127744
二乙胺 盐酸盐
ReagentPlus®, 99%
别名:
Diethylammonium chloride
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关于此项目
线性分子式:
(C2H5)2NH · HCl
化学文摘社编号:
分子量:
109.60
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-541-9
Beilstein/REAXYS Number:
3590084
MDL number:
产品名称
二乙胺 盐酸盐, ReagentPlus®, 99%
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
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Application
在氢氧化钠存在下，盐酸二乙胺与棉纤维反应，用于合成二乙基氨基乙基 (DEAE) 棉 。
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
存储类别
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
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
National Toxicology Program technical report series, (566)(566), 1-174 (2011-12-01)
Diethylamine is used mainly as a chemical intermediate to produce the corrosion inhibitor N,N-diethylethanolamine and a lesser amount is used to produce pesticides and insect repellants and in rubber processing. Diethylamine was nominated for study by the National Institute of
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
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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