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  2. Hydrochloric acid - Wikipedia

    en.wikipedia.org/wiki/Hydrochloric_acid

    They range from those of water at very low concentrations approaching 0% HCl to values for fuming hydrochloric acid at over 40% HCl. [31] [32] [33] Hydrochloric acid as the binary (two-component) mixture of HCl and H 2 O has a constant-boiling azeotrope at 20.2% HCl and 108.6 °C (381.8 K; 227.5 °F).

  3. Hydroxylamine - Wikipedia

    en.wikipedia.org/wiki/Hydroxylamine

    HO−S(=O) 2 −Cl + NH 2 OH → NH 2 −O−S(=O) 2 −OH + HCl. When heated, hydroxylamine explodes. A detonator can easily explode aqueous solutions concentrated above 80% by weight, and even 50% solution might prove detonable if tested in bulk. [16] [17] In air, the combustion is rapid and complete: 4 NH 2 OH + O 2 → 2 N 2 + 6 H 2 O

  4. Tin(II) chloride - Wikipedia

    en.wikipedia.org/wiki/Tin(II)_chloride

    A solution of tin(II) chloride containing a little hydrochloric acid is used for the tin-plating of steel, in order to make tin cans. An electric potential is applied, and tin metal is formed at the cathode via electrolysis. Tin(II) chloride is used as a mordant in textile dyeing because it gives brighter colours with some dyes e.g. cochineal ...

  5. Ammonia solution - Wikipedia

    en.wikipedia.org/wiki/Ammonia_solution

    In aqueous solution, ammonia deprotonates a small fraction of the water to give ammonium and hydroxide according to the following equilibrium: . NH 3 + H 2 O ⇌ NH + 4 + OH −.. In a 1 M ammonia solution, about 0.42% of the ammonia is converted to ammonium, equivalent to pH = 11.63 because [NH +

  6. Percentage solution - Wikipedia

    en.wikipedia.org/wiki/Percentage_solution

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  7. Triethylamine - Wikipedia

    en.wikipedia.org/wiki/Triethylamine

    The hydrochloride salt, triethylamine hydrochloride (triethylammonium chloride), is a colorless, odorless, and hygroscopic powder, which decomposes when heated to 261 °C. Triethylamine is soluble in water to the extent of 112.4 g/L at 20 °C. [3] It is also miscible in common organic solvents, such as acetone, ethanol, and diethyl ether.

  8. Methylamine - Wikipedia

    en.wikipedia.org/wiki/Methylamine

    Methylamine has been produced industrially since the 1920s (originally by Commercial Solvents Corporation for dehairing of animal skins). [4] This was made possible by Kazimierz Smoleński [] and his wife Eugenia who discovered amination of alcohols, including methanol, on alumina or kaolin catalyst after WWI, filed two patent applications in 1919 [5] and published an article in 1921.

  9. Hydroxylammonium nitrate - Wikipedia

    en.wikipedia.org/wiki/Hydroxylammonium_nitrate

    The compound is a salt with separated hydroxyammonium and nitrate ions. [2] Hydroxylammonium nitrate is unstable because it contains both a reducing agent (hydroxylammonium cation) and an oxidizer (), [3] the situation being analogous to ammonium nitrate.