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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. Spectral Database for Organic Compounds - Wikipedia

    en.wikipedia.org/wiki/Spectral_Database_for...

    Spectra were acquired using a pulse flip angle of 22.5 – 45 degrees and a pulse repetition time of 4 – 7 seconds. [4] Samples were prepared by dissolution in CDCl 3, D 2 O, or DMSO-d 6. [5] Each spectrum is accompanied by a list of the observed peaks with their respective chemical shifts in ppm and their intensities.

  5. Deuterated benzene - Wikipedia

    en.wikipedia.org/wiki/Deuterated_benzene

    The properties of deuterated benzene are very similar to those of normal benzene, however, the increased atomic weight of deuterium relative to protium means that the melting point of C 6 D 6 is about 1.3 °C higher than that of the nondeuterated analogue. The boiling points of both compounds, however, are the same: 80 °C.

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  7. Dimethyl sulfoxide (data page) - Wikipedia

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

    Phase behavior Triple point: 291.67 K (18.52 °C), ? Pa Critical point [2]: 720 K (447 °C), 5630 kPa Std enthalpy change of fusion, Δ fus H o: 14.37 kJ/mol Std entropy change

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