Jia, Hu team published research on Journal of Dispersion Science and Technology in | 1739-84-0

Product Details of C5H8N2, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Product Details of C5H8N2.

Jia, Hu;Kang, Zheng;Li, Zhijie research published 《 Using 1,2 dimethylimidazole to improve gel thermalstability for wellbore plugging in ultra-high temperature fractured reservoirs》, the research content is summarized as follows. Working fluid loss as well as formation damage is usually encountered as a big challenge during well completion and workover for fossil-fuel production Polymer gel is widely used for wellbore plugging to isolate the working fluid and the reservoir for controlling fluid loss and protecting the reservoir. However, with the increasing number of ultra-high temperature well (>180 °C) operations, the thermal stability of the gel plug is increasingly required. In this paper, 1,2 dimethylimidazole (C5H8N2) is first used to prepare a gel plug. The effects of C5H8N2on gel gelation at dynamic heating mode, viscosity, elasticity, thermal stability and temporary plugging performances are evaluated at 190 °C. It is found that the addition of C5H8N2does not affect the gelation, while a slightly viscosity-reducing effect is exhibited. At 190 °C, the gel without C5H8N2 broke down within 4 h and lost its temporary plugging performance, while the gel with 20% imidazole remained unbroken after 60 h. For the fractured core (5 cm in length) plugging experiments, the addition of 15% C5H8N2 significantly increased the breakthrough pressure of gels from 0.2 MPa to 1.9 MPa compared to pure gels (without C5H8N2). The enhancement mechanism of C5H8N2is investigated. Recommendations for the application of gels with C5H8N2 are given in the paper. This paper provides an avenue for the development of gel plug to deal with wellbore temporary plugging jobs in ultra-high temperature fractured reservoirs.

Product Details of C5H8N2, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem