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Isolasi dan Identifikasi Senyawa Flavonoid dari Daun Murbei (Morus alba Linn)

Indonesian Journal of Chemical Science · Vol. 8 No. 1 (2019) · pp. 16–22

DOI
10.15294/ijcs.v8i1.23035
ISSN
2502-6844, 2252-6951
Published
2019-02-15
Publisher
Universitas Negeri Semarang
Language
eng

Abstract

Mulberry leaves are used as traditional medicine because they contain secondary metabolites. Mulberry leaves are used as traditional medicine because they contain secondary metabolites. The purpose of this research is to know determine isolation method, identification, and class of flavonoid compounds from mulberry leaves. Sample were isolated using maceration method, liquid partition, gravitation column chromatography (GCC) technical, compound identification using FTIR and UV-Vis. Extraction of 3000 g dry powder of mulberry leaves using maceration method with n-hexane and ethanol solvent during 3x24 hours yielded 82.3538 g dark green ethanol extract, the phytochemical test showed that contained flavonoid compound. The ethanol extract was extracted with liquid partition using ethyl acetate: aquades (1: 1) yielded 38.4253 g ethyl acetate extract, that was TLC test eluted with n-hexane: ethyl acetate was obtained by the best eluent of 8:2. Isolation using column chromatography with silica gel and n-hexane: ethyl acetate eluent (9:1), (8:2), (7:3), and (6:4) gave 7 fractions, the phytochemical test showed that contained strong intensity flavonoid compound. Analysis of fraction 7 isolate using FTIR and UV-Vis. Infrared analysis showed that the isolate had bound -OH, CH aliphatic, C=O carbonil, C=C aromatic, CO alcohol, and CH aromatic groups. Analysis of fraction 7 isolate using UV-Visible gained 2 peaks at λ 324 nm (band I) and λ 291 nm (band II) which indicated the flavonoide groups of flavanone or dihydroflavonol. By using shifting reagent the fraction 7 isolate was suggested to contain dihydroflavonol group with substituent of ortho-dihydroxyl group on C-6 and C-7, ortho-dihydroxyl group on C-4 'and C-5', and hydroxyl group on C-3.

Collaboration network of the authors

40 authors · 169 co-authorship links · showing the 40 most connected

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  • State University of Semarang
  • Affiliation unknown
  • Different organisations
  • Same organisation
  • Affiliation unknown
  • Thicker line = more joint articles · bigger circle = more articles
Show as table
Co-authorOrganisationJoint articles
Supartono SupartonoAffiliation unknown11
Nanik WijayatiState University of Semarang7
Edy CahyonoState University of Semarang5
Harjono HarjonoAffiliation unknown4
Woro SumarniState University of Semarang3
Sri Susilogati SumartiState University of Semarang2
Sudarmin SudarminAffiliation unknown2
Kusoro SiadiAffiliation unknown2
Agung Tri PrasetyaState University of Semarang2
Bowo NurcahyoAffiliation unknown2
Sri NurhayatiAffiliation unknown2
Eko Budi SusatyoAffiliation unknown2
Endang SusilaningsihState University of Semarang2
Jumaeri JumaeriAffiliation unknown2
Aditya MariantiAffiliation unknown1
Nur Dina AmalinaAffiliation unknown1
Faya Nuralda SitompulAffiliation unknown1
Shafira Septiana FutriAffiliation unknown1
Legendra Gantar NegaraAffiliation unknown1
Intan Kharyna SholehahAffiliation unknown1
Dian Sri AsmorowatiAffiliation unknown1
Putri Dyah AstariAffiliation unknown1
Rangga Krisma PutraAffiliation unknown1
Denis Rahayu Yuna PratamaAffiliation unknown1
Ahmad NasrullohAffiliation unknown1
Puji RahayuState University of Semarang1
Harjito HarjitoAffiliation unknown1
Ishri Arju SyafangahAffiliation unknown1
Kumar PujiatiAffiliation unknown1
Lastri LastriAffiliation unknown1
Mita Megah Kurni PutriAffiliation unknown1
Ni'matul KhasanahAffiliation unknown1
SudarminState University of Semarang1
Amanah Galih AsihAffiliation unknown1
Intan CahyaningrumAffiliation unknown1
Kasmui KasmuiState University of Semarang1
Nisa Fathin MuslimahAffiliation unknown1

