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471593

Sigma-Aldrich

N,N-Diethylhydroxylamine

≥98%

Synonym(s):

N-Hydroxydiethylamine, DEHA, Diethylhydroxylamine

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About This Item

Linear Formula:
(CH3CH2)2NOH
CAS Number:
3710-84-7
Molecular Weight:
89.14
Beilstein/REAXYS Number:
1731349
EC Number:
223-055-4
MDL number:
MFCD00002126
UNSPSC Code:
12352100
PubChem Substance ID:
24870745
NACRES:
NA.22

vapor density

3.07 (vs air)

vapor pressure

4 mmHg ( 0 °C)

assay

≥98%

expl. lim.

10 %

refractive index

n20/D 1.420 (lit.)

bp

125-130 °C (lit.)

mp

−26-−25 °C (lit.)

density

0.867 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCN(O)CC

InChI

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

InChI key

FVCOIAYSJZGECG-UHFFFAOYSA-N

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General description

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.

Application

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.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

113.0 °F - closed cup

flash_point_c

45 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX0793
MKCV6525
MKCR2180
MKCQ0855
MKCL6464

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Surajit Jana et al.
Chemical communications (Cambridge, England), (38)(38), 3993-3995 (2006-09-28)
The first organometallic clusters of mixed hydrazide/hydroxylamide clusters of zinc, [Zn(MeZn)(4)(HNNMe(2))(2)(ONEt(2))(4)] and {Zn(EtZn)(4)[HNN(CH(2))(5)](2)(ONEt(2))(4)} were synthesized in one-pot synthesis protocols from dialkylzinc solutions, substituted hydrazines and N,N-diethylhydroxylamine; competing for the Zn atoms, the different binding properties of hydrazide and hydroxylamide ligands
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
J Heicklen et al.
Drug and chemical toxicology, 7(4), 315-327 (1984-01-01)
Groups of 20 male and 20 female CD-1(ICR)Br mice were treated either with 0, 3, 30, or 300 mg diethylhydroxylamine (DEHA)/kg-day (administered via the drinking water) from 57-112 days of age. For the four week period between 70 to 98
Elisabetta Damiani et al.
Free radical research, 38(1), 67-72 (2004-04-06)
Indolinonic aromatic nitroxides have been shown to efficiently inhibit free radical mediated oxidation reactions in biological systems. Since all antioxidants also possess pro-oxidant activity, possibly through a hydrogen abstraction process from suitable substrates, the relative hydrogen abstraction abilities of these
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