Aminoethylpiperazine

Aminoethylpiperazine

Names
Preferred IUPAC name 2-(Piperazin-1-yl)ethan-1-amine
Other names 2-(1-Piperazinyl)ethylamine, AEP, N-AEP, N-(2-Aminoethyl)piperazine, 2-Piperazinoethylamine, 1-(2-Aminoethyl)piperazine, 1-Piperazine ethanamine, 1-Aminoethylpiperazine
Identifiers
CAS Number	140-31-8 Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL209790 Y
ChemSpider	8465 Y
ECHA InfoCard	100.004.920
EC Number	205-411-0
PubChem CID	8795
RTECS number	TK8050000
UNII	I86052F9F6
UN number	2815
CompTox Dashboard (EPA)	DTXSID2021997
InChI InChI=1S/C6H15N3/c7-1-4-9-5-2-8-3-6-9/h8H,1-7H2 Y Key: IMUDHTPIFIBORV-UHFFFAOYSA-N Y InChI=1/C6H15N3/c7-1-4-9-5-2-8-3-6-9/h8H,1-7H2 Key: IMUDHTPIFIBORV-UHFFFAOYAV
SMILES NCCN1CCNCC1
Properties
Chemical formula	C6H15N3
Molar mass	129.207 g·mol−1
Appearance	Colourless to yellowish liquid
Density	0.984 g/cm3 at 20 °C
Melting point	−19 °C (−2 °F; 254 K)
Boiling point	222 °C (432 °F; 495 K)
Solubility in water	miscible
Vapor pressure	0.076 mmHg @ 20 °C
Hazards
Main hazards	harmful, corrosive, sensitizing
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H302, H312, H314, H317, H412
Precautionary statements	P260, P261, P264, P270, P272, P273, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P333+P313, P363, P405, P501
NFPA 704 (fire diamond)	2 2 0
Flash point	93 °C (199 °F; 366 K)
Autoignition temperature	315 °C (599 °F; 588 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y  (what is YN ?)
Infobox references

Aminoethylpiperazine is a derivative of piperazine. This ethyleneamine contains three nitrogen atoms; one primary, one secondary and one tertiary. It is a corrosive liquid and can cause second or third degree burns. Aminoethylpiperazine can also cause pulmonary edema as a result of inhalation.

Uses[]

Uses include inhibition of corrosion, epoxy curing, surface activation, and as an asphalt additive. When used as an epoxy resin curing agent, it is usually used in conjunction with other amines as an accelerator as it only has 3 amine hydrogens for cross-linking.

See also[]

• Piperazine

External links[]

• Catalytic method for the conjoint manufacture of N-aminoethylpiperazine
• Safety MSDS Data
• Safety data sheet
• Data sheet

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