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INDONESIA
Indonesian Journal of Chemistry
ISSN : 14119420     EISSN : 24601578     DOI : -
Indonesian Journal of Chemistry is an International, peer-reviewed, open access journal that publishes original research articles, review articles, as well as short communication in all areas of chemistry including applied chemistry. The journal is accredited by The Ministry of Research, Technology and Higher Education (RISTEKDIKTI) No : 21/E/KPT/2018 (in First Rank) and indexed in Scopus since 2012. Since 2018 (Volume 18), Indonesian Journal of Chemistry publish four issues (numbers) annually (February, May, August and November).
Arjuna Subject : -
Articles 1,956 Documents
SPECTROSCOPIC AND PHYSICOCHEMICAL METHODS FOR STUDYING THE INTERACTION OF METALLOPORPHYRIN WITH DNA Hidenari Inoue
Indonesian Journal of Chemistry Vol 2, No 3 (2002)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (109.773 KB) | DOI: 10.22146/ijc.21907

Abstract

In recent years studies on the interaction of porphyrin with DNA have received much attention because of the importance in DNA-probing and photodynamic therapy of cancer. A variety of spectroscopic methods, e.g. NMR, ESR, Mössbauer, UV-visible absorption, circular dichroism (CD), magnetic circular dichroism (MCD), IR and Raman spectroscopy, have been employed for studying interactions between porphyrin and DNA. Of these spectroscopic methods, only a few instrumental analytical techniques applicable to an aqueous buffer solution of DNA have been particularly developed to investigate porphyrin-DNA interactions. On the other hand, a number of physicochemical methods, e.g. gel electrophoresis, melting temperature measurements and hydrodynamic methods such as viscosity and sedimentation measurements, have been also used for determining the binding modes of porphyrin to DNA. The present lecture will focus on the application of visible absorption, CD and MCD spectroscopy as well as melting temperature and viscosity measurements to studies of porphyrin-DNA interactions.  
EXPLOITING A BENEFIT OF COCONUT MILK SKIM IN COCONUT OIL PROCESS AS NATA DE COCO SUBSTRATE Bambang Setiaji; Ani Setyopratiwi; Nahar Cahyandaru
Indonesian Journal of Chemistry Vol 2, No 3 (2002)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (48.167 KB) | DOI: 10.22146/ijc.21912

Abstract

A research to know influence of mixing concentration of coconut water and sucrose concentration to coconut milk skim as nata de coco substrate has been conducted. The variation was taken from mixing coconut water (0%, 25%, 35% and 50% and 100% as control) and the sucrose concentration (0.5%, 1%, 1.5% and 2%). Coconut milk skim boiled before used as substrat, yielded a coconut protein (blondo). The result of research showed that coconut milk skim can be used as nata de coco substrate with mixing coconut water and sucrose addition, mixing 50 % concentration coconut water representing optimum concentration. The content of crude fibre nata was yielded by higher concentration of sucrose, while mixing concentration coconut water do not influence crude fibre content.
SOLVATION STRUCTURE DETERMINATION OF Ni2+ ION IN WATER BY MEANS OF MONTE CARLO METHOD Tutik Arindah; Bambang Setiaji; Harno Dwi Pranowo
Indonesian Journal of Chemistry Vol 2, No 3 (2002)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (225.912 KB) | DOI: 10.22146/ijc.21915

Abstract

Determination of solvation structure of Ni2+ ion in water has been achieved using Monte Carlo method using canonic assemble (NVT constant). Simulation of a Ni2+ ion in 215 H2O molecules has been done under NVT condition (298.15 K). The results showed that number of H2O molecules surround Ni2+ ion were 8 molecules in first shell and 17 molecules in second shell, interaction energy of Ni2+-H2O in first shell was -68.7 kcal/mol and in second shell was -9.8 kcal/mol, and there were two angles of O-Ni2+-O, i.e. 74o and 142o. According to those results, the solvation structure of Ni2+ ion in water was cubic antisymetric.
STUDY OF THE EFFECT OF ETHANOL ADDITION AND SOLUTION HEATING ON THE DETERMINATION OF AMMONIA IN WATER BY INDOPHENOL BLUE METHOD Hasri Hasri; Mudasir Mudasir
Indonesian Journal of Chemistry Vol 2, No 2 (2002)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (88.782 KB) | DOI: 10.22146/ijc.21920

