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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:
75-04-7
Molecular Weight:
45.08
Beilstein:
505933
MDL number:
MFCD00008160
UNSPSC Code:
12352100
PubChem Substance ID:
24870703
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

200

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.[1] It is also used in the modification of poly(tetramethylene oxide)/silica hybrid composites.[2]

Signal Word

Danger

Hazard Statements

H225,H302,H311,H314,H335

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCL4938
MKCV5670
BCCL6686
BCCK8000
BCCL2680

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Synthesis of N-ethyl triazine-piperazine copolymer and flame retardancy and water resistance of intumescent flame retardant polypropylene.
Yang, Kun et al.
Polymer Degradation and Stability, 98(7), 1397-1406 (2013)
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)
Song Yang et al.
Journal of chromatography. A, 1216(15), 3280-3289 (2009-03-10)
Complementary methods using liquid chromatography-tandem quadrupole mass spectrometry (LC-MS/MS) and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry (GCxGC-TOF-MS) were developed and applied to determine targeted metabolites involved in central carbon metabolism [including tricarboxylic acid cycle, serine cycle, ethylmalonyl-coenzyme A (ethylmalonyl-CoA) pathway
Tracy A LeGreve et al.
The journal of physical chemistry. A, 113(2), 399-410 (2008-12-23)
Neutral serotonin-(H(2)O)(n) clusters with n = 1,2 have been studied under jet-cooled conditions using a combination of resonant two-photon ionization (R2PI), UV-UV hole-burning (UVHB), and resonant ion-dip infrared (RIDIR) spectroscopy. Serotonin (5-hydroxytryptamine, SERO) is a close analogue of tryptamine, differing
Yuying Shuai et al.
Journal of the science of food and agriculture, 90(15), 2563-2567 (2010-08-26)
Theanine, a unique amino acid found almost exclusively in tea plants, has various favourable physiological and pharmacological functions in humans. Gamma-glutamyltranspeptidase (GGT, EC 2.3.2.2) is considered to be the most effective enzyme for the production of theanine. In fact, GGT
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