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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. Gaylord Chemical Corporation - Wikipedia

    en.wikipedia.org/wiki/Gaylord_Chemical_Corporation

    The crude dimethyl sulfide product was purified by distillation and could then be used to produce DMSO. When Gaylord closed its Bogalusa plant in 2010, it changed its process technology to manufacture DMS from methanol and hydrogen sulfide gas via gas phase thioetherification. This is the dominant method used worldwide to make DMS and there are ...

  5. 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 ...

  6. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    Polyphenylene sulfide is a useful high temperature plastic. Coenzyme M, CH 3 SCH 2 CH 2 SO − 3, is the precursor to methane (i.e. natural gas) via the process of methanogenesis. Selected thioethers, from left: dimethylsulfide, coenzyme-M, the amino acid methionine, the vitamin biotin, and the engineering plastic polyphenylene sulfide.

  7. Organosulfur chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosulfur_chemistry

    The bond dissociation energies for dimethyl sulfide and dimethyl ether are respectively 73 and 77 kcal/mol (305 and 322 kJ/mol). Sulfides are typically prepared by alkylation of thiols. Alkylating agents include not only alkyl halides, but also epoxides, aziridines, and Michael acceptors. [6] They can also be prepared via the Pummerer ...

  8. 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.

  9. Category:Foul-smelling chemicals - Wikipedia

    en.wikipedia.org/wiki/Category:Foul-smelling...

    This page was last edited on 26 December 2023, at 01:54 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

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