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Usage

Uses

1-(2-Aminoethyl)-2-methyl-2-imidazoline is used as a chemical intermediate in the synthesis of various compounds due to its unique structure and reactivity. Its applications can be found in different industries, including pharmaceuticals, materials science, and chemical research.
Used in Pharmaceutical Industry:
1-(2-Aminoethyl)-2-methyl-2-imidazoline is used as a building block for the development of new drugs, taking advantage of its imidazoline structure to create potential therapeutic agents.
Used in Materials Science:
1-(2-Aminoethyl)-2-methyl-2-imidazoline is used as a component in the synthesis of advanced materials, such as polymers and composites, where its imidazoline ring can contribute to the desired properties of the final product.
Used in Chemical Research:
1-(2-Aminoethyl)-2-methyl-2-imidazoline is used as a research tool in the study of imidazoline chemistry, allowing scientists to explore new reactions and mechanisms involving this class of compounds.

InChI:InChI=1/C6H13N3/c1-6-8-3-5-9(6)4-2-7/h2-5,7H2,1H3

Upstream product

• 64-19-7 acetic acid 
• 111-40-0 3-azapentane-1,5-diamine 
• 112-24-3 triethylentetramine 

Relevant academic research and scientific papers

Metal corrosion inhibitor and preparation method thereof

The invention discloses a metal corrosion inhibitor and a preparation method thereof. The preparation method comprises the process steps of a natural gas storage CO2 liquid-phase corrosion inhibitor and a natural gas storage CO2 gas-phase corrosion inhibitor. The preparation method of the CO2 liquid-phase corrosion inhibitor for the natural gas storage comprises the following steps: S1, carrying out amidation and cyclization reaction on cis-octadecenoic acid-9-enoic acid and triethylenetetramine serving as main components, and dehydrating twice to form a five-membered heterocyclic imidazolineintermediate; s2, the imidazoline intermediate and benzyl chloride are subjected to quaternization, and oil solubility is converted into water-soluble imidazoline quaternary ammonium salt; and S3, reacting the imidazoline quaternary ammonium salt with ethyl sulfur nitrogen, and introducing an ethyl sulfur nitrogen polar group, so that the imidazoline quaternary ammonium salt has more active adsorption sites to obtain the natural gas storage CO2 liquid-phase corrosion inhibitor 2-ethylthio-amino-ethyl-benzyl-1-heptadecenyl-imidazoline quaternary ammonium salt. The corrosion inhibitor has gas-phase corrosion inhibition and liquid-phase corrosion inhibition functions at the same time, and the use concentration of the corrosion inhibitor can be reduced to a low degree on the premise that the function of the corrosion inhibitor is not affected.

Hydrolysis of 1,2-disubstituted imidazolines in aqueous media

The kinetics of hydrolysis of 1,2-disubstituted imidazolines in aqueous media was studied (pH 2.0 - 12.5, T = 25 - 90°C) by UV spectroscopy. The hydrolysis products were identified. The introduction of a branched substituent into position 2 of the imidazoline ring increases the hydrolytic stability of the compounds. The effect of the pH on the hydrolysis rate of imidazolines is discussed.