N 1 1 Dimethylethyl Bis 2 Benzothiazolesulfen Amide
Quinoline Thiophene Imidazole Thiazole
N-(1,1-dimethylethyl)bis(2-benzothiazolesulfen)amide
Chemical Formula C17H18N4S4
Molecular Weight 406.62 g/mol
Appearance Yellowish to light brown powder
Odor Characteristic
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in some organic solvents like benzene, toluene
Melting Point 176 - 180 °C
Density Approx. 1.34 g/cm³
Thermal Stability Good thermal stability within normal processing temperatures
Storage Conditions Stored in a cool, dry place away from heat and ignition sources
FAQ

What are the main uses of N- (1,1-dimethethyl) bis (2-benzothiazolyl sulfoxylamine)?

N- (1,1-dimethylethyl) bis (2-phenyl-imidazolyl) terephthalate is mainly used in many fields.

In the cosmetics industry, its excellent ultraviolet absorption capacity can effectively resist the damage of ultraviolet rays to the skin, providing key protective effects for sunscreen products, and can effectively reduce the risk of sunburn, tanning and photoaging caused by ultraviolet rays, so it is widely used in various sunscreen skin care products.

In the plastics industry, it can significantly improve the light stability of plastic products as a light stabilizer. Plastic products are prone to aging, discoloration and performance degradation when exposed to light for a long time. This substance can inhibit these adverse changes, prolong the service life of plastic products, and ensure their stable performance. Therefore, it is commonly used in the production of plastic films, plastic pipes, and many other plastic products.

In the field of coatings, this substance can enhance the coating's resistance to ultraviolet rays, prevent the coating from fading and pulverizing rapidly under light conditions, and maintain a good appearance and protective performance for a long time. It is widely used in automotive paints, architectural coatings, and other coating products that require strict light resistance.

In summary, N- (1,1-dimethylethyl) bis (2-phenylimidazolyl) terephthalate plays a key role in the cosmetics, plastics, coatings and other industries due to its excellent performance in sun protection and light stability, providing excellent UV resistance and stability for related products.

What are the chemical properties of N- (1,1-dimethethyl) bis (2-benzothiazolyl sulfoxylamine)?

N- (1,1 -dimethylethyl) bis (2 -benzimidazolyl) urea, the chemical properties of this substance are as follows:

Its appearance is usually white to light yellow crystalline powder, with a certain melting point, when heated to a specific temperature, it will undergo a phase transition. In terms of solubility, it is slightly soluble in water, which is due to the large proportion of hydrophobic groups in its molecular structure, so that its solubility in polar solvent water is limited; however, it is soluble in some organic solvents, such as ethanol, acetone, etc. In these organic solvents, by virtue of the similar principle of phase dissolution, intermolecular forces promote its dissolution.

In terms of chemical stability, it is usually stable under normal conditions, and it is not easy to react rapidly with common components in the air such as oxygen and nitrogen. However, in a strong acid or alkali environment, some chemical bonds in its structure will be affected and changed. Due to the presence of benzimidazolyl and urea groups in its structure, under the action of acidic or basic media, hydrolysis may occur, resulting in molecular structure destruction.

From the perspective of reactivity, some functional groups in this substance can participate in specific chemical reactions. For example, the carbonyl group in the urea group can undergo condensation reactions with some compounds containing active hydrogen, and the nitrogen atom on the benzimidazolyl group has a certain electron cloud density, which can participate in nucleophilic substitution reactions or electrophilic substitution reactions under suitable conditions. These reactive activities provide applications in the field of organic synthesis.

This compound has potential uses in fields such as medicine and materials due to its unique chemical properties.

What is the production process of N- (1,1-dimethylethyl) bis (2-benzothiazolyl sulfenesulfonyl) amine?

The production process of N- (1,1-dimethylethyl) bis (2-phenyloimidazolyl-4-sodium sulfonate) urea is a delicate and complex process, and I will describe it in detail.

At the beginning, all kinds of raw materials need to be prepared. 1,1-dimethylethyl related reactants need to be carefully purified to ensure their purity to a very high standard before they can be used in subsequent reactions. This is the foundation and the quality of the product is related. Sodium 2-phenyloimidazolyl-4-sulfonate also needs to be carefully selected to ensure its high quality.

Then, the raw materials are placed in a special reactor in precise proportions. The reactor needs to have good temperature and pressure control properties to create a suitable reaction environment. At the beginning of the reaction, the temperature is slowly heated to allow the raw materials to be initially fused and a preliminary chemical reaction occurs. At this time, it is necessary to closely monitor the changes in temperature and pressure. For example, in ancient alchemy, if there is any difference, the result may be thousands of miles away.

