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  2. Dimethyl sulfide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfide

    Beetroot, [26] asparagus, [27] cabbage, maize and seafoods produce dimethyl sulfide when cooked. Dimethyl sulfide is also produced by marine planktonic microorganisms such as the coccolithophores and so is one of the main components responsible for the characteristic odor of sea water aerosols, which make up a part of sea air.

  3. Flatulence - Wikipedia

    en.wikipedia.org/wiki/Flatulence

    [2] [28] Hydrogen sulfide, methyl mercaptan (also known as methanethiol), dimethyl sulfide, dimethyl disulfide and dimethyl trisulfide are present in flatus. The benzopyrrole volatiles indole and skatole have an odor of mothballs, and therefore probably do not contribute greatly to the characteristic odor of flatus.

  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. 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 ...

  6. 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.

  7. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    Azelaic acid and pelargonic acids are produced from ozonolysis of oleic acid on an industrial scale. An example is the ozonolysis of eugenol converting the terminal alkene to an aldehyde: [9] By controlling the reaction/workup conditions, unsymmetrical products can be generated from symmetrical alkenes: [10]

  8. Connecticut man allegedly killed a mother, her infant son ...

    www.aol.com/connecticut-man-allegedly-killed...

    A Connecticut man who allegedly killed a woman and her infant son in November targeted the woman because she owed him $400 for renting a vehicle of his, arrest reports said on Monday.

  9. Swern oxidation - Wikipedia

    en.wikipedia.org/wiki/Swern_oxidation

    The by-products are dimethyl sulfide ((CH 3) 2 S), carbon monoxide (CO), carbon dioxide (CO 2) and—when triethylamine is used as base—triethylammonium chloride (Et 3 NHCl). Of the volatile by-products, dimethyl sulfide has a strong, pervasive odour and carbon monoxide is acutely toxic, so the reaction and the work-up needs to be performed ...