123-84-2

Usage

Uses

Used in Adhesives, Resins, and Coatings Industry:
N-(2-Hydroxypropyl)ethylenediamine is used as a chelating agent and a building block for the production of adhesives, resins, and coatings. Its chelating properties help in improving the stability and performance of these materials.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, N-(2-Hydroxypropyl)ethylenediamine serves as an intermediate in the manufacturing process. Its role in the synthesis of various pharmaceutical compounds is crucial for the development of new drugs.
Used in Dye Production:
N-(2-HYDROXYPROPYL)ETHYLENEDIAMINE is also utilized in the production of dyes, where it contributes to the formation of colorants with specific properties, enhancing the quality and performance of the dyes.
Used in Surfactant Manufacturing:
N-(2-Hydroxypropyl)ethylenediamine is used as an intermediate in the production of surfactants, which are essential in a wide range of applications, including detergents, cleaners, and personal care products, due to its ability to form stable compounds with desired surfactant properties.
Used in Polymer Production:
Furthermore, it finds application in the production of certain polymers, where it is used to create polymers with specific characteristics, such as improved binding or reactivity properties.
Overall, N-(2-Hydroxypropyl)ethylenediamine is a multifaceted compound with applications across various industries, leveraging its unique ability to chelate and bind metal ions, as well as its role in the synthesis of diverse chemical products.

InChI:InChI=1/C5H14N2O/c1-5(8)4-7-3-2-6/h5,7-8H,2-4,6H2,1H3

Upstream product

• 75-04-7 ethylamine 
• 75-56-9 methyloxirane 
• 107-15-3 ethylenediamine 
• 57-55-6 propylene glycol 
• 10507-78-5 N,N,N'-tri(2-hydroxypropyl)ethylenediamine 

Downstream Products

• 38919-48-1 1-[2-(6-chloro-2-methoxy-acridin-9-ylamino)-ethylamino]-propan-2-ol; dihydrochloride 
• 3270-73-3 N,N′-bis(2-hydroxypropyl)ethylenediamine 
• 109-08-0 2-Methylpyrazine 
• 13925-00-3 2-ethylpyrazine 
• 290-37-9 1,4-pyrazine 
• 123-32-0 2,5-dimethyl-pyrazine 
• 693-98-1 2-methylimidazole 
• 15707-23-0 2-methyl-3-ethylpyrazine 
• 70788-93-1 1,4-Dihydroxy-5,8-bis-[2-(2-hydroxy-propylamino)-ethylamino]-anthraquinone 
• 109-07-9 (RS)-2-methylpiperazine 
• 292835-55-3 5-[(2S)-2-({(2S)-2-[(tert-Butoxycarbonyl)amino]-3-phenylpropanoyl}amino)-3-({2-[(2-hydroxypropyl)amino]ethyl}amino)-3-oxopropyl]-2-(carboxymethoxy)benzoic Acid 

Relevant academic research and scientific papers

Synthesis of amphiphilic amino alcohols

An efficient and general approach for the synthesis of amphiphilic 1,2-amino alcohols is reported. The use of N-benzyl protecting groups is essential for obtaining good yields when opening a long-chain terminal epoxide with an amine. Copyright Taylor & Francis Group, LLC.

Intermolecular and intramolecular cyclization over modified ZSM-5 and chromite catalysts to synthesize 2-methyl pyrazine and piperazine

The synthesis of methyl pyrazine and piperazine has been carried out over HZSM-5 and modified copper-chromite catalysts.The reaction occurs through the dehydrocyclization route at acidic centres.The Bronsted acidic centres at interstitial are particularly responsible for the conversion of propylene glycol, propylene oxide with ethylenediamine and β-hydroxy-propylethylenediamine to the N-containing heterocycles through intermolecular and intramolecular cyclization.In the formation of N-containing heterocycles, the steps involved are dehydration and cyclization.The important difference between these reactions and the methano-to-gasoline (MTG) process is the formation of olefinic compounds as intermediates in the latter.

KINETICS AND REACTION MECHANISM OF PROPYLENE OXIDE WITH ETHYLENEDIAMINE

Reaction rate constants were determined for propylene oxide addition to ethylenediamine resulting in successive substitution of all hydrogen atoms in amino groups.

Process for preparing nitrogen-containing heterocyclic compounds

Nitrogen-containing heterocyclic compounds are prepared by cyclization of a compound having the formula: EQU1 or EQU2 wherein X represents a hydrogen atom or --CH2 CHR-Y; R represents a hydrogen atom or methyl atom; Y represents an --OH group or --NH2 group; and n represents the integers 0 or 1 - 4; with a zeolite catalyst having the formula wherein M represents a cation selected from alkali metals, alkaline earth metals, zinc group elements, hydrogen and ammonium cations; n represents the valence of the cation; a is 1.0 ± 0.5 and m is 2 - 12.