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Usage

Uses

Used in Oil and Gas Industry:
2-Ethyl-2-imidazoline is used as a corrosion inhibitor to prevent metal degradation and maintain the integrity of drilling and production equipment, ensuring the smooth operation and longevity of oil and gas infrastructure.
Used as a Chemical Intermediate:
In the chemical industry, 2-Ethyl-2-imidazoline serves as a crucial intermediate in the production of surfactants, detergents, and textile softeners, contributing to the development of effective and eco-friendly cleaning and textile products.
Used in Pharmaceutical Industry:
2-Ethyl-2-imidazoline has potential applications in the pharmaceutical sector, where it may be utilized in the development of new drugs or as a component in existing medications, thanks to its unique chemical structure and properties.
Used as a Precursor in Organic Synthesis:
As a precursor, 2-Ethyl-2-imidazoline plays a significant role in the synthesis of various organic compounds, enabling the creation of new chemical entities for research and commercial applications.
Safety Precautions:
It is important to handle 2-Ethyl-2-imidazoline with care, as it can cause irritation to the skin, eyes, and respiratory system upon direct contact or inhalation. Proper safety measures should be taken to minimize exposure and ensure the well-being of individuals working with 2-Ethyl-2-imidazoline.

InChI:InChI=1/C5H10N2/c1-2-5-6-3-4-7-5/h2-4H2,1H3,(H,6,7)

Upstream product

• 925-58-6 N-(2-aminoethyl)propionamide 
• 3403-77-8 N,N'-ethanediyl-bis-propionamide 
• 107-15-3 ethylenediamine 
• 4231-35-0 methyl(diethylamino)acetylene 
• 107-12-0 propiononitrile 
• 137-40-6 sodium proprionate 

Downstream Products

• 84243-45-8 2-ethyl-1-[(2,6-dimethylphenyl)carbamoylmethyl]-2-imidazoline 
• 148560-07-0 C₁₉H₁₈N₂O₂ 
• 1072-62-4 2-Ethylimidazole 

Relevant academic research and scientific papers

Microwave-assisted facile synthesis of 2-substituted 2-imidazolines

A novel method for the synthesis of 2-substituted 2-imidazolines under microwave irradiation is reported. The yields of product obtained using this protocol are significantly high and the reaction time is reduced. ARKAT.

Use of Lanthanide(III) Ions as Catalysts for the Reactions of Amines with Nitriles

Catalytic amounts of lanthanide(III) triflates promote reactions between amines and nitriles leading to a variety of products.The Ln3+ ions activate weakly coordinating nitriles at large amine: Ln3+ mole ratios, even in the presence of amines that form thermodynamically stable complexes with Ln3+ ions.The reactions involving primary monoamines and diamines appear to be general and provide a viable synthetic route to N,N'-disubstituted amidines (2) and cyclic amidines (4), respectively.Symmetrically substituted triazines (8 or 9) are observed as byproducts in some of these systems when the reactions are carried out by using excess nitrile.Secondary alicyclic amines or dimethylamine reacts with acetonitrile to yield pyrimidines (6) and 2,4,6-trimethyl-s-triazine (8).Two routes to triazine have been proposed, one involving the reaction of ammonia with the nitrile and the second involving the reaction of an amidine (1 or 5) with the nitrile.The ability of Ln3+ ions to activate nitriles under conditions that oppose nitrile coordination is attributed to the lability of Ln3+ complexes derived from N-donors.

REACTION OF YNAMINES WITH BIFUNCTIONAL REAGENTS

The reaction of 1-diethylamino- and 1-(ethylphenylamino)-1-propynes with aromatic and aliphatic bifunctional reagents was invectigated.In the reactions of the ynamines with aromatic binucleophiles and also with ethenolamine and ethylenediamine heterocyclic compounds of the benzodioxole, benzimidazoline, benzoxazole, benzothiazole, oxazoline, and imidazoline series are formed.The reactions of the ynamines with ethylene glycol and dithioglycol gave amino(alkoxy)alkenes and amino(alkylthio)-alkenes.