Abstract

The effect of ethanol addition and solution heating on the analytical performance of the determination of ammonia in water by indophenol blue method was studied. The addition of ethanol and solution heating was intended to overcome the problem of reproducibility and sensitivity ussually found in the determination of ammonia by indophenol blue method which is carried out in 100 % aqueous media. The determination of ammonia was done indirectly by reacting ammonia in the sample with hypochloride and phenol using nitroprussida as catalyst to yield blue color-intense chromophore of indophenol. The chromophore was then detected by UV-Visible spectrophotometer. The proposed method was applied for the determination of ammonia in various samples of river water located in Yogyakarta and Makassar.             Results of the study showed that ethanol addition into analytical solution and solution heating enhanced the formation of indophenol blue. The optimal heating was achieved after 90 minutes of mixing. In ethanol/water medium (50/50, v/v), indophenol blue exhibited maximum absorbance at 648 nm. The analytical performance of ammonia determination by indophenol blue method in this medium is as followed: detection limit = 0.03 ppm, relative standard deviation (RSD) = 2.50 % and the calibration curve was linear in the concentration range of 0.0 - 0.4 ppm with correlation coefficient (r) = 0.9968. Results of ammonia determination in various samples of river water showed that the highest concentration of ammonia (2.421 ppm) was found in Tallo river, Makassar, while the lowest (0.359 ppm) was shown by the river near SGM factory, Yogyakarta.
EFFECT OF IMPREGNATION PROCEDURE OF Pt/γ-Al2O3 CATALYSTS UPON CATALYTIC OXIDATION OF CO Triyono Triyono
Indonesian Journal of Chemistry Vol 2, No 1 (2002)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (180.573 KB) | DOI: 10.22146/ijc.21927

Abstract

The oxidation of carbon monoxide by oxygen using two catalysts prepared by two different methods has been investigated. In the first method, catalyst prepared by immersing γ-Al2O3 into the hexa-chloroplatinic acid solution at 80oC for 4 h, resulted Pt/γ-Al2O3 catalyst having platinum highly dispersed on the support. While that of immersing γ-Al2O3 in the hexa-chloroplatinic acid solution at room temperature for 12 h, produced Pt/ γ-Al2O3 catalyst where platinum dispersion was much lower. Catalytic activity test showed that platinum well dispersed on the support enhanced the activity of oxidation of carbon monoxide. The platinum impregnated at room temperature resulted in the poor activity.
EXTRACTION OF PALM OIL’S FREE FATTY ACIDS BY TRIETHYLAMMINE (TEA) IN POLAR-NONPOLAR MIX-SOLVENT Endang Astuti; Winarto Haryadi; Sabirin Matsjeh
Indonesian Journal of Chemistry Vol 2, No 1 (2002)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (66.586 KB) | DOI: 10.22146/ijc.21932

Abstract

Palm oil contains unsaturated fatty acids that can be oxidated and can make rancidity of the palm oil. One of the trigliserida degradation products is free fatty acid. The usage of triethylammine (TEA) in the polar-nonpolar mix solvents could enhance the free fatty acids extraction efficiency. Free fatty acids extraction from palm oil was carried out for a minute with solvents ratio: TEA 0,00-0,20M in the following solvent: 0-99% diethyl ether + 99-0% ethanol + 1% water, % volume. The extraction was also performed in the following solvent: TEA 0,00-0,20M in 0-95% heptane + 95-0% isopropanol + 5% water, % volume. Reextraction was conducted for a minute by adding Na2SO4 1M. The alcohol layer which was rich with free fatty acid was taken out and the acid value was determined. As comparison, palm oil's free fatty acids was taken out with standard method by refluxing the sample in 95% alcohol for ten minutes. Identification of the free fatty acids was done by Gas Chromatography-Mass Spectrometer. The best solvent ratio for acid value determination was TEA 0,10-0,20M in the mix-solvent: 19% diethyl ether + 80% ethanol + 1% water, % volume and the extraction product contained 8 kind of free fatty acids. In addition, TEA 0,01M in the solvent: 95% isopropanol + 5% water, % volume could be obtained 8 kind of free fatty acids too. In contrary, the free fatty acid extraction by standard method contained 7 kind of fatty acids. Linoleic acid was the free fatty acid which could not be taken out by standard method. The usage of TEA in the proper polar-non polar mix-solvent was the complete method to determine free fatty acid contained in the palm oil.
IDENTIFICATION AND SEQUENCING BY NMR SPECTROSCOPY OF THE CARBOHYDRATE MOIETY IN A SAPONIN FROM Barringtonia asiatica Rymond J Rumampuk
Indonesian Journal of Chemistry Vol 1, No 3 (2001)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (87.941 KB) | DOI: 10.22146/ijc.21936

