Skip to main content
. 2013 Dec 3;6:337. doi: 10.1186/1756-3305-6-337

Table 2.

Chemical composition and oil yields of Cymbopogon species

KI exp a KI lit b ID c Compounds d Cymbopogon citratus
Cymbopogon giganteus
Cymbopogon schoenanthus
% % %
978
974
MS, RI
Sulcatone
0.5
 
 
982
988
MS, RI
Myrcene
12.4
 
 
984
988
MS, RI
2,3-Dehydro-1,8-cineole
 
0.1
0.1
995
1001
MS, RI
δ-2-Carene
 
0.1
15.5
998
1002
MS, RI
α-Phellandrene
 
 
0.2
1009
1014
MS, RI
α-Terpinene
 
 
0.2
1017
1020
MS, RI
p-Cymene
 
0.5
0.1
1020
1024
MS, RI
Limonene
 
9.6
3.6
1029
1032
MS, RI
Z-β-Ocimene
0.3
 
0.1
1039
1044
MS, RI
E-β-Ocimene
0.2
 
0.1
1081
1083
MS, RI
L-Fenchone
 
 
0.2
1082
1082
MS, RI
m-Cymenene
 
0.2
 
1085
1090
MS, RI
6,7-Epoxymyrcene
0.2
 
 
1093
1095
MS, RI
Linalool
1.1
 
 
1114
1118
MS, RI
Z-p-menth-2-en-1-ol
 
 
1.4
1116
1119
MS, RI
E - p -Mentha-2,8-dienol
 
19.3
 
1129
1133
MS, RI
Z - p -Mentha-2,8-dienol
 
10.2
 
1132
1136
MS, RI
E-p-menth-2-en-1-ol
 
 
0.7
1138
1144
MS, RI
Neo-Isopulegol
 
0.1
 
1145
1148
MS, RI
Citronellal
0.1
0.7
 
1148
 
MS
4-Isopropenylcyclohexanone
 
0.4
 
1160
1166
MS, RI
p-mentha-1,5-dien-8-ol
 
 
0.1
1168
1173
MS, RI
Rose furan epoxide
0.2
 
 
1180
1179
MS, RI
p-Cymen-8-ol
 
 
0.1
1183
1186
MS, RI
α-Terpineol
 
 
1.5
1183
1187
MS, RI
E -p-Mentha-1(7),8-dien-2-ol
 
19.6
 
1188
1195
MS, RI
Z-Piperitol
 
 
0.3
1194
 
MS
p-Menth-6-en-2,3-diol
 
3.2
 
1201
1209
MS, RI
E-Piperitol
 
 
0.2
1212
1215
MS, RI
E-Carveol
 
6.0
 
1216
1224
MS, RI
2,3-Epoxyneral
0.1
 
 
1224
1226
MS, RI
Z -Carveol
 
17.0
 
1225
1227
MS, RI
Z-p-Mentha-1(7),8-dien-2-ol
 
2.1
 
1237
1235
MS, RI
Neral
33.1
 
 
1237
1239
MS, RI
Carvone
 
3.2
 
1253
1249
MS, RI
Piperitone
 
0.1
58.9
1257
1249
MS, RI
Geraniol
1.0
 
 
1266
1269
MS, RI
Perilla aldehyde
 
0.8
 
1268
1264
MS, RI
Geranial
44.3
 
 
1286
1293
MS, RI
2-Undecanone
0.1
 
 
1351
1359
MS, RI
Geranic acid
0.1
 
 
1376
1379
MS, RI
Geranyl acetate
0.8
 
 
1382
1389
MS, RI
β-Elemene
 
 
0.4
1408
1417
MS, RI
E-Caryophyllene
0.1
 
1.1
1421
1431
MS, RI
β-Gurjunene
 
 
0.1
1443
1452
MS, RI
α-Humulene
 
 
0.1
1486
1495
MS, RI
2-Tridecanone
0.1
 
 
1490
1500
MS, RI
α-Muurolene
 
 
0.1
1503
1513
MS, RI
γ-Cadinene
 
 
0.1
1513
1522
MS, RI
δ-Cadinene
 
 
0.4
1540
1546
MS, RI
Elemol
 
 
5.3
1571
1582
MS, RI
Caryophyllene oxide
0.1
0.1
 
1595
1607
MS, RI
5-Epi-7-epi-α-eudesmol
 
 
0.3
1609
1622
MS, RI
10-Epi-γ-eudesmol
 
 
0.2
1609
1615
MS, RI
Selina-6-en-4-ol
0.4
 
 
1636
1640
MS, RI
Phenyl ethyl hexanoate
 
0.1
 
1623
1630
MS, RI
γ-Eudesmol
 
 
1.1
1626
1629
MS, RI
Eremoligenol
 
 
1.9
1634
1640
MS, RI
Hinesol
 
 
0.7
1643
1649
MS, RI
β-Eudesmol
 
 
1.2
1646
1652
MS, RI
α-Eudesmol
 
 
2.1
 
 
 
Yields
1.7
1.4
2.6
      Total identified 95.2 93.4 98.4

aKIexp = retention indices are determined using n-alkanes (C7-C17).

bKIlit = retention indices of reference compounds from literature.

cID = Identification methods; MS = comparison of the mass spectrum with those of the computer mass libraries, and Adams (2007); RI = comparison of calculated RI with those reported in the literature.

dCompounds are listed in order of their retention time; the names and the percentages of main compounds are indicated in bold.