Chemical Investigation of Polygonatum verticillatum
Rakesh Saini1*, Saurabh Chaturvedi1, M. Shahar Yar2, H. P. Bhartiya3 and Pratibha Singh3
1Pranveer Singh Institute of Technology, Bhauti, Kanpur (U.P)
2Jamiya Hamdard University, New Delhi
3 Govt. P.G. College Hamirpur (U.P)
*Corresponding Author E-mail: rakeshpsit.saini@gmail.com
ABSTRACT:
Polygonatum verticillatum, Convallariaceae erect glabrous herb upto 20 cm. in height with thick root stock. Upper part of the stem the leafy zig –zag grooved, leaves whorled sensible linear or lanceolate flowers 2-3 together, white, pinkish and white or pale green in whorled racemes fruits berries, red when ripe. Root stock is sweet, cooling, Emollient, Diuretic aphrodisiac, galactogogue, appetizing, tonic. It is useful in vitiated condition of pitas and vat, burning sensation fever, stongury, seminal weakness, anorexia and general debility. The author have done some work and isolated few higher fatty acids from the rhizome of this plant.
INTRODUCTION:
Polygonatum verticillatum; Common name: Whorled Solomon's seal; Family: Convallariaceae; Synonyms: Convallaria verticillata; Habitat: Margins of woods, clearings and shady rocky places, usually on acid soils, Perennial growing to 1.2m by 0.45m . It is hardy to zone 5. It is in flower from June to July. The flowers are hermaphrodite (have both male and female organs) and are pollinated by Bees. The plant is self-fertile.
The plant prefers light (sandy), medium (loamy) and heavy (clay) soils and requires well-drained soil. The plant prefers acid, neutral and basic (alkaline) soils and can grow in very acid soil. It can grow in full shade (deep woodland) or semi-shade (light woodland). It requires moist soil.
Extraction of oil:
The Shade dried rhizomes (500 gm) Power of Polygonatum verticillatum was used for essential oil extraction by Clevenger’s apparatus. The condensate was treated with n-Hexane. The n-Hexane layer was separated and dried over anhydrous Na2 SO4 and the solvent was evaporated under reduced pressure in a thin film rotatory evaporator at 300 C. The residual oil yield was 3 ml. we have identified five compounds A, B, C, D, E as below.
Gas Chromatographic Analysis: The oil was analyzed by gas. Chromatograph using flame ionization detector (FID). The temperature programming used is given below.
Injection Temperature : 240 0 c
Detector Temperature : 2800 c
Initial Temperature : 600 c
Programming run rate : 30/ min.
Total run time : 35 Min.
RESULT AND DISCUSSION:
GC-MS Screening of Essential Oil of Polygonatum verticillatum:
The essential oil Polygonatum verticillatum was analyzed by using GC-ms for identification of minor constituents of the essential oil which could not be isolated by means of repeated column chromatography and HPLC method . The gas chromatograph (table) showed the presence of various compounds the analysis revealed that the oil was dominated with long chain fatty acid and esters of compounds A, B, C, D and E. These were identified on the basis of GC-MS results Table and Literature search.
There was no literature report on essential oil of rhizomes of Polygonatum verticillatum so for. This is the first work on essential oil of rhizomes of this plant and first time isolated long chain fatty acids and esters from the Polygonatum verticillatum. Compounds were identified as follows.
Identified Compound- A.
Molecular formula- C12H24O2
Molecular weight- 200
Mass spectra- (M+) (200), 171, 157, 127, 115, 87 and 55.
GC-MS Data of oil of P. Verticilatum
|
Sr. No. |
Retention Time |
[M+] |
Major Fragments |
Compound |
|
A |
19.44 |
200 |
[ M+] (200),171,157,129,115, 87,(100) 55 |
CH3(CH2)10COOH |
|
B |
24.96 |
228 |
[ M+] (228),199,185,171,143,129 87,(100)115,41 |
CH3(CH2)12COOH |
|
C |
27.36 |
242 |
[ M+] (242),213,199,185,157,129 115,87,(100),55 |
CH3(CH2)13COOH |
|
D |
28.82 |
270 |
[ M+] (270),227,199, 171, (100), 143,87,55 |
CH3(CH2)15COOH |
|
E |
30.14 |
256 |
[ M+] (256),240,171,129,87 (100),,55 |
CH3(CH2)14COOH |
Melting Point - 44 0C (Lit.)
The above results led us to conclude the structure was compound A as – Dodecanoic acid or Lauric acid. CH3(CH2)10COOH
Structure-
Identified Compound - B
Molecular formula- C14H28O2
Molecular weight- 228
Mass spectra- (M+) (228), 199, 185, 171, 129, 115, 87 (100) and 115.
Melting Point - 58 0C (Lit.)
The above results led us to conclude the structure was compound B as – Tetra decanoic acid or myristic acid. CH3(CH2)12COOH
Structure-
Identified Compound- C
Molecular formula- C15H30O2
Molecular weight- 242
Mass spectra- (M+) (242), 213, 199, 185, 129, 115, 87 (100) ,55.
Melting Point - 62 0C (Lit.)
The above results led us to conclude the structure was compound C as – Penta decanoic acid. CH3 (CH2)13COOH
Structure-
Identified Compound - D
Molecular formula- C17H34O2
Molecular weight- 270
Mass spectra- (M+) (270), 227, 199, 171, (100) 143, 101, 87 and 55.
Melting Point - 66 0C (Lit.)
The above results led us to conclude the structure was compound C as – Penta dodecanoic acid. CH3(CH2)12COOH
Structure-
Identified Compound - E
Molecular formula- C16H32O2
Molecular weight- 256
Mass spectra- (M+) (256), 171, 129, 87 (100) and 55.
Melting Point - 64 0C (Lit.)
The above results led us to conclude the structure was compound E as – hexa decanoic acid or Palmitic acid. CH3(CH2)14COOH\
Structure-
ACKNOWLEDGEMENT:
The authors are highly thankful to the Central drug research Institute (CDRI) Lucknow and Dr. H.P Bhartiya (HOD) Govt. P.G. College Hamirpur (U.P) for providing necessary facilities.
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Received on 20.03.2009 Modified on 09.05.2009
Accepted on 12.06.2009 © AJRC All right reserved
Asian J. Research Chem. 3(1):Jan.-Mar. 2010 page 20-21