COMPARATIVE GC-MS ANALYSIS OF CYAMOPSIS TETRAGONOLOBA FRUIT EXTRACTS
HTML Full TextCOMPARATIVE GC-MS ANALYSIS OF CYAMOPSIS TETRAGONOLOBA FRUIT EXTRACTS
Priya Kumari Jain * and Shilpi Rijhwani
Department of Botany, ICG, The IIS University, Jaipur - 302020, Rajasthan, India.
ABSTRACT: Cyamopsis tetragonoloba is widely used by people and is found to have multiple medicinal utilities. Four (chloroform, ethyl acetate, methanolic and aqueous) extracts of Cyamopsis tetragonoloba fruit were therefore, analysed by Gas Liquid Chromatography and Mass Spectrometry analysis to assess their phytochemical constituents. The chloroform extract of Cyamopsis tetragonoloba fruits showed the presence of thirty one phytochemical constituents of which the major phytochemical compounds were Tetracontane and Stigmasterol. The ethyl acetate extract of Cyamopsis tetragonoloba fruit showed the presence of fifty phytochemical constituents. The important phytochemical compounds were stigmasterol and 4-tert-butylcalix [4] arene. Thirty eight phytochemicals were reported in the methanolic extract. The most important ones in term of peak area and retention time were mome inositol and 7-tetradecenal (Z). Mome inositol and 10, 12- Hexadecadien-1-ol was the primary components in a total of 30 phytochemicals obtained from the aqueous extract.
Keywords: |
Cyamopsis tetragonoloba, GC-MS, Phytochemicals, Extracts
INTRODUCTION: For thousands of years, medicine apparently depended exclusively on leaves, flowers and barks of plants because they consist of a wide variety of chemical compounds that offer a promising source of new drugs. The use and search for drugs and food supplements obtained from natural sources like plant extracts have increased in recent years 1. Records show that even today 80% of the world population depends on herbal traditional medicine for their primary health care. We know that plants produce chemicals to protect themselves but recent research demonstrates that they can also protect humans against diseases 2. Plants products are used for curing various diseases in developing countries because they are considered safer and better than synthetic drugs that create problems like side effects and carcinogenic effect 3.
The use of guar as a traditional plant for food and fodder has a long history. The resource base also suggests medicinal value of this plant in rural and tribal villages of India and abroad. In India, it is grown in Rajasthan, Gujarat, Haryana, Punjab, Uttar Pradesh, Madhya Pradesh and Orissa 4. Many people in arid and semi arid region of our country are dependent directly or indirectly on the production of guar.
In this modern age where a large number of people have seen diagnosed with life style disorders such as high blood pressure, cholesterol level and diabetes, Guar may play an important role for the alteration of symptoms related to these disease. Cyamopsis tetragonoloba is a rich source of secondary metabolites with known significant pharmacological effects. Guar gum which is a mucilaginous polysaccharide or the galactomannan layer of guar seeds have hypoglycemic, hypolipidemic and hypocholesterolemic effect on serum biochemical profile of human and non-human primates reducing total serum cholesterol, triglycerides, cardio vascular risk and increasing the high density lipoprotein cholesterol level and management of glycemic indices. This is because of its rich phytochemical profile like flavanoids- kaempferol, phenolic compounds- sinapic acid, chlorogenic acid, gallic acid, caffeic acid, ellagic acid, steroids- inositol, ethyl α-D glucopyranoside, stigmasterol and some amino acids like glutamine, arginine, aspartic acid and leucine. Guar is also used as a home remedy for the treatment of gastric problems, abdominal discomfort, asthma and inflammation; as laxative and as appetite depressor. It also used as an emulsifier, thickener and stabilizer in wide range of food and industrial applications. Guar can be highly regarded as crop of the future because of its nutritional, chemical and medicinal properties 5. The objective of the present study is to identify the phytochemical constituents of four different extract of Cyamopsis tetragonoloba fruit using GC-MS analysis.
