Table 1 GC-MS chemical composition (%) of the essential oil from P. racemosa grown in egypt.

From: Chemical profile of essential oil from Pimenta racemosa leaves, antioxidant potential, and its enzyme inhibitory properties

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

C10H16

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

C10H16

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

C10H12O2

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

  1. 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.