Affiliations come from OpenAlex; journal OAI-PMH metadata carries none. Authors without an OpenAlex ID are matched by name, which can merge or split people.

Metadata source: OAI-PMH (metadata jurnal) https://journal.unnes.ac.id/sju/index.php/ijcs/oai, first harvested 5 Nov 2026, last seen 8 Nov 2026.
Original metadata (oai_dc)
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	<dc:title xml:lang="en-US">Isolasi dan Identifikasi Senyawa Flavonoid dari Daun Murbei (Morus alba Linn)</dc:title>
	<dc:creator>Mabruroh, Eva Qomariyah</dc:creator>
	<dc:creator>Mursiti, Sri</dc:creator>
	<dc:creator>Kusumo, Ersanghono</dc:creator>
	<dc:description xml:lang="en-US">Mulberry leaves are used as traditional medicine because they contain secondary metabolites. Mulberry leaves are used as traditional medicine because they contain secondary metabolites. The purpose of this research is to know determine isolation method, identification, and class of flavonoid compounds from mulberry leaves. Sample were isolated using maceration method, liquid partition, gravitation column chromatography (GCC) technical, compound identification using FTIR and UV-Vis. Extraction of 3000 g dry powder of mulberry leaves using maceration method with n-hexane and ethanol solvent during 3x24 hours yielded 82.3538 g dark green ethanol extract, the phytochemical test showed that contained flavonoid compound. The ethanol extract was extracted with liquid partition using ethyl acetate: aquades (1 : 1) yielded 38.4253 g ethyl acetate extract, that was TLC test eluted with n-hexane : ethyl acetate was obtained by the best eluent of&amp;nbsp; 8:2. Isolation using column chromatography with silica gel and n-hexane: ethyl acetate eluent (9:1), (8:2), (7:3), and (6:4) gave 7 fractions, the phytochemical test showed that contained strong intensity flavonoid compound. Analysis of fraction 7 isolate using FTIR and UV-Vis. Infrared analysis showed that the isolate had bound -OH, CH aliphatic, C=O carbonil, C=C aromatic, CO alcohol, and CH aromatic groups. Analysis of fraction 7 isolate using UV-Visible gained 2 peaks at λ 324 nm (band I) and λ 291 nm (band II) which indicated the flavonoide groups of flavanone or dihydroflavonol. By using shifting reagent the fraction 7 isolate was suggested to contain dihydroflavonol group with substituent of ortho-dihydroxyl group on C-6 and C-7, ortho-dihydroxyl group on C-4 'and C-5', and hydroxyl group on C-3.</dc:description>
	<dc:publisher xml:lang="en-US">Universitas Negeri Semarang</dc:publisher>
	<dc:date>2019-02-15</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:type xml:lang="en-US">Peer-reviewed Article</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://journal.unnes.ac.id/sju/ijcs/article/view/23035</dc:identifier>
	<dc:identifier>10.15294/ijcs.v8i1.23035</dc:identifier>
	<dc:source xml:lang="en-US">Indonesian Journal of Chemical Science; Vol 8 No 1 (2019); 16-22</dc:source>
	<dc:source>2502-6844</dc:source>
	<dc:source>2252-6951</dc:source>
	<dc:source>10.15294/ijcs.v8i1</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://journal.unnes.ac.id/sju/ijcs/article/view/23035/12697</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2019 Indonesian Journal of Chemical Science</dc:rights>
</oai_dc:dc>