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  2. Methanesulfonyl fluoride - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_fluoride

    Repeated exposures to 1/10 of the LCt 50 did not produce overt systemic toxicity or significant pathology. [7] MSF can also cause severe skin burns and serious eye damage, if contact is made. It is a lachrymator and its vapor causes tears in eyes. [8] [2] Methanesulfonyl fluoride has a pungent odor.

  3. Mesylate - Wikipedia

    en.wikipedia.org/wiki/Mesylate

    Related to mesylate is the mesyl (Ms) or methanesulfonyl (CH 3 SO 2) functional group. The shortened term itself was coined by Helferich et al. in 1938 similarly to tosyl adopted earlier. [ 4 ] Methanesulfonyl chloride is often referred to as mesyl chloride.

  4. PMSF - Wikipedia

    en.wikipedia.org/wiki/PMSF

    PMSF does not inactivate all serine proteases. [1] The effective concentration of PMSF is between 0.1 - 1 mM. The half-life is short in aqueous solutions (110 min at pH 7, 55 min at pH 7.5, and 35 min at pH 8, all at 25 °C). [2] At 4˚C, pH 8, PMSF is almost completely degraded after 1 day. [2]

  5. Coumaphos - Wikipedia

    en.wikipedia.org/wiki/Coumaphos

    Coumaphos is a nonvolatile, fat-soluble phosphorothioate with ectoparasiticide properties: it kills insects and mites.It is well known by a variety of brand names as a dip or wash, used on farm and domestic animals to control ticks, mites, flies and fleas.

  6. Methylsulfonylmethane - Wikipedia

    en.wikipedia.org/wiki/Methylsulfonylmethane

    The LD 50 of MSM is greater than 17.5 grams per kilogram of body weight. [16] Extensive research in animal models indicates MSM has a very low toxicity when administered both orally and topically. [17] [18] [19] MSM is considered 'Possibly Safe' at therapeutic doses. [13] [20]

  7. Methanesulfonyl chloride - Wikipedia

    en.wikipedia.org/wiki/Methanesulfonyl_chloride

    Methanesulfonyl chloride is mainly used to give methanesulfonates by its reaction with alcohols in the presence of a non-nucleophilic base. [8] In contrast to the formation of toluenesulfonates from alcohols and p-toluenesulfonyl chloride in the presence of pyridine, the formation of methanesulfonates is believed to proceed via a mechanism wherein methanesulfonyl chloride first undergoes an ...

  8. A-242 - Wikipedia

    en.wikipedia.org/wiki/A-242

    A-242 has been added to Schedule 1 of the Annex on Chemicals of the Chemical Weapons Convention as of June 2020, and it has been explicitly named as an example compound for schedule 1.A.15. [ 2 ] [ 3 ] For chemicals listed in Schedule 1, the most stringent declaration and verification measures are in place combined with far-reaching limits and ...

  9. Fonofos - Wikipedia

    en.wikipedia.org/wiki/Fonofos

    This article about an ester is a stub. You can help Wikipedia by expanding it.