irmanida batubara - proceedings 2nd basic science international conference
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for conferenceTRANSCRIPT
~ s~~a- I
Basic Science International Conference
PROCEEDINGS
2nd BASIC SCIENCE International Co Malang
thFebruary 24-25 201
2nd Basic Science International Conference 2012 February 24 - 25th2012
Proceedings RESEARCH INNOVATION ON MODELlN6 SIMULATION
AND ITS APPLICATIONS
Editors Dr Wuryansari Muharini Kusumawinahyu
Danny Prasetyo Hartanto Rizka Firdausi
Mutya Fani Atsomya
Mathematics Department on Behalf of Faculty of Sciences
Brawijaya University
tclrometry -
-
u DlJCTlON
_
torant
(128) oIQ ) benzene
col (287)
--) [2J
_ u middoth as
_ _-ltJ2 cells in
_lh oxyci nnamate - rc ritical CO2
_ 0 [3 ]
_Igt
_
_ because it
middot_ r solvent is
L D T T Irawadi I Batuhara Basic Science International Conference 2012
GC-MS and NMR Analysis of ethyl-p-methoxycinnamate I olated From Kaemperia gaanga L Using Distillation Method
Lusiani Dewi Assaat Tun Tedja Ira wadi 2 Irmanida Batubara 3
Faculty aMathematics and Natural Sciences Education Sultan Ageng Tirtayasa University Serang Indonesia ussaalFuhoocull1
p Irtmenf oChemistry Faculty oMathematics and Nalllral Sciences Bogor Agriculture Uni versity Indonesia 11111 ledjawd1Ou CUI1l
partment 0Chemistry Faculty 0Mathematics and Natllral Sciences Bogor Agriculture University Indonesia imeba Illbara(al gl1lu il com
Abstract
poses of this research were to isolate and analyze ethyl-p-methoxycinnamate which is the main lit 0 Kaemperia galangu L Volatile oil 0 K gaanga L obtained by distilled fresh rhizome using
tillation method The main components of K galanga L volatile oil were ethy l-p-methoxycinnamate 1 Jmate and o-3-carelc The ethy l-p-methmJcinnamate compound analyzed using gas chromatography
(GC-MS) alld nuclear magnetic resonance (NMR) The result 0 GC-MS analysis showed p -methoxycinllamatc is the main component in the volatile oil (264) The structure then conJirmed vIR COSY HMQC and HMBC analysis in NMR
-p-lIIelhoxycinnamate GC-MS NMR
have a high 1 1 fat medicine
Kencur (Kael7Jl2eriagalOlya L) is one of the mes commonly used by people of Indonesia to
II MATERIAL D l ETH D_ I swelling rheumatism cough abdominal pain
bacterial infection and used as Plant materiab ients for preparing Jamu a local health tonic Tht 10- 1 y 3L
The main components of kencur volatile oils are wcre collected from pa ar md camphene (247) carvone rhizome determined b Herbanur (133) eucalyptol (959) Biology research cenrer Ll PI Bogor lnel n _I ~ methyl cinnamate (2323)
Mcane (641) and ethyl-p-methoxycinnamate Preparation of K gaiallga L distillate
Recently a lot of research established to led About 500 g K galanga L rhizome washed li lization of the main components of K galanga und cut into small pieces The rhizomes were
ethyl-p-methoxycinnamate Ethyl pshy distillated for 4 hours During the process solvent oxycinnamate eQuId inhibit the proliferation of temperature is set at 95-105 e
a dose-dependent manner by Water favor will carry the components of ~ing cells to enter into apoptosis Therefore it is volatile oil then the essential oil is collected From
rlant to choose the method how to isolate ethyl- the essential oil and residue we can collect a white from K galanga L crystals after left over night This white chrystals
extraction method was used to collected in the bottles for further analysis ethyl p-methoxycinnamate with yield about
Identification of compound