MATERIALS AND METHODS:
Collection of Plant Material: The fruits of M83 variety (notification number 22/11/1991-740 (E) of Cyamopsis tetragonoloba were collected from Rajasthan Agriculture Research Institute, Durgapura, Jaipur, India in the year 2014. The herbarium specimen was deposited in University for further reference.
Preparation of Powder and Extract: Cyamopsis tetragonoloba fruits were shade dried and washed in tap water and pulverized to fine powder in a mechanical grinder. The powder of Cyamopsis tetragonoloba fruit was extracted successively in the ratio of 1:10 (20 g of dry powder: 200 ml of solvent) in each of extracts viz. chloroform, ethyl acetate, methanol and water by Soxhlet extraction for relevant periods of time. All the extracts were concentrated to dryness in the oven. All the extracts were stored in a container for further GC-MS analysis.
Gas Chromatography - Mass Spectrometry: The GC-MS analysis of selected sample was performed with Shimadzu GC-MS - QP2010 Ultra.
ANALYTICAL LINE 1
Content | Value | Content | Value |
# of Rinses with Presolvent | 5 | Linear Velocity | 39.9 cm/sec |
# of Rinses with Solvent (post) | 8 | Purge Flow | 3.0 mL/min |
# of Rinses with Sample | 2 | Split Ratio | 10.0 |
Plunger Speed (Suction) | High | High Pressure Injection | OFF |
Viscosity Comp. Time | 0.2 sec | Carrier Gas Saver | OFF |
Plunger Speed (Injection) | High | Splitter Hold | OFF |
Syringe Insertion Speed | High | SPL1 Carrier | Yes |
Injection Mod | Normal | Column Oven | Yes |
Pumping Time | 5 | SPL1 | Yes |
Inj. Port Dwell Time | 0.0 sec | MS | Yes |
Terminal Air Gap | No | SPL1 Purge | Yes |
Plunger Washing Speed | High | External Wait | No |
Washing Volume | 6uL | Equilibrium Time | 0.5 min |
Syringe Suction Position | 0.0 mm | Ion Source Temp. | 230.00 °C |
Syringe Injection Position | 0.0 mm | Interface Temp. | 270.00 °C |
Solvent Selection | All A,B,C | Solvent Cut Time: | 5.50 min |
Column Oven Temp. | 60.0 °C | Detector Gain Mode | Relative |
Injection Temp. | 260.00 °C | Detector Gain | +0.00 kV |
Injection Mode | Split | Threshold | 1000 |
Flow Control Mode | Linear Velocity | Start Time | 6.00min |
Pressure | 72.3 kPa | End Time | 65.32min |
Total Flow | 16.2 mL/min | ACQ Mode | Scan |
Column Flow | 1.20 mL/min | Event Time | 0.20sec |
Scan Speed | 3333 | End m/z | 650.00 |
Start m/z | 40.00 | Sample Inlet Unit | GC |
Identification of compounds was conducted using the database of NIST08, WILEY8 and FAME Libraries. Mass spectrum of individual unknown compound was compared with the known compounds stored in the software database Libraries. The name, molecular weight and structure of the compounds of the test materials were insured.
RESULTS AND DISCUSSIONS: Gas chromatography mass spectrometry (GC-MS) is a method that blends the features of Gas Liquid Chromatography and Mass Spectrometry to identify diverse components within a test sample. Applications of GC-MS include explosives probe, environmental analysis, drug detection and identification of unknown samples.
GC-MS methods proved to be very effective and sensitive for the separation and detection of complex mixtures of phytoconstituents. GC-MS Chromatogram of the chloroform extract of Cyamopsis tetragonoloba fruit Fig. 1 showed 31 peaks indicating presence of thirty one phytochemical constituents. On comparison of the mass spectra of the constituents with the NIST08, WILET8 and FAME libraries the thirty one phytoconstituents were characterized and identified Table 1.
The major phytochemical constituents were Tetracontane and Stigmasterol. The ethyl acetate extract of Cyamopsis tetragonoloba fruit Fig. 2 showed 50 peaks indicating the presence of all fifty phytochemical constituents. On comparison of mass spectra, fifty phytoconstituents were characterized and identified Table 2.
