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. 2022 Jul 6;11(7):1330. doi: 10.3390/antiox11071330

Table 2.

Percentage (%) and relative concentrations (ng/mL) of the compounds of TEOs prepared at the beginning and at the end of the flowering period.

Percentage of Compound in the Thyme Essential Oils a Relative Concentration of Compound in the Experiments (ng/mL) b
Compounds MS Sim LRI Exp LRI Ref Beginning of Flowering End of Flowering Beginning of Flowering End of Flowering
Tricyclene 94 922 923 0.02 0.02 0.34 0.34
α-Thujene 98 925 927 0.99 0.99 18.51 18.51
α-Pinene 97 933 933 0.61 0.69 10.72 12.13
Camphene 97 949 953 0.39 0.50 7.02 9.00
Sabinene 95 972 972 0.02 0.01 0.36 0.18
Pent-4-enyl propanoate 94 974 974 0.03 0.01 0.50 0.17
β-Pinene 92 977 978 0.20 0.21 3.49 3.62
Vinyl amyl carbinol 95 979 978 0.27 0.42 4.52 7.03
Octan-3-one 93 984 986 0.03 0.03 0.48 0.48
Myrcene 96 988 991 1.45 1.28 23.20 20.48
Octan-3-ol 96 997 999 0.04 0.03 0.65 0.49
α-Phellandrene 96 1006 1007 0.15 0.10 2.53 1.69
δ-3-Carene 96 1009 1009 0.08 0.08 1.38 1.38
α-Terpinene 98 1017 1018 1.40 0.82 22.40 13.12
p-Cymene 96 1025 1025 12.89 20.64 221.71 355.01
Limonene 96 1029 1030 0.29 0.34 4.88 5.73
β-Phellandrene 94 1030 1031 0.07 0.08 1.15 1.31
Eucalyptol 97 1032 1032 0.62 0.75 11.42 13.82
(Z)-, β-Ocimene 90 1034 1035 0.01 0.01 0.16 0.16
(E)-, β-Ocimene 95 1045 1046 0.03 0.02 0.48 0.32
γ-Terpinene 95 1058 1058 15.18 6.01 24.29 9.62
3-Methylbut-2-enyl butanoate 90 1063 1068 0.06 0.06 1.00 1.00
(Z)-Sabinene hydrate 93 1070 1069 0.26 0.59 4.21 9.56
Terpinolene 96 1086 1086 0.09 0.08 1.62 1.44
p-Cymenene 94 1091 1093 0.01 0.02 0.17 0.35
Linalool 97 1099 1101 1.46 2.15 2.54 3.74
(E)-Sabinene hydrate 94 1102 1099 0.11 0.18 2.27 3.50
3-Methylbut-3-enyl 3-methylbutanoate 90 1110 1114 tr 0.02 0.00 0.36
(Z)-, p-Menth-2-en-1-ol 96 1126 1124 0.03 0.03 0.50 0.50
Camphor 97 1149 1149 0.27 0.36 5.40 7.20
Borneol 98 1173 1173 0.48 0.66 9.70 13.74
Terpinen-4-ol 92 1182 1184 0.66 0.63 12.32 11.76
Hex-(3Z)-enyl-Butyrate 92 1184 1187 0.01 0.03 0.18 0.54
p-Cymen-8-ol 93 1189 1189 0.02 0.05 0.40 1.00
α-Terpineol 97 1197 1195 0.12 0.15 2.26 2.82
(Z)-, Dihydro-carvone 94 1200 1198 0.03 0.05 0.56 0.93
n-Decanal 95 1206 1208 0.01 0.01 0.17 0.17
Thymol methyl ether 94 1230 1229 0.19 0.62 3.50 11.41
Carvacryl methyl ether 96 1239 1239 0.27 0.37 5.05 6.93
Neral 96 1242 1238 0.01 0.01 0.17 0.17
Carvone 95 1249 1246 0.01 0.02 0.18 0.36
Geranial 97 1274 1268 0.02 0.02 0.34 0.34
Thymol 94 1294 1293 55.81 54.21 1071.55 1040.83
Carvacrol 94 1302 1300 2.30 2.90 44.94 56.67
Thymol acetate 93 1345 1348 0.04 nd 0.80 0.00
Eugenol 95 1354 1357 0.05 0.12 1.06 2.54
Isobornyl propionate * 93 1376 1377 0.04 0.06 0.80 1.20
α-Copaene * 88 1377 1375
β-Bourbonene 95 1385 1382 0.02 0.03 0.36 0.54
(Z)-Jasmone 93 1394 1394 nd 0.01 0.00 0.19
(E)-Caryophyllene 97 1421 1424 1.56 1.92 28.08 34.56
β-Copaene 94 1431 1433 0.02 0.03 0.38 0.56
α-Humulene 97 1457 1454 0.05 0.06 0.85 1.02
(Z)-Muurola-4(14),5-diene 94 1464 1466 tr 0.01 0.00 0.18
Geranyl propanoate 97 1468 1471 0.09 0.05 1.62 0.90
γ-Muurolene 92 1476 1478 0.05 0.06 0.90 1.08
α-Amorphene 90 1481 1482 nd 0.01 0.00 0.18
Germacrene D 95 1482 1480 0.11 0.04 1.87 0.68
β-Selinene 94 1491 1492 tr 0.01 0.00 0.18
γ-Amorphene 87 1494 1490 0.02 0.02 0.36 0.36
α-Selinene 89 1497 1501 0.01 0.01 0.18 0.18
α-Muurolene 93 1500 1497 0.03 0.03 0.53 0.53
γ-Cadinene 95 1515 1512 0.06 0.10 1.08 1.80
δ-Cadinene 94 1520 1518 0.11 0.11 1.98 1.98
(E)-Calamenene 90 1522 1527 0.02 0.03 0.40 0.60
(E)-Cadina-1,4-diene 93 1534 1536 0.01 0.01 0.18 0.18
α-Cadinene 95 1539 1538 0.01 0.01 0.18 0.18
Geranyl butyrate 97 1554 1559 0.02 0.02 0.36 0.36
Caryophyllene oxide 93 1585 1587 0.27 0.47 5.40 9.40
Humulene epoxide II 89 1613 1613 tr 0.01 0.00 0.19
(Z)-Cubenol 89 1618 1614 0.01 0.02 0.19 0.38
epi-γ-Eudesmol 95 1626 1624 0.05 0.03 0.90 0.54
α-Cadinol 94 1645 1641 0.06 0.12 1.29 2.58
Cadin-4-en-10-ol 95 1658 1659 0.04 0.02 0.73 0.37
Total 99.77 99.65

Abbreviations: MS Sim, MS spectral similarity; LRI exp, experimental linear retention index; LRI ref, reference linear retention index; nd, not detected; tr, trace level; * indicates a coelution on SLB-5 ms column. a The volatile compounds are expressed in % values. b The relative concentrations were calculated based on the fact that the cells were treated with 200 μL essential oil emulsion.