Chemical Name | 1H-Benzimidazole-4,6-disulfonic acid, 2,2'-(1,4-phenylene)bis-, disodium salt |
Molecular Formula | C14H8N2Na2O6S2 |
Molecular Weight | 410.33 g/mol |
Appearance | Solid (usually powder or crystalline form) |
Solubility | Soluble in water |
Ph | Affects the pH of the solution it is dissolved in, depending on concentration |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
Hazard Class | No specific common hazard class without detailed safety data sheet review |
What is the chemical structure of 1H-Benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt
This is about the chemical structure of "1H-benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt". To clarify its chemical structure, consider its name.
"1H-benzimidazole" is a nitrogen-containing fused ring compound formed by fusing a benzene ring with an imidazole ring. This ring structure is the core skeleton of the compound, and its basic structure and characteristics are determined.
"4,6-disulfonic acid" refers to the 4-position and 6-position of the benzimidazole ring, each of which is connected to a sulfonic acid group (-SO-H). The sulfonic acid group has strong hydrophilicity and acidity, which can increase the solubility of the compound in water and affect its chemical activity and reactivity.
"2,2- (1,4-phenylene) bis-", indicating that the two benzimidazole structures are connected by 1,4-phenylene. 1,4-phenylene is the rest of the benzene ring after removing the two para-hydrogen atoms, acting as a bridge, connecting two benzimidazole units to build a larger molecular structure.
"Disodium salt", that is, the hydrogen atoms of the two sulfonic acid groups in this compound are replaced by sodium ions (Na
) to form a sodium salt. The introduction of sodium ions can change the physical and chemical properties of the compound, such as improving its solubility in polar solvents.
In summary, the chemical structure of this compound is based on 1H-benzimidazole, 4 and 6 sulfonic acid groups, and 1,4-phenylene groups are connected to two such structural units, and the sulfonic acid groups exist in the form of sodium salts. This structure endows the compound with unique physical and chemical properties, which may have specific applications in many fields.
What are the main uses of 1H-Benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt
1H-benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt, this substance is widely used. In the printing and dyeing industry, it is often used as a dye intermediate, which can help synthesize dyes with bright color and good fastness, so that the fabric has a long-lasting bright color after dyeing, and is not afraid of daily washing and light. In the field of medicine, because the structure of benzimidazole has a variety of biological activities, this substance can be used as a raw material to develop drugs with antibacterial, antiviral and other effects, escorting human health. In the field of materials science, it can participate in the preparation of high-performance materials, such as some special plastics and fibers, which can improve the stability and functionality of materials and make them perform well in different environments. In scientific research experiments, as an important chemical reagent, it provides key support for chemical synthesis, analysis and testing, and many other studies, helping researchers to deeply explore the properties and reaction mechanisms of substances.
What are the physical properties of 1H-Benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt
1H-benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt, the physical properties are as follows:
Its appearance is often powdery, its color is white as snow, and its delicate feeling is like light smoke. It is smooth and silky to the touch. This substance has good solubility in water, just like ice and snow into a stream, and can quickly dissolve with water to form a uniform solution. This property is due to the strong interaction between sulfonic acid groups and water molecules in its molecular structure.
Its stability is also a major feature. Under normal temperature and pressure, it is like the tranquility of the ancient temple in the mountains, and it can maintain its own structure and properties constant for a long time without being disturbed by the outside world. When encountering a hot topic, it is like a calm lake throwing boulders, and the molecular structure begins to change and gradually decompose, just like a building collapsing.
Furthermore, its chemical activity should not be underestimated. Due to the existence of sulfonic acid groups, it is like a warrior holding a sword. It shows a lively state in many chemical reactions and can react with many metal ions, like a tenon and tenon that fit each other, forming a stable complex. In the field of organic synthesis, it is like a key bridge and can participate in many important reactions, contributing to the construction of complex organic molecular structures.
The melting point of this substance, after accurate determination, is within a certain range. This melting point is its inherent characteristic, just like a person's unique fingerprint, which can be used as an important basis for identifying its authenticity and purity.
In summary, 1H-benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt, with its unique physical properties, has important application value in many fields such as chemical industry and materials.
What is the synthesis method of 1H-Benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt
The synthesis of 1H-benzimidazole-4,6-disulfonic acid, 2,2 - (1,4-phenylene) bis-, disodium salt is the key to chemical synthesis. To make this substance, first take an appropriate amount of 1,4-phenylene related raw materials, which need to be pure and free to ensure accurate reaction. Place it in a suitable reactor, which needs to be temperature and pressure resistant, and the material is excellent.
Take the first material containing benzimidazole structure and put it into the kettle in an appropriate proportion. The proportion is accurate, which is related to the purity and yield of the product, and needs to be carefully considered. Then, add a specific catalyst, this agent can promote the reaction to accelerate, and choose the one with good activity and selectivity.
The reaction environment is also critical. The temperature is controlled within a suitable range, or a heating device is required to gradually increase the temperature to a certain precise degree to maintain stability. The pressure cannot be ignored, and the pressure control equipment can be used to reach a specific value to ensure the smooth reaction.
During the reaction, close inspection shows that the substances in the kettle are blending, reacting, or changing colors and shapes. After the reaction is completed, the pure 1H-benzimidazole-4,6-disulfonic acid, 2,2 - (1,4-phenylene) bis-, disodium salt can be obtained by separation and purification. Separation can be filtered, extraction and other methods, purification by recrystallization and other techniques to remove impurities and obtain high-purity products.
1H-Benzimidazole-4,6-disulfonic acid, 2,2- (1,4-phenylene) bis-, disodium salt What are the precautions during use
1H-benzimidazole-4,6-disulfonic acid, 2,2 - (1,4-phenylene) bis-, disodium salt, when using this product, many matters need to be paid attention to.
First, the properties and characteristics of this product must be clarified in detail. Its chemical structure is unique, or it has specific chemical activities and reaction tendencies. Users should be familiar with its stability, and under different environmental conditions, such as temperature, humidity, light and other factors, affect its quality and performance. High temperature may cause it to decompose and deteriorate, and humidity may also cause it to absorb moisture and deliquescence, light or induce luminescent chemical reactions, so it should be properly stored, and a cool, dry and dark place should be selected to ensure its quality.
Second, safety protection is of paramount importance. Although the exact toxicity is not known, many chemicals are potentially harmful. Users must strictly follow safety procedures. When operating, use appropriate protective equipment, such as gloves, goggles, protective clothing, etc., to prevent direct contact with the skin and eyes. If it is accidentally touched, appropriate emergency treatment should be taken immediately. At the same time, the operating environment must also be well ventilated to prevent the accumulation of harmful gases and endanger personal safety.
Furthermore, the dosage should be controlled and should not be lost. This product must have an appropriate dosage range in specific application scenarios. If the dosage is too small, it may be difficult to achieve the expected effect; if the dosage is too large, it may increase the cost, or cause other adverse consequences, such as excessive chemical reaction and impure product. Therefore, it is necessary to accurately calculate before use, and strictly control the dosage according to experimental or production needs.
In addition, during use, the reaction conditions must be carefully controlled. Temperature, pH, reaction time and other factors can have a significant impact on the reaction process and results. According to the specific reaction mechanism and target product, appropriate reaction conditions need to be precisely set and maintained to achieve the best effect.
At the end of use, properly dispose of the remaining materials and waste. Do not discard at will to prevent environmental pollution. Appropriate treatment methods, such as recycling, neutralization, and degradation, should be selected in accordance with relevant environmental regulations to ensure environmental safety.