Skip to main content

Table 2 Chemical composition of D. muricatus volatile fractions extracted by HS-SPME

From: Biological activities and volatile constituents of Daucus muricatus L. from Algeria

     

Separated organse

Componentsa

lRIab

RIac

Aerial parts

Stems

Leaves

Flowers

Umbels

Roots

1a

Heptane

700

700

2.6 ± 0.07

7.9 ± 0.28

1.3 ± 0.11

1.1 ± 0.15

0.3 ± 0.04

0.2 ± 0.01

1b

3-Methyl butanol

709

705

0.3 ± 0.01

0.7 ± 0.01

0.2 ± 0.01

0.4 ± 0.01

0.2 ± 0.01

0.1 ± 0.01

1c

3-Methyl-pentan-2-ol

754

760

0.4 ± 0.14

0.4 ± 0.01

0.2 ± 0.01

0.5 ± 0.09

0.4 ± 0.01

0.7 ± 0.01

1d

Hexanal

780

771

0.2 ± 0.01

0.4 ± 0.01

0.1 ± 0.01

0.1 ± 0.01

0.3 ± 0.06

1.4 ± 0.07

1

Nonane

900

898

0.5 ± 0.07

0.5 ± 0.02

1.1 ± 0.22

0.4 ± 0.01

tr

0.1 ± 0.01

1e

Artemisiatriene

923

921

0.2 ± 0.01

-

-

0.3 ± 0.06

0.1 ± 0.01

-

2

α-Thujene

932

923

0.1 ± 0.01

-

0.1 ± 0.01

0.5 ± 0.04

0.1 ± 0.01

-

3

α-Pinene

936

931

13.2 ± 0.74

8.1 ± 0.36

16.1 ± 0.89

13.1 ± 0.97

15.5 ± 1.1

8.7 ± 0.14

4

Camphene

950

944

0.2 ± 0.01

tr

0.1 ± 0.01

0.3 ± 0.01

0.3 ± 0.08

0.4 ± 0.01

5a

Butyl butyrate

970

966

0.2 ± 0.01

-

0.2 ± 0.01

0.2 ± 0.01

0.2 ± 0.01

0.1 ± 0.01

6

Sabinene

973

967

2.9 ± 0.21

1.4 ± 0.14

2.3 ± 0.45

6.5 ± 0.33

1.5 ± 0.46

0.3 ± 0.01

7

β-Pinene

978

970

0.9 ± 0.06

0.7 ± 0.02

1.2 ± 0.56

1.1 ± 0.51

1.1 ± 0.13

1.6 ± 0.21

8

Myrcene

987

980

2.9 ± 0.13

1.5 ± 0.14

3.2 ± 0.21

2.9 ± 0.12

3.9 ± 0.66

0.1 ± 0.01

8a

Yomogi alcohol

991

981

0.4 ± 0.07

0.7 ± 0.01

0.4 ± 0.01

0.4 ± 0.01

0.4 ± 0.05

-

9

α-Phellandrene

1002

997

1.5 ± 0.13

-

3.1 ± 0.16

2 ± 0.29

1.1 ± 0.29

-

9a

3-Carene

1010

1005

0.1 ± 0.01

-

0.1 ± 0.01

0.1 ± 0.01

0.1 ± 0.01

