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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. International Chemical Safety Cards - Wikipedia

    en.wikipedia.org/wiki/International_Chemical...

    International Chemical Safety Cards (ICSC) are data sheets intended to provide essential safety and health information on chemicals in a clear and concise way.The primary aim of the Cards is to promote the safe use of chemicals in the workplace and the main target users are therefore workers and those responsible for occupational safety and health.

  4. Category:Thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Category:Thiocyanates

    Print/export Download as PDF; Printable version; In other projects ... Thiocyanate; Transition metal complexes of thiocyanate; A. Ammonium thiocyanate; B.

  5. 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 .

  6. File:Cr-Ac-OH-MSDS SigmaAldrich.pdf - Wikipedia

    en.wikipedia.org/wiki/File:Cr-Ac-OH-MSDS_Sigma...

    You are free: to share – to copy, distribute and transmit the work; to remix – to adapt the work; Under the following conditions: attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made.

  7. Transition metal complexes of thiocyanate - Wikipedia

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

    The 1:1 complex of thiocyanate and iron is deeply red. The effect was first reported in 1826. [15] The structure of this species has never been confirmed by X-ray crystallography. The test is largely archaic. Copper(I) thiocyanate is a reagent for the conversion of aryl diazonium salts to arylthiocyanates, a version of the Sandmeyer reaction.

  8. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  9. 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°.