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232831

Ethylamine hydrochloride

98%

Synonym(s):

N-Ethylammonium chloride, Ethylammonium chloride, Monoethylammonium chloride

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About This Item

Linear Formula:
C2H5NH2 · HCl
CAS Number:
557-66-4
Molecular Weight:
81.54
EC Number:
209-182-8
UNSPSC Code:
12352107
PubChem Substance ID:
24853934
Beilstein/REAXYS Number:
3589312
MDL number:
MFCD00012885
Assay:
98%
Form:
solid
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assay

98%

form

solid

mp

107-108 °C (lit.)

functional group

amine

SMILES string

Cl[H].CCN

InChI

1S/C2H7N.ClH/c1-2-3;/h2-3H2,1H3;1H

InChI key

XWBDWHCCBGMXKG-UHFFFAOYSA-N

Application

Ethylamine hydrochloride can be used as a reactant to synthesize:
  • Amino cellulose via reductive amination.
  • N-triethylborazine by reacting with metal tetrahydroborates.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK8019
STBK3422
STBK2199
STBJ8647
STBJ4971

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Abu Bin Ihsan et al.
International journal of molecular sciences, 20(18) (2019-09-20)
A series of N-substituted poly(Gly-alter-Val) peptides were successfully synthesized for the systematic evaluation of the micellization behavior of alternating peptides. Three-component polymerization employing an aldehyde, a primary ammonium chloride, and potassium isocyanoacetate afforded four alternating peptides in excellent yields. We
Mechanochemical synthesis of N-triethylborazine
Myakishev k, et al.
Russian Journal of Inorganic Chemistry, 54, 219-222 (2009)
Ae Ran Lim
Molecules (Basel, Switzerland), 25(8) (2020-04-25)
The thermal, physical, and molecular dynamics of layered hybrid type (C2H5NH3)2MCl4 (M = 59Co, 63Cu, 65Zn, and 113Cd) crystals were investigated by thermogravimetric analysis (TGA) and magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy. The temperatures of the onset
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Global Trade Item Number

SKUGTIN
232831-100G04061833545485