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N-(2-Aminoethyl)piperazine

Base Information Edit
  • Chemical Name:N-(2-Aminoethyl)piperazine
  • CAS No.:140-31-8
  • Deprecated CAS:935701-76-1
  • Molecular Formula:C6H15N3
  • Molecular Weight:129.205
  • Hs Code.: Oral, rat LD50: 2140 mg/kg
  • European Community (EC) Number:205-411-0,608-228-8
  • NSC Number:38968
  • UN Number:2815
  • UNII:I86052F9F6
  • DSSTox Substance ID:DTXSID2021997
  • Nikkaji Number:J35.446E
  • Wikipedia:Aminoethylpiperazine
  • Wikidata:Q3887815
  • ChEMBL ID:CHEMBL209790
  • Mol file:140-31-8.mol
N-(2-Aminoethyl)piperazine

Synonyms:1-aminoethylpiperazine;1-MAEP;aminoethylpiperazine;aminoethylpiperazine, monoacetate;monoaminoethylpiperazine

Suppliers and Price of N-(2-Aminoethyl)piperazine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 1-(2-Aminoethyl)piperazine
  • 100g
  • $ 150.00
  • TRC
  • 1-(2-Aminoethyl)piperazine
  • 10g
  • $ 110.00
  • TCI Chemical
  • N-(2-Aminoethyl)piperazine >99.0%(GC)(T)
  • 25mL
  • $ 20.00
  • TCI Chemical
  • N-(2-Aminoethyl)piperazine >99.0%(GC)(T)
  • 500mL
  • $ 48.00
  • Sigma-Aldrich
  • 2-(1-Piperazinyl)ethylamine for synthesis. CAS 140-31-8, pH 12 (100 g/l, H O, 20 °C)., for synthesis
  • 8003610250
  • $ 33.50
  • Sigma-Aldrich
  • 2-(1-Piperazinyl)ethylamine for synthesis
  • 250 mL
  • $ 32.10
  • Sigma-Aldrich
  • 1-(2-Aminoethyl)piperazine 99%
  • 100g
  • $ 23.80
  • Sigma-Aldrich
  • 1-(2-Aminoethyl)piperazine 99%
  • 500g
  • $ 54.90
  • Matrix Scientific
  • 2-(Piperazin-1-yl)ethanamine 95+%
  • 100g
  • $ 101.00
  • Matrix Scientific
  • 2-(Piperazin-1-yl)ethanamine 95+%
  • 10g
  • $ 24.00
Total 86 raw suppliers
Chemical Property of N-(2-Aminoethyl)piperazine Edit
Chemical Property:
  • Appearance/Colour:colorless liquid 
  • Vapor Pressure:0.05 mm Hg ( 20 °C) 
  • Melting Point:-19 °C 
  • Refractive Index:1.5000 
  • Boiling Point:220 °C at 760 mmHg 
  • PKA:10.11±0.10(Predicted) 
  • Flash Point:93.3 °C 
  • PSA:41.29000 
  • Density:0.958 g/cm3 
  • LogP:-0.18270 
  • Storage Temp.:Store below +30°C. 
  • Sensitive.:Air Sensitive 
  • Solubility.:>1000g/l 
  • Water Solubility.:soluble 
  • XLogP3:-1.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:129.126597491
  • Heavy Atom Count:9
  • Complexity:68.7
  • Transport DOT Label:Corrosive Poison
Purity/Quality:

99% *data from raw suppliers

1-(2-Aminoethyl)piperazine *data from reagent suppliers

Safty Information:
  • Pictogram(s): Corrosive
  • Hazard Codes:
  • Statements: 21/22-34-43-52/53 
  • Safety Statements: 26-36/37/39-45-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Nitrogen Compounds -> Piperazines
  • Canonical SMILES:C1CN(CCN1)CCN
  • Uses Used for studying corrosion inhibition 1-(2-Aminoethyl)piperazine is utilized in a variety of reactions for studying corrosion inhibition, biological activity and metal ligand effects on catalysis. It is used for epoxy curing, surface activation, and as an asphalt additive. It is used in lube oil and fuel additives, mineral processing aids, polyamide resins, urethane chemicals, wet strength resins.
Technology Process of N-(2-Aminoethyl)piperazine

There total 37 articles about N-(2-Aminoethyl)piperazine 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:
Guidance literature:
With hydrogen; at 120 ℃; under 150015 Torr; Concentration; Temperature; Pressure;
Guidance literature:
In water; at 300 ℃; for 15h; Product distribution; Mechanism; other polyamines, amino alcohols and amino ethers;
Refernces Edit
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