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Key Documents

127582

Sigma-Aldrich

N-(2-Hydroxyethyl)ethylenediamine

99%

Synonym(s):

2-(2-Aminoethylamino)ethanol, N-(2-Aminoethyl)ethanolamine

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About This Item

Linear Formula:
NH2CH2CH2NHCH2CH2OH
CAS Number:
Molecular Weight:
104.15
Beilstein:
506012
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3.6 (vs air)

Quality Level

Assay

99%

refractive index

n20/D 1.485 (lit.)

bp

238-240 °C/752 mmHg (lit.)

density

1.03 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

NCCNCCO

InChI

1S/C4H12N2O/c5-1-2-6-3-4-7/h6-7H,1-5H2

InChI key

LHIJANUOQQMGNT-UHFFFAOYSA-N

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Application

N-(2-hydroxyethyl)ethylenediamine (hydeten) or [N-(2-aminoethyl)ethanolamine] can be used as:
  • A precursor in the synthesis of room-temperature ionic liquids, acetate and formate ammonium salts of N-(2-hydroxyethyl)-ethylenediamine.
  • A ligand in the preparation of polymeric cyano-bridged platinum(II)complexes, ligand-copper(II)carbohydrate complexes and cyano-bridged Ni-Pt and Cu-Pt coordination polymers.

It can also be used to study the aerobic biodecomposition of amines in hypersaline wastewaters.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

291.2 °F

Flash Point(C)

144 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Investigation of Sugar-Binding Sites in Ternary Ligand- Copper (II)- Carbohydrate Complexes
Striegler S and Tewes E
European Journal of Inorganic Chemistry, 2002(2), 487-495 (2002)
C Foti et al.
Contact dermatitis, 45(3), 129-133 (2001-09-13)
Amphoacetates are organic compounds used in many industrial applications and in cosmetic formulations for the skin, hair and mucosa, as surfactants, mild foaming and cleansing agents in concentrations ranging from 0.1% to 50%. Despite the fact that they have been
Nigel P Moore et al.
Birth defects research. Part B, Developmental and reproductive toxicology, 95(2), 107-115 (2012-03-31)
N-(2-aminoethyl)ethanolamine (AEEA) caused aneurysms of the great vessels in rats exposed in utero and during the first days post partum, exacerbated by postnatal treatment of the lactating dams (Moore et al., 2012). The purpose of this work was to examine
Nigel P Moore et al.
Birth defects research. Part B, Developmental and reproductive toxicology, 95(2), 116-122 (2012-03-27)
N-(2-Aminoethyl)ethanolamine (AEEA) induced malformations of the great vessels in the offspring of rats treated during gestation and early lactation (Schneider et al., 2012. Birth Defects Res B Dev Reprod Toxicol [in press]). The aim of this study was to determine
Pablo Campo et al.
Chemosphere, 85(7), 1199-1203 (2011-09-20)
The treatment of hypersaline wastewaters represents a challenge since high salt concentrations disrupt bacteria present in normal biological treatments. This study was conducted to determine the fate of amines in two hypersaline wastewaters obtained from an industrial treatment plant processing

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