As a leading Disodium 5-[(4,6-Dichloro-1,3,5-Triazin-2-Yl)Amino]-4-Hydroxy-3-[(E)-Phenyldiazenyl]Naphthalene-2,7-Disulfonate 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 chemical structure of'Disodium 5- [ (4,6-Dichloro-1,3,5-Triazin-2-Yl) Amino] -4-Hydroxy-3- [ (E) -Phenyldiazenyl] Naphthalene-2,7-Disulfonate '?
This is the chemical name of "5 - [ (4,6 - dichloro - 1,3,5 - triazine - 2 - yl) amino] - 4 - hydroxy - 3 - [ (E) - phenylhydrazinyl] naphthalene - 2,7 - disodium disulfonate". Its chemical structure is quite complex, and it has a specific combination of atoms and groups.
In this compound, the naphthalene ring is the core structure, and the naphthalene ring is connected with sulfonic acid groups at the 2nd and 7th positions, and forms a sodium salt. This structure can give the compound a certain water solubility. The 3-position is connected with (E) -phenylhydrazine group, which contains nitrogen-nitrogen double bonds and imparts structure-specific chemical properties and reactivity. The 4-position is connected with hydroxyl groups, which can participate in a variety of chemical reactions, such as hydrogen bond formation. The 5-position is connected with an amino group derived from 4,6-dichloro-1,3,5-triazine-2-group. The structure of the triazine ring is stable, and the dichloro atom can participate in reactions such as nucleophilic substitution. Overall, this chemical structure fuses multiple functional groups, and each group interacts to determine the physical and chemical properties of the compound and its possible applications. It may have potential value in the fields of dyes, drug development, etc. Due to its structural complexity and multi-functional group characteristics, it can exhibit unique optical and chemical activities.
What is the main use of'Disodium 5- [ (4,6-Dichloro-1,3,5-Triazin-2-Yl) Amino] -4-Hydroxy-3- [ (E) -Phenyldiazenyl] Naphthalene-2,7-Disulfonate '?
"Disodium 5- [ (4,6-dichloro-1,3,5-triazine-2-yl) amino] -4-hydroxy-3- [ (E) -phenylazo] naphthalene-2,7-disulfonate" This material is often used in the dyeing and weaving industry. It is a type of azo dye compound. When the fabric is dyed, it can interact with the fabric fibers with its own specific chemical structure, firmly adhere to it, and then give the fabric rich color.
Looking back at the past, the dyeing and weaving technology has a long history. Since the ancient ancestors used natural plants and minerals as the source of dyeing, synthetic dyes have occupied an important position. This disodium compound, due to its good dyeing properties, has emerged in many synthetic dyes.
During the dyeing process, it can make the fabric evenly colored, and the dyed color has a certain light resistance and washing fastness. Therefore, in the textile industry, whether it is cotton, hemp and other natural fiber fabrics, or polyester and other chemical fiber fabrics, they all have their own uses, which can meet people's needs for long-lasting and beautiful fabric colors. And because of its specific chemical structure, it can also play a unique role in some special fabric treatment and printing processes, helping to present more complex and exquisite patterns and color effects.
How safe is Disodium 5- [ (4,6-Dichloro-1,3,5-Triazin-2-Yl) Amino] -4-Hydroxy-3- [ (E) -Phenyldiazenyl] Naphthalene-2,7-Disulfonate '?
"Disodium 5 - [ (4,6 - dichloro - 1,3,5 - triazine - 2 - yl) amino] - 4 - hydroxy - 3 - [ (E) - phenylazo] naphthalene - 2,7 - disulfonate" This product is related to its safety and needs to be observed from multiple angles.
To observe its chemical composition, it is complex and unique. 4,6 - dichloro - 1,3,5 - triazine - 2 - yl is related to structures such as naphthalene disulfonate. Such structures may cause it to exhibit different reactions in living organisms. In the past, many chemicals with similar complex structures were metabolized in organisms, or because they were difficult to degrade, they accumulated in the organs, causing physiological function. If there was a compound containing azo structure in the past, it would cause organ damage after long-term use.
Self-applied scenario theory, if used in industry, such as textile dyeing and other fields, in the production process, if workers are often exposed to this material, or affected by breathing or skin contact. The skin may be allergic, red and swollen, and the respiratory tract may feel uncomfortable or inflamed. If it flows into the environment, it will be in the aquatic ecology, or cause aquatic organisms to be poisoned, affecting the population reproduction and breaking the ecological balance. For example, in the past, a chlorine-containing organic compound flowed into the river, causing a large number of fish and shrimp to die.
