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Merck

473235

Sigma-Aldrich

N,N-Diethylhydroxylamine solution

85 wt. % in H2O

Sinónimos:

N-Hydroxydiethylamine, DEHA, Diethylhydroxylamine

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About This Item

Fórmula lineal:
(C2H5)2NOH
Número de CAS:
Peso molecular:
89.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

concentration

85 wt. % in H2O

refractive index

n20/D 1.419

bp

125-130 °C

mp

−25 °C

density

0.902 g/mL at 25 °C

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

General description

The product is 85wt.% solution of N,N-diethylhydroxylamine. The reaction of N,N-diethylhydroxylamine with tert-butylhydroperoxide has been studied. It participates in the preparation of symmetrical and an isomeric mixture of unsymmetrical phthalocyanines. It undergoes degradation on exposure to radiation and affords light hydrocarbons. Qualitative and quantitative analyses of the produced hydrocarbons have been reported. It also participates in the conversion of quinones and quinonemonosulfonimide to the corresponding hydroquinones and sulfonylaminophenols, respectively.

pictograms

FlameExclamation mark

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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Visite la Librería de documentos

Reduction of quinones and quinonemonosulfonimides with N, N-diethylhydroxylamine.
Fujita S and Sano K.
The Journal of Organic Chemistry, 44(15), 2647-2651 (1979)
Novel and Mild Route to Phthalocyanines and 3-Iminoisoindolin-1-ones via N, N-Diethylhydroxylamine-Promoted Conversion of Phthalonitriles and a Dramatic Solvent-Dependence of the Reaction.
Luzyanin KV, et al.
Advanced Synthesis & Catalysis, 350(1), 135-142 (2008)
Oxidation of N, N-dialkyl hydroxylamines with t-butyl hydroperoxide. A new synthesis for nitrones.
Mare HDL and Coppinger GM.
The Journal of Organic Chemistry, 28(4), 1068-1070 (1963)
Qualitative and quantitative analysis of the light hydrocarbons produced by radiation degradation of N, N-diethylhydroxylamine.
Wang J, et al.
J. Radioanal. Nucl. Chem., 262(2), 451-453 (2004)
Chronic inhalation study of mice subjected to diethylhydroxylamine, nitroethane, and diethylamine hydrogen sulfite.
J Heicklen et al.
Environmental research, 27(2), 277-289 (1982-04-01)

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