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. 2024 Mar 13;13(6):825. doi: 10.3390/plants13060825

Table 1.

Composition of the EO of A. arborescens.

KI a KI b % Identification c
Tricyclene 844 1047 0.3 1, 2
α-Thujene 850 1020 0.1 1, 2
α-Pinene 855 1036 2.3 1, 2, 3
Camphene 868 1075 6.0 1, 2, 3
Butanoic acid, 2-methylpropyl ester 870 1174 0.1 1, 2
Sabinene 891 1115 2.4 1, 2
β-Pinene 910 1120 0.8 1, 2, 3
α-Phellandrene 918 1177 1.8 1, 2, 3
α-Terpinene 929 1170 0.6 1, 2, 3
Propanoic acid, 2-methyl-, 3-methylbutyl ester 934 0.2 1, 2
p-Cymene 938 1250 2.4 1, 2, 3
Eucalyptol 942 1210 2.2 1, 2, 3
γ-Terpinene 970 1221 1.0 1, 2, 3
Terpinolene 997 1267 0.2 1, 2, 3
cis-Thujone 1009 1430 1.2 1, 2
trans-Thujone 1020 1442 24.2 1, 2
α-Campholenal 1032 1485 0.2 1, 2
allo-Ocimene 1041 1388 0.1 1, 2
Camphor 1050 1491 18.9 1, 2, 3
Pinocarvone 1063 1586 0.1 1, 2, 3
Borneol 1067 1715 0.2 1, 2, 3
Terpinen-4-ol 1079 1590 0.7 1, 2, 3
Isocitral 1084 1690 0.1 1, 2
α-Terpineol 1093 1661 0.3 1, 2
cis-Chrysantenyl acetate 1098 0.2 1, 2
4-Decen-1-ol 1133 0.2 1, 2
Thymol 1199 2172 0.6 1, 2, 3
δ-Elemene 1219 1479 0.1 1, 2
α-Copaene 1255 1477 0.4 1, 2
Isobornyl propanoate 1258 0.1 1, 2
β-Bourbonene 1263 1498 0.3 1, 2
β-Elemene 1266 1579 0.1 1, 2
β-Gurjunene 1273 1615 1.2 1, 2
Aromadendrene 1298 1631 6.5 1, 2
cis-Muurola-3,5-diene 1299 0.7 1, 2
α-Humulene 1322 1641 0.8 1, 2
γ-Gurjunene 1346 0.7 1, 2
Germacrene D 1350 1712 1.5 1, 2
cis-β-Guaiene 1354 1651 0.2 1, 2
trans-Muurola-4(14),5-diene 1365 0.3 1, 2
γ-Amorphene 1383 0.5 1, 2
δ-Amorphene 1393 1751 0.5 1, 2
α-Cadinene 1400 1753 0.1 1, 2
Caryophyllene oxide 1443 2000 3.0 1, 2
Aristolene epoxide 1453 0.2 1, 2
Caryophylla-4(12),8(13)-dien-5α-ol 1498 2324 0.8 1, 2
α-Cadinol 1507 2256 1.3 1, 2
Guaia-3,10(14)-dien-11-ol 1538 0.1 1, 2
cis-Z-α-Bisabolene epoxide 1550 0.1 1, 2
Cedren-13-ol, 8- 1837 2359 5.2 1, 2
trans-Nuciferol 1839 4.2 1, 2
Total 96.3
Monoterpene hydrocarbons 18.0
Oxygenated monoterpenes 49.0
Sesquiterpene hydrocarbons 13.9
Oxygenated sesquiterpenes 14.9
Others 0.5

a,b: Kovats retention indices determined relative to a series of n-alkanes (C10–C35) on the apolar HP-5 MS and the polar HP Innowax capillary columns, respectively; c: identification method: 1 = comparison of the Kovats retention indices with published data, 2 = comparison of mass spectra with those listed in the NIST 02 and Wiley 275 libraries and with published data, and 3 = coinjection with authentic compounds.