Chemical Name | Tetrasodium 2-[[8-[[3-[(5-chloro-2,6-difluoro-4-pyrimidinyl)amino]benzoyl]amino]-1-hydroxy-3,6-disulphonato-2-naphthyl]azo]naphthalene-1,5-disulphonate |
Chemical Name | Tetrasodium 2-[[8-[[3-[(5-chloro-2,6-difluoro-4-pyrimidinyl)amino]benzoyl]amino]-1-hydroxy-3,6-disulphonato-2-naphthyl]azo]naphthalene-1,5-disulphonate |
Chemical Formula | C34H19ClF2N8Na4O17S4 |
Molecular Weight | 1079.17 g/mol |
Solubility | Likely soluble in water considering multiple sulphonate groups |
Ph | May affect solution pH depending on sulphonate dissociation, but no data given |
Stability | Stability may be influenced by light, heat, and pH due to azo bond and other functional groups |
Toxicity | No data on toxicity, but pyrimidine, naphthalene and sulphonate - containing compounds may have various toxicity levels |
Chemical Name | Tetrasodium 2-[[8-[[3-[(5-chloro-2,6-difluoro-4-pyrimidinyl)amino]benzoyl]amino]-1-hydroxy-3,6-disulphonato-2-naphthyl]azo]naphthalene-1,5-disulphonate |
What is the chemical structure of Tetrasodium 2- [[8- [[3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amino] benzoyl] amino] -1-hydroxy-3,6-disulphonato-2-naphthyl] azo] naphthalene-1,5-disulphonate?
This is the name of a chemical substance, and its Chinese name is 2 - [8 - [[3 - [ (5 - chloro - 2,6 - difluoro - 4 - pyrimidinyl) amino] benzoyl] amino] - 1 - hydroxy - 3,6 - sodium disulfonate - 2 - naphthyl] azo] naphthalene - 1,5 - sodium disulfonate tetrasodium. This substance has a complex structure and contains groups such as pyrimidine, benzoyl, and naphthalene.
Its core structure may be initiated by a pyrimidine ring. The amino group of the 5-chloro-2,6-difluoro-4-pyrimidinyl group is connected to the benzene ring, and the other side of the benzene ring is combined with the formyl group to form a 3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amino] benzoyl moiety. The amino group of this part is in turn connected to the naphthalene group containing hydroxyl group and sodium sulfonate, which is connected to another naphthalene-1,5-disulfonate sodium through azo group, and exists in the form of tetrasodium as a whole. In this structure, the fluorine and chlorine atoms of the pyrimidine ring give specific chemical activities, the benzene ring and the naphthalene group build a rigid skeleton, and the sodium sulfonate group increases the water solubility of the substance. Each part interacts to determine its chemical properties and uses, or it is used for specific chemical reactions, material synthesis, or as a dye or auxiliary agent to play a role in the fields of chemical industry and materials.
What is the main use of Tetrasodium 2- [[8- [[3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amino] benzoyl] amino] -1-hydroxy-3,6-disulphonato-2-naphthyl] azo] naphthalene-1,5-disulphonate?
Tetrasodium 2 - [[8 - [[3 - [ (5 - chloro - 2,6 - difluoro - 4 - pyrimidinyl) amino] benzoyl] amino] - 1 - hydroxy - 3,6 - disulphonato - 2 - naphthyl] azo] naphthalene - 1,5 - disulphonate, is an organic compound. Its main use is commonly found in the field of dyes.
This compound has a unique structure and contains specific groups that give it unique color and chemical properties. In the textile industry, it can be used as a dye to dye fabrics with lasting and bright colors. Because of its good solubility and stability, it can be evenly dispersed in the dye liquid, making the fabric dyed evenly and bright in color.
It is also used in paper dyeing. It can make the paper get the desired color, improve the aesthetics and commercial value of the paper. At the same time, its stability helps to ensure that the color of the paper does not fade or fade during long-term storage.
It also plays an important role in the field of leather dyeing. It can make the leather show a rich and diverse color, and has little impact on the physical properties of the leather, maintaining the softness and toughness of the leather.
In addition, in some special industrial fields, such as ink manufacturing, or because of its unique chemical properties and color characteristics, it has become an important raw material, providing specific colors and properties for inks.
How safe is Tetrasodium 2- [[8- [[3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amino] benzoyl] amino] -1-hydroxy-3,6-disulphonato-2-naphthyl] azo] naphthalene-1,5-disulphonate?