[n this study the distillation method used to The chemical components of wh ite crystals eth yl p-methoxycinnamate By using this was determined by Agilent Technologies 6890 Gas
od on K galanga L rhizome essential oil from Chromatograph with Auto Sampler and 5973 1as ~iJI(nga L will be obtained which is expected to Selective Detector and Chemstation data sy remTh e
in eth yl p-methoxycinnamate with the highest operating parameters were as followsColumn HP 5 1 On other hand distillation method is a simple WAX Ionization mode EI electron energy 70 eV
is only use water as a solvent Capillary Column 30 m x 025 mm x 025 -tm Film ad of the other chemical solvents By using the Thickness interface temperature 280degC ion source
expected that isolated compound temperature 280degC inject volume I-tl column
Assaat L D T T Irawadi I Batubara Basic Science International Conference 2012
temperature 60degC-240degC The spectra were recorded and compared with the terpene library
Compound were identified by H-NMR COSY HMQC and HMBC Methanol-d3 was used as the NMR solvent These NMR measurements was performed by using JEOL EC600NMR
III RESULT AND DISCUSSION
Disti lation process of K galangal rhizome resulted K galanga L essential oil [n cold conditions a white crystal formed in the essential oil Its yield of white crystal is about 028 the white crystals were collected in a vial for further analysis GC-MS spectra showed that white crystal is a pure compound (Fig I)
Fig I The spectra for K galanga L essential oil (upper)
and white crystal (down)
GC-MS spectra sl10wed that main compound c- ent ial oi l were cthyl-p-methoxycinnamate ethyl middotlOnam~w and 6-cnrcne (upper) Chromatogram
fr m hite crystals spectra showed at retention 10 3 min CiC-vlS E Imlz 206 (M-I) (down) R ult f mass spectrulll analysis compared with Ii ra r inde mass spectrum Therefore the analysis as continucd using Nuclear Magnetic Resonance (NMR) White crystals analyzed using H-NMR COSY HMQC and HMBC White crystals H-NMR 063176 (I H d J= 165Hz H-2) 0 (I H d J= 165 Hz H-3) 074908 (2H d J=69Hz H-5 H-9) 669045 (2H d J=69Hz H-6 H-8) 037861 (3H s H-IO) 041898 (2H k H-II) 012807 (3H t H-12) 13C_ NMR 0167 74 (C-I) 011497 (C-2) 014456 (Cshy3) 012701 (C-4) 012959 (C-5) 011408 (C-6) 016179 (C-7) 011408 (C-8) 012959 (C-9) 05452 (C-I 0)06012 (C-II) 0 13 30 (C-12) Overall analysis is summarized in the following table
Table I The result of H-NMR spectrum analysis
0
Carbon
Chemical sh ifts
(0 ppm) Integration Multiplicity
Coupling constant IJ Hz)
2
-I 59 6S 7 10 II I~
63176 75 87 1
7-1 908 690-15
37861 41898 l280 i
Duple Duplet
Duplet Duplet
Singlet QU311et Triplet
165 1 6 ~
6 9 69
Below is a figure of a complete analytical result analysis of ethyl-p-methoxycinnamate
Fig 2 The result of H-NMR COSY HMQC all HMBC
IVCONCLUSION
Ethyl-p-methoxycinnamate compound isolated from K galunga L (2 shydistillation method The result of GC- I showed that the white crystals obtai _ distillation is ethyl-p-methoxyeinnamate - -~lao
ACKNOWLEDGEMET
We gratefully acknowledge the fun d = Directorate General of Higher Edueat of Indonesia for BPPS program and Mitsunaga and Kosei Yamauchi lor
spectroscopic analysis at Gifu Uniers
REFERENCES
[1) Tara S Chandra kala S Sachidananda
Smita S Ganesh S Wound healing JC
alcoholic extract of Ka empferia galallga
rats 2006 [ndioll J Physinl Plwl1Lcv l 20
3ti4-J90
L D T T Irawadi I Batubara Basic Science International Conference 2012
s Yuenyongsawad S Kummee S [3] Lill B Liu F Chen C Gao H Supercritical carbon jarllwan S Chemical components and dioxide extraction of ethyl p-methoxycinnamate from
