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301264

Sigma-Aldrich

Ethylamine

97%

Sinonimo/i:

Aminoethane, Monoethylamine

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About This Item

Formula condensata:
C2H5NH2
Numero CAS:
75-04-7
Peso molecolare:
45.08
Beilstein:
505933
Numero CE:
200-834-7
Numero MDL:
MFCD00008160
Codice UNSPSC:
12142100
ID PubChem:
24858175
NACRES:
NA.22

Densità del vapore

1.56 (15 °C, vs air)

Livello qualitativo

200

Tensione di vapore

874 mmHg ( 20 °C)

Saggio

97%

Temp. autoaccensione

721 °F

Limite di esplosione

14 %
3.5-14 %

P. eboll.

16.6 °C (lit.)

Punto di fusione

-81 °C (lit.)

Densità

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

Gruppo funzionale

amine

Stringa SMILE

CCN

InChI

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

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Categorie correlate

Descrizione generale

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.

Applicazioni

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.

Confezionamento

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

Note legali

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

Regolatore

N° Catalogo
Descrizione
Determinazione del prezzo

Avvertenze

Danger

Indicazioni di pericolo

H220,H280,H319,H332,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

2A - Gases

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

-34.6 °F - closed cup

Punto d’infiammabilità (°C)

-37 °C - closed cup

Dispositivi di protezione individuale

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

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Certificati d'analisi (COA)

Lot/Batch Number
SHBP0774
SHBN2131
SHBM7554
SHBM6277
SHBM0716

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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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