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  2. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    Thiocyanate [6] is known to be an important part in the biosynthesis of hypothiocyanite by a lactoperoxidase. [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.

  3. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  4. Argentometry - Wikipedia

    en.wikipedia.org/wiki/Argentometry

    An example of back titration, the Volhard method, named after Jacob Volhard, involves the addition of excess silver nitrate to the analyte; the silver chloride is filtered, and the remaining silver nitrate is titrated against ammonium thiocyanate, [1] with ferric ammonium sulfate as an indicator which forms blood-red [Fe(OH 2) 5 (SCN)] 2+ at the end point:

  5. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Fe(OH) 2: 5.255×10 −5: Iron(II) nitrate: Fe(NO 3) 2 ·6H 2 O: 113: 134: ... (SCN) 2: 0.553: Lead(II) thiosulfate: PbS 2 O 3: 0.0202: Lead(II) tungstate: PbWO 4: 0 ...

  6. Transition metal complexes of thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Ru(PPh 3) 2 (CO) 3 + (SCN) 2 → Ru(NCS) 2 (PPh 3) 2 (CO) 2 + CO, where Ph = C 6 H 5. Even though the reaction involves cleavage of the S-S bond in thiocyanogen, the product is the Ru-NCS linkage isomer. In another unusual method, thiocyanate functions as both a ligand and as a reductant in its reaction with dichromate to give [Cr(NCS) 4 (NH 3 ...

  7. Thiocyanogen - Wikipedia

    en.wikipedia.org/wiki/Thiocyanogen

    Thiocyanogen, (SCN) 2, is a pseudohalogen derived from the pseudohalide thiocyanate, [SCN] −, with behavior intermediate between dibromine and diiodine. [2] This hexatomic compound exhibits C 2 point group symmetry and has the connectivity NCS-SCN. [3] In the lungs, lactoperoxidase may oxidize thiocyanate to thiocyanogen [4] or ...

  8. Mercury (II) thiocyanate - Wikipedia

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

    The decomposition of Hg(SCN) 2 is exothermic on its own, and the CS 2 produced ignites easily and burns off. The C 3 N 4 product is a simplification; the actual product contains 0.5% hydrogen and is likely to consist of sheets of triazine rings linked by −N= and −NH− groups similar to g−C 3 N 4 and was found to contain nano-particles of ...

  9. Ammonium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Ammonium_thiocyanate

    Ammonium thiocyanate is used in the manufacture of herbicides, thiourea, and transparent artificial resins; in matches; as a stabilizing agent in photography; in various rustproofing compositions; as an adjuvant in textile dyeing and printing; as a tracer in oil fields; in the separation of hafnium from zirconium (important for the production of hafnium-free zircalloy for use in nuclear fuel ...