Skip to main content
. 2020 Nov 30;25(23):5654. doi: 10.3390/molecules25235654

Table 3.

List of compounds identified in hydrolate extracts from Laurus nobilis L.

CAS Compound RI % of Total Peak Area
HSD_SPE HHD_SPE
Oxidized Monoterpenes
470-67-7 1,4-Cineol 1014 <0.1 <0.1
470-82-6 1,8-Cineol 1030 56.4 54.0
78-70-6 Linalool 1099 0.3 0.5
29957-43-5 Hotrienol 1101 <0.1 <0.1
36262-12-1 Dehydrosabina ketone 1120 0.1 0.1
471-16-9 Sabinol 1136 <0.1 <0.1
1786-08-9 Nerol oxide 1151 <0.1 <0.1
513-20-2 Sabina ketone 1157 0.5 0.6
30460-92-5 Pinocarvone 1160 0.4 0.3
562-74-3 4-Terpineol 1178 6.0 7.1
13741-21-4 2,6-Dimethyl-3,7-octadiene-2,6-diol 1189 0.7 0.4
98-55-5 α-Terpineol 1193 5.0 6.4
80-57-9 Verbenone 1207 <0.1 <0.1
99-48-9 Carveol 1218 0.2 0.4
18679-48-6 2-Hydroxy-1,8-cineole 1225 0.4 0.5
22626-43-3 cis-p-Mentha-1(7),8-diene-2-ol 1228 0.5 0.8
494-99-5 Homoveratrole 1236 <0.1 <0.1
122-03-2 Cuminaldehyde 1240 <0.1 <0.1
51276-33-6 2,6-Dimethyl-1,7-octadien-3,6-diol 1272 0.4 0.2
536-60-7 Cumin alcohol 1288 0.7 1.3
89-83-8 Thymol 1298 0.2 0.1
22539-72-6 p-Mentha-1,4-dien-7-ol 1328 0.2 0.2
Others
100-52-7 Benzaldehyde 960 <0.1 <0.1
110-93-0 6-Methyl-5-hepten-2-one 985 <0.1 0.2
1073-11-6 Lavender lactone 1037 <0.1 0.1
6090-09-1 Limona ketone 1130 <0.1 <0.1
76-49-3 Bornyl acetate 1283 <0.1 <0.1
81781-24-0 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octan-5-yl acetate 1337 1.0 1.2
97-53-0 Eugenol 1350 2.2 2.4
57709-95-2 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octan-6-yl acetate 1357 0.1 0.1
121-33-5 Vanilin 1393 0.5 0.3
93-15-2 Methyleugenol 1399 1.8 1.7
17092-92-1 Dihydroactinidiolide 1524 0.2 <0.1

HHD_SPE—hydrolate obtained by hydrodistillation and 50× concentrated using solid phase extraction (SPE); HSD_SPE—hydrolate obtained by steam distillation and 50× concentrated using SPE; RI—retention index relative to n-alkanes on SLB-5ms capillary column.