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. 2019 Dec 12;2:33–40. doi: 10.1016/j.crfs.2019.11.005

Table 1.

Chemical composition of the Satureja montana (commercial sample) and Mentha longifolia (obtained from the population growing at the UPV, Valencia, Spain) essential oils (EOs).

COMPOUNDa RI (lineal) exp.b RI (lineal) ref.c S. montana
M. longifolia
Peak area %d Peak area %
Tricyclene 921 921 tre -f
α-thujene 925 924 1.1 ± 0.0
α-pinene 930 932 1.7 ± 0.0 1.0 ± 0.0
Camphene 945 946 0.5 ± 0.0 tr
Sabinene 969 969 0.1 ± 0.0 0.8 ± 0.0
β-pinene 974 974 tr 1.3 ± 0.0
Octen-2-ol 980 982 0.7 ± 0.0
Myrcene 991 988 3.1 ± 0.0 1.2 ± 0.0
2-octanol 997 994 0.4 ± 0.0
α-phellandrene 1004 1002 0.2 ± 0.0 tr
δ-3-carene 1010 1008 tr
α-terpinene 1016 1014 1.9 ± 0.0
p-cymene 1019 1020 14.2 ± 0.1
Limonene 1027 1024 1.8 ± 0.2 1.4 ± 0.0
1,8-cineole 1030 1026 0.7 ± 0.1 1.8 ± 0.0
(Z)-β-ocimene 1038 1032 0.2 ± 0.0 2.2 ± 0.0
(E)-β-ocimene 1049 1044 0.2 ± 0.0 0.2 ± 0.0
γ-terpinene 1055 1054 15.9 ± 0.1 2.4 ± 0.0
(Z)-sabinen hydrate 1067 1065 0.6 ± 0.0
Terpinolene 1088 1086 0.3 ± 0.0
Isopentyll 2-methyl butanoate 1099 1102 0.3 ± 0.0
Linalool 1102 1095 3.2 ± 0.0
3-octanol acetate 1120 1120 tr
Camphor 1142 1141 0.1 ± 0.0
Neomenthol 1158 1161 tr
Borneol 1166 1165 3.6 ± 0.0
δ-terpineol 1167 1162 0.2 ± 0.0
terpinen-4-ol 1177 1174 2.7 ± 0.0 tr
α-terpineol 1195 1186 0.2 ± 0.1 0.9 ± 0.0
Thymol, methyl ether 1235 1232 0.3 ± 0.0
Pulegone 1236 1233 tr
Carvone 1241 1239 tr
Carvacrol methyl ether 1246 1241 7.3 ± 0.1
Piperitone oxide 1248 1250 23.5 ± 0.3
(Z)-carvone oxide 1267 1259 0.1 ± 0.0
Isopiperitenone 1272 1272
Neryl formiate 1275 1280 0.1 ± 0.0
Thymol 1299 1289 3.0 ± 0.0
6-hydroxycarvotanacetone 1300 1300 0.1 ± 0.0
Carvacrol 1321 1298 24 ± 0.3
Piperitenone 1333 1340 tr
Thymol acetate 1357 1349 tr
Piperitenone oxide 1359 1366 52.7 ± 0.2
α-copaene 1376 1374 tr
β-bourbonene 1384 1387 tr
β-elemene 1387 1389 tr
(E)-jasmone 1400 1390 tr
(Z)-jasmone 1407 1392 0.1 ± 0.0
β-caryophyllene 1420 1417 9.1 ± 0.1 3.0 ± 0.0
(Z)-muurola-3,5-diene 1447 1448 0.4 ± 0.0
α-humulene 1452 1452 0.2 ± 0.0
(E)-β-farnesene 1458 1454
Germacrene-D 1474 1484 3.8 ± 0.2
Biciclogermacrene 1487 1500 0.2 ± 0.0
α-muurolene 1498 1500 0.1 ± 0.0
β- bisabolene 1508 1505 1.5 ± 0.0
γ-cadinene 1512 1513 0.1 ± 0.0
δ-cadinene 1522 1522 tr
Germacrene-D-4-ol 1568 1574 0.2 ± 0.0
Caryophyllene oxide 1580 1582 0.4 ± 0.0 tr
Muurolol epi-α 1647 1640 0.1 ± 0.0
α− cadinol 1655 1652 tr
TOTAL IDENTIFIED 98.9 98.5
a

Compounds listed according to their elution order in a ZB-5 column.

b

Experimental linear retention index.

c

Linear retention index according to Adams (2007).

d

Normalised peak area from the FID chromatogram (mean ± SD from triplicate runs).

e

tr = traces (% < 0.05).

f

Not detected.