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  2. 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 ...

  3. Deuterated solvent - Wikipedia

    en.wikipedia.org/wiki/Deuterated_solvent

    Deuterated solvents are a group of compounds where one or more hydrogen atoms are substituted by deuterium atoms. These isotopologues of common solvents are often used in nuclear magnetic resonance spectroscopy .

  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. Deuterated methanol - Wikipedia

    en.wikipedia.org/wiki/Deuterated_methanol

    Deuterated methanol (CD 3 OD), is a form (called an isotopologue) of methanol (CH 3 OH) in which the hydrogen atoms ("H") are replaced with deuterium (heavy hydrogen) isotope ("D"). [1] Deuterated methanol is a common solvent used in NMR spectroscopy .

  6. Deuterated benzene - Wikipedia

    en.wikipedia.org/wiki/Deuterated_benzene

    Deuterated benzene is a common solvent used in NMR spectroscopy. It is widely used for taking spectra of organometallic compounds, which often react with the cheaper deuterated chloroform. [3] A slightly more exotic application of C 6 D 6 is in the synthesis of molecules containing a deuterated phenyl group.

  7. 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.

  8. Deuterated acetone - Wikipedia

    en.wikipedia.org/wiki/Deuterated_acetone

    Deuterated acetone is prepared by the reaction of acetone with heavy water, 2 H 2 O or D 2 O, in the presence of a base. In this case, the base used is deuterated lithium hydroxide : [ 1 ] In order to fully deuterate the acetone, the process is repeated several times, distilling off the acetone from the heavy water, and re-running the reaction ...

  9. Category:Deuterated compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Deuterated_compounds

    Pages in category "Deuterated compounds" The following 26 pages are in this category, out of 26 total. This list may not reflect recent changes. 0–9.

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