Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nitrosophenylhydroxylamine, ammonium

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... [Pg.73]

CupaiitAF. See Mineral oil Cupferron. See Nitrosophenylhydroxylamine ammonium salt... [Pg.1101]

Firstcure NPAL. See Nitrosophenylhydroxylamine aluminum salt Firstcur NPHA. See Nitrosophenylhydroxylamine ammonium salt Firstcure ODAB. See Octyl dimethyl PABA Fir-wood oil. See Pine (Pinus sylvestris) needle oil... [Pg.1823]

Isopropanolamine 2-Mercaptoethanol 1-Methyl-3-phenyl-5-[3-(trifluoromethyl) phenyi]-4(1 H)-pyridinone a-Naphthylamine Nitrosophenylhydroxylamine ammonium salt Phenyl benzoate m-Phenylenedimaleimide N-Phenylmaleimide Phenyl mercuric bromide Potassium carbonate Potassium N-hydroxymethyl-N-methyldithiocarbamate Pyridine Silica, fused Tetrachlorophthalic acid Thiourea p-Toluic acid , N-Tridecyl-2,6-dimethylmorpholine Trimethyl phosphate agric. chemicals, maleic hydrazide Hydrazine agric. sprays Zinc sulfate monohydrate agric., biodegradable Poly (hydroxybutyrate-hydroxyvalerate) agriculture... [Pg.4806]

Mercaptopropionic acid Methylcyclohexanol Methyl ethyl ketoxime N-Nitrosodiethylamine N-Nitrosodimethylamine Nitrosophenylhydroxylamine ammonium salt Oat (Avena sativa) extract Octadecyl 3-mercaptopropionate Octylphenol 4,4(5H)-Oxazoledlmethanol, 2-(heptadecenyl)-Pansy (Viola tricolor) extract Phenyl neopentylene glycol phosphite Sodium citrate Sulfur dioxide a-Terpineol 2,2, 4,4 -Tetrahydroxy, 5,5 -di-t-butylbenzophenone Tetraisopropyl di (dioctylphosphito) titanate Thymol Toluhydroguinone 2,2,4-Trimethyl-1,2-dihydroquinoline Trimethyl quinoline 2,4,6-Tris (dimethylaminomethyl) phenol Ubiquinone Wheat (Triticum vulgare) germ oil Zeaxanthin Zinc dialkyl dithlophosphate antioxidant mfg. [Pg.4834]

Disodium manganous EDTA 5-Dodecyl salicylaldoxime Hexamethylene diamine tetra (methylene phosphonate) Humic acid 2-Hydroxy-5-nonylacetophenone oxime 4,4 -lsopropylidenediphenol alkyl (C12-15) phosphites Laureth-9 phosphate Lauroyl lysine Nitrosophenylhydroxylamine ammonium salt Potassium acid saccharate Sodium acid pyrophosphate Sodium cyanide Sodium N-hydroxyethylglycine Sodium polydimethylglycinophenolsulfonate Sodium sarcosinate... [Pg.4952]

Nitrosophenylhydroxylamine ammonium salt Nonylphenol Nuarimol 2-n-Octyl-4-lsothlazolin-3-one Oleyl hydroxyethyl imidazoline Paraformaldehyde Pentachlorophenol Phenoxyacetic acid Phenylacetic acid Phenylmercuric borate Phenylmercuric nitrate Phenylmercuric oleate p-Phenylphenol Phthalimide... [Pg.5338]

Laurylpyridinium bisulfate Methoxyethanol Myristalkonium chloride Nitrosophenylhydroxylamine ammonium salt PCA ethyl cocoyl arginate Phenylmercuric nitrate Phenylmercuric nitrate, basic Phenylmercuric oleate Silver nitrate Sodium arsenate Sodium hypochlorite Sodium lauroamphoacetate Sodium oleoamphopropionate Stearamine 2,2 -Thiobis (4,6-dichlorophenol) 3,5,5-Trimethylhexan-1-ol germicide (duckweed killer), petroleum Stearamine acetate... [Pg.5349]

Nitrosophenylhydroxylamine ammonium salt C6H9N9O3 Melamine cyanurate C6H9Na04S... [Pg.7042]

