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Sigma-Aldrich

Diethylamine hydrochloride

ReagentPlus®, 99%

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Synonym(s):
Diethylammonium chloride
Linear Formula:
(C2H5)2NH · HCl
CAS Number:
660-68-4
Molecular Weight:
109.60
Beilstein:
3590084
EC Number:
211-541-9
MDL number:
MFCD00012499
PubChem Substance ID:
24847795
NACRES:
NA.22

Quality Level

100

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)

SMILES string

Cl.CCNCC

InChI

1S/C4H11N.ClH/c1-3-5-4-2;/h5H,3-4H2,1-2H3;1H

InChI key

HDITUCONWLWUJR-UHFFFAOYSA-N

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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

Pictograms

CorrosionSkull and crossbones
GHS05,GHS06

Signal Word

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 Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
Jingfeng Chen et al.
Biochimica et biophysica acta, 1807(5), 491-502 (2011-03-17)
Mitochondria-derived oxygen-free radical(s) are important mediators of oxidative cellular injury. It is widely hypothesized that excess NO enhances O(2)(•-) generated by mitochondria under certain pathological conditions. In the mitochondrial electron transport chain, succinate-cytochrome c reductase (SCR) catalyzes the electron transfer
Roberto Cirilli et al.
Analytical chemistry, 81(9), 3560-3570 (2009-03-28)
Second-order rate constants of the diethylamine-promoted enantiomerization of 2-[2-(1-methyl-1H-pyrrol-2-yl)-2-oxo-1-phenylethyl]-isoindole-1,3-dione, a chiral alpha-substituted ketone endowed with high anti-MAO activity type-A, were measured by dynamic high-performance liquid chromatography (DHPLC), stopped-flow high-performance liquid chromatography (sf-HPLC), and a classical method based on enantioselective HPLC
Nathalie Hasler-Nguyen et al.
BMC research notes, 5, 321-321 (2012-06-23)
Rubbing a topical NSAID (non steroidal anti-inflammatory drug) on the skin may increase local drug permeation, affecting its distribution to the site of pain and inflammation. The present study evaluates this hypothesis, by assessing in vitro the effect on skin
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