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Merck

127744

Diethylamine hydrochloride

ReagentPlus®, 99%

Synonym(s):

Diethylammonium chloride

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About This Item

Linear Formula:
(C2H5)2NH · HCl
CAS Number:
660-68-4
Molecular Weight:
109.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847795
EC Number:
211-541-9
Beilstein/REAXYS Number:
3590084
MDL number:
MFCD00012499
Assay:
99%
Form:
solid

Key Documents

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InChI key

HDITUCONWLWUJR-UHFFFAOYSA-N

InChI

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

SMILES string

Cl.CCNCC

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

Quality Level

100

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Related Categories

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

Skull and crossbonesCorrosion
GHS06,GHS05

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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Certificates of Analysis (COA)

Lot/Batch Number
STBK5969
STBK4186
STBK2534
MKCK0327
STBJ1292

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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
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
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
Chunhe Yao et al.
Journal of separation science, 33(4-5), 475-483 (2010-01-12)
A novel kind of poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate)-based monolithic column was developed for LC by directing supramolecular self-assembly of high internal phase emulsion. Mercury intrusion porosimetry characterization and scanning electron microscope pictures showed that these monoliths presented micrometer-sized throughpores, unique
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