What is the chemical structure of 2-hexadecylsulfanyl-1H-benzimidazole-5-sulfonate?

The concept of "sodium; 2 - hexadecylsulfanyl - 1H - benzimidazole - 5 - sulfonate" is the English expression of chemical substances. Its meaning is sodium-containing 2 - hexadecylsulfanyl - 1H - benzimidazole - 5 - sulfonate.

In the structure of this compound, the core is a benzimidazole ring, which is fused by a benzene ring and an imidazole ring. It has a unique conjugated system and is planar in structure, giving the molecule certain stability and special electronic properties. 1H - means that the hydrogen atom is attached to the nitrogen atom at the 1st position of the imidazole ring.

At the 5th position, it is connected with a sulfonic acid group (-SO
), which has strong hydrophilicity and acidity, can dissociate the compound in water, exhibit ionic characteristics, and has a great impact on its solubility and chemical activity.

And the 2-position is connected to a hexadecyl thio group (-S-C H
), which is a long-chain alkyl group and has strong hydrophobicity. This long-chain alkyl group makes one end of the compound lipophilic, and cooperates with the hydrophilicity of the sulfonic acid group to give the compound surface activity, which can reduce the surface tension of the liquid and align it at the interface. < Br >
Sodium (sodium) in this compound is usually combined with the sulfonate anion (-SO 🥰) in the form of cation to form ionic bonds, maintain the electrical neutrality of the compound, and affect its physical and chemical properties, such as solubility, melting point, etc. The structural characteristics of this compound determine that it may have important applications in surfactants, drug carriers and other fields.

What are the physical properties of sodium 2-hexadecylsulfanyl-1H-benzimidazole-5-sulfonate?

This substance is a compound of sodium and 2-cetylthio-1H-benzimidazole-5-sulfonate. Its physical properties are as follows:

In terms of concept, it may be in a solid state, and due to the presence of sulfonate groups, it may have a certain water solubility. Capsulfonates are mostly hydrophilic, which can make the compound disperse or dissolve in water to a certain extent.

As for the melting point, it is difficult to determine accurately. However, it can be inferred that due to its molecular structure containing long chain alkyl and benzimidazole heterocycles, the structure is relatively complex, the intermolecular force is strong, and the melting point may be in a higher range.

In terms of solubility, in addition to a certain performance in water, it may also have a certain solubility in polar organic solvents. Due to the fact that there are both hydrophilic sulfonate parts and long-chain alkyl groups with certain lipophilicity in the molecule, it may be soluble in some polar organic solvents such as ethanol.

Its density is also difficult to know exactly, but it is based on compounds with similar structures, or similar to the density of common organic salts, which is slightly greater than the density of water.

In addition, its stability is also worth mentioning. The structure of the benzimidazole ring is relatively stable, but the long-chain alkyl part may be affected by external environments such as light and high temperature, triggering reactions such as oxidation, resulting in changes in the properties of the compound. And the sulfur atom in the compound may participate in the chemical reaction under specific conditions, which affects its stability.

The physical properties of this compound are closely related to the molecular structure, and each property is interrelated, showing a unique state in different environments.

Sodium; 2-hexadecylsulfanyl-1H-benzimidazole-5-sulfonate in which areas

Sodium; 2-cetylthio-1H-benzimidazole-5-sulfonate This compound has its uses in various fields.

In the field of medicine, its properties may help drug research and development. Due to the unique structure or specific biological activity of this compound, it can be used as a lead compound and modified by chemists to find new drugs with better efficacy and less side effects. For example, its thio-sulfonate structure may interact with specific targets in organisms to regulate physiological processes and provide new ways to overcome difficult diseases.

In the field of materials science, there are also extraordinary things. Special functional materials can be prepared by virtue of their unique chemical properties. If it is used to prepare materials with good ionic conductivity, it can be used in batteries, sensors and other devices. The long-chain alkyl group in its structure can improve the flexibility and hydrophobicity of the material and expand the application scenarios of the material.