bull 19ical activities of volatile oil of Kaemperia Kaell1peria galanga L rhi zome and its apoptotic middot III Linn 2005 Songkanakarin J Sci Techno induction in human HepG2 cells 2010 Natura ~ I -506 Product Research Vol 24 No 20 15 December
2010 1927- ~ 932
2nd Basic Science International Conference 2012 February 24 - 25th2012
Proceedings RESEARCH INNOVATION ON MODELlN6 SIMULATION
AND ITS APPLICATIONS
Editors Dr Wuryansari Muharini Kusumawinahyu
Danny Prasetyo Hartanto Rizka Firdausi
Mutya Fani Atsomya
Mathematics Department on Behalf of Faculty of Sciences
Brawijaya University
tclrometry -
-
u DlJCTlON
_
torant
(128) oIQ ) benzene
col (287)
--) [2J
_ u middoth as
_ _-ltJ2 cells in
_lh oxyci nnamate - rc ritical CO2
_ 0 [3 ]
_Igt
_
_ because it
middot_ r solvent is
L D T T Irawadi I Batuhara Basic Science International Conference 2012
GC-MS and NMR Analysis of ethyl-p-methoxycinnamate I olated From Kaemperia gaanga L Using Distillation Method
Lusiani Dewi Assaat Tun Tedja Ira wadi 2 Irmanida Batubara 3
Faculty aMathematics and Natural Sciences Education Sultan Ageng Tirtayasa University Serang Indonesia ussaalFuhoocull1
p Irtmenf oChemistry Faculty oMathematics and Nalllral Sciences Bogor Agriculture Uni versity Indonesia 11111 ledjawd1Ou CUI1l
partment 0Chemistry Faculty 0Mathematics and Natllral Sciences Bogor Agriculture University Indonesia imeba Illbara(al gl1lu il com
Abstract
poses of this research were to isolate and analyze ethyl-p-methoxycinnamate which is the main lit 0 Kaemperia galangu L Volatile oil 0 K gaanga L obtained by distilled fresh rhizome using
tillation method The main components of K galanga L volatile oil were ethy l-p-methoxycinnamate 1 Jmate and o-3-carelc The ethy l-p-methmJcinnamate compound analyzed using gas chromatography
(GC-MS) alld nuclear magnetic resonance (NMR) The result 0 GC-MS analysis showed p -methoxycinllamatc is the main component in the volatile oil (264) The structure then conJirmed vIR COSY HMQC and HMBC analysis in NMR
-p-lIIelhoxycinnamate GC-MS NMR
have a high 1 1 fat medicine
Kencur (Kael7Jl2eriagalOlya L) is one of the mes commonly used by people of Indonesia to
II MATERIAL D l ETH D_ I swelling rheumatism cough abdominal pain
bacterial infection and used as Plant materiab ients for preparing Jamu a local health tonic Tht 10- 1 y 3L
The main components of kencur volatile oils are wcre collected from pa ar md camphene (247) carvone rhizome determined b Herbanur (133) eucalyptol (959) Biology research cenrer Ll PI Bogor lnel n _I ~ methyl cinnamate (2323)
Mcane (641) and ethyl-p-methoxycinnamate Preparation of K gaiallga L distillate
Recently a lot of research established to led About 500 g K galanga L rhizome washed li lization of the main components of K galanga und cut into small pieces The rhizomes were
ethyl-p-methoxycinnamate Ethyl pshy distillated for 4 hours During the process solvent oxycinnamate eQuId inhibit the proliferation of temperature is set at 95-105 e
a dose-dependent manner by Water favor will carry the components of ~ing cells to enter into apoptosis Therefore it is volatile oil then the essential oil is collected From
rlant to choose the method how to isolate ethyl- the essential oil and residue we can collect a white from K galanga L crystals after left over night This white chrystals
extraction method was used to collected in the bottles for further analysis ethyl p-methoxycinnamate with yield about
Identification of compound