0.4 ± 0.01

10

α-Terpinene

1013

1008

0.8 ± 0.06

-

0.3 ± 0.01

2.8 ± 0.22

0.2 ± 0.01

0.1 ± 0.01

11

p-Cymene

1015

1012

3.2 ± 0.32

3.4 ± 0.12

3.1 ± 0.51

3.4 ± 0.51

3.2 ± 0.11

9.1 ± 0.76

12

Limonene

1025

1022

22.4 ± 1.28

13.3 ± 0.56

30.6 ± 0.99

19.1 ± 0.77

28.1 ± 0.82

6.9 ± 0.35

13

(Z)-β-Ocimene

1029

1025

0.2 ± 0.01

0.4 ± 0.01

0.1 ± 0.01

0.2 ± 0.02

0.1 ± 0.01

0.3 ± 0.01

13a

(E)-β-Ocimene

1041

1031

0.1 ± 0.01

0.1 ± 0.01

0.2 ± 0.02

0.2 ± 0.01

0.1 ± 0.01

0.3 ± 0.01

14

γ-Terpinene

1051

1049

3.2 ± 0.09

4.1 ± 0.54

2.5 ± 0.22

5.1 ± 0.55

1.3 ± 0.35

1.2 ± 0.01

14a

Octanol

1063

1052

0.3 ± 0.01

tr

0.6 ± 0.01

0.4 ± 0.08

0.3 ± 0.05

-

16

Nonan-2-one

1070

1073

0.6 ± 0.07

0.7 ± 0.02

0.5 ± 0.01

0.6 ± 0.08

0.6 ± 0.09

0.2 ± 0.01

17

p-Cymenene

1075

1077

0.3 ± 0.06

-

0.2 ± 0.01

0.4 ± 0.06

0.7 ± 0.03

3.1 ± 0.13

18

Terpinolene

1082

1079

0.7 ± 0.06

0.6 ± 0.01

0.9 ± 0.07

1.3 ± 0.23

0.4 ± 0.01

10.2 ± 0.86

19

Linalool

1083

1085

1.4 ± 0.08

3.2 ± 0.28

0.5 ± 0.01

1.1 ± 0.29

0.9 ± 0.1

0.2 ± 0.01

19a

α-Thujone

1089

1086

0.5 ± 0.04

1.8 ± 0.09

tr

0.5 ± 0.02

0.4 ± 0.02

0.1 ± 0.01

20

Undecane

1100

1100

8.9 ± 0.76

16.9 ± 0.89

6.1 ± 0.38

3.6 ± 0.14

7.4 ± 0.69

7.2 ± 0.26

20a

3-Octyl acetate

1113

1103

1.8 ± 0.12

0.7 ± 0.06

0.2 ± 0.01

0.3 ± 0.01

0.2 ± 0.01

0.2 ± 0.01

21a

Camphor

1123

1119

1.1 ± 0.07

2.9 ± 0.16

0.7 ± 0.01

0.6 ± 0.06

0.2 ± 0.01

0.5 ± 0.01

22

trans-Pinocarveol

1126

1120

0.4 ± 0.01

0.7 ± 0.01

0.3 ± 0.02

0.4 ± 0.01

0.6 ± 0.02

0.1 ± 0.01

22a

Citronellal

1129

1130

0.1 ± 0.01

tr

0.1 ± 0.01

0.1 ± 0.01

0.4 ± 0.05

-

22b

cis-Verbenol

1132

1132

0.1 ± 0.01

-

0.1 ± 0.01

0.1 ± 0.01

0.1 ± 0.01

-

24

