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Merck

127744

Sigma-Aldrich

Diethylamin -hydrochlorid

ReagentPlus®, 99%

Synonym(e):

Diethylammonium chloride

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About This Item

Lineare Formel:
(C2H5)2NH · HCl
CAS-Nummer:
Molekulargewicht:
109.60
Beilstein:
3590084
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Produktlinie

ReagentPlus®

Assay

99%

Form

solid

mp (Schmelzpunkt)

227-230 °C (lit.)

Löslichkeit

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

InChIKey

HDITUCONWLWUJR-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung

Diethylamine hydrochloride has been used in the synthesis of diethylaminoethyl (DEAE) cottons by reacting it with cotton cellulose in the presence of sodium hydroxide.

Rechtliche Hinweise

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Piktogramme

Skull and crossbonesCorrosion

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - Skin Sens. 1 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

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
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
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

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