ISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.)

Cassia fistula L. or trengguli is commonly found as an ornamental plant, pathways shade, and is often used as traditional medicine. The leaves in traditional medicines are used for laxative, fever, and skin remedy. Secondary metabolites have a role in the biological activity of a plant. One of ma...

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Main Author: Nurhayati, Nane
Format: Final Project
Language:Indonesia
Online Access:https://digilib.itb.ac.id/gdl/view/40411
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Institution: Institut Teknologi Bandung
Language: Indonesia
id id-itb.:40411
spelling id-itb.:404112019-07-02T11:41:33ZISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.) Nurhayati, Nane Indonesia Final Project Cassia fistula L., trengguli leaf, flavonoids. INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/40411 Cassia fistula L. or trengguli is commonly found as an ornamental plant, pathways shade, and is often used as traditional medicine. The leaves in traditional medicines are used for laxative, fever, and skin remedy. Secondary metabolites have a role in the biological activity of a plant. One of many secondary metabolites found in trengguli leaves is flavonoid, which is responsible for antioxidant and antibacterial activity. Therefore, this study aims to isolate and identify the flavonoid compounds in trengguli leaves. In this study, the leaves were extracted with methanol by continuous extraction using Soxhlet apparatus, fractionated by liquid-liquid extraction using nhexane, ethyl acetate, and water. The fractions were monitored by thin layer chromatography (TLC) with silica gel GF254 as a stationary phase and ethyl acetate-n-hexane-methanol (8:1:1) as the mobile phase, and visualized using UV ?254 nm, UV ?366 nm, and citroboric spray reagent. Result showed that the largest flavonoid content was in the ethyl acetate fraction. The ethyl acetate fraction was sub-fractionated by preparative TLC using similar mobile phase and stationary phase of fraction monitoring. The subfraction was purified by preparative TLC with silica gel GF254 as a stationary phase and ethyl acetate-n-hexane-methanol (3:3:0.5) as the mobile phase, and visualized using UV ?254 nm, UV ?366 nm, and citroboric spray reagent. The purity was tested by single development TLC using three different mobile phases and two-dimensional TLC. The isolate was characterized and identified by spectrophotodensitometry, two dimensional paper chromatography, and ammonia spray reagent. It was concluded that the isolate was supposed to be an isoflavone compound without free 5-OH. text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
description Cassia fistula L. or trengguli is commonly found as an ornamental plant, pathways shade, and is often used as traditional medicine. The leaves in traditional medicines are used for laxative, fever, and skin remedy. Secondary metabolites have a role in the biological activity of a plant. One of many secondary metabolites found in trengguli leaves is flavonoid, which is responsible for antioxidant and antibacterial activity. Therefore, this study aims to isolate and identify the flavonoid compounds in trengguli leaves. In this study, the leaves were extracted with methanol by continuous extraction using Soxhlet apparatus, fractionated by liquid-liquid extraction using nhexane, ethyl acetate, and water. The fractions were monitored by thin layer chromatography (TLC) with silica gel GF254 as a stationary phase and ethyl acetate-n-hexane-methanol (8:1:1) as the mobile phase, and visualized using UV ?254 nm, UV ?366 nm, and citroboric spray reagent. Result showed that the largest flavonoid content was in the ethyl acetate fraction. The ethyl acetate fraction was sub-fractionated by preparative TLC using similar mobile phase and stationary phase of fraction monitoring. The subfraction was purified by preparative TLC with silica gel GF254 as a stationary phase and ethyl acetate-n-hexane-methanol (3:3:0.5) as the mobile phase, and visualized using UV ?254 nm, UV ?366 nm, and citroboric spray reagent. The purity was tested by single development TLC using three different mobile phases and two-dimensional TLC. The isolate was characterized and identified by spectrophotodensitometry, two dimensional paper chromatography, and ammonia spray reagent. It was concluded that the isolate was supposed to be an isoflavone compound without free 5-OH.
format Final Project
author Nurhayati, Nane
spellingShingle Nurhayati, Nane
ISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.)
author_facet Nurhayati, Nane
author_sort Nurhayati, Nane
title ISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.)
title_short ISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.)
title_full ISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.)
title_fullStr ISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.)
title_full_unstemmed ISOLASI SENYAWA FLAVONOID DARI DAUN TRENGGULI (Cassia fistula L.)
title_sort isolasi senyawa flavonoid dari daun trengguli (cassia fistula l.)
url https://digilib.itb.ac.id/gdl/view/40411
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