Pinocarvone

1137

1135

0.1 ± 0.01

-

0.1 ± 0.01

0.1 ± 0.01

0.2 ± 0.02

0.7 ± 0.01

25

Borneol

1150

1149

0.5 ± 0.08

0.9 ± 0.01

0.4 ± 0.01

0.3 ± 0.04

0.4 ± 0.01

-

26

Cryptone

1160

1159

0.5 ± 0.06

0.5 ± 0.01

0.5 ± 0.08

0.4 ± 0.01

0.7 ± 0.09

3.8 ± 0.11

27

Terpinene-4-ol

1164

1160

1.4 ± 0.18

2.1 ± 0.43

0.9 ± 0.06

1.8 ± 0.36

1.1 ± 0.15

0.1 ± 0.01

27a

Myrtenal

1172

1163

0.1 ± 0.01

tr

0.1 ± 0.01

0.1 ± 0.01

0.1 ± 0.01

0.3 ± 0.02

27b

Estragole

1175

1169

1.1 ± 0.09

1.1 ± 0.58

1.3 ± 0.29

1.7 ± 0.12

0.6 ± 0.08

-

29

α-Terpineol

1176

1177

0.4 ± 0.05

0.5 ± 0.04

0.4 ± 0.08

0.4 ± 0.03

0.5 ± 0.01

0.2 ± 0.01

29a

Verbenone

1184

1178

0.3 ± 0.01

0.7 ± 0.01

0.1 ± 0.01

0.2 ± 0.01

0.1 ± 0.01

-

31

Decanal

1188

1185

0.1 ± 0.01

-

0.1 ± 0.01

0.1 ± 0.01

0.2 ± 0.01

-

33

Citronellol

1213

1211

1.1 ± 0.14

1.1 ± 0.22

1.1 ± 0.33

0.9 ± 0.06

1.5 ± 0.23

0.1 ± 0.01

34

Carvone

1214

1215

0.7 ± 0.07

1.1 ± 0.09

0.5 ± 0.01

0.6 ± 0.04

0.6 ± 0.02

0.1 ± 0.01

35

Pulegone

1215

1216

0.3 ± 0.01

0.8 ± 0.02

0.2 ± 0.01

0.2 ± 0.01

0.1 ± 0.01

-

37

Geraniol

1235

1235

0.2 ± 0.01

tr

0.1 ± 0.01

0.4 ± 0.02

0.1 ± 0.01

0.8 ± 0.05

38

trans-Myrtanol

1240

1236

0.1 ± 0.01

0.1 ± 0.01

tr

0.1 ± 0.01

0.3 ± 0.01

-

38a

Geranial

1244

1239

0.1 ± 0.01

tr

0.1 ± 0.01

0.1 ± 0.01

tr

-

39

cis-Chrysanthenyl acetate

1253

1242

0.1 ± 0.01

tr

0.1 ± 0.01

tr

0.1 ± 0.01

-

42

Bornyl acetate

1270

1266

0.6 ± 0.05

1.2 ± 0.11

0.4 ± 0.05

0.5 ± 0.06

0.6 ± 0.04

9.7 ± 0.55

43

Undecan-2-one

1273

1270

0.6 ± 0.08

0.8 ± 0.04

0.6 ± 0.08

0.4 ± 0.03

0.5 ± 0.01

0.3 ± 0.01

44

trans-Sabinyl acetate

1278

1271

5.1 ± 0.47

3.8 ± 0.26

2.6 ± 0.12

3.5 ± 0.38

9.6 ± 0.53

 