The major phytochemical constituents are stigmasterol and 4-tert-butylcalix [4] arene. The methanolic extract of Cyamopsis tetragonoloba fruit Fig. 3 showed 38 peaks indicating the presence of thirty eight phytochemical constituents. On comparison of mass spectra, thirty eight phytoconstituents were characterized and identified Table 3.
The major phytochemical constituents isolated were mome inositol and 7-tetradecenal, (Z). The aqueous extract of Cyamopsis tetragonoloba fruit Fig. 4 showed 30 peaks indicating the presence of thirty phytochemical constituents. On comparison of mass spectra, thirty phytoconstituents were characterized and identify Table 4. The major phytochemical constituents in this sample were 10, 12- Hexadecadien-1-ol and Mome inositol.
FIG. 1: GC-MS CHROMATOGRAM OF CHLOROFORM EXTRACT OF CYAMOPSIS TETRAGONOLOBA
FIG. 2: GC-MS CHROMATOGRAM OF ETHYL ACETATE EXTRACT OF CYAMOPSIS TETRAGONOLOBA
FIG. 3: GC-MS CHROMATOGRAM OF METHANOLIC EXTRACT OF CYAMOPSIS TETRAGONOLOBA
FIG. 4: GC-MS CHROMATOGRAM OF AQUEOUS EXTRACT OF CYAMOPSIS TETRAGONOLOBA
TABLE 1: PHYTOCHEMICALS IDENTIFIED IN CHLOROFORM EXTRACTS OF CYAMOPSIS TETRAGONOLOBA FRUIT BY GC-MS
Peak # | R. Time | Name of Compound | Molecular formula | Molecular weight | Peak area % |
1 | 26.749 | Tetradecanal | C14H28O | 212 | 0.17 |
2 | 27.794 | Tetradecanoic acid | C14H28O2 | 228 | 0.12 |
3 | 29.321 | 2,6,10-Trimethyl,14-ethylene-14-pentadecne | C20H38 | 278 | 0.45 |
4 | 30.198 | 3,7,11,15-Tetramethyl-2-hexadecen-1-ol | C20H40O | 296 | 0.12 |
5 | 32.096 | Hexadecanoic acid | C16H32O2 | 256 | 3.68 |
6 | 35.478 | 7-Tetradecenal,(Z)- | C14H26O | 210 | 3.46 |
7 | 35.830 | 9-Octadecenoic acid (Z)- | C18H34O2 | 282 | 0.45 |
8 | 38.264 | 9-Octadecenal,(Z)- | C18H34O | 266 | 0.43 |
9 | 38.663 | Oxalic acid, cyclohexyl tetradecyl ester | C22H40O4 | 368 | 0.28 |
10 | 40.787 | 4-(2-Tert-butyl-5-oxo-1,3-dioxolan-4-yl)butyl formamide | C12H21NO4 | 243 | 0.50 |
11 | 41.627 | 1,2 –Benzenediccarboxylic acid | C24H38O4 | 390 | 1.64 |
12 | 42.963 | 1-cyclohexyldimethylsilyloxybutane | C12H26OSi | 214 | 0.55 |
13 | 43.202 | Cyclohexaneacetic acid, alpha-methyl-alpha-propyl-,methyl ester | C13H24O2 | 212 | 0.41 |
14 | 43.424 | Tetratetracontane | C44H90 | 618 | 1.37 |
15 | 44.207 | Nonacosane | C29H60 | 408 | 0.42 |
16 | 44.295 | Squalene | C30H50 | 410 | 0.31 |
17 | 44.523 | 1-Triacontanol | C30H62O | 438 | 0.28 |
18 | 44.681 | Heptadecafluorononanoic acic, undecyl ester | C20H23F17O2 | 618 | 0.43 |
