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Merck

395072

Ethylamine solution

2.0 M in THF

Synonym(s):

Aminoethane, Monoethylamine

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About This Item

Linear Formula:
C2H5NH2
CAS Number:
75-04-7
Molecular Weight:
45.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24864640
MDL number:
MFCD00008160
Beilstein/REAXYS Number:
505933
Concentration:
2.0 M in THF
Form:
liquid

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InChI

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

SMILES string

CCN

InChI key

QUSNBJAOOMFDIB-UHFFFAOYSA-N

vapor pressure

17.14 psi ( 55 °C), 4.82 psi ( 20 °C)

form

liquid

concentration

2.0 M in THF

density

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

functional group

amine

Quality Level

100

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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

EUH019

Storage Class

3 - Flammable liquids

wgk

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ5580
MKCT9434
MKCS3569
MKCK3441
SHBK5624

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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)
A study on the aliphatic energetic plasticizers containing nitrate ester and nitramine
Min BS and Park YC
Journal of Industrial and Engineering Chemistry, 15(4), 595-601 (2009)
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
Riccardo Di Corato et al.
ACS nano, 5(2), 1109-1121 (2011-01-12)
Trifunctional polymer nanobeads are prepared by destabilization of a mixture of magnetic nanoparticles, quantum dots, and an amphiphilic polymer, followed by functionalization of the bead surface with folic acid molecules. The distribution of the nanoparticles within the nanobeads can be
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