Vedovello, Priscila team published research in SN Applied Sciences in 2021 | 1739-84-0

Recommanded Product: 1,2-Dimethyl-1H-imidazole, 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.

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Recommanded Product: 1,2-Dimethyl-1H-imidazole.

Vedovello, Priscila;de Oliveira Gomes, Ana Catarina;da Rocha Oliveira, Lucas Mendonca;Cruz, Sandra Andrea;Paranhos, Caio Marcio research published 《 Short alkyl chain length ionic liquid as organic modifier in polypropylene/clay nanocomposite: a thermal comparative study》, the research content is summarized as follows. The most common polymeric nanocomposites are constituted of organically-modified clays. Generally, these organic modifiers are based on quaternary ammonium salts. These systems have as disadvantage the low thermal resistance of its modifiers under processing. Ionic liquids (IL) with different mol. structures can be used as organic modifier in lamellar clays-based polymeric nanocomposites, being promising not only to increase interactions between the nanoclay and the matrix, but also to increase the thermal resistance. In this study, polypropylene-based/montmorillonite nanocomposites were compared from two different organic modifiers. The use of short alkyl chain length imidazolium-based IL as montmorillonite modifier was investigated in terms of the thermal stability when compared to the usual quaternary ammonium salt surfactant. Integral procedure decomposition temperature was employed to determine the effect of these two different organoclay modifiers in PP-nanocomposites. The activation energy for these samples was calculated using Flynn-Wall-Ozawa (FWO) method. It was also used the multiple linear regression anal. to calculate the activation energy in order to evaluate the accuracy of this method when applied to nanocomposites.

Recommanded Product: 1,2-Dimethyl-1H-imidazole, 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