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  2. Dimethyl sulfoxide (data page) - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_sulfoxide_(data_page)

    Printable version; In other projects Wikidata item; ... log 10 of dimethyl sulfoxide vapor pressure. ... 13.0 100.74: 90.00:

  3. Deuterated DMSO - Wikipedia

    en.wikipedia.org/wiki/Deuterated_DMSO

    13 C NMR Spectrum of DMSO-d 6. Pure deuterated DMSO shows no peaks in 1 H NMR spectroscopy and as a result is commonly used as an NMR solvent. [2] However commercially available samples are not 100% pure and a residual DMSO-d 5 1 H NMR signal is observed at 2.50ppm (quintet, J HD =1.9Hz). The 13 C chemical shift of DMSO-d 6 is 39.52ppm (septet ...

  4. 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.

  5. Gaylord Chemical Corporation - Wikipedia

    en.wikipedia.org/wiki/Gaylord_Chemical_Corporation

    Gaylord announced expanded DMSO production capacity in Tuscaloosa, Alabama, which came on-line in 2010. [ 2 ] Prior to being a subsidiary of Temple-Inland , Gaylord Chemical was a division of Gaylord Container Corporation , the successor (1986–2002) of the brown paper division of Crown Zellerbach (1928–86).

  6. 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 ]

  7. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Print/export Download as PDF; Printable version; In other projects Wikidata item; Appearance. move to sidebar hide ... [13] tert-Butanol: 82.5 [14] Chlorobenzene: 131.7

  8. Parikh–Doering oxidation - Wikipedia

    en.wikipedia.org/wiki/Parikh–Doering_oxidation

    The Parikh–Doering oxidation is an oxidation reaction that transforms primary and secondary alcohols into aldehydes and ketones, respectively. [1] The procedure uses dimethyl sulfoxide (DMSO) as the oxidant and the solvent, activated by the sulfur trioxide pyridine complex (SO 3 •C 5 H 5 N) in the presence of triethylamine or diisopropylethylamine as base.

  9. Solvent effects - Wikipedia

    en.wikipedia.org/wiki/Solvent_effects

    In the table above, it can be seen that water is the most polar-solvent, followed by DMSO, and then acetonitrile. Consider the following acid dissociation equilibrium: HA ⇌ A − + H + Water, being the most polar-solvent listed above, stabilizes the ionized species to a greater extent than does DMSO or Acetonitrile.