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  2. Topical gels - Wikipedia

    en.wikipedia.org/wiki/Topical_gels

    Consistency and viscosity affect the adhesion and retention property of the gel, and are important in ensuring the gel is retained at the site of application and effective delivery of the drug. [ 3 ] The ingredients in topical gel formulation can be broadly categorized into four types: gelator, solvent, drug, and excipients.

  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. Deuterated DMSO - Wikipedia

    en.wikipedia.org/wiki/Deuterated_DMSO

    Deuterated DMSO, also known as dimethyl sulfoxide-d 6, is an isotopologue of dimethyl sulfoxide (DMSO, (CH 3) 2 S=O)) with chemical formula ((CD 3) 2 S=O) in which the hydrogen atoms ("H") are replaced with their isotope deuterium ("D"). Deuterated DMSO is a common solvent used in NMR spectroscopy.

  5. Transition metal sulfoxide complex - Wikipedia

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

    Being weakly basic, sulfoxide ligands are generally labile, i.e. they are rapidly displaced by other more basic ligands. O-bonded sulfoxide ligands are susceptible to oxidation at sulfur. In this way, the weakly bonded ligand is converted into a leaving group, such as dimethylsulfone. Since dmso is susceptible to deprotonation by strong base ...

  6. Sulfoxide - Wikipedia

    en.wikipedia.org/wiki/Sulfoxide

    For example, dimethyl sulfide is oxidized to dimethyl sulfoxide and then further to dimethyl sulfone. Unsymmetrical sulfides are prochiral, thus their oxidation gives chiral sulfoxides. This process can be performed enantioselectively. [9] [10] Symmetrical sulfoxides can be formed from a diorganylzinc compound and liquid sulfur dioxide. [11]

  7. N-Methyl-2-pyrrolidone - Wikipedia

    en.wikipedia.org/wiki/N-Methyl-2-pyrrolidone

    It also belongs to the class of dipolar aprotic solvents such as dimethylformamide and dimethyl sulfoxide. It is used in the petrochemical, polymer and battery industries as a solvent, exploiting its nonvolatility and ability to dissolve diverse materials (including polyvinylidene difluoride , PVDF). [ 3 ]

  8. Dimethyl sulfoxide (data page) - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfoxide_(data_page)

    Phase behavior Triple point: 291.67 K (18.52 °C), ? Pa Critical point [2]: 720 K (447 °C), 5630 kPa Std enthalpy change of fusion, Δ fus H o: 14.37 kJ/mol Std entropy change

  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 ]

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