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  2. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    [7] [8] [9] Thus the complete absence of thiocyanate or reduced thiocyanate [10] in the human body, (e.g., cystic fibrosis) is damaging to the human host defense system. [11] [12] Thiocyanate is a potent competitive inhibitor of the thyroid sodium-iodide symporter. [13] Iodine is an essential component of thyroxine. Since thiocyanates will ...

  3. Iodine clock reaction - Wikipedia

    en.wikipedia.org/wiki/Iodine_clock_reaction

    The iodine clock reaction is a classical chemical clock demonstration experiment to display chemical kinetics in action; it was discovered by Hans Heinrich Landolt in 1886. [1] The iodine clock reaction exists in several variations, which each involve iodine species ( iodide ion, free iodine, or iodate ion) and redox reagents in the presence of ...

  4. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    In methyl thiocyanate, N≡C and C−S distances are 116 and 176 pm. By contrast, N=C and C=S distances are 117 and 158 pm in isothiocyanates. [7] Typical bond angles for C−S−C are 100°. [3] By contrast C−N=C in aryl isothiocyanates is 165°. Again, the thiocyanate isomers are quite different with C−S−C angle near 100°.

  5. Experimental: Create your own iodine clock reaction in 12 ...

    www.aol.com/news/experimental-create-own-iodine...

    Try this experiment at home with the kids to introduce them to the basic tenet of physics, kinetics! ... Transform iodine with a few simple ingredients: 3 plastic cups. 1000 MG Vitamin C.

  6. Organoiodine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiodine_chemistry

    Few organoiodine compounds are important industrially, at least in terms of large scale production. Iodide-containing intermediates are common in organic synthesis on the laboratory scale because of the easy formation and cleavage of the C–I bond. But the same lability of the C-I bond limits the applications of organoiodine compounds as drugs.

  7. Boom method - Wikipedia

    en.wikipedia.org/wiki/Boom_method

    Examples thereof are aqueous solution of: thiocyanate ion, iodine ion, perchlorate ion, nitrate ion, bromine ion, chlorine ion, acetate ion, fluorine ion, and sulfate ion, or mutual combinations therewith. According to the original Boom method, the chaotropic guanidinium salt employed is preferably guanidinium thiocyanate (GuSCN).

  8. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    Hydrogen iodide. The simplest compound of iodine is hydrogen iodide, HI.It is a colourless gas that reacts with oxygen to give water and iodine. Although it is useful in iodination reactions in the laboratory, it does not have large-scale industrial uses, unlike the other hydrogen halides.

  9. Mercury(II) thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Mercury(II)_thiocyanate

    Mercury(II) thiocyanate (Hg(SCN) 2) is an inorganic chemical compound, the coordination complex of Hg 2+ and the thiocyanate anion. It is a white powder. It is a white powder. It will produce a large, winding "snake" when ignited, an effect known as the Pharaoh's serpent .