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. 2014 Mar 28;67(3):531–543. doi: 10.1007/s10616-014-9713-4

Table 1.

Chemical compositions of Parmelia sulcata extract

Compounda 1tbR 2tbR Areac (%)
Acetic acid 430 1.30 0.94
Methyl 2,4-dihydroxy-3,6-dimethylbenzoate 1,875 2.37 20.65
3,7,11,15-Tetramethyl-2-hexadecen-1-ol 1,965 1.4 2.54
n-Hexadecanoic acid 2,240 1.455 2.43
Decalactone 2,385 1.92 0.13
9-Octadecynoic acid 2,405 1.885 0.23
Dodecanamide 2,440 1.82 0.42
Pentadecane 2,480 1.75 0.22
9-Octadecenal 2,580 1.78 4.65
Methyl isoheptadecanoate 2,760 1.485 0.26
2-Methylnonadecane 2,765 1.485 16.18
Farnesane 2,810 1.37 1.33
2-Nonadecanone 2,815 1.61 0.24
1-Acetoxynonadecane 2,835 1.475 0.47
Eicosane 2,900 1.365 24.43
Hexyl 2-phenylethyl ester-succinic acid 2,915 1.73 0.52
1-Heneicosanol 2,925 1.515 1.00
(E,E)-3,7,11-trimethyl-2,6-dodecadien-1-ol 2,945 1.49 5.60
Ethyl icosanoate 2,995 1.5 0.86
Allyl octadecyl oxalate 3,000 1.435 0.25
1-Docosanol, acetate 3,010 1.505 1.59
Squalene 3,015 1.58 0.26
2-Hexyl-1-octanol 3,070 1.4 0.25
2-Methyloctadecane 3,075 1.46 5.28
Heneicosane 3,080 1.57 4.66
Unknown 4.63

aAs identified by GCxGC–TOF/MS software; names according to NIST 2005 mass spectral library

btR and 2tR, retention times in the first and second dimension, respectively

cPercentage of each component is calculated as peak area of analyte divided by peak area of total ion chromatogram times 100