Methyl-2-Mercaptobenzimidazole CAS 53988-10-6
Factory wholesale Methyl-2-Mercaptobenzimidazole CAS 53988-10-6
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- Purity:99.8%
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Name: Methyl-2-Mercaptobenzimidazole
CAS: 53988-10-6
MOQ: 1KG
Directory Guidance on Methyl-2-Mercaptobenzimidazole
Chemical Structure
Basic Info:
| Melting Point | 300-304 °C(lit.) |
| Density | 1.25 |
| Vapor Pressure | 0.002Pa at 25℃ |
| Refractive Index | 1.5700 (estimate) |
Methyl-2-Mercaptobenzimidazole Introduction:
Methyl-2-Mercaptobenzimidazole is an organic compound with a unique chemical structure. Its molecular structure contains a benzimidazole ring and a thiol group. This special combination gives it many characteristics. From the perspective of chemical composition, the benzimidazole ring is an aromatic heterocycle composed of a benzene ring and an imidazole ring, which provides a relatively stable structural basis and a specific electron distribution for the compound. The introduction of the thiol group (-SH) brings it activity similar to that of a sulfhydryl group, and it can participate in a variety of chemical reactions, such as redox reactions and coordination reactions.
In terms of physical properties, Methyl-2-Mercaptobenzimidazole usually presents as a crystalline powder or solid substance with a specific melting point range, which enables the melting point tobe used as one of the bases for identification and quality control during operations such as separation and purification. Its solubility characteristics are quite prominent, and it has a certain solubility in some organic solvents such as dimethyl sulfoxide and ethanol, which provides convenience for its use in different application scenarios, such as in the dissolution and dispersion of drug preparations or as a reagent to participate in chemical reactions in the solution phase.
From a synthetic perspective, the preparation methods of Methyl-2-Mercaptobenzimidazole are diverse. Common synthetic routes may involve the derivatization reaction of benzimidazole. Through the reaction of appropriate starting materials such as benzimidazole compounds with methylating reagents containing thiol groups under specific reaction conditions, Gradually construct the target molecular structure.
Furthermore, the chemical stability of Methyl-2-Mercaptobenzimidazole has certain characteristics. Under conventional storage conditions, such as avoiding light, being dry, and in a cool environment, it can maintain the integrity of its chemical structure for a relatively long time. However, in certain special environments, such as high temperatures, strong acids, strong bases, or systems with strong oxidizing properties, its structure may change. The mercaptan group may be oxidized or the benzimidazole ring may undergo ring-opening reactions, etc. This has direct guiding significance for the selection of its application scope and storage conditions.
Nature and Specifications:
| Item | Specification |
| Product Name | Methyl-2-Mercaptobenzimidazole |
| CAS No. | 53988-10-6 |
| Appearance | Powder |
| Shelf Life | 2 years |
| Packing | As Your Requirements |
| Refractive Index | 1.5700 (estimate) |
| Water Solubility | 120mg/L at 20℃ |
| LogP | 0.4 at 25℃ |
Product service:
- Certificate Of Analysis (COA)
- Material Safety Data Sheet (MSDS)
- Route of synthesis (ROS)
- Method of Aanlysis (MOA)
- Nuclear Magnetic Resonance (NMR)
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- Free Sample
- Factory audit
The Application Situation Of Methyl-2-Mercaptobenzimidazole
In the field of medicine, Methyl-2-Mercaptobenzimidazole has broad application prospects. It can be used as a drug intermediate to synthesize some drug molecules with special efficacy. For example, it can participate in the synthesis of antibacterial drugs, and through its thiol group combined with certain antibacterial active groups, enhance the inhibitory effect of drugs on bacterial cell wall synthesis or interfere with the metabolic process of bacteria, thereby improving the efficacy and antibacterial spectrum of antibacterial drugs.
In materials science, Methyl-2-Mercaptobenzimidazole can be used as a ligand in the preparation of functional materials. Because its thiol group and the nitrogen atom on the benzimidazole ring have lone pairs of electrons, it can form stable coordination compounds with a variety of metal ions. For example, after coordination with transition metal ions such as copper ions and zinc ions, metal-organic framework materials (MOFs) with special optical, electrical or magnetic properties can be formed.
These materials have potential application value in the fields of gas adsorption and separation, catalytic reaction and sensor detection, such as being used to adsorb and separate specific gas molecules to improve the selectivity and efficiency of gas separation; or as catalyst carriers to provide an efficient and stable reaction environment for some organic catalytic reactions, enhancing the activity and selectivity of catalytic reactions.
