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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:
333-18-6
Molecular Weight:
133.02
Beilstein:
3665235
EC Number:
206-369-6
MDL number:
MFCD00012524
UNSPSC Code:
12352100
PubChem Substance ID:
24851714
NACRES:
NA.22

Quality Level

200

Assay

98%

form

solid

mp

>300 °C (lit.)

solubility

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

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

Exclamation markHealth hazard
GHS07,GHS08

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

Certificates of Analysis (COA)

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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)
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)
Self-assembled organogels based on two-component system.
Nam SR, et al.
Tetrahedron, 64(46), 10531-10537 (2008)
Kui Wu et al.
Journal of the American Society for Mass Spectrometry, 24(3), 410-420 (2013-02-14)
We report identification of the binding sites for an organometallic ruthenium anticancer complex [(η (6)-biphenyl)Ru(en)Cl][PF6] (1; en = ethylenediamine) on the 15-mer single-stranded oligodeoxynucleotides (ODNs), 5'-CTCTCTX7G8Y9CTTCTC-3' [X = Y = T (I); X = C and Y = A (II);
Maria V Babak et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(13), 4308-4318 (2013-01-24)
With the aim of systematically studying fundamental structure-activity relationships as a basis for the development of Ru(II) arene complexes (arene = p-cymene or biphenyl) bearing mono-, bi-, or tridentate am(m)ine ligands as anticancer agents, a series of ammine, ethylenediamine, and
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