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Merck
CN

471208

Ethylamine solution

66.0-72.0% in H2O

Synonym(s):

Aminoethane, Monoethylamine

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About This Item

Linear Formula:
C2H5NH2
CAS Number:
Molecular Weight:
45.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
505933
Concentration:
66.0-72.0% in H2O
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Product Name

Ethylamine solution, 66.0-72.0% in H2O

InChI

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

SMILES string

CCN

InChI key

QUSNBJAOOMFDIB-UHFFFAOYSA-N

concentration

66.0-72.0% in H2O

density

0.81 g/mL at 20 °C

functional group

amine

Quality Level

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Application

Ethylamine solution is used in the preparation of N-ethyl triazineepiperazine copolymer (ETPC), as a hydrophobic flame retardant material. It is also used in the modification of poly(tetramethylene oxide)/silica hybrid composites.

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Danger

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

3 - Flammable liquids

wgk

WGK 1

flash_point_f

71.6 °F

flash_point_c

22 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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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)
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
Câline Christine et al.
Organic & biomolecular chemistry, 10(46), 9183-9190 (2012-10-23)
The synthesis of a phosphonated acyclic bifunctional chelate L* for the labeling of biomaterial is described. L* is based on a pyridine backbone, functionalized in ortho positions by aminomethyl-bis-methylphosphonic acids, and, in the para position, by a side chain containing
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

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