3710-84-7 Usage
Description
N,N-Diethylhydroxylamine is a colorless and transparent liquid with a
boiling point of 125-130 °C and an ammonia odor. It is easily soluble in
water, soluble in ethanol, ether, chloroform and benzene.
Chemical Properties
liquid
Uses
Different sources of media describe the Uses of 3710-84-7 differently. You can refer to the following data:
1. N,N-Diethylhydroxylamine has the following various uses:1.As a vinyl monomer, used in efficient inhibitor agent of conjugate olefins. 2.In liquid or gas phase, if end gather seed is existed,it can be used as inhibitors of end gather. 3.It's a excellent end agent in process of Emulsion-polymerized styrene butadiene rubber. 4.It's a antioxidants of the unsaturated oil and resin. 5.In the environmental protection,it’s good photochemical smoke inhibitors. 6.It's used as corrosion inhibitors in the equipment of the boiler feed water and steam heat exchange. 7.It's used as antioxidant in photography screens potions.
2. Diethylhydroxylamine has been suggested as a stabilizer for color forma-tion for monoalkylphenols and phenolic antioxidants. It has also been reported to stabilize emulsions used in the latex industry and for Spandex rubber, as well as a reducing agent for quinones and a monomer stabilizer or inhibitor.
3. 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.
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.
Health effects
The effects of diethylhydroxylamine (DEHA), a potent free-radical scavenger, on lipid peroxidation of rat liver microsomes were investigated in vitro. DEHA strongly inhibited ascorbate-dependent nonenzymatic microsomal lipid peroxidation. It also completely inhibited nonenzymatic lipid peroxidation of heat-denatured microsomes, indicating that inhibition is protein-independent. DEHA only moderately inhibited NADPH-dependent enzymatic microsomal lipid peroxidation.
Safety Profile
Poison by skin contact.
Moderately toxic by ingestion and
intraperitoneal routes. Experimental
reproductive effects. Human mutation data
reported. When heated to decomposition it
emits toxic fumes of NOx. See also
AMINES.
Check Digit Verification of cas no
The CAS Registry Mumber 3710-84-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3710-84:
(6*3)+(5*7)+(4*1)+(3*0)+(2*8)+(1*4)=77
77 % 10 = 7
So 3710-84-7 is a valid CAS Registry Number.
InChI:InChI=1/C4H11NO.C2H2O4/c1-3-5(6)4-2;3-1(4)2(5)6/h6H,3-4H2,1-2H3;(H,3,4)(H,5,6)
3710-84-7Relevant articles and documents
Regio- and Enantioselective Formal Hydroamination of Enamines for the Synthesis of 1,2-Diamines
Yu, Lu,Somfai, Peter
supporting information, p. 8551 - 8555 (2019/05/21)
The asymmetric formal hydroamination of enamines using a CuH catalyst is reported. The method provides a straightforward and efficient approach to the synthesis of chiral 1,2-dialkyl amines in good yields with high levels of enantioselectivities for a broad range of substrates, and should have significant value for the preparation of molecules bearing a 1,2-diamine motif.
Selective Oxidation of Secondary Amines to N,N-Disubstituted Hydroxylamines by Choline Peroxydisulfate
Banan, Alireza,Valizadeh, Hassan,Heydari, Akbar,Moghimi, Abolghasem
, p. 2315 - 2319 (2017/10/06)
N,N-Disubstituted hydroxylamines were prepared directly from secondary amines by a reliable method using an oxidizing task-specific ionic liquid, choline peroxydisulfate. The operational simplicity, high selectivity, and green reaction conditions, make this method efficient and practical.
Catalytic method for preparing symmetrical and nonsymmetrical dialkylhydroxylamines
-
, (2008/06/13)
A process of forming N,N-dialkylhydroxylamines (a class of compounds useful as oxygen scavengers in boiler water feed) by contacting an N-alkylhydroxylamine with an alkyl carbonyl compound to form a nitrone in situ or, alternatively, using previously formed alkylnitrone which is subjected to H2 and a hydrogenation catalyst.