NMR Solvents

Solvent Formula 1H shifts 13C shifts mp °C     bp °C
Acetic Acid CD3COOD 2.2 21.1, 177.3 16.6 117.9
Acetone CD3COCD3 2.09 30.7, 205.1 -94.7 56.1
Acetonitrile CD3CN 2.0 0.3, 117.2 -43.8 81.6
Benzene C6D6 7.4 128.7 5.5 80.1
Carbon Disulphide CS2 none 192.8 -11.6 46.3
Carbon Tetrachloride CCl4 none 96.7 -23.0 76.8
Chloroform CDCl3 7.3 77.05 -63.5 61.3
Dichloromethane CD2Cl2 5.3 54.2 -95.1 40.8
Diethyl Ether (-100 °C) (CH3CH2)2O ?, 66.51 -116.3 34.6
Dimethyl Ether (-100 °C) CH3OCH3 3.2 60.08 -138.5 -23
Dimethylformamide Me2NCHO 31, 36, 162.4 -61.? 153.?
Dimethylsulfoxide CD3SOCD3 2.6 39.6 18.6 189.0
1,4-Dioxan (OCH2CH2)2    3.7 67.8 11.8 101.4
Ethanol CD3CD2OD 1.2, 7.3, 3.8     17.9, 57.3 - 78.3
Methanol CD3OD 3.5 49.3 -97.8 64.6
Nitrobenzene C6D5NO2 7.5, 7.7, 8.1 123, 129, 135 5.7 210.8
Nitromethane CD3NO2 4.3 57.3 -28.6 101.2
Pyridine C5D5N 7.1, 7.6, 8.8 123.9, 135.9, 150.2      -41.6 115.3
1,1,2,2-Tetrachloroethane CHCl2CHCl2 ? 75.5 -43.8 146.3
Tetrahydrofuran C4H8O 1.8, 3.7 26.7, 68.6 -108.5 65.4
Tetrahydrofuran -100 °C ?, 67.96
Toluene C6D5CD3 2.1, 7.0-7.1 20.4, 124-137 -94.9 110.6
Trichlorofluoromethane CFCl3 none 117.6 -111 23.7
Trifluoroacetic Acid CF3COOD ~10 99-136,162-167 -15.3 72.4
Water D2O 4.8 none 0.0 100.0
Solvent Formula 1H shifts 13C shifts mp °C     bp °C
More detail, actual spectra