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  2. Deuterium NMR - Wikipedia

    en.wikipedia.org/wiki/Deuterium_NMR

    Deuterium NMR has a range of chemical shift similar to proton NMR but with poor resolution, due to the smaller magnitude of the magnetic dipole moment of the deuteron relative to the proton. It may be used to verify the effectiveness of deuteration: a deuterated compound will show a strong peak in 2 H NMR but not proton NMR.

  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. Trimethylsilylpropanoic acid - Wikipedia

    en.wikipedia.org/wiki/Trimethylsilylpropanoic_acid

    Trimethylsilylpropanoic acid (TMSP or TSP) is a chemical compound containing a trimethylsilyl group. It is used as internal reference in nuclear magnetic resonance for aqueous solvents (e.g. D 2 O). For that use it is often deuterated (3-(trimethylsilyl)-2,2,3,3-tetradeuteropropionic acid or TMSP- d 4 ). [ 1 ]

  5. DSS (NMR standard) - Wikipedia

    en.wikipedia.org/wiki/DSS_(NMR_Standard)

    It is the sodium salt of trimethylsilylpropanesulfonic acid. A white, water-soluble solid, it is used as a chemical shift standard for proton NMR spectroscopy of aqueous solutions. [1] The chemical shift, specifically the signal for the trimethylsilyl group, is relatively insensitive to pH. [2]

  6. Heteronuclear single quantum coherence spectroscopy - Wikipedia

    en.wikipedia.org/wiki/Heteronuclear_single...

    In a typical HSQC spectrum, the NH 2 peaks from the sidechains of asparagine and glutamine appear as doublets on the top right corner, and a smaller peak may appear on top of each peak due to deuterium exchange from the D 2 O normally added to an NMR sample, giving these sidechain peaks a distinctive appearance. The sidechain amine peaks from ...

  7. Deuterated chloroform - Wikipedia

    en.wikipedia.org/wiki/Deuterated_chloroform

    Commercial chloroform-d does, however, still contain a small amount (0.2% or less) of non-deuterated chloroform; this results in a small singlet at 7.26 ppm, known as the residual solvent peak, which is frequently used as an internal chemical shift reference. In carbon-13 NMR spectroscopy, the sole carbon in deuterated chloroform shows a ...

  8. 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 .

  9. Deuterium - Wikipedia

    en.wikipedia.org/wiki/Deuterium

    Deuterium is often represented by the chemical symbol D. Since it is an isotope of hydrogen with mass number 2, it is also represented by 2 H. IUPAC allows both D and 2 H, though 2 H is preferred. [8] A distinct chemical symbol is used for convenience because of the isotope's common use in various scientific processes.

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