. 2015 Mar 12;4(1):185–203. doi: 10.3390/antiox4010185

Table 2.

Phytochemical analysis of the N. jatamansi hexane extract.

No.	RT (min)	Compound Name	Chemical Formula	Mass	Area (%)	Hit
1	9.62	Dodecane	C₁₂H₂₆	170.204	1.615	1
2	11.22	2-Furanmethanol, tetrahydro-5-methyl-trans	C₆H₁₂O	116.084	0.031	1
3	13.98	Linalool	C₁₀H₁₈O	154.135	0.362	1
4	15.30	Benzenemethanol, a-methyl-propanoate	C₁₁H₁₄O₂	178.099	0.705	1
5	15.68	1H-Cyclopropa(a)naphthalene, 1a,2,3,5,6,7,7a,7b-octahydro-1,1,7,7a-tetramethyl-(1aR-(1aa,7a,7aa,7ba))	C₁₅H₂₄	204.188	1.061	1
6	16.02	a-Muurolene	C₁₅H₂₄	204.188	14.071	1
7	16.39	1H-Cycloprop(e)azulene,1a,2,3,4,4a,5,6,7b-octahydro-1,1,4,7-tetramethyl-(1aR-(1aa,4a,4aa,7ba))	C₁₅H₂₄	204.188	9.184	5
8	16.69	l-calamenene	C₁₅H₂₂	202.172	0.065	1
9	17.11	Α-ionone	C₁₃H₂₀O	192.151	0.643	1
10	17.41	Bicyclo(3.3.1)nonan-2-one,1-methyl-9-(1-methylethylidene)	C₁₃H₂₀O	192.151	8.329	1
11	17.63	Neoisolongifolene,8,9-dehydro	C₁₅H₂₂	202.172	2.002	1
12	17.81	(−)-à-Panasinsen	C₁₅H₂₄	204.188	1.716	1
13	18.13	Neoisolongifolene,8,9-dehydro	C₁₅H₂₂	202.172	10.86	1
14	18.96	Bicyclo(2.2.2)octa-2,5-diene, 1,2,3,6-tetramethyl	C₁₂H₁₈	162.141	3.643	1
15	19.15	Isolongifolene,4,5,9,10-dehydro	C₁₅H₂₀	200.157	1.24	1
16	19.76	trans-Nerolidol	C₁₅H₂₆O	222.198	4.781	1
17	19.88	para-methoxyphenylpiperazine	C₁₁H₁₆N₂O	192.1263	5.576	1
18	20.2	Cyclolongifolene oxide, dehydro	C₁₅H₂₂O	218.167	1.368	1
19	21.51	1(2H)-Naphthalenone,octahydro-4a,8a-dimethyl-7-(1-ethylethyl)-, (4aR-(4aa,7a,8aa))	C₁₅H₂₆O	222.198	0.329	1
20	22.05	2-tetradecenal	C₁₄H₂₆O	210.1984	4.873	1
21	30.1	Palmitic acid	C₁₆H₃₂O₂	256.24	1.537	1
22	31.64	Oleic acid	C₁₈H₃₄O₂	282.256	5.499	1
23	32.86	2,8,9-Trioxa-5-aza-1-silabicyclo(3.3.3)undecane,1-methoxy	C₇H₁₅NO₄Si	205.077	0.165	1
24	37.22	Tridecanoic acid, methyl ester	C₁₄H₂₈O₂	228.209	0.625	1
25	39.71	Heptacosane	C₂₇H₅₆	380.438	2.664	1