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  2. Methanethiol - Wikipedia

    en.wikipedia.org/wiki/Methanethiol

    CH 3 SH + CH 3 ONa → CH 3 SNa + CH 3 OH. The resulting thiolate anion is a strong nucleophile. It can be oxidized to dimethyl disulfide: 2CH 3 SH + [O] → CH 3 SSCH 3 + H 2 O. Further oxidation takes the disulfide to two molecules of methanesulfonic acid, which is odorless. Bleach deodorizes methanethiol in this way.

  3. Dimethyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfide

    Dimethyl sulfide has a characteristic odor commonly described as cabbage-like.It becomes highly disagreeable at even quite low concentrations. Some reports claim that DMS has a low olfactory threshold that varies from 0.02 to 0.1 ppm [clarification needed] between different persons, but it has been suggested that the odor attributed to dimethyl sulfide may in fact be due to disulfides ...

  4. Dimethylsulfoniopropionate - Wikipedia

    en.wikipedia.org/wiki/Dimethylsulfoniopropionate

    One of its breakdown products is methanethiol (CH 3 SH), which is assimilated by bacteria into protein sulfur. Another volatile breakdown product is dimethyl sulfide (CH 3 SCH 3 ; DMS). There is evidence that DMS in seawater can be produced by cleavage of dissolved (extracellular) DMSP [ 7 ] [ 8 ] by the enzyme DMSP-lyase , although many non ...

  5. Methylated-thiol-coenzyme M methyltransferase - Wikipedia

    en.wikipedia.org/wiki/Methylated-thiol-coenzyme...

    This enzyme involved in methanogenesis from methylated thiols, such as methanethiol, dimethyl sulfide, and 3-S-methylmercaptopropionate. References

  6. Dimethyl trisulfide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_trisulfide

    Dimethyl trisulfide (DMTS) is an organic chemical compound and the simplest organic trisulfide, with the chemical formula CH 3 SSSCH 3. [ 2 ] [ 3 ] It is a flammable liquid with a foul odor, which is detectable at levels as low as 1 part per trillion.

  7. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    The two organic substituents are indicated by the prefixes. (CH 3) 2 S is called dimethylsulfide. Some sulfides are named by modifying the common name for the corresponding ether. For example, C 6 H 5 SCH 3 is methyl phenyl sulfide, but is more commonly called thioanisole, since its structure is related to that for anisole, C 6 H 5 OCH 3.

  8. Dimethyl-sulfide monooxygenase - Wikipedia

    en.wikipedia.org/wiki/Dimethyl-sulfide_monooxygenase

    Dimethyl-sulfide monooxygenase (EC 1.14.13.131, dimethylsulfide monooxygenase) is an enzyme with systematic name dimethyl sulfide,NADH:oxygen oxidoreductase. [1] This enzyme catalyses the following chemical reaction. dimethyl sulfide + O 2 + NADH + H + methanethiol + formaldehyde + NAD + + H 2 O

  9. Methanomethylovorans hollandica - Wikipedia

    en.wikipedia.org/wiki/Methanomethylovorans...

    Methanomethylovorans hollandica is a species of methylotrophic methanogen able to grow on dimethyl sulfide and methanethiol. It is the type species of its genus. It is obligately anaerobic. [1] It was the first strictly anaerobic archeaon isolated from freshwater sediments in which dimethyl sulfide is the sole source of carbon. It is not a ...