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  2. Methanethiol - Wikipedia

    en.wikipedia.org/wiki/Methanethiol

    Cylinder of methanethiol gas. Methanethiol is mainly used to produce the essential amino acid methionine, which is used as a dietary component in poultry and animal feed. [10] Methanethiol is also used in the plastic industry as a moderator for free-radical polymerizations [10] and as a precursor in the manufacture of pesticides.

  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

    DMSP is broken down by marine microbes to form two major volatile sulfur products, each with distinct effects on the environment. 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).

  5. Ellman's reagent - Wikipedia

    en.wikipedia.org/wiki/Ellman's_reagent

    This reaction is rapid and stoichiometric, with the addition of one mole of thiol releasing one mole of TNB. The TNB 2− is quantified in a spectrophotometer by measuring the absorbance of visible light at 412 nm, using an extinction coefficient of 14,150 M −1 cm −1 for dilute buffer solutions, [4] [5] and a coefficient of 13,700 M −1 cm −1 for high salt concentrations, such as 6 M ...

  6. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    The nonbonding electrons on sulfur are delocalized into the π-system. As a consequence, thiophene exhibits few properties expected for a sulfide – thiophene is non-nucleophilic at sulfur and, in fact, is sweet-smelling. Upon hydrogenation, thiophene gives tetrahydrothiophene, C 4 H 8 S, which indeed does behave as a typical sulfide.

  7. Borane dimethylsulfide - Wikipedia

    en.wikipedia.org/wiki/Borane_dimethylsulfide

    B 2 H 6 + 2 S(CH 3) 22 BH 3 ·S(CH 3) 2. It can be purified by bulb to bulb vacuum transfer. Although a structure of BMS has not been determined crystallographically, (pentafluorophenyl)-borane dimethylsulfide (C 6 F 5 BH 2 ·S(CH 3) 2), has been examined by X-ray crystallography. [4] The boron atom adopts a tetrahedral molecular geometry.

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