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Acids peroxymonosulfuric acid

Combustible when exposed to heat, flame, or oxidizers. Potentially explosive reaction with aluminum chloride + nitromethane (at 110°C/100 bar), formaldehyde, peroxydisulfuric acid, peroxymonosulfuric acid, sodium nitrite + heat. Violent reaction with aluminum chloride + nitrobenzene (at... [Pg.1093]

PHENOCHLOR (1336-36-3) see PCBs or polychlorinated biphenyls. PHENOL(108-95-2) CgHjOH Combustible solid, smelt (molten), or liquid [explosion limits in air (% by volume when heated) 3 to 10 flash point 174°F/79°C autoignition tenq) 1319°F/715°C Fire Rating 2]. Violent reaction with butadiene, strong oxidizers. Reacts, possibly violently, with strong acids caustics, aliphatic amines amides, oxidizers, calcium hypochlorite formaldehyde, lead diacetate menthol, y -naphthol, peroxydisulfuric acid peroxymonosulfuric acid potassiiun hydroxide sodium nitrite 1,2,3-trihydroxybenzene. Liquid attacks some... [Pg.844]

Peroxynitrite (ONOO ) is generated intracellularly from NO and superoxide anion. Ketones have been found to catalyse its decomposition via dioxirane intermediates. Decomposition of Caro s acid (peroxymonosulfuric acid, H2SO5) is similarly catalysed. Kinetics of the decomposition catalysed by acetones with strongly electron-withdrawing substituents (e.g. fluoro, 1,1,1-trifluoro and hexafiuoro) show evidence of the involvement of the ketone hydrate (i.e. the 1,1-diol) and its anion. ... [Pg.41]

Sulfuric acid, H2SO4, the most important commercial sulfur compound (see Sulfuric acid and sulfur trioxide), and peroxymonosulfuric acid [7722-86-3] (Caro s acid), H2SO, are discussed elsewhere (see Peroxides and peroxide compounds, inorganic). The lower valent sulfur acids are not stable species at ordinary temperatures. Dithionous acid [15959-26-9] H2S2O4, sulfoxyHc acid [20196-46-7] H2SO2, and thiosulfuric acid [13686-28-7] H2S2O2 are unstable species. A discussion of efforts to isolate and characterize the unstable sulfur acids is given (330). [Pg.148]

Peracids. Peracids are compounds containing the functional group —OOH derived from an organic or inorganic acid functionaHty. Typical stmctures include CH2C(0)OOH derived from acetic acid and H0S(0)200H (peroxymonosulfuric acid) derived from sulfuric acid. Peracids have... [Pg.146]

Peroxymonosulfuric acid (historically known as Caro s acid), H2S05, results when peroxydisulfuric acid reacts with a limited amount of water,... [Pg.542]

Oxone Peroxymonosulfuric acid, monopotassium salt, mixt. with dipotassium sulfate and potassium hydrogen sulfate (9) (37222-66-5)... [Pg.260]

The displacement of alkoxy groups from polynitroarylenes has been used for the indirect synthesis of some highly nitrated polynitroarylenes. Holleman synthesized 2,3,4,6-tetranitrotoluene (57) by treating 3-methoxy-2,4,6-trinitrotoluene (132) with ammonia in methanol, followed by oxidation of the resulting product (56) with peroxymonosulfuric acid. [Pg.171]

Synonyms peroxymonosulfuric acid persulfuric acid sulfomonoperacid... [Pg.197]

The peroxyacids containing —O-OH groups, are formed with all the transition elements in groups 4, 5, 6 of the periodic tabic, with main group elements 4 and 5 as well as elements of atomic numbers from boron to sulfur, inclusive. Representative peroxyacids are peroxymonosulfuric acid,... [Pg.1189]

Oxone Peroxymonosulfuric acid, monopotassium salt, mixt. with dipotassium sulfate and potassium hydrogen sulfate (37222-66-5), 69, 160, 229 Oxonium, trimethyl-, tetrafluoroborate (1-), 65,140 (1-OXO-2-PROPENYL)TRIMETHYLSILANE, 66,14-16,18 3-(1-Oxopropyl)-4-(S)-phenylmethyl-2-oxazolidinone 2-Oxazolidinone, 3-(1-oxopropyl)-4-(phenylmethyl)-, (S)- (101711-78-8), 68, 83 Ozone (10028-15-6), 65, 183... [Pg.155]

See other pages where Acids peroxymonosulfuric acid is mentioned: [Pg.214]    [Pg.566]    [Pg.745]    [Pg.808]    [Pg.844]    [Pg.855]    [Pg.856]    [Pg.261]    [Pg.282]    [Pg.214]    [Pg.566]    [Pg.745]    [Pg.808]    [Pg.844]    [Pg.855]    [Pg.261]    [Pg.282]    [Pg.739]    [Pg.146]    [Pg.289]    [Pg.1629]    [Pg.541]    [Pg.685]    [Pg.150]    [Pg.152]    [Pg.152]    [Pg.1020]    [Pg.1020]    [Pg.739]    [Pg.240]    [Pg.1571]    [Pg.464]    [Pg.1698]    [Pg.1629]   
See also in sourсe #XX -- [ Pg.130 , Pg.133 ]



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Oxone: Peroxymonosulfuric acid, monopotassium salt, mixt. with dipotassium sulfate

Peroxymonosulfuric acid compounds

Peroxymonosulfuric acid oxidant

Peroxymonosulfuric acid preparation

Peroxymonosulfuric acids

Sulfur peroxymonosulfuric acids

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