[n this study the distillation method used to The chemical components of wh ite crystals eth yl p-methoxycinnamate By using this was determined by Agilent Technologies 6890 Gas
od on K galanga L rhizome essential oil from Chromatograph with Auto Sampler and 5973 1as ~iJI(nga L will be obtained which is expected to Selective Detector and Chemstation data sy remTh e
in eth yl p-methoxycinnamate with the highest operating parameters were as followsColumn HP 5 1 On other hand distillation method is a simple WAX Ionization mode EI electron energy 70 eV
is only use water as a solvent Capillary Column 30 m x 025 mm x 025 -tm Film ad of the other chemical solvents By using the Thickness interface temperature 280degC ion source
expected that isolated compound temperature 280degC inject volume I-tl column
Assaat L D T T Irawadi I Batubara Basic Science International Conference 2012
temperature 60degC-240degC The spectra were recorded and compared with the terpene library
Compound were identified by H-NMR COSY HMQC and HMBC Methanol-d3 was used as the NMR solvent These NMR measurements was performed by using JEOL EC600NMR
III RESULT AND DISCUSSION
Disti lation process of K galangal rhizome resulted K galanga L essential oil [n cold conditions a white crystal formed in the essential oil Its yield of white crystal is about 028 the white crystals were collected in a vial for further analysis GC-MS spectra showed that white crystal is a pure compound (Fig I)
Fig I The spectra for K galanga L essential oil (upper)
and white crystal (down)
GC-MS spectra sl10wed that main compound c- ent ial oi l were cthyl-p-methoxycinnamate ethyl middotlOnam~w and 6-cnrcne (upper) Chromatogram
fr m hite crystals spectra showed at retention 10 3 min CiC-vlS E Imlz 206 (M-I) (down) R ult f mass spectrulll analysis compared with Ii ra r inde mass spectrum Therefore the analysis as continucd using Nuclear Magnetic Resonance (NMR) White crystals analyzed using H-NMR COSY HMQC and HMBC White crystals H-NMR 063176 (I H d J= 165Hz H-2) 0 (I H d J= 165 Hz H-3) 074908 (2H d J=69Hz H-5 H-9) 669045 (2H d J=69Hz H-6 H-8) 037861 (3H s H-IO) 041898 (2H k H-II) 012807 (3H t H-12) 13C_ NMR 0167 74 (C-I) 011497 (C-2) 014456 (Cshy3) 012701 (C-4) 012959 (C-5) 011408 (C-6) 016179 (C-7) 011408 (C-8) 012959 (C-9) 05452 (C-I 0)06012 (C-II) 0 13 30 (C-12) Overall analysis is summarized in the following table
Table I The result of H-NMR spectrum analysis
0
Carbon
Chemical sh ifts
(0 ppm) Integration Multiplicity
Coupling constant IJ Hz)
2
-I 59 6S 7 10 II I~
63176 75 87 1
7-1 908 690-15
37861 41898 l280 i
Duple Duplet
Duplet Duplet
Singlet QU311et Triplet
165 1 6 ~
6 9 69
Below is a figure of a complete analytical result analysis of ethyl-p-methoxycinnamate
Fig 2 The result of H-NMR COSY HMQC all HMBC
IVCONCLUSION
Ethyl-p-methoxycinnamate compound isolated from K galunga L (2 shydistillation method The result of GC- I showed that the white crystals obtai _ distillation is ethyl-p-methoxyeinnamate - -~lao
ACKNOWLEDGEMET
We gratefully acknowledge the fun d = Directorate General of Higher Edueat of Indonesia for BPPS program and Mitsunaga and Kosei Yamauchi lor
spectroscopic analysis at Gifu Uniers
REFERENCES
[1) Tara S Chandra kala S Sachidananda
Smita S Ganesh S Wound healing JC
alcoholic extract of Ka empferia galallga
rats 2006 [ndioll J Physinl Plwl1Lcv l 20
3ti4-J90
L D T T Irawadi I Batubara Basic Science International Conference 2012
s Yuenyongsawad S Kummee S [3] Lill B Liu F Chen C Gao H Supercritical carbon jarllwan S Chemical components and dioxide extraction of ethyl p-methoxycinnamate from
