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NMR impurities in DMSO-d₆

Common impurity peaks observed in DMSO-d₆ (solvent residual ¹H: 2.50 (quint); ¹³C: 39.52). Full solvent residual table: NMR solvent residual peaks.

Trace solvents, drying agents, and workup residues often appear as extra signals beside your compound. The tables below list typical ¹H chemical shifts (δ, ppm) reported for common impurities in each deuterated solvent. Values are taken from the Gottlieb (1997) and Fulmer (2010) compilations (DOI 10.1021/jo971176v, 10.1021/om100106e). Shifts drift slightly with temperature, concentration, and water content—compare nearby runs on the same instrument when assigning peaks.

To reduce impurity signals: use fresh solvent, avoid silicone grease near the NMR tube, dry glassware, and remove volatile solvents (EtOAc, DCM, ether, THF) on a rotary evaporator before dissolving the sample. Residual water appears at solvent-dependent chemical shifts; see the water-in-solvents table on the solvent residual peaks page.

Impurity¹H peaks (ppm)
Solvent residual2.50
H₂O / HOD3.33
CH₂Cl₂5.76
CHCl₃8.32
MeOH3.16
EtOH3.44 / 1.06
acetone2.09
MeCN2.07
EtOAc4.03 / 1.99 / 1.17
Et₂O3.38 / 1.09
THF3.60 / 1.76
DMF7.95 / 2.89 / 2.73
DMSO2.50 (overlaps solvent)
acetic acid1.91
n-hexane / grease1.25 / 0.86
silicone grease0.08
TMS0.00
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