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  2. 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 ...

  3. Tetramethylammonium hydroxide - Wikipedia

    en.wikipedia.org/wiki/Tetramethylammonium_hydroxide

    Tetramethylammonium hydroxide (TMAH or TMAOH) is a quaternary ammonium salt with molecular formula N(CH 3) 4 + OH −. It is commonly encountered in form of concentrated solutions in water or methanol. TMAH in solid state and its aqueous solutions are all colorless, but may be yellowish if impure.

  4. Nickel(II) thiocyanate - Wikipedia

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

    Nickel(II) thiocyanate is a coordination polymer with formula Ni(SCN) 2. [1] It is a green-brown solid and its crystal structure was determined first in 1982. [ 1 ]

  5. 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 ...

  6. Sigma-Aldrich - Wikipedia

    en.wikipedia.org/wiki/Sigma-Aldrich

    Sigma Advanced Genetic Engineering (SAGE) Labs is a division within Sigma-Aldrich that specializes in genetic manipulation of in vivo systems for special research and development applications. It was formed in 2008 to investigate zinc finger nuclease technology and its application for disease research models.

  7. Category:Thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Category:Thiocyanates

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  8. 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°.

  9. Barium thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Barium_thiocyanate

    Barium thiocyanate is prepared by mixing barium hydroxide and ammonium thiocyanate in water. [4] 2 NH 4 SCN + Ba(OH) 2 → Ba(SCN) 2 + 2 NH 3 + 2 H 2 O. According to X-ray crystallography, the anhydrous salt is a coordination polymer. The Ba 2+ ions are each bonded to eight thiocyanate anions, with four Ba-S and four Ba-N

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