bull 19ical activities of volatile oil of Kaemperia Kaell1peria galanga L rhi zome and its apoptotic middot III Linn 2005 Songkanakarin J Sci Techno induction in human HepG2 cells 2010 Natura ~ I -506 Product Research Vol 24 No 20 15 December
2010 1927- ~ 932
tclrometry -
-
u DlJCTlON
_
torant
(128) oIQ ) benzene
col (287)
--) [2J
_ u middoth as
_ _-ltJ2 cells in
_lh oxyci nnamate - rc ritical CO2
_ 0 [3 ]
_Igt
_
_ because it
middot_ r solvent is
L D T T Irawadi I Batuhara Basic Science International Conference 2012
GC-MS and NMR Analysis of ethyl-p-methoxycinnamate I olated From Kaemperia gaanga L Using Distillation Method
Lusiani Dewi Assaat Tun Tedja Ira wadi 2 Irmanida Batubara 3
Faculty aMathematics and Natural Sciences Education Sultan Ageng Tirtayasa University Serang Indonesia ussaalFuhoocull1
p Irtmenf oChemistry Faculty oMathematics and Nalllral Sciences Bogor Agriculture Uni versity Indonesia 11111 ledjawd1Ou CUI1l
partment 0Chemistry Faculty 0Mathematics and Natllral Sciences Bogor Agriculture University Indonesia imeba Illbara(al gl1lu il com
Abstract
poses of this research were to isolate and analyze ethyl-p-methoxycinnamate which is the main lit 0 Kaemperia galangu L Volatile oil 0 K gaanga L obtained by distilled fresh rhizome using
tillation method The main components of K galanga L volatile oil were ethy l-p-methoxycinnamate 1 Jmate and o-3-carelc The ethy l-p-methmJcinnamate compound analyzed using gas chromatography
(GC-MS) alld nuclear magnetic resonance (NMR) The result 0 GC-MS analysis showed p -methoxycinllamatc is the main component in the volatile oil (264) The structure then conJirmed vIR COSY HMQC and HMBC analysis in NMR
-p-lIIelhoxycinnamate GC-MS NMR
have a high 1 1 fat medicine
Kencur (Kael7Jl2eriagalOlya L) is one of the mes commonly used by people of Indonesia to
II MATERIAL D l ETH D_ I swelling rheumatism cough abdominal pain
bacterial infection and used as Plant materiab ients for preparing Jamu a local health tonic Tht 10- 1 y 3L
The main components of kencur volatile oils are wcre collected from pa ar md camphene (247) carvone rhizome determined b Herbanur (133) eucalyptol (959) Biology research cenrer Ll PI Bogor lnel n _I ~ methyl cinnamate (2323)
Mcane (641) and ethyl-p-methoxycinnamate Preparation of K gaiallga L distillate
Recently a lot of research established to led About 500 g K galanga L rhizome washed li lization of the main components of K galanga und cut into small pieces The rhizomes were
ethyl-p-methoxycinnamate Ethyl pshy distillated for 4 hours During the process solvent oxycinnamate eQuId inhibit the proliferation of temperature is set at 95-105 e
a dose-dependent manner by Water favor will carry the components of ~ing cells to enter into apoptosis Therefore it is volatile oil then the essential oil is collected From
rlant to choose the method how to isolate ethyl- the essential oil and residue we can collect a white from K galanga L crystals after left over night This white chrystals
extraction method was used to collected in the bottles for further analysis ethyl p-methoxycinnamate with yield about
Identification of compound
[n this study the distillation method used to The chemical components of wh ite crystals eth yl p-methoxycinnamate By using this was determined by Agilent Technologies 6890 Gas
od on K galanga L rhizome essential oil from Chromatograph with Auto Sampler and 5973 1as ~iJI(nga L will be obtained which is expected to Selective Detector and Chemstation data sy remTh e
