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  2. Biuret - Wikipedia

    en.wikipedia.org/wiki/Biuret

    The parent compound can be prepared by heating urea at 150 °C for ~6 hours until it gets slightly cloudy, then recrystallizing from water.After that, it can be recrystallized repeatedly from 2% sodium hydroxide solution and water to finally get base-free crystalline needles of the monohydrate which are free of cyanuric acid.

  3. 1,3,5-Triazine - Wikipedia

    en.wikipedia.org/wiki/1,3,5-Triazine

    Another important derivative is 1,3,5-triazine-2,4,6-triol better known as cyanuric acid. Cyanuric chloride (2,4,6-trichloro-1,3,5-triazine) is the starting point for the manufacture of many herbicides such as Simazine and atrazine.

  4. 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. This white, odorless solid finds use as a precursor or a component of bleaches, disinfectants, and herbicides.

  5. Oxidizing agent - Wikipedia

    en.wikipedia.org/wiki/Oxidizing_agent

    The international pictogram for oxidizing chemicals. Dangerous goods label for oxidizing agents. An oxidizing agent (also known as an oxidant, oxidizer, electron recipient, or electron acceptor) is a substance in a redox chemical reaction that gains or "accepts"/"receives" an electron from a reducing agent (called the reductant, reducer, or electron donor).

  6. 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 ...

  7. 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.

  8. Hexahydro-1,3,5-triazine - Wikipedia

    en.wikipedia.org/wiki/Hexahydro-1,3,5-triazine

    Structure of (Me 3 TACH)ScCl 3 viewed down the three-fold symmetry axis (color scheme: blue = N, green = Cl, gray = C). [6] Trimers of isocyanates are sometimes labeled as 2,4,6-trioxohexahydro-1,3,5-triazines. They have the formula (RNC(O)) 3 and based on the isocyanuric (trione) tautomer of cyanuric acid.

  9. Reducing agent - Wikipedia

    en.wikipedia.org/wiki/Reducing_agent

    The table below shows a few reduction potentials, which can be changed to oxidation potentials by reversing the sign. Reducing agents can be ranked by increasing strength by ranking their reduction potentials. Reducers donate electrons to (that is, "reduce") oxidizing agents, which are said to "be reduced by" the reducer. The reducing agent is ...

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