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  2. 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.

  3. 1-Iodohexane - Wikipedia

    en.wikipedia.org/wiki/1-Iodohexane

    Solubility in water. ... data are given for materials in their standard state (at 25 °C ... The compound can also be prepared by treating 1-hexanol with iodine and ...

  4. Hildebrand solubility parameter - Wikipedia

    en.wikipedia.org/wiki/Hildebrand_solubility...

    The principal limitation of the solubility parameter approach is that it applies only to associated solutions ("like dissolves like" or, technically speaking, positive deviations from Raoult's law); it cannot account for negative deviations from Raoult's law that result from effects such as solvation or the formation of electron donor ...

  5. Iodine - Wikipedia

    en.wikipedia.org/wiki/Iodine

    Elemental iodine is slightly soluble in water, with one gram dissolving in 3450 mL at 20 °C and 1280 mL at 50 °C; potassium iodide may be added to increase solubility via formation of triiodide ions, among other polyiodides. [25] Nonpolar solvents such as hexane and carbon tetrachloride provide a higher solubility. [26]

  6. Hexane - Wikipedia

    en.wikipedia.org/wiki/Hexane

    Hexane and other volatile hydrocarbons (petroleum ether) present an aspiration risk. [26] n-Hexane is sometimes used as a denaturant for alcohol, and as a cleaning agent in the textile, furniture, and leather industries. It is slowly being replaced with other solvents. [27] Like gasoline, hexane is highly volatile and is an explosion risk.

  7. Hypervalent organoiodine compounds - Wikipedia

    en.wikipedia.org/wiki/Hypervalent_organoiodine...

    In iodane chemistry, carbon is considered more electronegative than iodine, despite the Pauling electronegativities of those respective atoms. [2] Thus iodobenzene (C 6 H 5 I) is an iodine(I) compound, (dichloroiodo)benzene (C 6 H 5 ICl 2) and iodosobenzene (C 6 H 5 IO) iodine(III) compounds, and iodoxybenzene (C 6 H 5 IO 2) an iodine(V) compound.

  8. Organoiodine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiodine_chemistry

    This application exploits the X-ray absorbing ability of the heavy iodine nucleus. A variety of agents are available commercially, many are derivatives of 1,3,5-triiodobenzene and contain about 50% by weight iodine. For most applications, the agent must be highly soluble in water and, of course, non-toxic and readily excreted.

  9. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    Liquid iodine trichloride conducts electricity, possibly indicating dissociation to ICl + 2 and ICl − 4 ions. [9] Iodine pentafluoride (IF 5), a colourless, volatile liquid, is the most thermodynamically stable iodine fluoride, and can be made by reacting iodine with fluorine gas at room temperature. It is a fluorinating agent, but is mild ...

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