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. 2020 Nov 28;31(12):116. doi: 10.1007/s10856-020-06455-w

Table 2.

Results of gas chromatography–mass spectrometry analysis

Retention time (min) Compounds % Area
1 3.448 6,7-Dimethyl-4-hydroxycoumarin 4.78
2 3.907 6-Methylchromanone 0.87
3 4.199 3,4,5-Trimethoxycinnamic acid 0.86
4 4.572 o-Cymene 0.63
5 4.633 α-Pinene 11.01
6 5.092 7-Methoxy-3-(4-methoxyphenyl)coumarin 1.99
7 5.724 Limonene 2.53
8 6.232 Terpinolene 1.77
9 6.741 Myrtenol 2.46
10 7.163 p-Mentha-3,8-diene 1.63
11 7.364 α-Thujenal 3.73
12 8.184 Bornyl acetate 1.41
13 8.93 α-Terpineol 3.02
14 9.25 α-Selinene 4.34
15 9.406 δ-Guaiene 0.94
16 9.964 Humulene 1.18
17 10.099 Longifolene 4.2
18 10.23 γ-Gurjunene 1.76
19 10.956 cis-Sesquisabinene hydrate 0.99
20 11.161 Farnesol 1.45
21 11.342 Himbaccol 2.65
22 13.441 β-Santalol 2.28
23 13.667 Lanceol, cis 4.65
24 13.888 α-Terpinyl acetate 2.77
25 13.966 3,6,3′,4′-Tetrahydroxyflavone 2.01
26 14.512 Kaur-16-ene 1.41
27 14.815 Squalene 4.33
28 14.922 Ledol 15.51
29 15.11 7,3′,4′,5′-Tetramethoxyflavanone 2.22
30 15.398 Quercetin 3′-methyl ether 2
31 16.566 p-Cresol, 2,2′-methylenebis(4-methyl-6-tert-butylphenol) 1.76
32 17.657 Apigenin 8-C-glucoside 0.65
33 18.006 2′-Hydroxy-2,4,4′,5-tetramethoxychalcone 0.9
34 18.309 Juniperol 1.29
35 18.752 Isovitexin 0.17
36 19.814 6,2′,3′-Trimethoxyflavone 1.39
37 22.546 7-Hydroxychromanone 0.94
38 22.878 4-Hydroxy-7-methoxy-3-(4-methoxyphenyl) coumarin 1.56