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301264

Sigma-Aldrich

Ethylamine

97%

Sinónimos:

Aminoethane, Monoethylamine

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About This Item

Fórmula lineal:
C2H5NH2
Número de CAS:
75-04-7
Peso molecular:
45.08
Beilstein:
505933
Número CE:
200-834-7
Número MDL:
MFCD00008160
Código UNSPSC:
12142100
ID de la sustancia en PubChem:
24858175
NACRES:
NA.22

densidad de vapor

1.56 (15 °C, vs air)

Nivel de calidad

200

presión de vapor

874 mmHg ( 20 °C)

Análisis

97%

temp. de autoignición

721 °F

lim. expl.

14 %
3.5-14 %

bp

16.6 °C (lit.)

mp

-81 °C (lit.)

densidad

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

grupo funcional

amine

cadena SMILES

CCN

InChI

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

Clave InChI

QUSNBJAOOMFDIB-UHFFFAOYSA-N

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Descripción general

Ethylamine, also known as ethanamine is commonly employed as a precursor in the synthesis of organic compounds. It is a corrosive primary amine, which is found naturally in many vegetables and fruits. It is also present as a constituent of tobacco smoke. Ethylamine is known to affect the lungs and kidney when a person is exposed to it.

Aplicación

Ethylamine can be used as a reagent:
  • In the hydroamination reaction to prepare ethylamine derivatives by addition reaction with alkynes using the Ind2TiMe2 catalyst.
  • To prepare Schiff base ligands, which are reacted with various metal cations to obtain mono- or binuclear ethylamine metal complexes.
  • To synthesize ethylamine-modified montmorillonite, which is used as a novel material for the removal of radiocesium from radioactive wastewater.

Envase

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:
  • Aldrich® Sure/Pac™ station for liquefied gases Z566446
  • PTFE Sealing tape Z104388 or Z221880
  • Stainless steel hose adapter Z146838
  • Aldrich® mini gas regulator Z513547

Información legal

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

Opcional

Referencia del producto
Descripción
Precios

Palabra de señalización

Danger

Frases de peligro

H220,H280,H319,H332,H335

Clasificaciones de peligro

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

Órganos de actuación

Respiratory system

Código de clase de almacenamiento

2A - Gases

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

-34.6 °F - closed cup

Punto de inflamabilidad (°C)

-37 °C - closed cup

Equipo de protección personal

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)

Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
SHBP0774
SHBN2131
SHBM7554
SHBM6277
SHBM0716

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Visite la Librería de documentos

Ethylamine
Encyclopedia of Toxicology (2014)
Synthesis and Spectroscopic Studies of a Novel Schiff Base Derived from o-Acetoacetylphenol and Ethylamine and Its Metal Complexes
Salib KAR, et al.
Synth. React. Inorg. Met.-Org. Chem. , 33(9), 1667-1687 (2003)
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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