123-84-2 Usage
Description
N-(2-Hydroxypropyl)ethylenediamine, with the molecular formula C5H14N2O, is a colorless to pale yellow liquid that exhibits a faint odor. It is a versatile chemical compound primarily recognized for its role as a chelating agent and as a building block in the synthesis of a variety of chemical compounds. Its ability to bind and remove metal ions from solutions is particularly noteworthy.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 123-84-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 123-84:
(5*1)+(4*2)+(3*3)+(2*8)+(1*4)=42
42 % 10 = 2
So 123-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H14N2O/c1-5(8)4-7-3-2-6/h5,7-8H,2-4,6H2,1H3
123-84-2Relevant articles and documents
Synthesis of amphiphilic amino alcohols
Toom, Lauri,Villo, Piret,Liblikas, Ilme,Vares, Lauri
experimental part, p. 4295 - 4313 (2009/04/11)
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.
KINETICS AND REACTION MECHANISM OF PROPYLENE OXIDE WITH ETHYLENEDIAMINE
Plucinski, Janusz,Prystasz, Henryka
, p. 2201 - 2208 (2007/10/02)
Reaction rate constants were determined for propylene oxide addition to ethylenediamine resulting in successive substitution of all hydrogen atoms in amino groups.
