Skip to main content
. 2019 Aug 14;24(16):2941. doi: 10.3390/molecules24162941

Table 2.

Chemical composition of EO from P. vera L. var. Bronte hull.

Compound Name Area (%) KI a Identification b
1 Bornylene 0.03 916 1,2
2 Tricyclene 0.72 923 1,2
3 α-Pinene 22.65 935 1,2,3
4 Camphene 3.88 950 1,2,3
5 β-Pinene 1.02 978 1,2,3
6 β-Myrcene 2.43 993 1,2,3
7 2-Carene 1.05 995 1,2,3
8 α-Phellandrene 0.47 1006 1,2
9 δ-3-Carene 7.98 1011 1,2,3
10 α-Terpinene 2.33 1018 1,2,3
11 p-Cymene 1.42 1027 1,2
12 D-Limonene 8.50 1031 1,2,3
13 trans-β-Ocimene 0.48 1050 1,2
14 cis-β-Ocimene 0.35 1056 1,2
15 γ-Terpinene 0.58 1061 1,2
16 4-Carene 32.03 1082 1,2
17 α-Pinene oxide 0.69 1096 1,2
18 Linalool 0.38 1101 1,2,3
19 2-Fenchanol 0.44 1107 1,2
20 1,3,8-p-Menthatriene 0.17 1130 1,2
21 Camphor 0.22 1148 1,2
22 Menthone 0.35 1150 1,2
23 Borneol 1.03 1169 1,2
24 p-Cymen-8-ol 0.74 1188 1,2
25 α-Terpineol 3.99 1194 1,2,3
26 Myrtenal 0.03 1197 1,2
27 Myrtenol 0.06 1202 1,2
28 α-Methylcynnamaldehyde 0.05 1210 1,2
29 Piperitone 0.53 1250 1,2
30 Nerol 0.34 1232 1,2
31 Bornyl acetate 2.37 1285 1,2,3
32 Nerol acetate 0.18 1365 1,2
33 β-Bisabolene 0.05 1513 1,2
34 γ-Selinene 0.09 1525 1,2
35 δ-Cadinene 0.07 1530 1,2
36 cis-5-Dodecenoic acid 0.13 1568 1,2
37 1,13-Tetradecadiene 1.43 1810 1,2
38 1-Hexadecanol 0.13 1880 1,2
39 Palmitic acid 0.05 1957 1,2
40 1,15-Hexadecadiene 0.43 2549 1,2
Total 99.87
Monoterpene hydrocarbons 86.20
Oxygenated monoterpenes 11.37
Sesquiterpene hydrocarbons 0.21
Oxygenated sesquiterpenes 0.00
Others 2.22
Essential oil yield % (v/w) 0.3

a Linear retention index on an HP-5MS column; b Identification method: 1 = linear retention index; 2 = identification based on the comparison of mass spectra; 3 = Co-injection with standard compounds.