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Sigma-Aldrich E26266 Ethylenediamine ReagentPlus®, ≥99% 500 mL

Stok Kodu
LB.SA.E26266-500ML
Kısa Bilgi
Synonym(s): 1,2-Diaminoethane Linear Formula: NH2CH2CH2NH2 CAS Number: 107-15-3 Molecular Weight: 60.10 Beilstein: 605263 EC Number: 203-468-6 MDL number: MFCD00008204 eCl@ss: 39030201 PubChem Substance ID: 24894477 NACRES: NA.21
Ön Siparişli Ürün
Sigma-Aldrich E26266 Ethylenediamine ReagentPlus®, ≥99% 500 mL
Synonym(s): 1,2-Diaminoethane
Linear Formula:
NH2CH2CH2NH2
CAS Number:
107-15-3
Molecular Weight:
60.10
Beilstein:
605263
EC Number:
203-468-6
MDL number:
MFCD00008204
eCl@ss:
39030201
PubChem Substance ID:
24894477
NACRES:
NA.21
Sigma-Aldrich E26266 Ethylenediamine ReagentPlus®, ≥99%%  
PROPERTIES
vapor density 2.07 (vs air)
Quality Level
200
vapor pressure
10 mmHg ( 20 °C)
product line
ReagentPlus®
Assay
≥99%
form
liquid
autoignition temp.
716 °F
expl. lim.
16 %
refractive index
n20/D 1.4565 (lit.)
bp
118 °C (lit.)
mp
8.5 °C (lit.)
solubility
H2O: soluble at
density
0.899 g/mL at 25 °C (lit.)
SMILES string
NCCN
InChI
1S/C2H8N2/c3-1-2-4/h1-4H2
InChI key
PIICEJLVQHRZGT-UHFFFAOYSA-N
Gene Information
human ... FNTA(2339)
 
DESCRIPTION
General description
Ethylenediamine (en) is a linear aliphatic diamine that can be synthesized by reacting ethanolamine and ammonia in the presence of zeolite catalyst.[1] Its effect as an allergen has been investigated.[2] It participates in the synthesis of metal chalcogenides[3] and thiogallates.[4]
Application
Ethylenediamine (1,2-Diaminoethane, DAE) can be used as a reagent to prepare various metal ion complexes. For instance, DAE reacts with chromium(II) salts forms a Cr(II)/DAE complex, which is used as an efficient reducing agent for the reduction of primary alkyl halides to alkanes, and aryl bromides or iodides to arenes. This complex is also used to reduce β-substituted alkyl halides and epoxides to alkenes.[5] DAE can also be used in the following reduction reactions:
DAE/Borane (1:1) complex is used as a highly selective reducing agent for the conversion of cinnamaldehyde to cinnamyl alcohol.[5]
DAE/Li complex is used as an efficient reagent for the reduction of alkenes, aromatic hydrocarbons, phenols, and alcohols.[5]
Ethylenediamine (en) has been used in the following process:
Synthesis of nucleus pulposus (NP)-like collagen-glycosaminoglycans (CG) core.[6]
Surface modification of epoxy-activated cryogel.[7]
Alteration of the surface of carbon nanoparticles (CNPs) to generate CNPs-ethylene.[8]
It may be used in the following studies:
Surface modification of triazolate-bridged metal-organic framework.[9]
As a solvent in the synthesis of ZnS (zinc sulfide) and ZnSe (zinc selenium) precursors by solvothermal process.[10]
As a reactant in the synthesis of Pd/C-ethylenediamine complex catalyst.[11]
As a chelating agent in the synthesis of β-Co(OH)2 nanocrystals.[12]
Synthesis of ethylenediamine-templated iron arsenates and fluoroarsenates.[13]
As a template agent and coordination agent in the synthesis of CdS (cadmium sulfide) nanocrystals.[14]
Legal Information
ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC
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Sigma-Aldrich E26266 Ethylenediamine ReagentPlus®, ≥99%
Sigma-Aldrich E26266 Ethylenediamine ReagentPlus®, ≥99% 500 mL Linear Formula: NH2CH2CH2NH2, CAS Number: 107-15-3, Molecular Weight: 60.10, Beilstein: 605263, EC Number: 203-468-6, MDL number: MFCD00008204 LB.SA.E26266-500ML
Sigma-Aldrich E26266 Ethylenediamine ReagentPlus®, ≥99% 500 mL

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