15068
Ethylenediamine solution
technical, 75-80%
Synonym(s):
1,2-Diaminoethane
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About This Item
Linear Formula:
NH2CH2CH2NH2
CAS Number:
Molecular Weight:
60.10
Beilstein:
4123523
MDL number:
UNSPSC Code:
12352100
eCl@ss:
39030201
PubChem Substance ID:
NACRES:
NA.21
Recommended Products
grade
technical
Assay
75-80%
form
liquid
SMILES string
NCCN
InChI
1S/C2H8N2/c3-1-2-4/h1-4H2
InChI key
PIICEJLVQHRZGT-UHFFFAOYSA-N
Gene Information
human ... FNTA(2339)
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General description
Ethylenediamine solution is a valuable reagent that can be used in a variety of organic synthesis reactions. It is a versatile solvent, a strong nucleophile, and a catalyst. It is also used as a chelating agent to bind metal ions in solution. This can be useful for a variety of applications, including metal recovery, wastewater treatment, and analytical chemistry.
Application
Ethylenediamine solution can be used as a building block for the synthesis of multi-amine dendritic poly(amidoamine) macromolecules. It is also used as a functionalization agent in cubic ZIF-8 metal-organic framework synthesis. Additionally, ethylenediamine is used for amide functionalization of MWNT/nylon 6, 6 composite nanofibers fabrication.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
93.2 °F - closed cup
Flash Point(C)
34 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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J Zuidema
Pharmaceutisch weekblad. Scientific edition, 7(4), 134-140 (1985-08-23)
Ethylenediamine is an excipient with many industrial and pharmaceutical uses. It is included in creams as a stabilizer and in aminophylline as the counter ion of theophylline. Ethylenediamine is one of the most frequent contact sensitizers, producing local and generalized
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
Ana Carolina M S Dias et al.
Biosensors & bioelectronics, 44, 216-221 (2013-02-23)
An immunosensor for the non-structural protein 1 (NS1) of the dengue virus based on carbon nanotube-screen printed electrodes (CNT-SPE) was successfully developed. A homogeneous mixture containing carboxylated carbon nanotubes was dispersed in carbon ink to prepare a screen printed working
Kavita Sablok et al.
Journal of hazardous materials, 248-249, 322-328 (2013-02-19)
Binding of electron-deficient trinitrotoluene (TNT) to the electron rich amine groups on a substrate form specific charge-transfer Jackson-Meisenheimer (JM) complex. In the present work, we report formation of specific JM complex on amine functionalized reduced graphene oxide/carbon nanotubes- (a-rGO/CNT) nanocomposite
Changhai Xu et al.
Carbohydrate polymers, 92(1), 249-253 (2012-12-12)
There exists a misunderstanding on the TAED-activated peroxide system in the textile industry that H(2)O(2) used in excess of the stoichiometric amount could produce an addition effect on bleaching of cotton under alkaline conditions. In this study, a critical reinvestigation
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