N-(2-Aminoethyl)-N'-(2-(1-piperazinyl)ethyl)ethylenediamine

Base Information

• Chemical Name: N-(2-Aminoethyl)-N'-(2-(1-piperazinyl)ethyl)ethylenediamine
• CAS No.: 31295-49-5
• Molecular Formula: C10H25 N5
• Molecular Weight: 215.342
• Hs Code.: 2933599090
• European Community (EC) Number: 250-556-5
• DSSTox Substance ID: DTXSID2067610
• Nikkaji Number: J278.086K
• Wikidata: Q81994230
• Mol file: 31295-49-5.mol

Synonyms:31295-49-5;EINECS 250-556-5;N-(2-Aminoethyl)-N'-(2-(1-piperazinyl)ethyl)ethylenediamine;N-(2-Aminoethyl)-N'-[2-(1-piperazinyl)ethyl]ethylenediamine;N-(2-Aminoethyl)-N-(2-(1-piperazinyl)ethyl)-1,2-ethanediamine;1,2-Ethanediamine, N-(2-aminoethyl)-N'-(2-(1-piperazinyl)ethyl)-;1,2-Ethanediamine, N-(2-aminoethyl)-N'-[2-(1-piperazinyl)ethyl]-;1,2-Ethanediamine, N1-(2-aminoethyl)-N2-(2-(1-piperazinyl)ethyl)-;SCHEMBL600834;DTXSID2067610;EN300-9305615;N-(2-Aminoethyl)-N'-[2-(1-piperazinyl)ethyl]-1,2-ethanediamine;Piperazine, 1-[2-[[2-[(2-aminoethyl)amino]ethyl]amino]ethyl]-;{2-[(2-AMINOETHYL)AMINO]ETHYL}[2-(PIPERAZIN-1-YL)ETHYL]AMINE

Chemical Property of N-(2-Aminoethyl)-N'-(2-(1-piperazinyl)ethyl)ethylenediamine

Chemical Property:

• Boiling Point: 346.8°Cat760mmHg
• Flash Point: 163.5°C
• PSA: 65.35000
• Density: 0.985g/cm³
• LogP: -0.22170
• XLogP3: -2.2
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 8
• Exact Mass: 215.21099582
• Heavy Atom Count: 15
• Complexity: 136

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C1CN(CCN1)CCNCCNCCN

Technology Process of N-(2-Aminoethyl)-N'-(2-(1-piperazinyl)ethyl)ethylenediamine

There total 2 articles about N-(2-Aminoethyl)-N'-(2-(1-piperazinyl)ethyl)ethylenediamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

piperazine (110-85-0) + 1-<2-<(2-aminoethyl)amino>ethyl>aziridine (23435-23-6) → N-(2-aminoethyl)-N'-[2-(1-piperazinyl)ethyl]ethylenediamine (31295-49-5)

Guidance literature:

With hydrogen cation; In water; at 50 - 70 ℃; Rate constant; Thermodynamic data; E_a, ΔH;

Reference yield:

ethyleneimine (151-56-4,9002-98-6) + 1-<2-(2-aminoethyl)aminoethyl>piperazine (24028-46-4) → 1-(2-aminoethyl)-4-<(2-aminoethyl)aminoethyl> piperazine (31295-54-2) + N-(2-aminoethyl)-N'-[2-(1-piperazinyl)ethyl]ethylenediamine (31295-49-5)

Guidance literature:

With hydrogenchloride; In water; at 25 ℃; Kinetics; Thermodynamic data; acid-catalyzed ring opening reactions at various temperature, E_a, ΔH are given;

upstream raw materials:

piperazine

1-<2-<(2-aminoethyl)amino>ethyl>aziridine

ethyleneimine

1-<2-(2-aminoethyl)aminoethyl>piperazine