19 | 44.788 | Cyclohexaneacetic acid, alpha-methyl-alpha-propyl-, methyl ester | C13H24O2 | 212 | 0.24 |
20 | 45.893 | Tremulone | C29H46O | 410 | 0.31 |
21 | 46.084 | Stigmasterol acetate | C31H50O2 | 454 | 0.30 |
22 | 46.605 | Tetracontane | C40H82 | 562 | 15.85 |
23 | 46.897 | Octacosanoic acid, methyl ester | C29H58O2 | 438 | 0.37 |
24 | 48.182 | Campesterol | C28H48O | 400 | 1.06 |
25 | 48.509 | Stigmasterol | C29H48O | 412 | 10.94 |
26 | 49.086 | 2-Nonadecanone | C19H38O | 282 | 0.66 |
27 | 49.297 | Gamma-sitosterol | C29H50O | 414 | 5.57 |
28 | 49.935 | beta-Amyrone | C30H48O | 424 | 2.53 |
29 | 50.604 | Betulin | C30H50O2 | 442 | 2.27 |
30 | 52.286 | 2-Hexadecanone | C16H32O | 240 | 0.56 |
31 | 52.700 | Phytol, acetate | C22H42O2 | 338 | 0.71 |
TABLE 2: PHYTOCHEMICALS IDENTIFIED IN ETHYL ACETATE EXTRACTS OF CYAMOPSIS TETRAGONOLOBA FRUIT BY GC- MS
Peak # | R. Time | Name of Compound | Molecular formula | Molecular weight | Peak area % |
1 | 19.018 | 3-Hexadecene, (Z)- | C16H32 | 224 | 0.23 |
2 | 22.366 | Cyclohexene, 3-(1,5-dimethyl-4-hexenyl)-6-methylene-[S-(R*,S*)]- | C15H24 | 204 | 0.86 |
3 | 23.975 | 1- Hexadecene | C16H32 | 224 | 0.42 |
4 | 26.471 | Curlone | C15H22O | 218 | 0.32 |
5 | 26.746 | Tetradecanal | C14H28O | 212 | 0.33 |
6 | 29.320 | 2,6,10-Trimethyl,14-ethylene-pentadecne | C20H38 | 278 | 0.72 |
7 | 29.546 | Tetradecanoic acid, trimethylsilyl ester | C17H36O2Si | 300 | 2.05 |
8 | 30.194 | 2-Hexadecen-1-ol,3,7,11,15-tetramethyl-[R-[R*,R*-(E)]]- | C20H40O | 296 | 0.21 |
9 | 31.516 | n-Pentadecanoic acid,trimethylsilyl ester | C18H38O2Si | 314 | 0.21 |
10 | 32.463 | 1-Octadecene | C18H36 | 252 | 0.86 |
11 | 33.415 | Hexadecanoic acid,trimethylsilyl ester | C19H40O2Si | 328 | 1.88 |
12 | 36.159 | 1-Heneicosanol | C21H44O | 312 | 2.90 |
13 | 36.260 | Eicosane | C20H42 | 282 | 0.22 |
14 | 38.234 | 9- Octadecenal, (Z)- | C18H34O | 266 | 0.64 |
15 | 38.637 | Oxalic acid, cyclohexyl tetradecyl ester |
C22H40O4 |
368 | 0.38 |
16 | 38.740 | 4,8,12,16-Tetramethylheptadecan-4-olide | C21H40O2 | 324 | 0.32 |
17 | 39.551 | n-Tetracosanol-1 | C24H50O | 354 | 5.12 |
18 | 40.773 | 4-(2-Tert-butyl-5-oxo-1,3-dioxolan-4-yl)butyl formamide | C12H21NO4 | 243 | 0.48 |
19 | 41.615 | 1,2 –Benzenedicarboxylic acid | C24H38O4 | 390 | 3.00 |
20 | 42.028 | 4- Octadecenal | C18H34O | 266 | 0.20 |
21 | 42.902 | 1-Cyclohexyldimethylsilyloxybutane | C12H26OSi | 214 | 0.13 |
22 | 42.948 | 6-Ethyl-3-trimethylsilyloxydecane | C15H34OSi | 258 | 0.31 |
23 | 43.410 | Tetratetracontane | C44H90 | 618 | 1.00 |
