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:
Molecular Weight:
81.54
Beilstein:
3589312
EC Number:
MDL number:
UNSPSC Code:
12352107
PubChem Substance ID:
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Assay
98%
form
solid
mp
107-108 °C (lit.)
SMILES string
Cl[H].CCN
InChI
1S/C2H7N.ClH/c1-2-3;/h2-3H2,1H3;1H
InChI key
XWBDWHCCBGMXKG-UHFFFAOYSA-N
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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 Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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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
Koji Osawa et al.
Structural dynamics (Melville, N.Y.), 6(6), 064703-064703 (2019-12-24)
Deep eutectic solvents (DESs) prepared by mixing hydrogen-bond donor and acceptor molecules have been found to be of use in several applications. Recently, it was shown that DESs can enhance the peroxidation activity of cytochrome c. Here, to elucidate the
Amino-modified cellulose nanocrystals with adjustable hydrophobicity from combined regioselective oxidation and reductive amination
Sirvio J, et al.
Carbohydrate Polymers, 136 (2016)
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
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