47a

Neryl acetate

1342

1335

2.0 ± 0.31

2.4 ± 0.36

3.4 ± 0.65

1.3 ± 0.35

0.9 ± 0.1

0.3 ± 0.01

48

δ-Elemene

1340

1337

0.3 ± 0.02

0.7 ± 0.06

0.3 ± 0.05

0.1 ± 0.01

tr

0.1 ± 0.01

49

Geranyl acetate

1362

1360

0.1 ± 0.01

tr

tr

0.2 ± 0.01

tr

0.2 ± 0.01

50

Undecanol

1363

1365

0.1 ± 0.01

tr

tr

tr

tr

1.9 ± 0.01

51

α-Copaene

1379

1377

0.7 ± 0.01

1.1 ± 0.12

0.4 ± 0.02

0.6 ± 0.03

0.9 ± 0.08

0.4 ± 0.01

51a

Daucene

1380

1379

0.5 ± 0.02

0.9 ± 0.08

0.1 ± 0.01

0.2 ± 0.01

0.7 ± 0.01

0.7 ± 0.06

54

Dodecanal

1389

1395

0.2 ± 0.01

0.3 ± 0.01

0.1 ± 0.01

0.1 ± 0.01

0.1 ± 0.01

1.3 ± 0.01

54a

Tetradecane

1400

1399

0.1 ± 0.01

0.2 ± 0.02

0.1 ± 0.01

0.1 ± 0.01

tr

-

56

trans-Caryophyllene

1424

1422

2.3 ± 0.23

1.4 ± 0.13

3.1 ± 0.25

3.8 ± 0.26

1.2 ± 0.15

1.9 ± 0.18

58

β-Copaene

1430

1430

0.3 ± 0.02

0.4 ± 0.01

0.6 ± 0.05

0.3 ± 0.01

0.3 ± 0.01

0.4 ± 0.01

59

α-Humulene

1455

1450

0.4 ± 0.05

-

0.1 ± 0.01

0.9 ± 0.08

0.1 ± 0.01

0.1 ± 0.01

61

Dodecanol

1472

1468

tr

tr

tr

tr

tr

3.4 ± 0.28

62

γ-Muurolene

1473

1471

1.3 ± 0.13

0.5 ± 0.01

0.6 ± 0.01

1.5 ± 0.42

1.9 ± 0.21

4.3 ± 0.16

63

Germacrene D

1479

1476

0.4 ± 0.04

0.5 ± 0.06

0.2 ± 0.01

0.4 ± 0.02

0.3 ± 0.01

0.2 ± 0.01

64

trans-β-Bergamotene

1480

1475

tr

tr

tr

tr

tr

0.5 ± 0.03

65

6-epi-Shyobunone

1481

1480

0.1 ± 0.01

tr

0.1 ± 0.01

0.2 ± 0.01

0.2 ± 0.01

-

65a

β-Selinene

1486

1481

0.2 ± 0.01

0.2 ± 0.01

0.2 ± 0.02

0.1 ± 0.01

0.2 ± 0.03

0.5 ± 0.02

69

Shyobunone

1500

1501

0.1 ± 0.01

tr

0.1 ± 0.01

0.1 ± 0.01

0.1 ± 0.01

0.7 ± 0.01

70

δ-Cadinene

1520

1515

0.6 ± 0.04

0.5 ± 0.01

0.3 ± 0.04

0.1 ± 0.01

1.3 ± 0.16

0.9 ± 0.07

71

(E)-α-Bisabolene

1531

1526

1.1 ± 0.31

0.5 ± 0.02

1.4 ± 0.12

0.9 ± 0.1

1 ± 0.45

0.4 ± 0.01

72

Isochavicol isobutyrate

1541

1538

0.3 ± 0.05

tr

0.3 ± 0.01

0.9 ± 0.06

0.1 ± 0.01

0.1 ± 0.1

76

Caryophyllene oxide

1578

1582

0.2 ± 0.01

-

0.1 ± 0.01

0.4 ± 0.01

0.1 ± 0.01

0.7 ± 0.01

77

Tridecanol

1580

1586

tr

tr

tr

tr

tr

1.1 ± 0.07

87

Eudesma-4(15),7-dien-1β-ol

1671

1672

tr

-

tr

tr

tr

0.6 ± 0.01

89

Heptadecane

1700

1699

0.4 ± 0.13

-

1.3 ± 0.65

0.2 ± 0.01

0.2 ± 0.01

-

 

Total identification (%)

  

97.8

95.4

99.1

94.3

97.6

90.6

 

GC-FID Total area 105

  

103

22

154

108

107

68

 

Monoterpene hydrocarbons

  

52.9

33.6

64.1

59.3

57.8

42.8

 

Oxygenated monoterpenes

  

20.6

25.6

14.4

16

20.5

17.6

 

Sesquiterpene hydrocarbons

  

8.1

5.8

7.2

8.7

7.2

10.4

 

Oxygenated sesquiterpenes

  

0.4

-

0.3

0.7

0.4

2.0

 

Phenylpropanoids

  

0.3

-

0.3

0.9

0.1

0.1

 

Non-terpenic compounds

  

15.5

30.4

12.8

8.7

11.6

17.7

  1. a Order of elution is given on apolar column (Rtx-1). Numbers correspond to those in Table 1. The volatile components identified exclusively from the HS-fractions were affected by a letter, b Retention indices of literature on the apolar column (lRIa) reported from König et al., 2001., c Retention indices on the apolar Rtx-1 column (RIa), d Percentages (means of three analyses) obtained by GC-FID (on RTX-1: apolar column) under optimized HS-SPME parameters: temperature: 70°C, equilibrium time: 120 min; extraction time: 30 min.