2Department of Chemistry, G.I.C Garkha, Distt-Pithoragarh, Uttrakhand.
Methods: The plant Boenninghausenia albiflora Reichb including leaves, stem, and flowers were extracted by hydro distillation method for 6 hours using Clevenger apparatus. The hydro-distilled essential oil of Boenninghausenia albiflora Reichb has been examined by means of gas chromatography-mass spectrometry (GC-MS).
Results: A total of 54 components of the essential oil of Boenninghausenia albiflora Reichb. were identified, accounting for 97 % of the total oil. The main compounds found were cinnamyl propyl ether 22 %, linalool 22 %, (E)-cinnamaldehyde 15 %, (E) cinnamyl alcohol 5 %.
Keywords: Boenninghausenia albiflora; Essential oil; Gas Chromatography; Mass Spectrometry;
Essential oils and their volatile constituents are used to prevent and treat human disease. The possible role and mode of action of these natural products is discussed with regard to the prevention and treatment of cancer, cardiovascular diseases including atherosclerosis and thrombosis, as well as their bioactivity as antibacterial, antiviral, antioxidants and antidiabetic agents. The pharmaceutical properties of aromatic plants are partially attributed to essential oils [7].
The identification of the chemical constituents was assigned on the basis of comparison of their retention indices and mass spectra with those given in the literature. Retention indices (RI) were determined with reference to a homologous series of normal alkanes, by using the following formula [7,8].
t0 – the retention time of solvent (dead time)
tR – the retention time of the compound.
CN – Number of Carbons in longer chain of alkane
Cn– number of Carbons in shorter chain of alkane
n - Is the number of carbon atoms in the smaller alkane
N - Is the Number of carbon atoms in the larger alkane
S.N. |
Compound |
Area % |
Mol. formula |
RI |
Mode of identification |
1. |
α-Thujene |
0.10 |
C10H16 |
927 |
a,b |
2. |
α-Pinene |
2.24 |
C10H16 |
936 |
a,b |
3. |
Benzaldehyde |
3.02 |
C7H6O |
946 |
a,b |
4. |
Camphene |
1.35 |
C10H16 |
953 |
a,b |
5. |
β-Pinene |
1.10 |
C10H16 |
978 |
a,b |
6. |
1-Propylcyclopentanol |
0.08 |
C8H16O |
1010 |
a,b |
7. |
δ-3-Carene |
0.12 |
C10H16 |
1012 |
a,b |
8. |
p-Cymene |
2.12 |
C10H14 |
1015 |
a,b |
9. |
Limonene |
0.54 |
C10H16 |
1030 |
a,b |
10. |
Salicylaldehyde |
0.16 |
C7H6 O2 |
1044 |
a,b |
11. |
4-Methyl-4-vinylbutyrolactone |
0.13 |
C7H10 O2 |
1050 |
a,b |
12. |
Cineole |
0.81 |
C10H18O |
1058 |
a,b |
13. |
Acetophenone |
0.11 |
C8H8O |
1068 |
a,b |
14. |
cis-Linalool oxide |
3.74 |
C10H18O2 |
1069 |
a,b |
15. |
Trans-Linalool Oxide |
3.62 |
C10H18O2 |
1075 |
a,b |
16. |
β-Linalool |
22.56 |
C10H18O |
1082 |
a,b |
17. |
α-Campholenal |
0.10 |
C10H16O |
1125 |
a,b |
18. |
Nopinone |
0.15 |
C9H14O |
1138 |
a,b |
19. |
t-Pinocarveol |
0.18 |
C10H16O |
1140 |
a,b |
20. |
t-Verbenol |
0.05 |
C10H16O |
1145 |
a,b |
21. |
Linderol |
0.44 |
C10H18O |
1149 |
a,b |
22. |
Hydrocinnamaldehyde |
0.45 |
C9H10O |
1165 |
a,b |
23. |
pyranoid |
0.93 |
C10H18O2 |
1170 |
a,b |
24. |
α-Terpineol |
0.36 |
C10H18O |
1176 |
a,b |
25. |
3,7-Dimethyloct-1,5-dien-3,7-diol |
0.56 |
C10H18O2 |
1192 |
a,b |
26. |
(Z)-Cinnamaldehyde |
0.17 |
C9H8O |
1218 |
a,b |
27. |
Bornyl formate |
0.07 |
C11H18O2 |
1275 |
a,b |
28. |
(E)-cinnamaldehyde |
15.06 |
C9H8O |
1280 |
a,b |
29. |
Bornyl acetate |
1.31 |
C12H20O2 |
1285 |
a,b |
30. |
(E)-Cinnamyl alcohol |
5.65 |
C9H10O |
1308 |
a,b |
31. |
cis-2,3-Pinanediol |
0.33 |
C10H18O2 |
1321 |
a,b |
32. |
ethyl-Hydrocinnamate |
0.24 |
C11H14O2 |
1351 |
a,b |
33. |
Cinnamyl formate |
0.39 |
C10H10O2 |
1352 |
a,b |
34. |
cis-Cinnamic acid |
0.44 |
C9H8O2 |
1357 |
a,b |
35. |
α-Copaene |
0.36 |
C15H24 |
1375 |
a,b |
36. |
Hydrocinnamyl acetate |
0.77 |
C11H14O2 |
1377 |
a,b |
37. |
Cinnamyl propyl ether |
22.61 |
C12H16O |
1380 |
a,b |
38. |
(Z)-ethyl-Cinnamate |
0.30 |
C11H12O2 |
1381 |
a,b |
39. |
Isopropyl 3-phenylpropanoate |
0.17 |
C12H16O2 |
1390 |
a,b |
40. |
α- Amorphene |
0.19 |
C15H24 |
1477 |
a,b |
41. |
β-selinene |
0.26 |
C15H24 |
1486 |
a,b |
42. |
Guaia-1(10),11-diene |
0.10 |
C15H24 |
1490 |
a,b |
43. |
α-Muurolene |
0.08 |
C15H24 |
1497 |
a,b |
44. |
γ-Cadinene |
0.07 |
C15H24 |
1512 |
a,b |
45. |
Trans-Calamenene |
0.07 |
C15H22 |
1527 |
a,b |
46. |
Spathulenol |
0.09 |
C15H24O |
1536 |
a,b |
47. |
Caryophyllene oxide |
1.59 |
C15H24O |
1580 |
a,b |
48. |
Humulene epoxide II |
0.23 |
C15H24O |
1610 |
a,b |
49. |
Caryophylla-4(12),8(13)-dien-5-alpha-ol |
0.30 |
C15H2O |
1642 |
a,b |
50. |
Cadin-4-en-10-ol |
0.07 |
C15H26O |
1659 |
a,b |
51. |
α- Costol |
0.28 |
C15H24O |
1770 |
a,b |
52. |
Kaur-16-ene |
0.75 |
C20H32 |
2030 |
a,b |
53. |
Linalyl cinnamate |
0.06 |
C19H24O2 |
2115 |
a,b |
54. |
9-Dodecynyl 3-phenylpropanoate |
0.14 |
C21H30O2 |
2370 |
a,b |
|
|
97.17 |
|
|
|
• GC-MS Gas Chromatography-Mass Spectrometry.
• GC-FID Gas Chromatography-Flame Ionization Detector.
• RI: Retention Index.
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