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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

    R-CH=CH 2 + H-SR' → R-CH 2-CH 2-S-R' This reaction is often catalysed by free radicals produced from a photoinitiator. [6] Sulfides can also be prepared by many other methods, such as the Pummerer rearrangement. Trialkysulfonium salts react with nucleophiles with a dialkyl sulfide as a leaving group: Nu − + R 3 S + → Nu-R + R 2 SR 1

  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 disulfide - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_disulfide

    Dimethyl disulfide (DMDS) is an organic chemical compound with the molecular formula CH 3 SSCH 3. It is a flammable liquid with an unpleasant, garlic -like odor resembling that of "leaking gas". The compound is colorless although impure samples often appear yellowish.

  9. 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.