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Merck

395072

Sigma-Aldrich

Ethylamine solution

2.0 M in THF

Sinónimos:

Aminoethane, Monoethylamine

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About This Item

Fórmula lineal:
C2H5NH2
Número de CAS:
Peso molecular:
45.08
Beilstein/REAXYS Number:
505933
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

17.14 psi ( 55 °C)
4.82 psi ( 20 °C)

Quality Level

form

liquid

concentration

2.0 M in THF

density

0.81 g/mL at 20 °C
0.856 g/mL at 25 °C

SMILES string

CCN

InChI

1S/C2H7N/c1-2-3/h2-3H2,1H3

InChI key

QUSNBJAOOMFDIB-UHFFFAOYSA-N

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General description

Ethylamine is a simple aliphatic primary amine used as a chemical intermediate in organic synthesis.

Application

Ethylamine solution (2.0 M in THF) can be used as a reagent:     
  • In amination reactions.      
  • To synthesize N-ethyl-4-hydroxybutanamide by reacting with γ-butyrolactone.      
  • To prepare an anthracene-based tripodal chemosensor for the selective detection of Zn(II) ions.

Ethylamine solution can also be used as a reaction medium in the synthesis of large-scale flower-like CuS microspheres using Cu(S2CNEt2)2 as a precursor.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

target_organs

Central nervous system, Respiratory system

supp_hazards

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

-23.8 °F - closed cup

flash_point_c

-31 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves


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Selective sensing of Zn (II) ion by a simple anthracene-based tripodal chemosensor
Ghosh K and Saha I
Tetrahedron Letters, 51(38), 4995-4999 (2010)
Self-assembly of CuS nanoflakes into flower-like microspheres: synthesis and characterization.
Shen X-P, et al.
Journal of Physics and Chemistry of Solids, 70(2), 422-427 (2009)
Seán D McDermott et al.
Forensic science international, 212(1-3), 13-21 (2011-07-22)
During the analysis of "seized samples", suspected of containing 4-methylmethcathinone (mephedrone) and N-ethylcathinone (ethcathinone) additional compounds were observed in the GCMS chromatogram. These compounds were suspected to be the corresponding phenylacetone isomers of mephedrone and ethcathinone respectively. These isomers are
Aurore Thibon et al.
Dalton transactions (Cambridge, England : 2003), (43)(43), 9587-9594 (2009-10-28)
The new ligand L(6)(2)4E (N,N,N',N'-tetrakis(5-ethyl-2-pyridylmethyl)ethane-1,2-diamine) was designed as a more robust analog of TPEN (N,N,N',N'-tetrakis(2-pyridylmethyl)ethane-1,2-diamine) for which the ability at stabilizing high valent Fe-Oxo and Fe-(hydro)peroxo has been reported. With respect to the latter, the pyridyl beta-substituents in L(6)(2)4E do
Steven J Enoch et al.
Chemical research in toxicology, 22(8), 1447-1453 (2009-07-21)
Certain types of low molecular weight chemicals have the ability to cause respiratory sensitization via haptenation of carrier proteins. It has been suggested that such chemicals must contain multiple "reactive" functional groups to elicit an immune response. In contrast to

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