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195804

Sigma-Aldrich

Ethylenediamine dihydrochloride

98%

Synonym(s):

1,2-Diaminoethane dihydrochloride

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About This Item

Linear Formula:
NH2CH2CH2NH2 · 2HCl
CAS Number:
Molecular Weight:
133.02
Beilstein:
3665235
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

solid

mp

>300 °C (lit.)

solubility

water: soluble 100 mg/mL, clear, colorless to very faintly yellow

functional group

amine

SMILES string

Cl[H].Cl[H].NCCN

InChI

1S/C2H8N2.2ClH/c3-1-2-4;;/h1-4H2;2*1H

InChI key

OHHBFEVZJLBKEH-UHFFFAOYSA-N

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Application

Ethylenediamine dihydrochloride was used in modified ethylenediamine condensation method for fluorimetric determination of catecholamines. It was used to investigate the luminescence properties of complexes of EuIII and TbIII with ethylenediamine. It was used in the synthesis of 1,3,5-tris(4,5-dihydro-1H-imidazol-2-yl)benzene.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Self-assembled organogels based on two-component system.
Nam SR, et al.
Tetrahedron, 64(46), 10531-10537 (2008)
Luminescence spectroscopic study of europium (III) and terbium (III) with ethylenediamine in dimethyl sulfoxide.
Wang Z, et al.
J. Chem. Soc., Dalton Trans., 18, 2791-2796 (1993)
Modified ethylenediamine condensation method and its application in the analysis of catecholamines by ion-exchange chromatography.
Seki T.
Journal of Chromatography A, 155(2), 415-420 (1978)
Shinichi Mochizuki et al.
Biochimica et biophysica acta, 1828(2), 412-418 (2012-10-25)
Gene therapy is expected to treat various incurable diseases including viral infections, autoimmune disorders, and cancers. Cationic lipids (CL) have been used as carriers of therapeutic DNAs for gene therapy because they can form a complex with DNA and such
M A Barakat et al.
Journal of environmental management, 117, 50-57 (2013-01-29)
Generation 4 polyamidoamine (PAMAM) dendrimers with ethylenediamine cores (G4-OH) were immobilized on titania (TiO(2)) and examined as novel metal chelation materials. Characterization results indicate both the effective immobilization of dendrimers onto titania and retention of the dendrimer on titania following

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