Table 1 Characteristics of 1H NMR anomeric signals of monosaccharides, their esterification, and degradation products

From: Development of a 1H qNMR method for the identification and quantification of monosaccharides in dietary fibre fractions

Compound

δ (ppm)

Multiplicitya and integration

J1-2 couplings (Hz)

No. H

 

Anomer

 
 

α

β

α

β

α

β

 

Glucose

5.24

4.66

d, half peak*2

d, half peak*2

3.74

7.99

1

Fructose

-

4.13

-

m, whole peak

-

-

2b

Galactose

5.29

4.60

d, whole peak

d, half peak*2

3.88

7.95

1

Ribose

4.86

4.97

d, whole peak

d, whole peak

1.85

6.17

1c

Arabinose

4.53

5.26

d, whole peak

d, half peak*2

7.84

3.66

1

Rhamnose

5.13

4.87

d, whole peak

d, whole peak

1.01

1.72

1

Fucose

5.22

4.57

d, whole peak

d, half peak*2

3.92

7.90

1

Mannose

5.20

4.91

d, half peak*2

d, whole peak

1.76

1.04

1

Xylose

5.21

4.59

d, half peak*2

d, half peak*2

3.68

7.88

1

Galacturonic acid

5.36

4.64

d, whole peak

d, half peak*2

3.82

7.94

1

Glucuronic acid

5.30

4.72

d, whole peak

d, half peak*2

3.77

7.94

1

Glucuronic acid lactone

4.74

5.05

m, peak-half β-GlcA

m, whole peak

-

-

3d

Acetate

2.10

s, whole peak

 

3

Methanol

3.37

s, whole peak

 

3

Formic acid

8.25

s, whole peak

 

1

Furfural

9.48

s, whole peak

 

1

Hydroxymehylfurfural

9.43

s, whole peak

 

1

  1. aMultiplicity: s singlet, d doublet, and m multiplet.
  2. bH3 + H4 of fructofuranose (22.6% of the total fructose).
  3. cα and β pyranosidic forms (60.2% of the total ribose).
  4. dComplex signal of three non-anomeric protons.