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Table 1 1H NMR assignment of metabolites in wines

From: Quality evaluation of different varieties of dry red wine based on nuclear magnetic resonance metabolomics

Keys

Compound

1H-NMR chemical shift

Group

1

Valine

0.88(d), 1.02(d)

C4H3,C5H3

2

2,3-Butanediol

1.15(d)

C1H3+C4H3

3

Ethanol

1.19(t), 3.56(q)

C2H3,C1H2

4

Proline

2.00(m), 2.07(m), 2.35(m), 3.35(m), 3.42(m), 4.16(m)

γ-CH2,β-CH,β’-CH,δ-CH,δ-CH,α-CH

5

Succinic acid

2.65(s)

C2H2+C3H2

6

Ethyl acetate

1.26(t), 4.16(q)

C4H3, C3H2

7

Tartaric acid

4.51(s)

C2H+C3H

8

β-Glucose

4.61 (d)

βC1H

9

α-Glucose

5.33(d)

αC1H

10

Gallic acid

7.14(s)

C2H+C6H

11

Glycerol

3.58(q), 3.67(m), 3.81(m)

C2H2,C3H2,C1H

12

Lactic acid

1.39(d), 4.16(m)

C3H3,C2H

13

Choline

3.20(s)

N-CH3

14

α-d-Glucuronic acid

5.35(d)

C1H

15

Malic acid

2.74(dd), 2.87(dd), 4.46(q)

βCH2,β’CH2, CH

16

Citric acid

2.82(d), 2.94(d)

C2Ha+C4Ha,C2Hb+C4Hb

17

Alanine

1.51(d)

βCH3

18

Tyrosine

6.86(d),7.19(d)

C2H,C3H

19

D-Sucrose

5.46(d), 3.55(dd), 3.72(dd), 3.90(dd), 4.215(d), 4.05(dd), 3.88(dd)

C1H,C2H,C3H,C4H,C1′H,C2′H,C3′H

20

γ-Aminobutyric acid

2.50(t), 1.96(m), 3.05(t)

α-CH2,β-CH2, γ-CH2

  1. Letters in parentheses indicate the peak multiplicities: s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet) and dd (doublet of doubles)