SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES

Zinc-difattyalkyldithiocarbamates are organosulfur compounds with many functions, including as an antioxidant in a lubrication system. They were synthesized by reacting secondary fatty amine with ZnCl2 and CS2 giving result zinc-difattyalkyldithiocarbamates of around 77-87%. The synthesized products...

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Main Authors: Komar Sutriah, Zainal Alim Mas’ud, Tun Tedja Irawadi
Format: Article
Language:English
Published: Universitas Gadjah Mada 2012-06-01
Series:Indonesian Journal of Chemistry
Subjects:
Online Access:https://jurnal.ugm.ac.id/ijc/article/view/21362
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spelling doaj-3990d393c47143a590da2ecd197f02ab2020-11-24T23:52:44ZengUniversitas Gadjah MadaIndonesian Journal of Chemistry1411-94202460-15782012-06-0112218919410.22146/ijc.2136214460SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIESKomar Sutriah0Zainal Alim Mas’ud1Tun Tedja Irawadi2Department of Agriculture Engineering, Bogor Agricultural University, Kampus Dramaga, Bogor 16680Department of Chemistry, Bogor Agricultural University, Kampus Dramaga, Bogor 16680Department of Chemistry, Bogor Agricultural University, Kampus Dramaga, Bogor 16680Zinc-difattyalkyldithiocarbamates are organosulfur compounds with many functions, including as an antioxidant in a lubrication system. They were synthesized by reacting secondary fatty amine with ZnCl2 and CS2 giving result zinc-difattyalkyldithiocarbamates of around 77-87%. The synthesized products were characterized using infrared (IR) spectroscopic techniques. The IR spectra of zinc-difattyalkyldithiocarbamates showed sharp bands at 1450-1550 cm-1 for thioureida v (C-N), 950-1050 cm-1 for v (C-S), and in the far-red area 300-400 cm-1 for sulfur-metal bond. Products recovery was evaluated by AAS and the purity was analyzed by HPLC. Seven variants of zinc-difattyalkyldithiocarbamates were obtained. Antioxidant activity was evaluated by rancimat test regarding their induction time. At 125 ppm levels all variants showed higher value in each of their induction time as compared to those of butylated hydroxyanisole and butylated hydroxytoluene, commercial antioxidants No.1, and commercial antioxidants no.2. Three variants, i.e. Zn-bis(dilauryl)dithiocarbamate, Zn-bis(laurylpalmityl)dithiocarbamate, and Zn-bis(laurylstearyl)dithiocarbamate had higher values in their induction time than the other variants. The values are 16.67, 26.54, and 16.11 h, respectively.https://jurnal.ugm.ac.id/ijc/article/view/21362antioxidantsdithiocarbamate complexZn-difattyalkyldithiocarbamate
collection DOAJ
language English
format Article
sources DOAJ
author Komar Sutriah
Zainal Alim Mas’ud
Tun Tedja Irawadi
spellingShingle Komar Sutriah
Zainal Alim Mas’ud
Tun Tedja Irawadi
SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES
Indonesian Journal of Chemistry
antioxidants
dithiocarbamate complex
Zn-difattyalkyldithiocarbamate
author_facet Komar Sutriah
Zainal Alim Mas’ud
Tun Tedja Irawadi
author_sort Komar Sutriah
title SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES
title_short SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES
title_full SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES
title_fullStr SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES
title_full_unstemmed SYNTHESIS OF ZINC-DIFATTYALKYLDITHIOCARBAMATES AND THEIR ANTIOXIDANT ACTIVITIES
title_sort synthesis of zinc-difattyalkyldithiocarbamates and their antioxidant activities
publisher Universitas Gadjah Mada
series Indonesian Journal of Chemistry
issn 1411-9420
2460-1578
publishDate 2012-06-01
description Zinc-difattyalkyldithiocarbamates are organosulfur compounds with many functions, including as an antioxidant in a lubrication system. They were synthesized by reacting secondary fatty amine with ZnCl2 and CS2 giving result zinc-difattyalkyldithiocarbamates of around 77-87%. The synthesized products were characterized using infrared (IR) spectroscopic techniques. The IR spectra of zinc-difattyalkyldithiocarbamates showed sharp bands at 1450-1550 cm-1 for thioureida v (C-N), 950-1050 cm-1 for v (C-S), and in the far-red area 300-400 cm-1 for sulfur-metal bond. Products recovery was evaluated by AAS and the purity was analyzed by HPLC. Seven variants of zinc-difattyalkyldithiocarbamates were obtained. Antioxidant activity was evaluated by rancimat test regarding their induction time. At 125 ppm levels all variants showed higher value in each of their induction time as compared to those of butylated hydroxyanisole and butylated hydroxytoluene, commercial antioxidants No.1, and commercial antioxidants no.2. Three variants, i.e. Zn-bis(dilauryl)dithiocarbamate, Zn-bis(laurylpalmityl)dithiocarbamate, and Zn-bis(laurylstearyl)dithiocarbamate had higher values in their induction time than the other variants. The values are 16.67, 26.54, and 16.11 h, respectively.
topic antioxidants
dithiocarbamate complex
Zn-difattyalkyldithiocarbamate
url https://jurnal.ugm.ac.id/ijc/article/view/21362
work_keys_str_mv AT komarsutriah synthesisofzincdifattyalkyldithiocarbamatesandtheirantioxidantactivities
AT zainalalimmasud synthesisofzincdifattyalkyldithiocarbamatesandtheirantioxidantactivities
AT tuntedjairawadi synthesisofzincdifattyalkyldithiocarbamatesandtheirantioxidantactivities
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