Furthermore, in the field of surfactants, the compound can also be used. Because it contains hydrophilic sulfonate groups and hydrophobic hexadecyl groups, it has the characteristics of surfactants. It can reduce the surface tension of liquids, improve the surface wettability of liquids and solids, and play a role in detergents, emulsifiers and other products to improve cleaning and dispersion properties.

In addition, in some special chemical reactions, it can be used as a catalyst or ligand. Its unique structure can stabilize the reaction intermediates, promote the smooth progress of the reaction, improve the reaction efficiency and selectivity, and open up new possibilities for organic synthetic chemistry. In short, sodium; 2-cetylthio-1H-benzimidazole-5-sulfonate has broad application prospects in many fields, which need to be further explored and excavated by researchers.

Sodium; what is the preparation method of 2-hexadecylsulfanyl-1H-benzimidazole-5-sulfonate

The preparation of 2-cetylthio-1H-benzimidazole-5-sodium sulfonate requires specific steps and procedures. First, prepare all the required raw materials, such as hexadecyl mercaptan, 5-amino-2-mercaptobenzimidazole and suitable sulfonating reagents, bases, etc.

First, hexadecyl mercaptan and 5-amino-2-mercaptobenzimidazole are mixed in a suitable reaction solvent, catalyzed by an appropriate amount of catalyst, and controlled the temperature and reaction time to carry out thioalkylation. In this process, pay attention to the uniformity of stirring, so that the reactants are fully contacted, and the reaction is smooth.

After the thioalkylation reaction is completed, the pure 2-cetylthio-1H-benzimidazole is obtained through separation and purification. Then, it is sulfonated with a sulfonating agent. This step requires precise control of the reaction conditions, and the degree of sulfonation is closely related to the quality of the product.

After the sulfonation reaction is completed, the sulfonic acid is converted into sodium sulfonate by reacting with alkali substances. At last, 2-cetylthio-1H-benzimidazole-5-sodium sulfonate is refined by recrystallization, filtration, drying and other processes. The whole preparation process requires fine control of reaction conditions and strict compliance with operating specifications to obtain high-quality products.

How safe is sodium 2-hexadecylsulfanyl-1H-benzimidazole-5-sulfonate?

Sodium; 2-cetylthio-1H-benzimidazole-5-sulfonate, the safety of this substance is related to the health of everyone and the tranquility of the environment, so it needs to be investigated in detail.

First discuss its chemical structure, 2-cetylthio-1H-benzimidazole-5-sulfonate, benzimidazole ring has a certain stability, but the cetylthio-sulfonate group will affect its properties. Cetylthio increases its lipid solubility, and the sulfonate group makes it water-soluble, so the amphiphilic property may affect its behavior in different media.

In terms of toxicity, it is difficult to assert without sufficient research data. However, similar compounds containing benzimidazole and sulfonate structures may be toxic to organisms. For example, some pesticides containing benzimidazole structure may affect the biological endocrine system and interfere with the normal physiological activities of organisms. If this substance enters the human body, after being absorbed by the digestive system, it may interact with biological macromolecules such as proteins and nucleic acids in the body, disrupting the normal metabolism of cells.

Look at its impact on the environment, because it is amphiphilic, or easy to accumulate at the interface between water bodies and soils. In water bodies, or change the surface tension of water bodies, affect the living environment of aquatic organisms, and interfere with the respiration, feeding and other behaviors of aquatic organisms. In the soil, or affect the structure and function of soil microbial community, hinder the material cycle and energy conversion in the soil.

Review its stability. Under different environmental conditions, the stability of this substance varies. Light, temperature, pH can cause its decomposition or transformation. For example, in a strong acid or alkali environment, benzimidazole rings or sulfonate groups may react such as hydrolysis to form new substances, and the safety of new substances also needs to be considered.

In summary, although there is currently no detailed data to conclusively prove the safety of sodium; 2-cetylthio-1H-benzimidazole-5-sulfonate, due to its structure and similar compound characteristics, its biological and environmental or latent risks, follow-up experimental studies are required to ensure its safety, biological and environmental safety.