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471208

Sigma-Aldrich

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

Quality Level

concentration

66.0-72.0% in H2O

density

0.81 g/mL at 20 °C

functional group

amine

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

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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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)
Synthesis of N-ethyl triazine-piperazine copolymer and flame retardancy and water resistance of intumescent flame retardant polypropylene.
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Paige E Mahaney et al.
Journal of medicinal chemistry, 51(13), 4038-4049 (2008-06-19)
Further exploration of the cycloalkanol ethylamine scaffold, of which venlafaxine ( 1) is a member, was undertaken to develop novel and selective norepinephrine reuptake inhibitors (NRIs) for evaluation in a variety of predictive animal models. These efforts led to the
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Surface functionalization of semiconductors has been the backbone of the newest developments in microelectronics, energy conversion, sensing device design, and many other fields of science and technology. Over a decade ago, the notion of viewing the surface itself as a
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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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