43175-57-1

Usage

Uses

Used in the Oil and Gas Industry:
N-(2-Methoxyethyl)-N-propylamine is used as a corrosion inhibitor to protect equipment and infrastructure from the damaging effects of corrosive substances, thereby extending the service life and ensuring the smooth operation of industrial processes.
Used as a Solvent:
N-(2-METHOXYETHYL)-N-PROPYLAMINE serves as a solvent in various applications, leveraging its ability to dissolve a range of substances, which is crucial in numerous chemical processes and formulations.
Used in Adhesives and Sealants:
N-(2-Methoxyethyl)-N-propylamine is incorporated as a component in adhesives and sealants, enhancing their performance characteristics such as adhesion strength, flexibility, and durability.
Used in the Production of Surfactants:
As a chemical intermediate, N-(2-METHOXYETHYL)-N-PROPYLAMINE contributes to the synthesis of surfactants, which are essential in a variety of consumer products and industrial applications for their properties to reduce surface tension and stabilize emulsions.
Used in the Production of Quaternary Ammonium Compounds:
N-(2-Methoxyethyl)-N-propylamine is also utilized in the creation of quaternary ammonium compounds, which have broad applications in the formulation of disinfectants, sanitizers, and fabric softeners due to their antimicrobial and softening properties.
While stable under normal conditions, it is imperative to handle and store N-(2-Methoxyethyl)-N-propylamine with appropriate safety measures to prevent inhalation, skin contact, and ingestion, ensuring the well-being of individuals and the integrity of the environment.

Upstream product

• 107-10-8 propylamine 
• 6482-24-2 2-Bromoethyl methyl ether 
• 106-94-5 propyl bromide 
• 109-85-3 2-methoxyethylamine 
• 98829-72-2 N-(2-Methoxy-ethyl)-propionamide 

Downstream Products

• 209334-19-0 8-(4-Benzyloxy-phenyl)-3-methyl-7-oxo-3,7-dihydro-imidazo[4,5-a]-quinolizine-10-carboxylic acid (2-methoxy-ethyl)-propyl-amide 
• 1227262-25-0 C₂₃H₂₇N₅O₅S 
• 1224595-20-3 C₂₄H₃₁FN₂O₅ 
• 1197371-58-6 C₂₁H₂₈N₆O₂ 
• 1197371-55-3 C₂₁H₂₉N₅O₃ 
• 1197371-54-2 C₂₁H₂₉N₅O₂ 
• 444325-32-0 [6-Chloro-2-trifluoromethyl-7-(2,4,6-trimethyl-phenyl)7Himidazo[1,2-a]imidazol-3-ylmethyl]-(2-methoxy-ethyl)-propyl-amine 

Relevant academic research and scientific papers

COUMARAN GROUP CONTAINING AMINE COMPOUNDS AND THEIR ACID ADDITION SALTS AND QUATERNARY AMMONIUM SALTS AND THE USE THEREOF AS ANTI ARRHYTHMIC AGENTS AND AS PSYCHOTROPIC AGENTS

Amine represented by the following formula (1), or their acid addition salts or their quaternary ammonium salts. STR1 The amines of formula (1) or their pharmaceutically acceptable acid addition salts or quaternary ammonium salts are useful for the treatment and prevention of heart diseases of animals, particularly arrhythima, myocardial infarction, angina pectoris and heart failure and psychoneurological diseases.

Alkene Loss from Metastable Methyleneimmonium Ions: Unusual Inverse Secondary Isotope Effect in Ion-Neutral Complex Intermediate Fragmentations

The mechanism of propene elimination from metastable methyleneimmonium ions is discussed.The first field-free region fragmentations of complete sets of isotopically labelled methyleneimmonium ions (H2C=N+R1R2 : R1 = R2 = n-C3H7; R1 = R2 = i-C3H7; R1 = n-C3H7; R2 = C2H5; R1 = n-C3H7; R2 = CH3; R1 = n-C3H7; R2 = H) were used to support the mechanism presented.The relative amounts of H/D transferred are quantitatively correlated to two distinct mathematical concepts which allow information to be deduced about influences on reaction pathways that cannot be measured directly.Propene loss from the ions examined proceeds via ion-neutral complex intermediates.For the di-n-propyl species rate-determining and H/D distribution-determining steps are clearly distinct.Whereas the former corresponds to a 1,2-hydride shift in a 1-propyl cation coordinated to an imine moiety, the latter is equivalent to a proton transfer to the imine occurring from the 2-propyl cation generated by the previous step.For the diisopropyl-substituted ions which directly form the 2-propyl cation-containing complex, the rate-determining hydride shift vanishes.The 2-propyl cation-containing complex can decompose directly or via an intermediate proton-bridged complex.Competition of these routes is not excluded by the experimental results.Assuming a 2:1:3 distribution, a preference for the α- and β-methylene of the initial n-propyl chain as the source of the hydrogen transferred is detected for n-propylimmonium ions containing a second alkyl chain R2.This preference shows a clear dependence on the steric influence of R2.During the transfer step isotopic substitution is found to affect the H/D distribution strongly.For the alternative route of McLafferty rearrangement leading to C2H4 loss, specific γ-H transfer is observed.