24 | 43.774 | Fumaric acid, 2-heptyl octadecyl ester | C29H54O4 | 466 | 0.28 |
25 | 44.174 | Eicosyl pentafluoropropionate | C23H41F52O2 | 444 | 3.78 |
26 | 44.291 | Squalene | C30H50 | 410 | 0.23 |
27 | 44.365 | Isomucronulatol | C17H18O5 | 302 | 0.34 |
28 | 44.670 | 1-Tricontanol | C30H62O | 438 | 0.69 |
29 | 44.979 | 1-Docosanol | C22H46O | 326 | 0.31 |
30 | 45.062 | 2-Pentadecanone,6,10,14-trimethyl- | C18H36O | 268 | 0.10 |
31 | 45.126 | Nonadecyl pentafluoropropionate | C22H39F5O2 | 430 | 0.23 |
32 | 45.319 | Delta-Tocopherol | C27H46O2 | 402 | 0.42 |
33 | 45.447 | 1-Nonadecene | C19H38 | 266 | 0.22 |
34 | 45.885 | Stigmasta-4,7,22-trien-3-ol | C29H46O | 410 | 0.64 |
35 | 46.010 | Nonahexacontanoic acid | C69H138O2 | 998 | 0.06 |
36 | 46.067 | Stigmasterol acetate | C31H50O2 | 454 | 0.27 |
37 | 46.203 | gamma-Tocopherol | C28H48O2 | 416 | 0.87 |
38 | 46.634 | gamma-Sitosterol | C29H50O | 414 | 0.27 |
39 | 46.936 | alpha-Tocopherol | C29H5O2 | 430 | 1.49 |
40 | 47.533 | Hexacosyl pentafluoro
Propionate |
C29H53F5O2 | 528 | 0.27 |
41 | 48.231 | Campesterol | C28H48O | 400 | 1.41 |
42 | 48.505 | Stigmasterol | C29H48O | 412 | 16.49 |
43 | 49.297 | gamma-Sitosterol | C29H50O | 414 | 9.34 |
44 | 49.585 | 3-(1-[2-(1,2-Dimethylpropyl)cyclopropyl]ethyl)-3a,5b-dimethyl hexadecahydro-1H-cyclopenta [a]cyclopropa[t]phenanthren-8-ol | C30H50O | 426 | 0.49 |
45 | 49.956 | beta-Amyrone | C30H48O | 424 | 5.98 |
46 | 50.455 | Tremulone | C29H46O | 410 | 0.19 |
47 | 51.057 | Sitostenone | C29H48O | 412 | 0.40 |
48 | 51.578 | 17-Pentatriacontene | C35H70 | 490 | 0.43 |
49 | 52.699 | Phytol,acetate | C22H42O2 | 338 | 1.52 |
50 | 53.178 | 4-Tert-butylcalix[4]arene | C44H56O4 | 648 | 11.04 |
TABLE 3: PHYTOCHEMICALS IDENTIFIED IN METHANOLIC EXTRACTS OF CYAMOPSIS TETRAGONOLOBA FRUIT BY GC- MS
Peak # | R. Time | Name of Compound | Molecular formula | Molecular weight | Peak area % |
1 | 7.297 | 2,5 Dimethyl-2,4-dihydroxy-3(2H)-furanone | C6H8O4 | 144 | 0.19 |
2 | 9.086 | Pantolactone | C6H10O3 | 130 | 0.06 |
3 | 9.816 | 2,5 Dimethyl-3(2H)-furanone | C6H8O3 | 128 | 0.38 |
4 | 10.519 | Cyclopentane,1-acetyl-1,2-epoxy- | C7H10O2 | 126 | 0.38 |
5 | 12.013 | Acetic acid, hexyl ester | C8H16O2 | 144 | 0.22 |
6 | 12.267 | 2,3-Dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one | C6H8O4 | 144 | 2.02 |
7 | 14.523 | Coumaran | C8H8O | 120 | 0.10 |
8 | 14.946 | 5-Hydroxymethylfurfural | C6H6O3 | 126 | 5.01 |
9 | 16.717 | 5-Acetoxy methyl-2- furaldehyde | C8H8O4 | 168 | 0.07 |
10 | 16.884 | Trimethylsilyl 3- methyl -2- furoate | C9H14O3Si | 198 | 0.37 |
