- (6-Amino-1-Oxo-3-Sulfonatonaphthalen-2 (1H) -Ylidene) Hydrazinyl] -6-Sulfonatonaphthalen-1-Yl}} Diazenyl] Naphthalene-1-Yl} What is Diazenyl] Naphthalene-1,5-Disulfonate?
This is a rather complex chemical called tetrasodium 3- [ (E) - {4 - [ (E) - {4 - [ (2E) -2 - (6-amino-1-oxo-3-sulfonaphthalene-2 (1H) -subunit) hydrazine] -6-sulfonaphthalene-1-yl}] diazonaphthalene-1-yl}] diazonaphthalene-1,5-disulfonate. The concept of its nomenclature is based on the combination of many specific groups and structures. "Tetrasodium" indicates that the compound contains four sodium ions, which play a role in charge balance in the structure of the compound. And "3 - [ (E) - {4 - [ (E) - {4 - [ (2E) -2 - (6-amino-1-oxo-3-sulfonaphthalene-2 (1H) -subunit) hydrazine] -6-sulfonaphthalene-1-yl}] diazynaphthalene-1-yl}] diazynaphthalene-1,5-disulfonate" part, the main organic structure is carefully outlined. Among them, the naphthalene ring structure appears many times, and there are different functional groups such as amino, sulfonyl, diazynyl, and hydrazine. Diazo groups often have active chemical properties, or affect the activity and route of the substance to participate in chemical reactions. Sulfonyl groups can impart certain water solubility and ionic properties to compounds. Amino groups also contribute to the acid-base properties and reactivity of compounds. The combination of these complex structures and functional groups may give the substance specific physical and chemical properties, or show unique functions in specific fields, such as dyes, drug development, etc. However, it is difficult to know its exact properties and uses in detail based on the name alone. More experimental data and research data are needed to gain a comprehensive understanding.
Tetrasodium 3- [ (E) - {4- [ (E) - {4- [ (2E) -2- (6-Amino-1-Oxo-3-Sulfonatonaphthalen-2 (1H) -Ylidene) Hydrazinyl] -6-Sulfonatonaphthalen-1-Yl}} Diazenyl] Naphthalene-1-Yl} What are the main uses of Diazenyl] Naphthalene-1,5-Disulfonate?
This is the name of an organic compound, its scientific name is tetrasodium 3- [ (E) - {4 - [ (E) - {4 - [ (2E) -2 - (6-amino-1-oxo-3-sulfonaphthalene-2 (1H) -subunit) hydrazine] -6-sulfonaphthalene-1-yl}] diazo] naphthalene-1-yl} diazo] naphthalene-1,5-disulfonate. This compound is mostly used in the field of dyes and pigments.
In the production of dyes, its structure gives it unique color properties, can produce bright colors, and has good affinity and adhesion to fiber materials, which can make the dyeing effect uniform, long-lasting, washable and light-resistant. Like the dyeing process of the textile industry, it is often used to meet the needs of rich colors.
In terms of pigments, with its own chemical stability and color characteristics, it can be used in the production of inks, coatings, etc. When making inks, it can ensure that the color of the printing pattern is bright and clear; when used in paints, it can provide good hiding power and color stability, and improve the decorative and protective properties of the coating.
Overall, this compound, with its unique chemical structure, plays a key role in the dye and pigment-related industries, contributing to the ideal color and performance of many products.
Tetrasodium 3- [ (E) - {4- [ (E) - {4- [ (2E) -2- (6-Amino-1-Oxo-3-Sulfonatonaphthalen-2 (1H) -Ylidene) Hydrazinyl] -6-Sulfonatonaphthalen-1-Yl}} Diazenyl] Naphthalene-1-Yl} How safe is Diazenyl] Naphthalene-1,5-Disulfonate?
This substance is called tetrasodium 3- [ (E) - {4 - [ (E) - {4 - [ (2E) -2 - (6-amino-1-oxo-3-sulfonaphthalene-2 (1H) -subunit) hydrazine] -6-sulfonaphthalene-1-yl}] diazenyl] naphthalene-1-yl}] diazenyl] naphthalene-1,5-disulfonate, and its safety needs to be considered from many aspects.
Looking at its name, it can be known as a complex organic compound, containing various elements such as nitrogen and sulfur and special groups. Generally speaking, sulfonate groups are soluble or better in water, and such structures may be surface active or can reduce surface tension.