in eth yl p-methoxycinnamate with the highest operating parameters were as followsColumn HP 5 1 On other hand distillation method is a simple WAX Ionization mode EI electron energy 70 eV
is only use water as a solvent Capillary Column 30 m x 025 mm x 025 -tm Film ad of the other chemical solvents By using the Thickness interface temperature 280degC ion source
expected that isolated compound temperature 280degC inject volume I-tl column
Assaat L D T T Irawadi I Batubara Basic Science International Conference 2012
temperature 60degC-240degC The spectra were recorded and compared with the terpene library
Compound were identified by H-NMR COSY HMQC and HMBC Methanol-d3 was used as the NMR solvent These NMR measurements was performed by using JEOL EC600NMR
III RESULT AND DISCUSSION
Disti lation process of K galangal rhizome resulted K galanga L essential oil [n cold conditions a white crystal formed in the essential oil Its yield of white crystal is about 028 the white crystals were collected in a vial for further analysis GC-MS spectra showed that white crystal is a pure compound (Fig I)
Fig I The spectra for K galanga L essential oil (upper)
and white crystal (down)
GC-MS spectra sl10wed that main compound c- ent ial oi l were cthyl-p-methoxycinnamate ethyl middotlOnam~w and 6-cnrcne (upper) Chromatogram
fr m hite crystals spectra showed at retention 10 3 min CiC-vlS E Imlz 206 (M-I) (down) R ult f mass spectrulll analysis compared with Ii ra r inde mass spectrum Therefore the analysis as continucd using Nuclear Magnetic Resonance (NMR) White crystals analyzed using H-NMR COSY HMQC and HMBC White crystals H-NMR 063176 (I H d J= 165Hz H-2) 0 (I H d J= 165 Hz H-3) 074908 (2H d J=69Hz H-5 H-9) 669045 (2H d J=69Hz H-6 H-8) 037861 (3H s H-IO) 041898 (2H k H-II) 012807 (3H t H-12) 13C_ NMR 0167 74 (C-I) 011497 (C-2) 014456 (Cshy3) 012701 (C-4) 012959 (C-5) 011408 (C-6) 016179 (C-7) 011408 (C-8) 012959 (C-9) 05452 (C-I 0)06012 (C-II) 0 13 30 (C-12) Overall analysis is summarized in the following table
Table I The result of H-NMR spectrum analysis
0
Carbon
Chemical sh ifts
(0 ppm) Integration Multiplicity
Coupling constant IJ Hz)
2
-I 59 6S 7 10 II I~
63176 75 87 1
7-1 908 690-15
37861 41898 l280 i
Duple Duplet
Duplet Duplet
Singlet QU311et Triplet
165 1 6 ~
6 9 69
Below is a figure of a complete analytical result analysis of ethyl-p-methoxycinnamate
Fig 2 The result of H-NMR COSY HMQC all HMBC
IVCONCLUSION
Ethyl-p-methoxycinnamate compound isolated from K galunga L (2 shydistillation method The result of GC- I showed that the white crystals obtai _ distillation is ethyl-p-methoxyeinnamate - -~lao
ACKNOWLEDGEMET
We gratefully acknowledge the fun d = Directorate General of Higher Edueat of Indonesia for BPPS program and Mitsunaga and Kosei Yamauchi lor
spectroscopic analysis at Gifu Uniers
REFERENCES
[1) Tara S Chandra kala S Sachidananda
Smita S Ganesh S Wound healing JC
alcoholic extract of Ka empferia galallga
rats 2006 [ndioll J Physinl Plwl1Lcv l 20
3ti4-J90
L D T T Irawadi I Batubara Basic Science International Conference 2012
s Yuenyongsawad S Kummee S [3] Lill B Liu F Chen C Gao H Supercritical carbon jarllwan S Chemical components and dioxide extraction of ethyl p-methoxycinnamate from
bull 19ical activities of volatile oil of Kaemperia Kaell1peria galanga L rhi zome and its apoptotic middot III Linn 2005 Songkanakarin J Sci Techno induction in human HepG2 cells 2010 Natura ~ I -506 Product Research Vol 24 No 20 15 December
2010 1927- ~ 932