By establishing a suitable detection system and using the quantitative relationship between the color change degree or fluorescence intensity change produced by the reaction of Methyl-2-Mercaptobenzimidazole with the target metal ions and the metal ion concentration, rapid and sensitive detection of the metal ion content in the sample can be achieved. It has practical application needs in many fields such as environmental monitoring, food quality testing and biological sample analysis, and provides an effective technical means for accurately determining the metal ion content.
In the field of corrosion and rust prevention, Methyl-2-Mercaptobenzimidazole also shows certain application potential. It can be adsorbed on the metal surface to form a protective film, thereby preventing the metal from directly contacting the corrosive media in the external environment such as water and oxygen, thereby playing a role in slowing down metal corrosion and rust prevention.
In industrial production, this characteristic can be applied to short-term rust prevention in the metal processing process, or added as an additive to anti-corrosion coatings, lubricants and other products to improve their anti-corrosion performance, extend the service life of metal materials, and reduce economic losses and safety hazards caused by corrosion.
The Advantages Of Methyl-2-Mercaptobenzimidazole
From the perspective of chemical reactivity, Methyl-2-Mercaptobenzimidazole has significant advantages. The activity of its thiol groups enables it to participate in various important chemical reactions, and the reaction conditions are relatively mild, allowing for reactions to occur at some room temperature or slightly heated conditions, greatly improving its operability and reaction efficiency in practical applications such as chemical synthesis.
For example, when performing thiol exchange reactions, compared with some thiol compounds with lower reactivity, it can react with compounds containing active groups faster to generate target products, thereby saving reaction time and cost. In fields such as drug synthesis and material modification that require a large number of chemical reactions, this high reactivity can effectively improve the efficiency and economy of the entire production process.
In terms of biocompatibility, Methyl-2-Mercaptobenzimidazole exhibits good properties. When used in the field of biomedicine, such as as a drug intermediate to synthesize drugs or for biosensor detection, its own chemical structure has low toxicity to organisms and can adapt to the physiological environment in the body to a certain extent.
This means that drugs or detection systems containing this compound will not cause serious toxic side effects or immune reactions when used in vivo, improving the safety of drugs and the acceptability of detection methods in the biomedical field, and providing a strong guarantee for the development of safer and more effective biomedical application products.
From the perspective of chemical reactivity, Methyl-2-Mercaptobenzimidazole has significant advantages. The activity of its thiol groups enables it to participate in various important chemical reactions, and the reaction conditions are relatively mild, allowing for reactions to occur at some room temperature or slightly heated conditions, greatly improving its operability and reaction efficiency in practical applications such as chemical synthesis.
For example, when performing thiol exchange reactions, compared with some thiol compounds with lower reactivity, it can react with compounds containing active groups faster to generate target products, thereby saving reaction time and cost. In fields such as drug synthesis and material modification that require a large number of chemical reactions, this high reactivity can effectively improve the efficiency and economy of the entire production process.
In terms of biocompatibility, Methyl-2-Mercaptobenzimidazole exhibits good properties. When used in the field of biomedicine, such as as a drug intermediate to synthesize drugs or for biosensor detection, its own chemical structure has low toxicity to organisms and can adapt to the physiological environment in the body to a certain extent.
This means that drugs or detection systems containing this compound will not cause serious toxic side effects or immune reactions when used in vivo, improving the safety of drugs and the acceptability of detection methods in the biomedical field, and providing a strong guarantee for the development of safer and more effective biomedical application products.
From the perspective of the feasibility of synthesis and preparation, the synthesis method of Methyl-2-Mercaptobenzimidazole is relatively mature and has many selectivities, which provides favorable conditions for its large-scale production and industrial application. Whether it is through traditional chemical synthesis methods or some new green synthesis technologies, it is relatively easy to obtain products with higher purity.
Most of the raw materials involved in its synthesis process are from a wide range of sources and are relatively reasonably priced, which plays a key role in reducing production costs. In addition, the diversity of synthetic routes also allows researchers to flexibly select the most suitable synthesis process according to different production scales and specific requirements, further optimize various parameters in the production process, improve product quality and output, and meet the market’s growing demand for it.
In terms of product stability, Methyl-2-Mercaptobenzimidazole has unique advantages. Under conventional storage and usage environments, its chemical structure can remain stable for a long time and is not easily decomposed or deteriorated, ensuring the reliability of product quality and performance. For products that require long-term storage or transportation under different environmental conditions, this stability is crucial to reduce losses and risks caused by unstable product quality.
In terms of functional expansion, Methyl-2-Mercaptobenzimidazole has great potential. Since there are multiple sites in its molecular structure that can be chemically modified, such as the substitution position on the benzimidazole ring and the thiol group, it can be functionalized to introduce various functional groups, thereby giving it new chemical and physical properties and developing new products with different application functions.
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Related References:
Chemicalbook-Methyl-2-Mercaptobenzimidazole
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