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724033

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
UNSPSC Code:
12142100
NACRES:
NA.22
PubChem Substance ID:
329764053
EC Number:
200-834-7
Beilstein/REAXYS Number:
505933
MDL number:
MFCD00008160
Assay:
99.0%
Form:
gas
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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

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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Danger

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

2A - Gases

wgk

WGK 1

flash_point_f

-34.6 °F - closed cup

flash_point_c

-37 °C - closed cup

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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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