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395072

Sigma-Aldrich

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
Beilstein:
505933
MDL number:
MFCD00008160
UNSPSC Code:
12352100
PubChem Substance ID:
24864640
NACRES:
NA.22

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

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.

Signal Word

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

Supplementary Hazards

EUH019

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

-23.8 °F - closed cup

Flash Point(C)

-31 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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