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Merck

471593

Sigma-Aldrich

N,N-Diethylhydroxylamin

≥98%

Synonym(e):

N-Hydroxydiethylamine, DEHA, Diethylhydroxylamine

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About This Item

Lineare Formel:
(CH3CH2)2NOH
CAS-Nummer:
Molekulargewicht:
89.14
Beilstein:
1731349
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdichte

3.07 (vs air)

Dampfdruck

4 mmHg ( 0 °C)

Assay

≥98%

Expl.-Gr.

10 %

Brechungsindex

n20/D 1.420 (lit.)

bp

125-130 °C (lit.)

mp (Schmelzpunkt)

−26-−25 °C (lit.)

Dichte

0.867 g/mL at 25 °C (lit.)

SMILES String

CCN(O)CC

InChI

1S/C4H11NO/c1-3-5(6)4-2/h6H,3-4H2,1-2H3

InChIKey

FVCOIAYSJZGECG-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

N,N-Diethylhydroxylamine (diethylhydroxylamine, DEHA, (C2H5)2NOH) is a N,N-dialkylhydroxylamine. Its interaction with the surface of clean silicon(100)-2x1 has been studied by various theoretical and spectroscopic methods. H2O2 along with superoxide and diethylnitroxide radicals have been reported to be formed during the photochemical oxidation of DEHA.

Anwendung

N,N-Diethylhydroxylamine may be employed as a ligand in the preparation of unsymmetric mixed ligand oxadiazoline and/or imine platinum complexes. It may be used in the synthesis of organometallic clusters of mixed hydrazide/hydroxylamide clusters of zinc.

Piktogramme

FlameExclamation mark

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

113.0 °F - closed cup

Flammpunkt (°C)

45 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Hyunsung Mun et al.
Polymers, 11(6) (2019-06-15)
In the tire industry, solution styrene butadiene rubber (SSBR), which can introduce a functional group with good reactivity to silica at chain ends, is used to increase rolling resistance performance by considering fuel economy. However, this is not environmentally friendly
Jamal Lasri et al.
Dalton transactions (Cambridge, England : 2003), (30)(30), 3259-3266 (2007-09-26)
Iminoacylation of acetone oxime Me(2)C[double bond, length as m-dash]NOH upon reaction with trans-[PtCl(2)(NCCH(2)CO(2)Me)(2)] and [2 + 3] cycloaddition of acyclic nitrone (-)O(+)N(Me) = C(H)(C(6)H(4)Me-4) to a nitrile ligand in lead to the formation of mono-imine trans-[PtCl(2)(imine-a)(NCCH(2)CO(2)Me)] [imine-a = NH[double bond
P Bilski et al.
Photochemistry and photobiology, 58(1), 11-18 (1993-07-01)
The photooxidation of N,N-diethylhydroxylamine (DEHA) by Rose Bengal (RB) has been investigated in micellar and nonmicellar aqueous solutions. We measured the quantum yield of oxygen consumption forming H2O2 and monitored two intermediates, the superoxide and diethylnitroxide radicals. When the pH
E Kurisaki et al.
The American journal of forensic medicine and pathology, 12(1), 54-58 (1991-03-01)
A 39-year-old man committed suicide by ingesting a large quantity of SH792. SH792 is a silicone resin precursor used as a hardener for waterproof paints. It is polymerized in water; this process is then followed by the formation of silicone
Gino A DiLabio et al.
Physical chemistry chemical physics : PCCP, 9(13), 1629-1634 (2007-04-13)
Incorporating diversity into structures constructed from the organic modification of silicon surfaces requires the use of molecules that contain multiple substituents of different types. In this work we examine the possible dissociation pathways of diethylhydroxylamine (DEHA, (C(2)H(5))(2)NOH) on the surface

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