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  2. Methylsulfonylmethane - Wikipedia

    en.wikipedia.org/wiki/Methylsulfonylmethane

    Dimethyl sulfone (DMSO 2) is an organosulfur compound with the formula (CH 3) 2 SO 2. It is also known by several other names including methyl sulfone and (especially in alternative medicine) methylsulfonylmethane (MSM). [4] This colorless solid features the sulfonyl functional group and is the simplest of the sulfones. It is relatively inert ...

  3. Methyl methanesulfonate - Wikipedia

    en.wikipedia.org/wiki/Methyl_methanesulfonate

    Ethyl methanesulfonate, dimethyl sulfone, dimethyl sulfate Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify ( what is Y N ?)

  4. CEA-List: Laboratory for Integration of Systems and Technology

    en.wikipedia.org/wiki/CEA-LIST:_Laboratory_for...

    CEA-List, work on radiations control for health is held by two entities of reference: The Henry-Becquerel National Laboratory (LNHB) National French reference laboratory for metrology; DOSEO platform is unique in France as it consists of advanced technological equipment for imaging and radiotherapy. [7] [8] [9]

  5. Dimethyl sulfate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfate

    Impure dimethyl sulfate was prepared in the early 19th century. [4] J. P. Claesson later extensively studied its preparation. [5] [6]It was investigated for possible use in chemical warfare in World War I [7] [8] in 75% to 25% mixture with methyl chlorosulfonate (CH 3 ClO 3 S) called "C-stoff" in Germany, or with chlorosulfonic acid called "Rationite" in France.

  6. Category:Laboratories in France - Wikipedia

    en.wikipedia.org/.../Category:Laboratories_in_France

    Pages in category "Laboratories in France" The following 26 pages are in this category, out of 26 total. ... Laboratory for Analysis and Architecture of Systems;

  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. Sulfonamide - Wikipedia

    en.wikipedia.org/wiki/Sulfonamide

    Sulfonamides can be prepared in the laboratory in many ways. The classic approach entails the reaction of sulfonyl chlorides with an amine. [citation needed] RSO 2 Cl + R' 2 NH → RSO 2 NR' 2 + HCl. A base such as pyridine is typically added to absorb the HCl that is generated. Illustrative is the synthesis of sulfonylmethylamide. [3]

  9. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    It also maintains List I of chemicals and List II of chemicals, which contain chemicals that are used to manufacture the controlled substances/illicit drugs. The list is designated within the Controlled Substances Act [ 1 ] but can be modified by the U.S. Attorney General as illegal manufacturing practices change.