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. 2017 Jan 26;22(2):203. doi: 10.3390/molecules22020203

Table 5.

Chemical composition (%) of TEOCG extracted in October.

# 1 Name Sample 2
O1h O2h O3h O6h O12h O24h
3 3-metilcicloesanone - - - - 0.9 ± 0.06 1.9 ± 0.13
4 3-octanol 2.1 ± 0.19 1.0 ± 0.09 0.6 ± 0.05 0.3 ± 0.03 0.3 ± 0.03 0.7 ± 0.06
5 terpinen-4-ol 0.6 ± 0.03 0.7 ± 0.03 0.9 ± 0.04 0.9 ± 0.04 1.1 ± 0.05 0.8 ± 0.04
14 caryophyllene oxide - - 1.0 ± 0.06 1.2 ± 0.07 1.8 ± 0.11 1.7 ± 0.11
17 crysanthenone 1.3 ± 0.11 2.3 ± 0.19 3.3 ± 0.28 5.3 ± 0.44 5.4 ± 0.45 13.4 ± 1.12
19 limonene 9.2 ± 0.51 2.1 ± 0.11 0.6 ± 0.03 0.7 ± 0.04 0.8 ± 0.04 0.9 ± 0.05
21 iso-caryophyllene 0.4 ± 0.02 0.6 ± 0.04 0.5 ± 0.03 0.7 ± 0.04 2.0 ± 0.12 3.5 ± 0.21
23 isopulegone 1.0 ± 0.05 1.0 ± 0.05 1.2 ± 0.06 1.1 ± 0.06 1.3 ± 0.07 1.0 ± 0.05
25 menthol 4.3 ± 0.25 4.4 ± 0.25 6.3 ± 0.36 5.5 ± 0.32 5.3 ± 0.31 4.2 ± 0.24
26 menthone 35.4 ± 3.01 27.8 ± 2.36 23.6 ± 2.01 10.9 ± 0.93 7.0 ± 0.59 6.8 ± 0.58
31 piperitenone oxide 1.4 ± 0.14 1.9 ± 0.18 3.3 ± 0.32 3.6 ± 0.35 0.5 ± 0.05 5.2 ± 0.51
32 p-menth-1-en-8-ol 0.3 ± 0.02 0.3 ± 0.02 0.5 ± 0.03 0.8 ± 0.05 1.4 ± 0.09 2.3 ± 0.15
36 pulegone 42.5 ± 2.17 57.5 ± 2.93 53.3 ± 2.72 68.2 ± 3.48 68.8 ± 3.51 51.8 ± 2.64
Unidentified compounds 1.5 ± 0.13 0.4 ± 0.03 4.9 ± 0.43 0.8 ± 0.07 3.4 ± 0.29 5.8 ± 0.51

1 # indicate the compound identification number; 2 Samples’ names were obtained by merging the first letter of the month and the extraction time as reported in Table 1. Compounds are not listed in order of elution.