10563-26-5 Usage
Description
N,N'-BIS(3-AMINOPROPYL)ETHYLENEDIAMINE, also known as 1,2-bis(3-aminopropylamino)ethane or 3,3′-ethylenediiminodipropylamine, is a chemical compound resulting from the condensation reaction with 4,6-dibenzofurandicarbaldehyde. It is a clear, colorless to pale yellow liquid with unique chemical properties that make it suitable for various applications across different industries.
Uses
Used in Chemical Synthesis:
N,N'-BIS(3-AMINOPROPYL)ETHYLENEDIAMINE is used as a chemical intermediate for the synthesis of various compounds due to its reactive amine groups, which can participate in a range of chemical reactions, including condensation, substitution, and addition reactions.
Used in Pharmaceutical Industry:
N,N'-BIS(3-AMINOPROPYL)ETHYLENEDIAMINE is used as a building block for the development of new pharmaceutical compounds, particularly those with potential therapeutic applications. Its versatile structure allows for the creation of diverse molecular frameworks with potential biological activities.
Used in Material Science:
In the field of material science, N,N'-BIS(3-AMINOPROPYL)ETHYLENEDIAMINE is used as a component in the development of novel materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance. Its amine groups can form strong interactions with other molecules, contributing to the overall performance of the material.
Used in Analytical Chemistry:
N,N'-BIS(3-AMINOPROPYL)ETHYLENEDIAMINE can be employed as a reagent in analytical chemistry for the detection, separation, or quantification of various compounds. Its amine groups can form complexes with metal ions or other analytes, enabling selective detection and analysis.
Used in Environmental Applications:
N,N'-BIS(3-AMINOPROPYL)ETHYLENEDIAMINE may be utilized in environmental applications, such as the removal of heavy metals from contaminated water or soil. Its amine groups can chelate with metal ions, facilitating their removal and reducing the environmental impact of these contaminants.
Hazard
A poison by skin contact.Moderately toxic
by ingestion.
Flammability and Explosibility
Nonflammable
Safety Profile
A poison by skin contact. Moderately toxic by ingestion. When heated to decomposition it emits toxic vapors of NOx.
Check Digit Verification of cas no
The CAS Registry Mumber 10563-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,6 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10563-26:
(7*1)+(6*0)+(5*5)+(4*6)+(3*3)+(2*2)+(1*6)=75
75 % 10 = 5
So 10563-26-5 is a valid CAS Registry Number.
10563-26-5Relevant articles and documents
Brubaker,Schaefer
, p. 968,969 (1971)
Near-infrared photoswitching of cyclodextrin-guest complexes using lanthanide-doped LiYF4 upconversion nanoparticles
M?ller, Nadja,Hellwig, Tim,Stricker, Lucas,Engel, Sabrina,Fallnich, Carsten,Ravoo, Bart Jan
, p. 240 - 243 (2017)
This communication reports a new type of supramolecular cyclodextrin-guest complexes using cyclodextrin coated upconversion nanoparticles as hosts and monovalent and divalent azobenzenes and arylazopyrazoles as guests. A potentially biocompatible photocontrol of the interaction by isomerization of the azobenzene or arylazopyrazole was achieved by laser irradiation at 980 nm and a very low light intensity of 0.22 W cm-2
BENZYLATED MANNICH BASE CURING AGENTS, COMPOSITIONS, AND METHODS
-
Paragraph 0139; 0140, (2017/09/08)
Compositions and curing agents comprising a benzylated Mannich base composition. The benzylated Mannich base composition includes a reaction product of (a) a substituted phenolic compound having at least one substituent of formula (I): wherein R1 is each independently a linear or branched alkyl group having 1 to 4 carbon atoms, and R2 is hydrogen, methyl, ethyl or phenyl, with (b) a benzylated polyalkylene polyamine (II): wherein RA is substituted or unsubstituted benzyl; RB is each independently RA, or a hydrogen atom, or a group selected from C1-C16 linear, cyclic, and branched alkyl, alkenyl, and alkaryl groups; X, Y, and Z are independently selected from C2-C10 alkylene, and cycloalkylene groups; y is an integer from 0 to 7, and z is an integer from 0 to 4; and, optionally, (c) a multifunctional amine. Amine-epoxy compositions and articles produced from these compositions are also disclosed.
Phenylglyoxal for polyamines modification and cyclam synthesis
Tripier, Rapha?l,Chuburu, Fran?oise,Le Baccon, Michel,Handel, Henri
, p. 4573 - 4579 (2007/10/03)
The bis-aminals obtained by tetraamine and phenylglyoxal condensation display various behaviours such as equilibrium between different configurations, rearrangements that lead to lactam derivatives, or amine deprotection. Our investigations about them were focused on three different linear amines, and then extended to polyazacycloalkanes cyclen and cyclam. Cyclam was also synthesised with the bis-aminals issued from condensation of linear polyamines with phenylglyoxal. The lactam derivatives described here were moreover, employed for the mono-N-functionalisation of tetraamines by phenyl-acetic acid group.