The formation of the ammonium salt and the analytical application of nitrosophenylhydroxylamine as a reagent for the determination of iron and copper show that compounds of this kind are acidic. [Pg.177]

Soon after the introduction of dimethylglyoxime as a specific reagent for nickel by Tschugaeff-Kraut-Brunck (1905-1907), Baudisch discovered a compound which precipitates copper and iron quantitatively from acid solutions.82 He appropriately named this reagent as cupferron . It is the water soluble ammonium salt of nitrosophenylhydroxylamine (5). When dissolved in chloroform, the whitish-grey copper compound gives a bright yellow solution and the brown yellow iron(III) compound a deep red solution. This behaviour reveals the inner complex character of these derivatives (6). [Pg.509]

Figure 11.1 presents a scheme for the radioanalytical determination of 55Fe in water, biota, and sediment samples.11 This procedure is based on the separation of Fe from other metals (especially Cd, Cs, Cu, Ni, and Zn) on an anion exchange resin. The iron is then purified by coprecipitation with cupferron (the ammonium salt of nitrosophenylhydroxylamine). [Pg.243]

Cupferron reagent, the ammonium salt of nitrosophenylhydroxylamine, C6H5N(NO)ONH4. reddish-brown precipitate is formed in the presence of hydrochloric acid ... [Pg.247]

NITROSOPHENYLHYDROXYLAMINE see AN0500 AMMONIUM OXALATE see ANO750 AMMONIUM PARAMOLYBDATE see ANM750 AMMONIUM PENTADECAFLUOROOCTANATE see ANP625... [Pg.1512]

TETRACLORURO de ZIRCONIO (Spanish) (10026-11-6) Decomposes in the presence of moist air, forming a dense white cloud and hydrogen chloride fumes may ignite spontaneously. Reacts with water, steam, releasing heat, a dense white cloud, and hydrogen chloride. Violent reaction with bromine pentafluoride, lithium, oxygen difluoride, tetrahydrofuran. Contact with alkali metals may cause explosions. Incompatible with ammonium-V-nitrosophenylhydroxylamine. Attacks many plastics, rubber, and coatings. [Pg.1131]

ZIRCAT (7440-67-7) Finely divided material is spontaneously flammable in air may ignite and continue to bum under water. Violent reactions with oxidizers, alkali hydroxides, alkali metals (and their compounds), carbon tetrachloride, cupric oxide, lead, lead oxide, lead peroxide (combined material can burn explosively, and is sensitive to friction and static electricity), nitryl fluoride, oxygen difluoride, phosphoms, potassium, potassium compounds (potassium chlorate, potassium nitrate), sodium borate, sodium hydroxide. Explodes if mixed with hydrated borax when heated. Contact with lithium chromate may cause explosion above 752°F/450°C. Forms explosive mixture with potassium chlorate. Dusts of zirconium ignite and explode in a carbon dioxide atmosphere. Contact with ammonium-V-nitrosophenylhydroxylamine above 104°F/40°C forms an explosive material. Incompatible with boron, carbon, nitrogen, halogens, lead, platinum, potassium nitrate. In case of fire, use approved Class D extinguishers or smothering quantities of dry sand, crushed limestone, clay. [Pg.1253]


See other pages where Nitrosophenylhydroxylamine, ammonium is mentioned: [Pg.721]    [Pg.1809]    [Pg.163]    [Pg.270]    [Pg.2840]    [Pg.3798]    [Pg.5020]    [Pg.5133]    [Pg.5556]    [Pg.5596]    [Pg.5737]    [Pg.5749]    [Pg.6119]    [Pg.6762]    [Pg.721]    [Pg.1809]    [Pg.163]    [Pg.270]    [Pg.2840]    [Pg.3798]    [Pg.5020]    [Pg.5133]    [Pg.5556]    [Pg.5596]    [Pg.5737]    [Pg.5749]    [Pg.6119]    [Pg.6762]    [Pg.118]    [Pg.440]    [Pg.440]    [Pg.61]    [Pg.92]    [Pg.92]    [Pg.523]    [Pg.61]    [Pg.542]    [Pg.66]    [Pg.416]    [Pg.326]    [Pg.1096]    [Pg.1096]    [Pg.1097]    [Pg.538]   


SEARCH



Nitrosophenylhydroxylamine

© 2024 chempedia.info