1072-03-3

Usage

Uses

Used in Pharmaceutical Industry:
2-(ethylamino)ethyl hydrogen sulphate is used as a pharmaceutical compound for its potential applications in drug formulations and development. Its unique chemical structure allows it to interact with various biological systems, making it a valuable component in the creation of new medications.
Used in Detergent Manufacturing:
In the detergent industry, 2-(ethylamino)ethyl hydrogen sulphate is used as a surfactant or a component in the formulation of cleaning agents. Its water solubility and ability to form micelles make it effective in removing dirt and stains from various surfaces.
Used in Textile Industry:
2-(ethylamino)ethyl hydrogen sulphate is utilized in the textile industry as a dye fixative or a softening agent. Its chemical properties enable it to improve the colorfastness of dyed fabrics and provide a softer feel to the textiles.
It is crucial to handle 2-(ethylamino)ethyl hydrogen sulphate with care due to its potential hazards if not used properly. Proper safety measures should be taken to minimize risks during its production, storage, and application in various industries.

InChI:InChI=1/C4H11NO4S/c1-2-5-3-4-9-10(6,7)8/h5H,2-4H2,1H3,(H,6,7,8)

Upstream product

• 110-73-6 2-(Ethylamino)ethanol 

Downstream Products

• 3484-90-0 N-ethyl-1,3-thiazoline-2-thione 
• 155595-62-3 N-Ethyl-N'-phenyl-ethane-1,2-diamine 

Relevant academic research and scientific papers

Synthesis and characterization of novel ionic liquids: N-substituted aziridinium salts

Ionic liquids based on three-membered ring aziridinium cations have been synthesized for the first time using a straightforward synthetic route. N-butyl-N-methylaziridinium bis(trifluoromethanesulfonyl)imide, N-propyl-N-ethylaziridinium bis(trifluoromethanesulfonyl)imide, N-butyl-N-[2-(2-methoxyethoxy)ethyl]aziridinium bis(trifluoromethanesulfonyl) imide, N-butyl-N-methylaziridinium dicyanamide, and N-butyl-N-ethylaziridinium dicyanamide were thus obtained in good yields and satisfactory purity and fully characterized.

Disproportionation reactions from glyoxal and difunctional basic molecules

Glyoxal was reacted with basic difunctional molecules in order to study the disproportionation reaction.Symmetrical and unsymmetrical 1,2-diamines gave rise to piperazinones; their 1,3-diamine analogues yielded hexahydrodiazepinones; and β-aminoalcohols yielded morpholinones and hydroxyamino acids.Aminoamides gave the expected piperazinediones in low yields and no reaction was observed with diamides.The first step of the reaction consists of the formation of dihydroxy compounds, from which the more basic function assists the departure of OH, providing the expected more stable iminium ion.The observed regioselectivity is consistent with the relative basicities of the two functions; a 100percent regioselectivity is observed with aminoalcohols (giving way to morpholinones and not to amides), a good regiposelectivity with most of N-alkyl-N'-aryl-diamines and a rather low one with N-methyl-N'-ethyl- or N-methyl-N'-p-methoxyphenyl-diamines.Geometry factors were related to the better yield obtained with 1,2-diamines compared with 1,3-diamines.The mechanism was investigated.When deutared glyoxal and diamines were reacted in D2O, incorporation of deuterium was observed, in accordance with the formation of an enolate in the course of the oxidoreduction.The low reactivity of aminoamides and the observed regioselectivities could be related to both the weak basicity of the function that is supposed to allow the formation of the iminium ion and the basicity of the other function that accepts a positive charge and which, if too weak, impedes the reaction because of the instability of the intermediate iminium ion. glyoxal / disproportionation rules / basic difunctional molecules