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  2. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    In the table above, it can be seen that water is the most polar-solvent, followed by DMSO, and then acetonitrile. Consider the following acid dissociation equilibrium: HA ⇌ A − + H + Water, being the most polar-solvent listed above, stabilizes the ionized species to a greater extent than does DMSO or Acetonitrile.

  3. Dimethyl sulfoxide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfoxide

    Dimethyl sulfoxide (DMSO) is an organosulfur compound with the formula (CH 3) 2 S O.This colorless liquid is the sulfoxide most widely used commercially. It is an important polar aprotic solvent that dissolves both polar and nonpolar compounds and is miscible in a wide range of organic solvents as well as water.

  4. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    DMSO is widely used as an alternative to water because it has a lower dielectric constant than water, and is less polar and so dissolves non-polar, hydrophobic substances more easily. It has a measurable pK a range of about 1 to 30. Acetonitrile is less basic than DMSO, and, so, in general, acids are weaker and bases are stronger in this solvent.

  5. Acetonitrile - Wikipedia

    en.wikipedia.org/wiki/Acetonitrile

    Acetonitrile is used mainly as a solvent in the purification of butadiene in refineries. Specifically, acetonitrile is fed into the top of a distillation column filled with hydrocarbons including butadiene, and as the acetonitrile falls down through the column, it absorbs the butadiene which is then sent from the bottom of the tower to a second separating tower.

  6. Solvent - Wikipedia

    en.wikipedia.org/wiki/Solvent

    Acetonitrile 0.786 Ethanol 0.789 Acetone 0.790 Methanol 0.791 Methyl isobutyl ketone 0.798 Isobutyl alcohol 0.802 1-Propanol 0.803 Methyl ethyl ketone 0.805 2-Butanol 0.808 Isoamyl alcohol 0.809 1-Butanol 0.810 Diethyl ketone 0.814 1-Octanol 0.826 p-Xylene 0.861 m-Xylene 0.864 Toluene 0.867 Dimethoxyethane 0.868 Benzene 0.879 Butyl acetate 0.882

  7. Transition metal sulfoxide complex - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_sulfoxide...

    All such derivatives feature O-bonded sulfoxides. The tricationic complex in [Rh(dmso) 6](O 3 SCF 3) 3 features one S-bonded and five O-bonded sulfoxide ligands. [10] The complex [Cu(Ph 2 SO) 4] 2+ is square planar, in contrast to the derivative with dmso ligands. The square planar d 8 complex [Rh(dmso) 4] + features a pairs of S- and O-bonded ...

  8. Swern oxidation - Wikipedia

    en.wikipedia.org/wiki/Swern_oxidation

    Humans can detect this compound in concentrations as low as 0.02 to 0.1 parts per million. [13] A simple remedy for this problem is to rinse used glassware with bleach or oxone solution, which will oxidize the dimethyl sulfide back to dimethyl sulfoxide or to dimethyl sulfone , both of which are odourless and nontoxic.

  9. Methylsulfonylmethane - Wikipedia

    en.wikipedia.org/wiki/Methylsulfonylmethane

    Dimethyl sulfone (DMSO 2) is an organosulfur compound with the formula (CH 3) 2 SO 2. It is also known by several other names including methyl sulfone and (especially in alternative medicine) methylsulfonylmethane (MSM). [4] This colorless solid features the sulfonyl functional group and is the simplest of the sulfones. It is relatively inert ...

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