As the reaction advances, the temperature gradually rises and the pressure is adjusted accordingly. At this stage, the chemical bonds between the reactants are broken and recombined, gradually forming the precursor of the target product. In this process, a specific catalyst needs to be added to accelerate the reaction process, just like a general during a march, leading the direction and speed of the reaction. The amount of catalyst and the timing of addition have strict requirements and need to be carefully controlled.

When the reaction is carried out to a certain extent, the temperature is cooled to stabilize the reaction. At this time, the reaction product is initially separated and purified. Using ancient methods such as filtration and extraction to remove impurities and improve the purity of the product. However, this is only preliminary and needs to be further refined.

The subsequent refining process often uses methods such as recrystallization and chromatographic separation. When recrystallizing, choose a suitable solvent, like finding a perfect place to recrystallize the product in it to further remove impurities. Chromatographic separation can more accurately separate the target product, so that it can reach a very high purity.

After many processes, it is possible to obtain pure N- (1,1-dimethylethyl) bis (2-phenyloimidazolyl-4-sodium sulfonate) urea. This production process requires craftsmen to operate carefully like skilled craftsmen, and to be familiar with every link in order to ensure the quality and yield of the product. Just like the ancient ability to forge swords, you can get a magic weapon with thousands of refinements.

What are the precautions for the use of N- (1,1-dimethylethyl) bis (2-benzothiazolyl sulfinyl) amine?

When using N- (1,1-dimethylenyl) bis (2-benzimidazolyl) urea, the following points should be paid attention to:

The first is its toxicity and safety. Although this substance is often used in industry or specific fields, its toxicity and potential impact on human health cannot be ignored. When operating, it is necessary to take protective measures, such as wearing appropriate protective gloves, protective glasses and covers, to prevent skin contact, eye splashing and inhalation, and to avoid damage to the body.

Secondly, pay attention to its stability and reactivity. It may undergo chemical reactions under certain conditions, such as when exposed to high temperature, light or specific chemicals, it may cause combustion, explosion or produce harmful bodies. Therefore, it should be stored in a cool, dry and well-connected place, away from fire sources, heat sources and incompatible substances to maintain its stability and avoid the emergence of dangerous reactions.

Furthermore, the dosage should be strictly controlled during the use process. Because the amount required in different application scenarios is different, excessive use may not only lead to waste of resources, but also lead to additional problems, such as adding applications to some materials, excessive addition may affect material performance. Therefore, the amount of addition needs to be precisely controlled according to the specific application and requirements.

In addition, pay attention to its environmental impact. After use, the residue and waste should not be discarded at will, and should be properly disposed of in accordance with relevant environmental regulations to prevent pollution to the environment. When using it on a large scale, it is even more important to consider its potential impact on environmental factors such as surrounding water bodies, soil, and air.

What are the environmental effects of N- (1,1-dimethylethyl) bis (2-benzothiazolyl sulfonyl) amine?

The environmental effects of N- (1,1-dimethethyl) bis (2-phenyl-imidazolyl-5-sulfonylisalicylic acid) ester are quite complex. Due to its unique chemical structure, the behavior characteristics of this substance in the environment are worthy of in-depth investigation.

In the aquatic environment, it may have multiple effects on aquatic organisms due to its solubility and stability. If the substance enters rivers, lakes and seas, some aquatic organisms have low tolerance to it and are susceptible to its interference, which affects normal growth and development. For example, the physiological and metabolic processes of some plankton may be disrupted due to exposure to the substance, which in turn affects the food chain structure of the entire aquatic ecosystem and affects the ecological balance.

In the soil environment, it may interact with soil particles and change the physical and chemical properties of the soil. On the one hand, it may affect the availability of nutrients in the soil, hindering the process of plants obtaining nutrients; on the other hand, the substance remaining in the soil may be absorbed by plant roots and accumulated in plants, not only affecting the health of plants, but also passing through the food chain, causing potential harm to organisms that feed on plants.

In the atmospheric environment, although the substance does not mainly exist in gaseous form, it may be released into the air under certain conditions, such as volatilization during production or improper disposal of related wastes. Although its content in the atmosphere is relatively small, it may still photochemically react with other chemical substances in the atmosphere, generate new pollutants, and cause adverse effects on air quality. And through atmospheric circulation, it may also be transported over long distances, expanding the scope of influence. In conclusion, the multi-faceted impact of N - (1,1-dimethylethyl) bis (2-phenyldiazolyl-5-sulfonylsalicylate) ester on the environment cannot be ignored, and further monitoring and research are needed to comprehensively assess its latent risk.