4-(2-aminoethyl)-1-Piperazineacetic acid

Base Information

Chemical Name:4-(2-aminoethyl)-1-Piperazineacetic acid
CAS No.:87980-97-0
Molecular Formula:C₈H₁₇N₃O₂
Molecular Weight:187.242
Hs Code.:2933599090
DSSTox Substance ID:DTXSID60475038
Wikidata:Q82305275
Mol file:87980-97-0.mol

Synonyms:87980-97-0;4-(2-aminoethyl)-1-Piperazineacetic acid;2-(4-(2-Aminoethyl)piperazin-1-yl)acetic acid;2-[4-(2-aminoethyl)piperazin-1-yl]acetic Acid;SCHEMBL34418;DTXSID60475038;AKOS012964173;[4-(2-Aminoethyl)piperazin-1-yl]acetic acid

Suppliers and Price of 4-(2-aminoethyl)-1-Piperazineacetic acid

Supply Marketing:

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

AccelPharmtech
4-(2-aminoethyl)-1-Piperazineaceticacid 93.00%
25G
$ 3020.00

AccelPharmtech
4-(2-aminoethyl)-1-Piperazineaceticacid 93.00%
10G
$ 1450.00

AccelPharmtech
4-(2-aminoethyl)-1-Piperazineaceticacid 93.00%
5G
$ 870.00

AccelPharmtech
4-(2-aminoethyl)-1-Piperazineaceticacid 93.00%
1G
$ 330.00

Total 5 raw suppliers

Chemical Property of 4-(2-aminoethyl)-1-Piperazineacetic acid

Chemical Property:

Boiling Point:350.0±32.0 °C(Predicted)
PKA:4.24±0.10(Predicted)
PSA：69.80000
Density:1.155±0.06 g/cm3(Predicted)
LogP:-0.77660
XLogP3:-3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:187.132076794
Heavy Atom Count:13
Complexity:167

Purity/Quality:

95% ^*data from raw suppliers

4-(2-aminoethyl)-1-Piperazineaceticacid 93.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CN(CCN1CCN)CC(=O)O

Technology Process of 4-(2-aminoethyl)-1-Piperazineacetic acid

There total 4 articles about 4-(2-aminoethyl)-1-Piperazineacetic acid 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:

: 127178-04-5
N-carboxymethyl-N'-(β-aminoethyl)piperazine trihydrochloride

: 87980-97-0
N-carboxymethyl-N'-(β-aminoethyl)piperazine

Guidance literature:: With potassium hydroxide; In ethanol; Ambient temperature;

Reference yield:

: 127178-03-4
N-(β-carboxyethyl)-N'-(β-salicylideneaminoethyl)-piperazine

: 87980-97-0
N-carboxymethyl-N'-(β-aminoethyl)piperazine

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / conc. HCl / 90 - 105 °C / pH 1.5

2: KOH / ethanol / Ambient temperature

With hydrogenchloride; potassium hydroxide; In ethanol;

Reference yield:

: 93968-73-1
2-(((2-(piperazin-1-yl)ethyl)imino)methyl)phenol

: 87980-97-0
N-carboxymethyl-N'-(β-aminoethyl)piperazine

Guidance literature:: Multi-step reaction with 3 steps

1: base / 4 h / 50 - 55 °C / pH 9-10

2: 71 percent / conc. HCl / 90 - 105 °C / pH 1.5

3: KOH / ethanol / Ambient temperature

With hydrogenchloride; potassium hydroxide; In ethanol;