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  2. Cyanuric acid - Wikipedia

    en.wikipedia.org/wiki/Cyanuric_acid

    Cyanuric acid or 1,3,5-triazine-2,4,6-triol is a chemical compound with the formula (CNOH) 3. Like many industrially useful chemicals, this triazine has many synonyms.

  3. The Avenues, Salt Lake City - Wikipedia

    en.wikipedia.org/wiki/The_Avenues,_Salt_Lake_City

    Map of the Avenues. The Avenues neighborhood lies on the "north east bench" of the Wasatch Mountains in Salt Lake City. The southern boundary of the Avenues is South Temple Street (1st Avenue is the next street north). Heading north, the Avenues neighborhood is built up onto the lower slopes of the mountains.

  4. Melamine cyanurate - Wikipedia

    en.wikipedia.org/wiki/Melamine_cyanurate

    Melamine cyanurate, also known as melamine–cyanuric acid adduct or melamine–cyanuric acid complex, is a crystalline complex formed from a 1:1 mixture of melamine and cyanuric acid. The substance is not a salt despite its non-systematic name melamine cyanurate .

  5. Thiocyanuric acid - Wikipedia

    en.wikipedia.org/wiki/Thiocyanuric_acid

    Thiocyanuric acid precipitates from warm, acidic solutions of thiocyanic acid. A modern synthesis begins instead with a preformed ring: cyanuric chloride reacts with sodium hydrosulfide to give table salt and thiocyanuric acid. [3] The compound is mildly acidic, with pKa's of 5.7, 8.4, and 11.4. [3] Various salts of (HNC=S) − 3 have been ...

  6. Potassium cyanate - Wikipedia

    en.wikipedia.org/wiki/Potassium_cyanate

    KOCN is prepared by heating urea with potassium carbonate at 400 °C: . 2 OC(NH 2) 2 + K 2 CO 3 → 2 KOCN + (NH 4) 2 CO 3. The reaction produces a liquid. Intermediates and impurities include biuret, cyanuric acid, and potassium allophanate (KO 2 CNHC(O)NH 2), as well as unreacted starting urea, but these species are unstable at 400 °C.

  7. Cyanuric chloride - Wikipedia

    en.wikipedia.org/wiki/Cyanuric_chloride

    Cyanuric chloride is employed as a reagent in organic synthesis for the conversion of alcohols into alkyl chlorides, [8] and carboxylic acids into acyl chlorides: [9]. It is also used as a dehydrating agent, e.g. in the conversion of amides to nitriles, [10] and for the activation of carboxylic acids for reduction to alcohols.

  8. Sodium dichloroisocyanurate - Wikipedia

    en.wikipedia.org/wiki/Sodium_dichloroisocyanurate

    Sodium dichloroisocyanurate (INN: sodium troclosene, troclosenum natricum or NaDCC or SDIC) is a chemical compound widely used as a cleansing agent and disinfectant. [1] It is a colorless, water-soluble solid, produced as a result of reaction of cyanuric acid with chlorine.

  9. Dichloroisocyanuric acid - Wikipedia

    en.wikipedia.org/wiki/Dichloroisocyanuric_acid

    Dichloroisocyanuric acid is an oxidizer, reacting with water to form chlorine gas. [2]Although the bleaching agent in most chlorine based bleach is sodium hypochlorite, the sodium salt of dichloroisocyanuric acid, sodium dichloroisocyanurate, is the active ingredient in commercial disinfectant bacteriocides, algicides, and cleaning agents [3] such as the pulverized cleanser Comet.