Assaat L D T T Irawadi I Batubara Basic Science International Conference 2012
temperature 60degC-240degC The spectra were recorded and compared with the terpene library
Compound were identified by H-NMR COSY HMQC and HMBC Methanol-d3 was used as the NMR solvent These NMR measurements was performed by using JEOL EC600NMR
III RESULT AND DISCUSSION
Disti lation process of K galangal rhizome resulted K galanga L essential oil [n cold conditions a white crystal formed in the essential oil Its yield of white crystal is about 028 the white crystals were collected in a vial for further analysis GC-MS spectra showed that white crystal is a pure compound (Fig I)
Fig I The spectra for K galanga L essential oil (upper)
and white crystal (down)
GC-MS spectra sl10wed that main compound c- ent ial oi l were cthyl-p-methoxycinnamate ethyl middotlOnam~w and 6-cnrcne (upper) Chromatogram
fr m hite crystals spectra showed at retention 10 3 min CiC-vlS E Imlz 206 (M-I) (down) R ult f mass spectrulll analysis compared with Ii ra r inde mass spectrum Therefore the analysis as continucd using Nuclear Magnetic Resonance (NMR) White crystals analyzed using H-NMR COSY HMQC and HMBC White crystals H-NMR 063176 (I H d J= 165Hz H-2) 0 (I H d J= 165 Hz H-3) 074908 (2H d J=69Hz H-5 H-9) 669045 (2H d J=69Hz H-6 H-8) 037861 (3H s H-IO) 041898 (2H k H-II) 012807 (3H t H-12) 13C_ NMR 0167 74 (C-I) 011497 (C-2) 014456 (Cshy3) 012701 (C-4) 012959 (C-5) 011408 (C-6) 016179 (C-7) 011408 (C-8) 012959 (C-9) 05452 (C-I 0)06012 (C-II) 0 13 30 (C-12) Overall analysis is summarized in the following table
Table I The result of H-NMR spectrum analysis
0
Carbon
Chemical sh ifts
(0 ppm) Integration Multiplicity
Coupling constant IJ Hz)
2
-I 59 6S 7 10 II I~
63176 75 87 1
7-1 908 690-15
37861 41898 l280 i
Duple Duplet
Duplet Duplet
Singlet QU311et Triplet
165 1 6 ~
6 9 69
Below is a figure of a complete analytical result analysis of ethyl-p-methoxycinnamate
Fig 2 The result of H-NMR COSY HMQC all HMBC
IVCONCLUSION
Ethyl-p-methoxycinnamate compound isolated from K galunga L (2 shydistillation method The result of GC- I showed that the white crystals obtai _ distillation is ethyl-p-methoxyeinnamate - -~lao
ACKNOWLEDGEMET
We gratefully acknowledge the fun d = Directorate General of Higher Edueat of Indonesia for BPPS program and Mitsunaga and Kosei Yamauchi lor
spectroscopic analysis at Gifu Uniers
REFERENCES
[1) Tara S Chandra kala S Sachidananda
Smita S Ganesh S Wound healing JC
alcoholic extract of Ka empferia galallga
rats 2006 [ndioll J Physinl Plwl1Lcv l 20
3ti4-J90
L D T T Irawadi I Batubara Basic Science International Conference 2012
s Yuenyongsawad S Kummee S [3] Lill B Liu F Chen C Gao H Supercritical carbon jarllwan S Chemical components and dioxide extraction of ethyl p-methoxycinnamate from
bull 19ical activities of volatile oil of Kaemperia Kaell1peria galanga L rhi zome and its apoptotic middot III Linn 2005 Songkanakarin J Sci Techno induction in human HepG2 cells 2010 Natura ~ I -506 Product Research Vol 24 No 20 15 December
2010 1927- ~ 932
L D T T Irawadi I Batubara Basic Science International Conference 2012
s Yuenyongsawad S Kummee S [3] Lill B Liu F Chen C Gao H Supercritical carbon jarllwan S Chemical components and dioxide extraction of ethyl p-methoxycinnamate from
bull 19ical activities of volatile oil of Kaemperia Kaell1peria galanga L rhi zome and its apoptotic middot III Linn 2005 Songkanakarin J Sci Techno induction in human HepG2 cells 2010 Natura ~ I -506 Product Research Vol 24 No 20 15 December
2010 1927- ~ 932