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Ammonium salicylate

AMMO 2.5 EC , cypermetlu-in, 13 Ammonia, 13 Ammonium acetate, 13 Ammonium arsenate, 13 Ammonium benzoate, 13 Ammonium bicarbonate, 13 Ammonium bifluoride, 14 Ammonium bisulfite, 14 Ammonium carbamate, 14 Ammonium carbonate, 14 Ammonium chloride, 14 Ammonium chlorplatmate, 14 Ammonium clu omate, 14 Ammonium citrate, 14 Ammonium diclu omate, 14 Ammonium fluoride, 14 Ammonium fomiate, 15 Ammonium hexafluorosilicate, 15 Ammonium hydroxide, 15 Ammonium metavanadate, 15 Ammonium molybdate, 15 Ammonium nitrate, 15 Ammonium oxalate, 15 Ammonium perfluorooctanoate, 15 Ammonium persulfate, 15 Ammonium phosphate, 15 Ammonium picrate, 16 Ammonium salicylate, 16... [Pg.321]

Ammonium acetate Ammonium adipate Ammonium benzoate Ammonium bicarbonate Ammonium biflluoride Ammonium binoxalate Ammonium bisulfate Ammonium bitartrate Ammonium tetraborate Ammonium bromide Ammonium carbonate Ammonium chloride Ammonium citrate Ammonium diclnomate Ammonium fluoride Ammonium fluorosilicate Ammonium gluconate Ammonium iodide Ammonium molybdate Ammonium nitrate Ammonium oxalate Ammonium perchlorate Ammonium picrate Ammonium polysulfide Ammonium salicylate Ammonium stearate Ammonium sulfate Ammonium sulfide (hydrosulfide) Ammonium tartrate Ammonium tliiocyanate Ammonium thiosulfate... [Pg.262]

Many of these salts melt or sublime before or during decomposition and reaction temperatures generally increase with molar mass. Thermal analyses for a selection of ammonium carboxylates have been given by Erdey et al. [915] who conclude that the base strength of the anion increases with temperature until it reaches that of NH3. Decompositions of ammonium acetate (>333 K) and ammonium oxalate (>473 K) proceed through amide formation. Ammonium benzoate and ammonium salicylate sublime (>373 K) without decomposition but ammonium citrate decomposes (>423 K) to yield some residual carbon. [Pg.203]

Salicylate Ammonium salicylate NH4C7H5O3, white solid, soluble, formed by reaction of NH4OH and salicylic acid, and then evaporating. [Pg.86]

As in the case of the concentration dependence of the chemical shift, the H and 13C band shapes of the surfactant resonance peaks are also concentration dependent. Analysis of H NMR band shapes for large aggregates of a cetyl trimethyl ammonium bromide-water system results in a CMC of 1.0 mM this is consistent with the value measured by other methods.57 The H NMR bands of alkyl trimethyl ammonium salicylate and hexadecyl pyridinium salicylate aqueous systems start to broaden at concentrations just above the CMC. The broadening continues up to a concentration above which the band shape is almost constant, as the concentration is further increased.-58 I3C NMR linewidth analysis of sodium octanoate in aqueous solution gives reasonable estimated CMC values.59... [Pg.150]

Ammonium salicylate NH3C,H303 628-94-9 166.161 wh cry powder vs H,0 s FtOH... [Pg.697]

The effect of cis versus trans configuration of oleyl (cis) and elaidyl (trans) trimethyl ammonium salicylate systems was studied by Qi and Zakin [2002]. Little difference in the temperature ranges for effective DR were found at = 1.0 and 1.5. However, the kinked chain of the cis (oleic) stmcture with its larger volume results in a larger packing parameter (p = Ve/aolc, where Ve is the effective volume of the... [Pg.108]

Ammonium nitrate Ammonium nitrite Ammonium oxalate Ammonium salicylate Ammonium sulfate Ammonium sulfide Ammonium sulfite Ammonium thiosulfate Amyl acetate Amyl alcohol Amyl chloride Amyl mercaptan Amyl naphthalene Amyl nitrate Amyl nitrite Amyl phenol Aniline hydrdochloride Aniline sulfate Aniline sulfite Animal fats Animal oils Anthraquinone Antimony sulfate Antimony tribromide Antimony trichloride Antimony trioxide Aqua regia Arsenic oxide Arsenic trichloride Arsenic trioxide Arsenic trisulfide Ascorbic acid Barium carbonate Barium chlorate Barium chloride, aqueous Barium cyanide Barium hydroxide Barium iodide Barium nitrate Barium oxide Barium peroxide Barium salts Beet sugar liquors Benzaldehyde Benzene... [Pg.550]

Figure 6.13 Ion-pair chromatographic separation of inorganic anions with indirect photometric detection. Separator column Waters C18 Radiai-PAK, 5 m eluent 0.4mmol/L tetrabutyl-ammonium salicylate (pH 462) flow rate 2miy min detection indirect UV (288 nm) injection... Figure 6.13 Ion-pair chromatographic separation of inorganic anions with indirect photometric detection. Separator column Waters C18 Radiai-PAK, 5 m eluent 0.4mmol/L tetrabutyl-ammonium salicylate (pH 462) flow rate 2miy min detection indirect UV (288 nm) injection...
Ammonium salicylate NH,C2H503 528-94-9 155.151 whcry powder vs H)0 s EtOH... [Pg.744]

See other pages where Ammonium salicylate is mentioned: [Pg.50]    [Pg.835]    [Pg.324]    [Pg.312]    [Pg.1215]    [Pg.288]    [Pg.16]    [Pg.199]    [Pg.50]    [Pg.835]    [Pg.320]    [Pg.1513]    [Pg.15]    [Pg.41]    [Pg.86]    [Pg.203]    [Pg.245]    [Pg.254]    [Pg.1071]    [Pg.1088]    [Pg.1089]    [Pg.432]    [Pg.87]    [Pg.87]    [Pg.31]    [Pg.284]    [Pg.78]    [Pg.176]    [Pg.515]    [Pg.515]    [Pg.677]    [Pg.18]    [Pg.324]   
See also in sourсe #XX -- [ Pg.16 ]

See also in sourсe #XX -- [ Pg.86 ]

See also in sourсe #XX -- [ Pg.150 ]

See also in sourсe #XX -- [ Pg.31 ]

See also in sourсe #XX -- [ Pg.16 ]

See also in sourсe #XX -- [ Pg.176 ]



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Ammonium salicylate sulphate

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