127744
Diethylamine hydrochloride
ReagentPlus®, 99%
Synonym(s):
Diethylammonium chloride
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About This Item
Linear Formula:
(C2H5)2NH · HCl
CAS Number:
Molecular Weight:
109.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-541-9
Beilstein/REAXYS Number:
3590084
MDL number:
Assay:
99%
Form:
solid
Quality Segment
product line
ReagentPlus®
assay
99%
form
solid
mp
227-230 °C (lit.)
solubility
H2O: soluble 50 mg/mL, clear, colorless, H2O: soluble, clear, colorless (50 mg/mL)
functional group
amine
SMILES string
Cl.CCNCC
InChI
1S/C4H11N.ClH/c1-3-5-4-2;/h5H,3-4H2,1-2H3;1H
InChI key
HDITUCONWLWUJR-UHFFFAOYSA-N
Application
Diethylamine hydrochloride has been used in the synthesis of diethylaminoethyl (DEAE) cottons by reacting it with cotton cellulose in the presence of sodium hydroxide.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
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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Related Content
Hebeish A and El-Hilw ZH.
Journal of Applied Polymer Science, 67(4) (1998)
Min-Jon Lin et al.
Biochemical and biophysical research communications, 365(4), 724-728 (2007-11-24)
In this study, we investigated the effect of NO donor, diethylamine/nitric oxide (DEA/NO), on the electrophysiological behavior of human skeletal muscle chloride channel (CLCN1). The wild-type and variants of CLCN1, including one polymorphism (P727L) and four mutants (T631I, D644G, G482R
Helmut Görner
The journal of physical chemistry. A, 115(29), 8208-8215 (2011-06-22)
The photoreduction of 6-nitrospiro[2H-1-benzopyran-2,2'-indoline] (N1) and two derivatives (N2 and N3) by diethylamine or triethylamine (TEA) in solution was studied by pulsed and steady-state photolysis. The quantum yield of coloration of the ring-closed Sp form, due to photoinduced ring opening