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About This Item
Linear Formula:
C2H5NH2
CAS Number:
Molecular Weight:
45.08
Beilstein:
505933
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
vapor pressure
10.07 psi ( 20 °C)
19.16 psi ( 55 °C)
Quality Level
form
liquid
concentration
2.0 M in methanol
density
0.81 g/mL at 20 °C
0.783 g/mL at 25 °C
functional group
amine
storage temp.
2-8°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 an alkali. Ethylamine modified vermiculite (Ethyl-VER) was prepared, which was used to remove cesium from aqueous solution. The oxidation of ethylamine on platinum single crystal electrodes in an acidic medium has been studied by cyclic voltammetry (CV) and Fourier transform infrared reflection-absorption spectroscopy (FT-IRRAS).
Application
Ethylamine solution may be employed as reaction medium in the synthesis of large-scale flower-like CuS microspheres.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 1
Target Organs
Eyes,Central nervous system
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
48.2 °F - closed cup
Flash Point(C)
9 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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Oxidation of methylamine and ethylamine on Pt single crystal electrodes in acid medium.
Huerta F, et al.
Journal of Electroanalytical Chemistry, 469(2), 159-169 (1999)
Hang Long et al.
Journal of colloid and interface science, 428, 295-301 (2014-06-10)
Ethylamine modified vermiculite (Ethyl-VER) with high specific surface area and excellent pore structure was prepared to remove cesium from aqueous solution. The physic-chemical properties of the pristine and modified vermiculite were analyzed by X-ray diffraction (XRD), Fourier-transform infrared (FTIR), specific
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)
Câline Christine et al.
Organic & biomolecular chemistry, 10(46), 9183-9190 (2012-10-23)
The synthesis of a phosphonated acyclic bifunctional chelate L* for the labeling of biomaterial is described. L* is based on a pyridine backbone, functionalized in ortho positions by aminomethyl-bis-methylphosphonic acids, and, in the para position, by a side chain containing
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
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