Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
C2H5NH2
CAS Number:
Molecular Weight:
45.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
505933
Concentration:
2.0 M in THF
Form:
liquid
Quality Level
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
SMILES string
CCN
InChI
1S/C2H7N/c1-2-3/h2-3H2,1H3
InChI key
QUSNBJAOOMFDIB-UHFFFAOYSA-N
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:
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.
- 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.
Still not finding the right product?
Explore all of our products under Ethylamine solution
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
WGK 1
flash_point_f
-23.8 °F - closed cup
flash_point_c
-31 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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



