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. 2025 Aug 21;15:30705. doi: 10.1038/s41598-025-15542-3

Table 1.

GC-MS chemical composition (%) of the essential oil from P. racemosa grown in egypt.

No. Compound name a Retention time
(tR)
Molecular formula RI Peak area
(%)
Method of identification Ref.
Experimental Reported
1. α-Pinene 7.17 C10H16 931 932 0.32 RI, MS 18,54
2. β -Myrcene 8.94 C 10 H 16 992 992 12.88 RI, MS 4,45
3. α-Phellandrene 9.29 C10H16 1003 1005 0.54 RI, MS 40,43
4. p-Cymene 9.92 C10H14 1024 1026 1.12 RI, MS 46
5. D-Limonene 10.06 C 10 H 16 1028 1029 8.35 RI, MS 18
6. (E)-β-Ocimene 10.68 C10H16 1048 1050 0.20 RI, MS 41
7. β-Linalool 12.28 C10H18O 1100 1100 2.14 RI, MS 18
8. Terpinen-4-ol 14.67 C10H18O 1178 1177 0.19 RI, MS 45
9. Chavicol 17.05 C9H10O 1258 1259 1.48 RI, MS 18
10. Eugenol 20.08 C 10 H 12 O 2 1366 1365 70.87 RI, MS 51
11. α-Copaene 20.46 C15H24 1379 1376 0.13 RI, MS 11
12. (E)-β-Caryophyllene 21.65 C15H24 1423 1423 0.28 RI, MS 51
13. α-Murolene 23.13 C15H24 1480 1481 0.15 RI, MS 45
14. 3-Cyclohexene-1-carboxaldehyde, 4-(4-methyl-3-pentenyl)- 24.20 C13H20O 1509 1522 0.29 RI, MS 41,46
15. δ-Cadinene 24.33 C15H24 1527 1530 0.50 RI, MS 30
16. (E)-β-Caryophyllene oxide 25.88 C15H24O 1590 1590 0.16 RI, MS 18
17. τ-Cadinol 27.27 C15H26O 1648 1648 0.16 RI, MS 41
Total identified 99.76%
Phenylpropanoids 72.35%
Hydrocarbon monoterpenes 23.41%
Oxygenated monoterpenes 2.33%
Hydrocarbon sesquiterpenes 1.06%
Oxygenated sesquiterpenes 0.32%
Others 0.29

a Compounds are arranged according to their elution. RI: Kovats retention index on TG-5MS capillary column. MS, identification based on mass spectral data and fragmentation profile.