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. 2013 Oct 2;2013:536490. doi: 10.1155/2013/536490

Table 2.

Chemical composition of M. longifolia essential oil.

Componentsb RIc Molecular mass % Compositiona Mode of identificationd Quality (%)e
Monoterpene  hydrocarbons (7.31)
α-Pinene 939 136 0.76 ± 0.06 RT, RI, MS 97
β-Pinene 979 136 2.14 ± 0.19 RT, RI, MS 96
 Limonene 1029 136 1.80 ± 0.19 RT, RI, MS 94
cis-β-Ocimene 1037 136 1.98 ± 0.11 RT, RI, MS 97
δ-Terpinene 1089 136 0.63 ± 0.04 RI, MS 96
Oxygenated monoterpenes (67.24)
 1,8-Cineol 1031 154 2.00 ± 0.17 RT, RI, MS 98
 Linalool 1097 154 0.98 ± 0.10 RT, RI, MS 98
 Borneol 1169 154 5.96 ± 0.44 RT, RI, MS 96
α-Terpineol 1189 154 1.17 ± 0.09 RT, RI, MS 98
 Thymol 1290 150 2.85 ± 0.20 RT, RI, MS 99
 Piperitenone 1343 150 24.9 ± 1.34 RT, RI, MS 97
 Thymol acetate 1352 192 1.08 ± 0.08 RI, MS 94
 Piperitenone oxide 1370 166 28.3 ± 1.6 RT, RI, MS 96
Sesquiterpene hydrocarbons (17.19)
α-Gurjunene 1410 204 1.11 ± 0.18 RI, MS 96
β-Caryophyllene 1421 204 5.94 ± 0.32 RT, RI, MS 99
 Germacrene D 1485 204 8.16 ± 1.01 RT, RI, MS 99
 Calamenene 1540 202 1.98 ± 0.17d RT, RI, MS 98
Oxygenated sesquiterpenes (5.05)
cis-Jasmone 1393 164 1.13 ± 0.11a RT, RI, MS 96
 Caryophyllene oxide 1583 220 3.92 ± 0b RT, RI, MS 97

Total 96.79

aValues are mean ± standard deviation of three samples of M. longifolia essential oil, analyzed individually in triplicate.

bCompounds are listed in order of elution from a HP-5MS column; cretention indices relative to C9–C24   n-alkanes on the HP-5MS column; dmode of identifications; RT: identification based on retention time; RI: identification based on retention index; MS: identification based on comparison of MS data compared with those from the NIST02.L and WILEY7n.L mass spectral libraries; ematching percentage with the NIST02.L and WILEY7n.L mass spectral libraries.