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724033

Sigma-Aldrich

Ethylamine

99.0%

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
EC Number:
200-834-7
MDL number:
MFCD00008160
UNSPSC Code:
12142100
PubChem Substance ID:
329764053
NACRES:
NA.22

vapor density

1.56 (15 °C, vs air)

Quality Level

100

vapor pressure

874 mmHg ( 20 °C)

Assay

99.0%

form

gas

autoignition temp.

721 °F

expl. lim.

14 %
3.5-14 %

bp

16.6 °C (lit.)

mp

-81 °C (lit.)

density

0.680 g/mL at 20 °C (lit.)
0.689 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCN

InChI

1S/C2H7N/c1-2-3/h2-3H2,1H3

InChI key

QUSNBJAOOMFDIB-UHFFFAOYSA-N

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Packaging

Supplied in a Sure/Pac™ cylinder and has a 316 stainless steel needle valve with a male 1/4" NPTF outlet thread installed . Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.

Compatible with the following:

Legal Information

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC

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Signal Word

Danger

Hazard Statements

H220,H280,H319,H332,H335

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Gas 1 - Press. Gas Liquefied gas - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

2A - Gases

WGK

WGK 1

Flash Point(F)

-34.6 °F - closed cup

Flash Point(C)

-37 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
SHBQ6123
SHBN0143
SHBK7179
SHBK6599
SHBK6300

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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
Stacey F Bent et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(3), 956-960 (2010-11-12)
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
Riccardo Di Corato et al.
ACS nano, 5(2), 1109-1121 (2011-01-12)
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
Veronica Sandgren et al.
Bioorganic & medicinal chemistry, 20(14), 4377-4389 (2012-06-16)
A series of P1-P3 linked macrocyclic BACE-1 inhibitors containing a hydroxyethylamine (HEA) isostere scaffold has been synthesized. All inhibitors comprise a toluene or N-phenylmethanesulfonamide P2 moiety. Excellent BACE-1 potencies, both in enzymatic and cell-based assays, were observed in this series
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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