471208
Ethylamine solution
66.0-72.0% in H2O
Synonym(s):
Aminoethane, Monoethylamine
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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
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Quality Level
concentration
66.0-72.0% in H2O
density
0.81 g/mL at 20 °C
SMILES string
CCN
InChI
1S/C2H7N/c1-2-3/h2-3H2,1H3
InChI key
QUSNBJAOOMFDIB-UHFFFAOYSA-N
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Application
Ethylamine solution is used in the preparation of N-ethyl triazineepiperazine copolymer (ETPC), as a hydrophobic flame retardant material. It is also used in the modification of poly(tetramethylene oxide)/silica hybrid composites.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
71.6 °F
Flash Point(C)
22 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of N-ethyl triazine-piperazine copolymer and flame retardancy and water resistance of intumescent flame retardant polypropylene.
Yang, Kun et al.
Polymer Degradation and Stability, 98(7), 1397-1406 (2013)
Modification of an inorganic-organic hybrid composite: effect of ethylamine.
Brennan, Anthony B and Miller, Thomas M
Chemistry of Materials, 6(3), 262-267 (1994)
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
Masayasu Taki et al.
Biochemistry, 47(29), 7726-7733 (2008-07-17)
During the catalytic reaction of copper amine oxidase, one of the two prochiral hydrogen atoms at the C1 position of substrate amine is stereoselectively abstracted by a conserved Asp residue serving as a general base. Using stereospecifically deuterium-labeled enantiomers of
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