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.)
functional group
amine
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
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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
Konstantina Kyritsi et al.
Hepatology (Baltimore, Md.), 71(3), 990-1008 (2019-07-26)
Serotonin (5HT) is a neuroendocrine hormone synthetized in the central nervous system (CNS) as well as enterochromaffin cells of the gastrointestinal tract. Tryptophan hydroxylase (TPH1) and monoamine oxidase (MAO-A) are the key enzymes for the synthesis and catabolism of 5HT
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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