Abstract

A trisaccharide chain in a saponin from the seeds of Barringtonia asiatica has been identified and sequenced as {[b-D-galactopyranosyl(1®3)- b-D-glucopyranosyl(1®2)]-b-D-glucuronopyranosyloxy} using a combination of homonuclear and heteronuclear correlation NMR spectroscopy. The 1H and 13C NMR signals of the sugar residues can be determined and distinguished from one other by use of the HMQC-TOCSY technique. Anomeric configurations were unambiguously assigned from the vicinal coupling constants 3JH-1,H-2 of the anomeric protons. Inter-glycosidic linkage assignments were elucidated using  HMBC.
SYNTHESIS of 3.4-METHYLENEDIOXYPHENYL-2-PROPANONE from SAFROLE Hanoch J Sohilait; Hardjono Sastrohamidjojo; Sabirin Matsjeh; J Stuart Grossert
Indonesian Journal of Chemistry Vol 1, No 3 (2001)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (69.382 KB) | DOI: 10.22146/ijc.21941

Abstract

The Synthesis of 3.4-methylenedioxyphenyl-2-propanone from safrole has been achieved through conversion of allyl group to secondary alcohol, followed by oxidation with pyridinium chlorochromate(PCC).  The secondary alcohol has been achieved by two methods. The first method was formic acid adition reaction, followed by hydrolysis in aqueous ethanolic solution of potassium hydroxide.  The second method was the oxymercuration-demercuration reaction of safrole. The addition reaction of safrole with formic acid yield safrylformate (34,70%). The hydrolysis of safrylformate with 3M KOH produced safrylalchohol (73,29%). The oxymercuration-demercuration reaction of safrole with Hg(OAc)2-NaBH4 gave (74,37%) of safrylalcohol.  The oxidation of safryalcohol with PCC gave 3.4-methylenedioxyphenyl-2-propanone as a main target in 71,83%. The structure elucidations of these products were analyzed by  FTIR , 1H-NMR,  13C-NMR and MS.
GOLD IS EARNED FROM THE PRODUCTION OF THAI GOLD LEAF Dirk Bax
Indonesian Journal of Chemistry Vol 1, No 3 (2001)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (68.065 KB) | DOI: 10.22146/ijc.21943

Abstract

Thai people like to cover sacred objects or things dear to them with gold leaf.. Statues of Buddha are sometimes covered with so many layers of gold leaf that they become formless figures, that can hardly be recognized. Portraits of beloved ancestors, statues of elephants and grave tombs are often covered with gold leaf. If one considers the number of Thai people and the popularity of the habit, the amount of gold involved could be considerable.
Study of the Gold Extraction Using Tetra N-Butyl Ammonium Chloride-Chloroform Yuli Puspito Rini; Agus Kuncaka; Ngatidjo Hadipranoto
Indonesian Journal of Chemistry Vol 1, No 2 (2001)
Publisher : Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (5022.747 KB) | DOI: 10.22146/ijc.21947

Abstract

The existence of the AuCl4- ion in the solution as the function of pH before performing the extraction of gold in the system of tetra N-butylammonium chloride (TBACI) -chloroform has been studied. The experimental data showed that AuCl4- ion was hydrolyzed at pH 5-10 and, an amorf dark-brown precipitate was appeared at pH 11-14. Amount of gold in the solution at pH 14 before extraction was around 70%. Study of the extraction has been carried out by investigating the influence of pH and TBACI concentration on the extraction efficiency. The experimental result indicated that TBACI was very efficient extractant for the extraction of gold from aqueous halide with the efficiency higher than 99%. The extraction of Gold in the TBACI-chloroform was effective at pH 0-4 with minimum concentration of TBACI 10-3 M, and the calculated Kex (extraction constant) was 5.07x10-4.

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