Tetrasodium 2 - [[8 - [[3 - [ (5 - chloro - 2,6 - difluoro - 4 - pyrimidinyl) amino] benzoyl] amino] -1 - hydroxy - 3,6 - disulphonato - 2 - naphthyl] azo] naphthalene - 1,5 - disulphonate, this is a complex organic compound. In terms of its safety, it is necessary to consider more.
The chemical structure of the concept contains halogen elements such as chlorine and fluorine, and aromatic ring structures such as pyrimidine and naphthalene. Under specific conditions, halogen elements may undergo chemical reactions to form harmful substances. The aromatic ring is structurally stable, but it is also difficult to degrade in the environment, or accumulate and cause latent risk.
From the perspective of toxicology, it may have certain biological activity. When in contact with biological bodies, or interact with biological macromolecules such as proteins and nucleic acids, interfering with normal physiological and biochemical processes. Or because the structure is similar to some key molecules in biological bodies, occupy receptor sites and cause adverse effects.
For environmental safety, such compounds are discharged into the environment because of their complex structure, which is difficult for microorganisms to decompose, or cause water and soil pollution. And they may be transmitted through the food chain and enriched in biological bodies, endangering the ecosystem.
However, it is difficult to accurately determine their safety based on the structure alone. It is necessary to undergo rigorous experiments, such as acute toxicity, chronic toxicity, teratogenicity, carcinogenicity, mutagenicity, and environmental behavior studies, in order to determine the degree of harm to organisms and the environment, and to determine safe use norms and protective measures.
What are the production methods of Tetrasodium 2- [[8- [[3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amino] benzoyl] amino] -1-hydroxy-3,6-disulphonato-2-naphthyl] azo] naphthalene-1,5-disulphonate?
The method of this dyeing is to investigate the method. The method first takes 5-chloro-2,6-difluoro-4-pyrimidine, a benzyl compound containing a specific group, and puts it in a suitable reaction kettle in an appropriate ratio. There is a medium in the kettle that can promote the reaction of the two, or a solution, or a catalyst, so that the two can generate amination reaction, generating 3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amine] benzyl compound.
However, the 1-group-3,6-disulfonic-2-naphthalene compound of this product is mixed and placed in the reverse environment again. In this case, it is necessary to control the degree and force of the two, so that the two can be combined and reacted to generate 8- [3 - [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amine] benzyl] amine] -1-group-3,6-disulfonic-2-naphthalene derivatives.
Next, this derivative is introduced into the diazotization reversal process. The amount of diazonium is taken, and the derivatives are mixed according to a certain step. Under specific conditions, it is formed into diazonium.
This is the same, and the naphthalene-1,5-disulfonic acid is taken. When the diazonium is formed, the naphthalene-1,5-disulfonic acid is added quickly, and the coupling is reversed. In this step, it is necessary to precisely control the factors such as the resistance and degree of resistance, so that the two can be coupled together to generate Tetrasodium 2- [[8- [3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amine] benzyl] amine] -1-alkyl-3,6-disulfonic-2-naphthyl] azo] naphthalene-1,5-disulfonic acid.
The most, a series of refined lifting processes such as washing, washing, and dryness, remove the waste left in the reaction, and obtain high-quality objects. The whole process requires tolerance and step-by-step steps to get good products.
How competitive is Tetrasodium 2- [[8- [[3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amino] benzoyl] amino] -1-hydroxy-3,6-disulphonato-2-naphthyl] azo] naphthalene-1,5-disulphonate in the market?
Today, there is a substance called Tetrasodium + 2 - [ [ 8 - [ [ 3- [ (5-chloro-2,6-difluoro-4-pyrimidinyl) amino] benzoyl] amino] -1-hydroxy-3,6-sodium disulfonate-2-naphthyl] azo] naphthalene-1,5-sodium disulfonate. This substance is in the market, and its competitive status, I should be Ru Shi Zhi.
Looking at this substance, its chemical structure is unique, or it has specific properties and uses. In the chemical industry, materials and other fields, the unique chemical structure is often the key. If this substance has excellent performance in a specific reaction or application, it can solve the difficult problems in the industry, or it can emerge.
However, the competition it faces should not be underestimated. There are many congeneric products in the market, each with its own strengths. If other competing products have already occupied the market and performed well in terms of cost and performance stability, this substance needs to be outstanding.
If its developer can rely on superb technology to properly control costs and ensure stable quality, it may have advantages in price and quality, or it may gain a place in the market competition. And if its promotion is effective, so that many wold-be users know its unique ability, it can also add to the competitiveness.
Overall, the competitiveness of this substance in the market depends not only on its own performance, cost control, but also on many factors such as publicity and promotion. Only when all factors cooperate can we set sail in the tide of competition.