473235
N,N-Diethylhydroxylamine solution
85 wt. % in H2O
Synonym(s):
N-Hydroxydiethylamine, DEHA, Diethylhydroxylamine
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About This Item
Linear Formula:
(C2H5)2NOH
CAS Number:
Molecular Weight:
89.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-055-4
MDL number:
InChI key
FVCOIAYSJZGECG-UHFFFAOYSA-N
InChI
1S/C4H11NO/c1-3-5(6)4-2/h6H,3-4H2,1-2H3
SMILES string
CCN(O)CC
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
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.
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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
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
Regulatory Information
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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)
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)
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)
J Heicklen
Annals of the New York Academy of Sciences, 502, 145-159 (1987-01-01)
Photochemical smog is caused by a free-radical chain mechanism which converts NO to NO2. The NO2 further reacts to produce ozone, nitric acid, and peracylnitrates. This chain mechanism can be inhibited by suitable free-radical scavengers. The chemistry and toxicology of
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