11 | 19.026 | 1- Tridecene | C13H26 | 182 | 0.24 |
12 | 22.369 | beta- Sesquiphellandrene | C15H24 | 204 | 0.18 |
13 | 23.241 | Butylated hydroxyanisole | C11H16O2 | 180 | 0.13 |
14 | 23.828 | 1,5- Dibromohexane | C6H12Br2 | 242 | 0.13 |
15 | 24.250 | N (beta Hydroxyethyl)-4-(gamma-hydroxypropyl)piperidine | C10H21NO2 | 187 | 0.12 |
16 | 28.433 | 3- Eicosene | C20H40 | 280 | 0.11 |
17 | 32.036 | Mome inositol | C7H14O6 | 194 | 76.09 |
18 | 34.292 | 9,12-Octadecadienoic acid, methyl ester | C19H34O2 | 294 | 0.13 |
19 | 34.419 | 9- Octadecenoic acid(Z)-, methyl ester | C19H36O2 | 296 | 0.21 |
20 | 35.347 | 7-Tetradecenal,(Z)- | C14H26O | 210 | 8.30 |
21 | 35.722 | Stearic acid | C18H36O2 | 284 | 1.04 |
22 | 36.737 | Bombykol | C16H30O | 238 | 0.07 |
23 | 37.679 | Fumaric acid, 2-dimethyl aminoethyl octadecyl ester | C26H49NO4 | 439 | 0.07 |
24 | 39.072 | Eicosanoic acid | C20H40O2 | 312 | 0.14 |
25 | 39.287 | Dihydroegotamine | C33H37N5O5 | 583 | 0.08 |
26 | 40.529 | Fumaric acid, 2 dimethyl aminoethyl nonyl ester | C17H31NO4 | 313 | 0.05 |
27 | 41.609 | 1,2 –Benzenediccarboxylic acid | C24H38O4 | 390 | 0.23 |
28 | 44.289 | Squalene | C30H50 | 410 | 0.04 |
29 | 44.366 | Mucronulatol | C17H18O5 | 302 | 0.06 |
30 | 44.676 | Tricontyl pentafluoropropionate | C33H61F5O2 | 584 | 0.05 |
31 | 45.879 | Tremulone | C29H46O | 410 | 0.09 |
32 | 46.183 | gamma-Tocopherol | C28H48O2 | 416 | 0.10 |
33 | 46.909 | alpha-Tocopherol | C29H5O2 | 430 | 0.17 |
34 | 48.160 | Campesterol | C28H48O | 400 | 0.13 |
35 | 48.459 | Stigmasterol | C29H48O | 412 | 1.66 |
36 | 49.250 | gamma-Sitosterol | C29H50O | 414 | 0.80 |
37 | 49.899 | beta-Amyrone | C30H48O | 424 | 0.44 |
38 | 50.569 | Betulin | C30H50O2 | 442 | 0.33 |
TABLE 4: PHYTOCHEMICALS IDENTIFIED IN AQUEOUS EXTRACTS OF CYAMOPSIS TETRAGONOLOBA FRUIT BY GC- MS
Peak # | R. Time | Name of Compound | Molecular formula | Molecular weight | Peak area % |
1 | 11.989 | Acetic acid, hexyl ester | C8H16O2 | 144 | 0.26 |
2 | 12.232 | 2,3-dihydro-3, 5-dihydroxy-6-methyl-4H-pyran-4-one | C6H8O4 | 144 | 1.45 |
3 | 14.759 | 5-Hydroxymethylfurfural | C6H6O3 | 126 | 0.16 |
4 | 16.534 | Carvacrol | C10H14O | 150 | 0.10 |
5 | 19.056 | 1-Dodecanol | C12H26O | 186 | 0.13 |
6 | 21.434 | Xanthosine | C10H12N4O6 | 284 | 3.33 |
7 | 22.098 | 10-Dicahydroquinolinol | C9H17NO | 155 | 0.25 |
8 | 23.297 | Butylated hydroxyanisole | C11H16O2 | 180 | 0.11 |
9 | 24.017 | 1-Hexadecene | C16H32 | 224 | 0.20 |
10 | 25.991 | alpha Santalol | C15H24O | 220 | 0.38 |
