N-Nitrosophenylhydroxylamine

Monomers like N-methylol acrylamide or N-methylol methacrylamide [1081] also have been suggested. Inhibitors can be phenol derivatives [1079] such as N-nitrosophenylhydroxylamine salt [1179]. 

Different from the metallic nanoparticles, iron-oxide nanoparticles are chemically much more stable and readily synthesized. They can be prepared via high-temperature organic-phase decomposition of FeCup3, where Cup represents N-nitrosophenylhydroxylamine, C6H5N(N0)0 [30], decomposition ofFe(CO)s followed by oxidation [31-33], and decomposition of iron carboxylate [34, 35]. They can also be synthesized from partial reduce-tion/decomposition of Fe(acac)3 or Fe(acac)3 and M(acac)2 [36-38]. 

SYNS CUPFERRON N-HYDROXY-N-NITROSO-BENZENAMINE, AMMONIUM SALT KUPFERRON (CZECH) NCI-C03258 N-NITROSOFENYL-HYDROXYLAMIN AMONNY (CZECH) N-NITROSOPHENYLHYDROXYLAMIN AMMONIUM SALZ (GERMAN) N-NITROSOPHENYLHYDRO-XYLAMINE AMMONIUM SALT... 

Q-1300,-1301. [WakoChem.USA] N-Nitrosophenylhydroxylamine salts analytical reagents, radical polymerization inhibitor, chelating agent, antioxidant, r ric. chemicals, germicides, fungicides. 

N-Nitrosophenylhydroxylamine, ammonium salt. See Nitrosophenylhydroxylamine ammonium salt... 

N-nitrosophenylhydroxylamine or cupferron has been used as a precipitating agent for many metal ions for many years, and the solubility of these complexes, in non-polar solvents such as chloroform was recognized at an early date. The extraction reaction is analogous to Eq. 1, although little quantitative work has been done on 138... 

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