From a toxicological point of view, such compounds containing complex nitrogen heterostructures and sulfonates, although it is difficult to reach a general conclusion, some substances containing similar structures may be ingested orally, metabolized in the body or affect physiological functions due to complex structures. If it comes into contact with the skin, it may cause irritation due to its possible surface activity or change the normal physiological state of the skin. If it comes into contact with the eyes, or due to solubility and chemical activity, it may cause irritation or even damage to the eye mucosa.
In terms of environmental safety, due to its sulfonate content, if a large amount enters the water body, or affects the surface tension of the water body, interferes with the survival of aquatic organisms, and may also accumulate in the environment due to its refractory degradability, destroying the ecological balance.
When using, be sure to follow relevant safety procedures and take protective measures to prevent adverse effects on the human body and the environment.
Tetrasodium 3- [ (E) - {4- [ (E) - {4- [ (2E) -2- (6-Amino-1-Oxo-3-Sulfonatonaphthalen-2 (1H) -Ylidene) Hydrazinyl] -6-Sulfonatonaphthalen-1-Yl}} Diazenyl] Naphthalene-1-Yl} Diazenyl] Naphthalene-1,5-Disulfonate What are the production methods?
To obtain Tetrasodium+3-%5B%28E%29-%7B4-%5B%28E%29-%7B4-%5B%282E%29-2-%286-Amino-1-Oxo-3-Sulfonatonaphthalen-2%281H%29-Ylidene%29Hydrazinyl%5D-6-Sulfonatonaphthalen-1-Yl%7D%7DDiazenyl%5DNaphthalen-1-Yl%7DDiazenyl%5DNaphthalene-1%2C5-Disulfonate, the method is as follows:
First prepare the required raw materials, such as naphthalene compounds containing specific structures, diazotization reagents, coupling reagents, etc. Select suitable naphthalene derivatives, and specific substituents are required, such as 6-amino-1-oxo-3-sodium sulfonate naphthalene-2 (1H) -subunit, etc., to ensure the accurate structure of the product.
First diazotization of naphthalene derivatives containing amino groups. In a low temperature and acidic environment, the amino group is converted into diazo salts by treating with sodium nitrite and inorganic acid. This process requires temperature control to prevent the decomposition of diazo salts, which affects the yield and purity.
Another naphthalene derivative with suitable substituents is taken as the coupling component. Under basic or weakly acidic conditions, the diazonium salt is slowly added to the coupling component solution and stirred to promote the coupling reaction. Pay attention to the pH and temperature of the system during the reaction, because they have a great influence on the reaction rate and product structure. Appropriate pH and temperature can ensure the correct formation of azo bonds to obtain the target structural product.
After the reaction is completed, separate and purify the product by appropriate methods. Or use filtration, extraction, recrystallization and other methods to remove impurities such as unreacted raw materials and by-products to obtain high purity Tetrasodium+3-%5B%28E%29-%7B4-%5B%28E%29-%7B4-%5B%282E%29-2-%286-Amino-1-Oxo-3-Sulfonatonaphthalen-2%281H%29-Ylidene%29Hydrazinyl%5D-6-Sulfonatonaphthalen-1-Yl%7D%7DDiazenyl%5DNaphthalen-1-Yl%7DDiazenyl%5DNaphthalene-1%2C5-Disulfonate.
When recrystallizing, select a suitable solvent to dissolve the product in a hot solvent, and crystallize and precipitate after cooling to further improve the purity. Every step requires fine operation, from raw material selection to product purification, all links are closely related to the successful preparation of this compound.
Tetrasodium 3- [ (E) - {4- [ (E) - {4- [ (2E) -2- (6-Amino-1-Oxo-3-Sulfonatonaphthalen-2 (1H) -Ylidene) Hydrazinyl] -6-Sulfonatonaphthalen-1-Yl}} Diazenyl] Naphthalene-1-Yl} Diazenyl] Naphthalene-1,5-Disulfonate What are the common brands in the market?
This is the name of a chemical substance, and it is difficult for ordinary people to know its common brands in the market. I have searched all over the classics, but there is no exact record. The name of this chemical is so complicated, or it is a substance for specific fields and professional purposes, and it is not a well-known and common product. Or it is applied in profound fields such as chemical industry and scientific research, but it is difficult to describe its common brands in detail. Although I have tried my best, I have not been able to obtain the exact information of common brands in the market, but I still hope Haihan.