11 | 28.876 | Mome inositol | C7H14O6 | 194 | 52.15 |
12 | 31.161 | Hexadecanoic acid, methyl ester | C17H34O2 | 270 | 0.14 |
13 | 31.729 | Dibutyl phthalate | C16H22O4 | 278 | 0.21 |
14 | 32.065 | Hexadecanoic acid | C16H32O2 | 256 | 6.87 |
15 | 34.348 | 9,12-Octadecadienoic acid, methyl ester | C19H34O2 | 294 | 0.32 |
16 | 34.481 | 9- Octadecenoic acid(Z)-, methyl ester | C19H36O2 | 296 | 0.22 |
17 | 35.327 | Bombykol | C16H30O | 238 | 8.28 |
18 | 35.428 | Cis-Vaccenic acid | C18H34O2 | 282 | 2.96 |
19 | 35.782 | Stearic acid | C18H36O2 | 284 | 1.18 |
20 | 36.793 | 1,E-11,Z-13-Octadecatriene | C18H32 | 248 | 0.35 |
21 | 37.040 | 9,12-Octadecadienoyl chloride,(Z,Z)- | C18H31ClO | 298 | 0.27 |
22 | 37.936 | 15-Hydroxypentadecanoic acid | C15H30O3 | 258 | 0.27 |
23 | 38.637 | Ambrettolide | C16H28O2 | 252 | 0.20 |
24 | 39.977 | 1-Monolinolein | C21H38O4 | 354 | 0.18 |
25 | 40.839 | 9- Octadecenal, (Z)- | C18H34O | 266 | 0.40 |
26 | 41.664 | 1,2 –Benzenediccarboxylic acid | C24H38O4 | 390 | 0.41 |
27 | 43.845 | Sebacic acid, di(dec-4-enyl) ester | C30H54O4 | 478 | 0.57 |
28 | 48.619 | Hexadecanoic acid, 1,3-propanediyl ester | C35H68O4 | 552 | 0.54 |
29 | 52.726 | Stigmasterol acetate | C31H50O2 | 454 | 1.73 |
30 | 57.479 | Ergostane-3,5,6,12,25-pentol,25-acetate,(3 beta, 5 alpha, 6 beta, 12 beta) | C30H52O6 | 508 | 3.02 |
CONCLUSION: GC-MS analysis is the primary step towards understanding the nature of bioactive compounds of plant and this type of analysis will be helpful for further elaborated study. GC-MS analysis of phytochemicals in Cyamopsis tetragonoloba gives a clear image of its pharmaceutical properties because here, we are able to identify some of secondary metabolites that were present in high amounts than others. tetracontane, stigmasterol, 4, Tert butylcalix[4] arene, mome inositol, 7 tetradecenal and 10, 12 Hexadecadien-1-ol that are repeatedly present in the plant extracts and have reported hypoglycemic, hycholesterolemic, antioxidant, anticancerous and thyroid inhibiting properties.
ACKNOWLEDGEMENT: I would like to thank my family, my supervisor and the management of The IIS University, Jaipur for their support and guidance.
CONFLICT OF INTEREST: Nil
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How to cite this article:
Jain PK and Rijhwani S: Comparative GC-MS analysis of Cyamopsis tetragonoloba fruit extracts. Int J Pharm Sci & Res 2018; 9(10): 4236-42. doi: 10.13040/IJPSR.0975-8232.9(10).4236-42.
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