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  2. 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 ...

  3. Bergstrom Nutrition - Wikipedia

    en.wikipedia.org/wiki/Bergstrom_Nutrition

    Bergstrom Nutrition (originally named Cardinal Associates) was founded in 1988 by George Bergstrom and Bob Cowan, chemical engineers who worked with dimethylsulfoxide (DMSO) and dimethyl sulfone (DMSO2)/methylsulfonylmethane (MSM). The founders were first to introduce MSM as a dietary supplement to both the animal and human markets. [citation ...

  4. Dimethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfate

    Dimethyl sulfate (DMS) is a chemical compound with formula (CH 3 O) 2 SO 2. As the diester of methanol and sulfuric acid , its formula is often written as ( CH 3 ) 2 SO 4 or Me 2 SO 4 , where CH 3 or Me is methyl .

  5. 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.

  6. Organosulfur chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosulfur_chemistry

    Humans and other animals have an exquisitely sensitive sense of smell toward the odor of low-valent organosulfur compounds such as thiols, sulfides, and disulfides. Malodorous volatile thiols are protein-degradation products found in putrid food, so sensitive identification of these compounds is crucial to avoiding intoxication.

  7. Sulfone - Wikipedia

    en.wikipedia.org/wiki/Sulfone

    Sulfone is a relatively inert functional group, typically less oxidizing and 4 bel more acidic than sulfoxides. In the Ramberg–Bäcklund reaction and the Julia olefination, sulfones are converted to alkenes by the elimination of sulfur dioxide. [13] However, sulfones are unstable to bases, eliminating to give an alkene. [14]

  8. Phenytoin/pentobarbital - Wikipedia

    en.wikipedia.org/wiki/Phenytoin/pentobarbital

    Phenytoin/pentobarbital (trade name Beuthanasia-D Special) is an animal drug product used for euthanasia, which contains a mixture of phenytoin and pentobarbital. [1] It is administered as an intravenous injection to give animals a quick and humane death.

  9. Methyl methanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Methyl_methanesulfonate

    Ethyl methanesulfonate, dimethyl sulfone, dimethyl sulfate Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify ( what is Y N ?)