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  2. Acetone (data page) - Wikipedia

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

    The handling of this chemical may incur notable safety precautions. It is highly recommended that you seek the Material Safety Datasheet for this chemical from a reliable source and follow its directions. Mallinckrodt Baker; Science Stuff

  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).

  4. Chemical shift - Wikipedia

    en.wikipedia.org/wiki/Chemical_shift

    Chemical shift δ is usually expressed in parts per million (ppm) by frequency, because it is calculated from [5] =, where ν sample is the absolute resonance frequency of the sample, and ν ref is the absolute resonance frequency of a standard reference compound, measured in the same applied magnetic field B 0.

  5. Proton nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Proton_nuclear_magnetic...

    The total area of the 1 ppm CH 2 peak will be twice that of the 2.5 ppm CH peak. The CH 2 peak will be split into a doublet by the CH peak—with one peak at 1 ppm + 3.5 Hz and one at 1 ppm − 3.5 Hz (total splitting or coupling constant is 7 Hz). In consequence the CH peak at 2.5 ppm will be split twice by each proton from the CH 2. The first ...

  6. Isotopic shift - Wikipedia

    en.wikipedia.org/wiki/Isotopic_shift

    In NMR spectroscopy, isotopic effects on chemical shifts are typically small, far less than 1 ppm, the typical unit for measuring shifts. The 1 H NMR signals for 1 H 2 and 1 H 2 H ("HD") are readily distinguished in terms of their chemical shifts. The asymmetry of the signal for the "protio" impurity in CD 2 Cl

  7. 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 ...

  8. Dimethyldioxirane - Wikipedia

    en.wikipedia.org/wiki/Dimethyldioxirane

    Dimethyldioxirane (DMDO) is the organic compound with the formula (CH 3) 2 CO 2. [1] It is the dioxirane derived from acetone and can be viewed as the monomer of acetone peroxide.It is a powerful selective oxidizing agent that finds some use in organic synthesis.

  9. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone (>C=O).It is a colorless, highly volatile, and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops.