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Table 3 Chemical composition of the essential oils extracted from the leaves of O. basilicum and T. algeriensis

From: Chemical composition and bioactivity of essential oils and Ethanolic extracts of Ocimum basilicum L. and Thymus algeriensis Boiss. & Reut. from the Algerian Saharan Atlas

Constituents

LRI

O. basilicum

(%)

T. algeriensis

(%)

Method of identificationb

α-pinene

941

0.3

6.8

MS; LRI; RC

camphene

955

- a

0.8

MS; LRI; RC

sabinene

977

0.4

0.7

MS; LRI; RC

β-pinene

982

0.6

1.2

MS; LRI; RC

myrcene

993

1.3

1.2

MS; LRI; RC

3-octanol

994

-a

- a

MS; LRI; RC

α-terpinene

1020

- a

- a

MS; LRI; RC

p-cymene

1028

- a

0.3

MS; LRI; RC

limonene

1032

- a

2.7

MS; LRI; RC

1,8-cineole

1034

9.2

4.1

MS; LRI; RC

(Z)-β-ocimene

1042

0.7

- a

MS; LRI; RC

(E)-β-ocimene

1052

0.5

1.5

MS; LRI; RC

γ-terpinene

1063

- a

- a

MS; LRI; RC

cis-sabinene hydrate

1070

- a

- a

MS; LRI; RC

terpinolene

1090

0.2

0.4

MS; LRI; RC

linalool

1101

52.1

1.2

MS; LRI; RC

nonanal

1104

- a

- a

MS; LRI; RC

pentylisovalerate

1108

0.1

- a

MS; LRI

1-octen-3-yl acetate

1111

0.1

0.4

MS; LRI; RC

cis-p-menth-2-en-1-ol

1123

- a

- a

MS; LRI

3-octyl acetate

1126

0.2

- a

MS; LRI; RC

α-campholenal

1127

- a

0.5

MS; LRI

camphor

1145

- a

1.1

MS; LRI; RC

trans-verbenol

1147

- a

0.5

MS; LRI; RC

δ-terpineol

1172

0.2

- a

MS; LRI

4-terpineol

1179

0.1

0.5

MS; LRI; RC

α-terpineol

1191

5.7

4.9

MS; LRI; RC

cis-dihydrocarvone

1195

- a

- a

MS; LRI; RC

trans-carveol

1219

- a

0.4

MS; LRI; RC

(Z)-3-hexenyl isovalerate

1238

- a

- a

MS; LRI; RC

pulegone

1239

0.2

- a

MS; LRI; RC

neral

1242

- a

0.2

MS; LRI; RC

carvone

1244

- a

0.3

MS; LRI; RC

linalyl acetate

1259

19.1

- a

MS; LRI; RC

bornyl acetate

1287

- a

3.1

MS; LRI; RC

dihydroedulan IA

1292

- a

- a

MS; LRI

isodihydrocarvyl acetate

1329

- a

- a

MS; LRI

α-terpinyl acetate

1352

- a

47.4

MS; LRI; RC

cis-carvyl acetate

1364

- a

- a

MS; LRI; RC

neryl acetate

1365

1.8

9.6

MS; LRI; RC

geranyl acetate

1383

3.6

0.9

MS; LRI; RC

β-elemene

1392

- a

- a

MS; LRI

(Z)-jasmone

1395

- a

- a

MS; LRI; RC

β-caryophyllene

1419

1.0

0.6

MS; LRI; RC

β-copaene

1430

- a

- a

MS; LRI

aromadendrene

1440

- a

- a

MS; LRI; RC

α-humulene

1455

0.1

- a

MS; LRI; RC

(E)-β-farnesene

1458

0.1

- a

MS; LRI; RC

cis-muurola-4(14), 5-diene

1463

0.1

- a

MS; LRI

germacrene D

1482

- a

0.6

MS; LRI

bicyclogermacrene

1496

- a

MS; LRI

germacrene A

1505

- a

- a

MS; LRI

δ-cadinene

1524

- a

- a

MS; LRI

(E)-α-bisabolene

1542

- a

0.2

MS; LRI

(E)-nerolidol

1564

- a

3.5

MS; LRI

spathulenol

1577

- a

- a

MS; LRI

caryophyllene oxide

1582

0.1

0.9

MS; LRI; RC

viridiflorol

1591

0.4

- a

MS; LRI

1, 10-di-epi-cubenol

1615

0.1

- a

MS; LRI

T-cadinol

1641

- a

- a

MS; LRI

T-muurolol

1642

- a

- a

MS; LRI

Monoterpene hydrocarbons

 

4.0

15.6

 

Oxygenated monoterpenes

 

92.0

74.7

 

Sesquiterpene hydrocarbons

 

1.3

1.4

 

Oxygenated sesquiterpenes

 

0.6

4.4

 

Apocarotenes

 

0.0

0.0

 

Non-terpene derivatives

 

0.4

0.4

 

Total identified

 

98.3

96.5

 
  1. a: not detected in the sample
  2. bmethod of identification: MS Mass spectrum, LRI Linear retention index, RC Reference compound