. 2014 Apr;4(2):97–103. doi: 10.1016/S2222-1808(14)60323-6

Table 3. Chemical composition of P. halepensis essential oils from West Northern of Algeria.

Compounds	IR^a LIT	IR^b app	IR^c pol	Collective Oil^d Simple Oils^e			Identification
Compounds	IR^a LIT	IR^b app	IR^c pol	%	%Min	%Max	Identification
α-Thujene	922	923	1021	0.7	0.4	1.0	RI, MS
α-Pinene	931	932	1023	16.8	12.2	24.5	RI, MS
Camphene	943	944	1066	0.2	0.1	0.3	RI, MS
Sabinene	964	966	1118	4.2	1.5	6.3	RI, MS
β-Pinene	970	971	1108	1.9	1.7	2.2	RI, MS
Myrcene	970	983	1159	25.2	15.2	32.0	RI, MS
α-Phelandrene	997	998	1157	0.1	nd	0.2	RI, MS
3-Carene	1005	1006	1147	1.6	0.6	5.5	RI, MS
α-Terpinene	1008	1010	1175	0.9	0.1	1.8	RI, MS
p-Cymene	1010	1012	1259	0.6	0.2	1.8	RI, MS
β-Phelandrene	1021	1021	1204	0.4	0.7	1.4	RI, MS
Limonene	1020	1021	1195	0.9	0.6	1.4	RI, MS
Z-β-Ocimene	1024	1025	1225	0.4	nd	1.4	RI, MS
E-β-ocimene	1034	1036	1241	1.4	0.52	3.4	RI, MS
γ-Terpinene	1047	1049	1237	1.4	0.2	2.6	RI, MS
Terpinolene	1078	1082	1247	8.3	1.8	13.8	RI, MS
Linalool	1080	1084	1529	0.4	0.1	0.8	RI, MS
Perillene	1090	1099	1414	0.1	tr	0.1	RI, MS
Cis-p-menth-2-en-1-ol	1108	1107	1600	0.2	0.1	0.3	RI, MS
Trans-p-menth-2-en-1-ol	1113	1117	1612	0.1	tr	0.2	RI, MS
Terpinene-4-ol	1161	1164	1583	4.2	1.0	8.2	RI, MS
α-Terpinolene	1179	1175	1688	0.4	tr	0.7	RI, MS
Bornyl acetate	1269	1268	1475	0.1	tr	0.3	RI, MS
Citronellyl acetate	1331	1333	1645	0.1	tr	0.1	RI, MS
Neryl acetate	1342	1342	1409	0.1	0.1	0.2	RI, MS
Geranyl acetate	1361	1360	1740	0.2	tr	0.5	RI, MS
α-Copaene	1379	1373	1475	0.2	0.1	0.3	RI, MS
E-β-Caryophyllene	1424	1418	1583	10.9	7.0	17.1	RI, MS
α-Humulene	1456	1449	1651	2.1	1.3	3.4	RI, MS
2-Phenylethyl isovanerate	1463	1468	1973	7.7	4.8	10.9	RI, MS
Germacrene D	1480	1474	1692	0.2	0.1	0.2	RI, MS
α-muurolene	1496	1492	1709	0.2	tr	0.6	RI, MS
δ-Cadinene	1516	1513	1738	0.3	tr	0.5	RI, MS
E-α-Bisabolene	1532	1532	1740	0.2	0.1	0.3	RI, MS
Phenylethyl Tiglate E	1547	1546	2141	0.1	nd	0.2	RI, MS
Phenylethyl Tiglate Z	1559	1568	2145	0.8	tr	3.3	RI, MS
Caryophyllene oxide	1576	1583	1898	0.8	0.2	2.2	RI, MS
Guaiol	1591	1592	2070	0.2	0.1	0.5	RI, MS
Humulene epoxyde	1601	1613	2035	0.1	tr	0.1	RI, MS
Epi-Cubenol	1624	1625	2043	0.1	0.1	0.2	RI, MS
Tau-Cadinol	1632	1633	2163	0.2	tr	0.1	RI, MS
T-Muurolol	1634	1638	2141	0.1	0.1	0.3	RI, MS
α-Cadinol	1645	1640	2163	0.2	tr	0.3	RI, MS
Bulnesol	1659	1666	2195	0.1	nd	0.1	RI, MS
Cembrene	1938	1940	2185	0.4	0.1	1.6	RI, MS, Ref.
m-Camphorene	1947	1939	2234	0.2	nd	0.4	RI, MS, Ref.
Cembrene A	1962	1951	2227	0.1	nd	0.3	RI, MS, Ref.
p-Camphorene	1980	1974	1987	0.3	nd	1.1	RI, MS, Ref.
Geranyl Linalool	2037	2037	2540	1.5	nd	3.0	RI, MS
Total Identification %				97.9
Yields % (w/w)				0.26	0.10	0.63
Hydrocarbon compounds				80.6
Monoterpene hydrocarbons				65.5
Sesquiterpene hydrocarbons				14.1
diterpenic hydrocarbons				1.0
Oxygenated compounds				17.3
Oxygenated monoterpenes				5.4
Oxygenated sesquiterpenes				1.8
Oxygenated diterpenes				1.5
Non-terpenic oxygenated compounds				8.6

^a: Retention indices of literature on the apolar column (/RI_Lit) reported from König et al., 2001; ^b: Retention indices on the apolar Rtx-1 column; ^c: Retention indices on the polar Rtx-Wax column; ^d: Normalized percentages abundance are given on the apolar column except for components with identical RI (percentages are given on the polar column), tr=trace (<0.05%). ^e: Minimum and maximum normalized percentages abundance from simple oils; RI: Retention indices; MS: Mass spectra in electronic impact mode; Ref.: compounds identified from literature data: König et al., 2001).