However, if this thing has been rigorously studied, there is a complete security evaluation, it can be used under specific conditions, or its risk can be controlled. But before detailed research and analysis, its safety must not be ignored, and it must be cautious to ensure the safety of all living beings and the environment.
'Disodium 5- [ (4,6-Dichloro-1,3,5-Triazin-2-Yl) Amino] -4-Hydroxy-3- [ (E) -Phenyldiazenyl] Naphthalene-2,7-Disulfonate 'What are the production methods?
"'Disodium 5- [ (4,6-Dichloro-1,3,5-Triazin-2-Yl) Amino] -4-Hydroxy-3- [ (E) -Phenyldiazenyl] Naphthalene-2,7-Disulfonate' is an organic compound. The method of its preparation, described in ancient books, has many ways.
First, it can be started from naphthalene compounds. First, a specific naphthol derivative is used as a base, and a sulfonated acid group is introduced at a specific position in the naphthalene ring through sulfonation. In this step, the temperature, time and amount of sulfonating agent of the reaction need to be carefully controlled in order to obtain accurate positioning of the sulfonated product. Then, the obtained sulfonated naphthol meets the chlorine-containing triazine compound, and in the alkaline environment, it is bonded by the substitution reaction of amino groups and chlorine atoms. The key to this process is the fine regulation of the strength of the base and the reaction conditions to promote a smooth and efficient reaction.
Furthermore, the method of diazo coupling can also be used. First prepare the diazo salt containing phenyl groups, which is the key to the diazo reaction. It is necessary to strictly observe the conditions of low temperature and suitable pH to ensure the stability of the diazo salt. Then, the diazo salt is mixed with the naphthalene intermediate obtained above, and a coupling reaction occurs in an appropriate buffer system, thereby introducing a specific azo structure on the naphthalene ring.
There are improved methods. During the reaction process, selecting a suitable catalyst can accelerate the rate of the reaction and improve the yield and purity of the product. And the choice of solvent is also important. Different solvents affect the selectivity and rate of the reaction. It takes many tests to determine the best solvent system. In short, the preparation of this compound can only achieve the desired effect when it is carefully operated according to the characteristics of each method.
Which products are similar to'Disodium 5- [ (4,6-Dichloro-1,3,5-Triazin-2-Yl) Amino] -4-Hydroxy-3- [ (E) -Phenyldiazenyl] Naphthalene-2,7-Disulfonate '?
"What are the products similar to'Disodium 5 - [ (4,6 - Dichloro - 1,3,5 - Triazin - 2 - Yl) Amino] - 4 - Hydroxy - 3 - [ (E) - Phenyldiazenyl] Naphthalene - 2,7 - Disulfonate '?" This substance is a chemical substance. In the era of "Tiangong Kaiwu", the modern chemical system has not yet been formed, so it is difficult to directly list similar products in the language and perspective of "Tiangong Kaiwu". However, we can speculate and imagine in the style of ancient classical Chinese from the perspective of related uses and characteristics.
This chemical may be involved in dyeing, chemical and other uses. In ancient dyes, commonly used plant dyes, such as bluegrass, are contained in "Tiangong Kaiwu · Zhangshi": "All five kinds of blue can be indigo." Indigo can be obtained from bluegrass through fermentation and other processes for fabric dyeing. Although its chemical composition is different from the above chemicals, they all have the effect of dyeing.
Another example is ancient alum, such as alum, which is also mentioned in "Tiangong Kaiwu". Alum is used for water purification, tanning, printing and dyeing, etc. In printing and dyeing, it can be used as a mordant to help dyes adhere to fabrics. This may be similar to the chemical applications mentioned above, and they are all materials that assist related processes.
Another example is the ancient lead powder, which is used for makeup and painting. Lead powder has been refined in a complex manner, and the method is recorded in "Tiangong Kaiwu". Although it is essentially different from modern chemicals in some uses, it may be comparable in terms of the application of substances to specific fields. However, it needs to be clear that ancient materials and modern chemicals are very different in molecular structure, preparation process and other aspects, and only a slight analogy is made from the perspective of application function.