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  • | OtherCations = [[Potassium nitrite]]<br/>[[Ammonium nitrite]] ...[[azo compound|diazo]] [[dye]]s, [[nitroso compound]]s, and other organic compounds; in dyeing and printing textile fabrics and bleaching fibers; in [[photogra
    21 KB (3,046 words) - 16:45, 27 September 2010
  • ...s and [[sodium hydroxide|sodium]], [[potassium hydroxide|potassium]], or [[ammonium hydroxide]]: {{Magnesium compounds}}
    11 KB (1,555 words) - 16:49, 27 September 2010
  • [[Category:Aromatic compounds]] [[Category:Quaternary ammonium compounds]]
    5 KB (580 words) - 16:49, 27 September 2010
  • | OtherCpds = [[Ammonium nitrate]]<br/>[[Azide]] Nitrous oxide is most commonly prepared by careful heating of [[ammonium nitrate]], which decomposes into nitrous oxide and water vapor.<ref>{{cite
    61 KB (8,728 words) - 16:50, 27 September 2010
  • ...ound some 1,443 times more potent than morphine, stronger than the Bentley compounds such as [[etorphine]]. ...ined at the last extraction step, the alkaloids are precipitated by either ammonium hydroxide or sodium carbonate. The last step is purifying and separating mo
    87 KB (12,376 words) - 16:51, 27 September 2010
  • ...then [[pyrolysis]] at 400 to 450 °C in order to remove all non-diamondoid compounds <ref>Diamondoids are thermodynamically very stable and will survive this py ...]. Pentamantane can also react with [[tetrabromomethane]] and [[Quaternary ammonium cation|tetra-n-butylammonium]] Bromide (TBABr) in a [[free radical reaction
    8 KB (1,136 words) - 10:07, 20 September 2010
  • ...tching. For example, to etch a hydrogen-terminated silicon(111) surface, [[ammonium fluoride]] aqueous solution or [[boiling]] water is usually used. ...roup]]s. The reaction is called [[hydrosilylation]]. Many kinds of organic compounds with various functions can be introduced onto the silicon surface by the hy
    2 KB (231 words) - 10:08, 20 September 2010
  • ...ee to [[polymerize]]. In the branched cases some monomers are missing the ammonium anion and instead link to three other monomers. ...able than longer chains (n>1000),<ref>[http://www.sinoharvest.com/products/Ammonium-Polyphosphate.shtml]</ref> but short polymer chains (''e.g.'' pyro-, tripol
    3 KB (473 words) - 10:09, 20 September 2010
  • ...erobic bacteria can be utilized by autotrophic bacteria to reduce oxidized compounds and CO<sub>2</sub> to form either acetic acid or methane. ...h monovalent cations, low molecular weight amines, and quaternary ammonium compounds. It becomes water-insoluble in the presence of polyvalent cations such as C
    68 KB (9,959 words) - 10:10, 20 September 2010
  • ...[alum]], [[ferrous sulfate]], and [[gypsum]]; and [[ammonium chloride]], [[ammonium phosphate]], [[borax]], and various [[acids]]. These early attempts found a ..., A. A.; Talinli, N.; Akar, A. Ladder type polymers from dihydroxyaromatic compounds and dialdehydes. ''Angew. Makrom. Chem.'' '''1999,''' ''271'' (1), 8-10. IS
    17 KB (2,260 words) - 10:10, 20 September 2010
  • ...ated by anchoring antimicrobial species, such as [[phosphonium]] salts, [[ammonium]] salts, or [[phenol]] groups via quaternization, [[substitution]] of chlor | Active group: [[Quaternary ammonium]] group.<ref>{{cite journal|last=Ward|first=M.|coauthors=Sanchez, M.|date=2
    26 KB (3,675 words) - 10:11, 20 September 2010
  • ...bn = 0751404136}}</ref> The first method to precipitate the ruthenium with ammonium chloride is similar to the procedure that [[Smithson Tennant]] and [[Willia ==Chemical compounds==
    39 KB (5,430 words) - 10:13, 20 September 2010
  • ...orption (chemistry)|absorbent]], whereas the other method involved using [[ammonium chloride]] (''sal ammoniac''). The distillation process was to be repeated
    26 KB (3,820 words) - 10:18, 20 September 2010
  • ...butyllithium]]. Methylating agents attack the amine to give the quaternary ammonium salt:<ref>{{OrgSynth | | author = J. Jacques and A. Marquet | title = Selec ...mposites Australia</ref> DMA is also used as a precursor to other organic compounds.
    4 KB (538 words) - 13:10, 20 September 2010
  • ...; or in the form of its [[acetyl]] derivative by heating 2-naphthol with [[ammonium]] [[acetate]] to 270-280 °C. It forms odorless, colorless plates which mel
    3 KB (377 words) - 13:10, 20 September 2010
  • [[Category:Quaternary ammonium compounds]]
    772 bytes (91 words) - 13:12, 20 September 2010
  • As with most [[fluorescent]] [[Chemical compound|compounds]], ethidium bromide is [[aromatic]]. Its core [[heterocyclic]] moiety is ge ...lth implications of its own including increased skin absorption of organic compounds<ref>{{cite journal |author=Singer VL, Lawlor TE, Yue S. |title=Comparison o
    15 KB (1,980 words) - 13:13, 20 September 2010
  • ...]], ethanolamines, simple and complex glycols, polyglycol ethers and other compounds. It is also a common gas-phase [[disinfectant]] which is widely used in hos ...ular, its propensity to join the addition reactions typical of unsaturated compounds, had long been a matter of debate. Only in 1893, the heterocyclic triangula
    82 KB (11,709 words) - 21:31, 20 September 2010
  • ...th 2-acetylpyridine forms the related 1,5-diketone, which condenses with [[ammonium acetate]] to form a terpyridine. Treatment of this derivative with [[Raney ...transition metal]] [[ion]] as do other [[polypyridine complex|polypyridine compounds]], such as [[2,2'-bipyridine]] and 1,10-phenanthroline. Complexes containin
    4 KB (504 words) - 20:14, 21 September 2010
  • ...nal benzene derivatives, catechol readily condenses to form [[heterocyclic compounds]]. Cyclic [[ester]]s are formed upon treatment with [[phosphorus trichlori Catechols produce [[quinones]] with the addition of [[ceric ammonium nitrate]] (CAN).
    11 KB (1,437 words) - 20:14, 21 September 2010

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