Preparation Of 2-Aminoethylsulfonic Acid

Preparation process of 2-aminoethylsulfonic acid (taurine) from ethanolamine, sulfuric acid and sodium sulfite has beenstudied. The process involves two steps of reactions, the first was esterification of ethanolamine (H2N-CH2-CH2-OH)with sulfuric acid to produce the intermediate product of 2-aminoe...

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Main Authors: Ngadiman, Ermawan, L. Broto Sugeng Kardono, Siti Isnijah, Muhammad Hanafi, Galuh Widiyarti, Andini Sundowo
Format: Article
Language:English
Published: Universitas Indonesia 2009-04-01
Series:Makara Seri Sains
Subjects:
Online Access:http://journal.ui.ac.id/science/article/view/383
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spelling doaj-ddcd49e3b8d541e1adc2ec22dda9fd422020-11-25T00:59:59ZengUniversitas IndonesiaMakara Seri Sains1693-66712009-04-011315558Preparation Of 2-Aminoethylsulfonic AcidNgadimanErmawanL. Broto Sugeng KardonoSiti IsnijahMuhammad HanafiGaluh WidiyartiAndini SundowoPreparation process of 2-aminoethylsulfonic acid (taurine) from ethanolamine, sulfuric acid and sodium sulfite has beenstudied. The process involves two steps of reactions, the first was esterification of ethanolamine (H2N-CH2-CH2-OH)with sulfuric acid to produce the intermediate product of 2-aminoethyl ester (H2N-CH2-CH2-OSO3H) which then wasextended to the second step by sulfonation with sodium sulfite to produce 2-aminoethylsulfonic acid (H2N-CH2-CH2-SO3H). These two process conditions were observed by varying mole ratio of reactants, temperature and time period ofreactions. Taurine product was qualitatively analyzed using 1H-NMR and LC-MS. Physical-chemical analysis weredone by observing its melting point and determining its water, chloride and sulfate contents. Its melting point, watercontent, and sulfate content were 290oC, 0.303%, and 3 ppm, respectively, while its chloride content was undetected.After purification, the yield of process was 25.57%.http://journal.ui.ac.id/science/article/view/3832-aminoethylsulfonic acidesterificationsulfonation1H-NMRLC-MS
collection DOAJ
language English
format Article
sources DOAJ
author Ngadiman
Ermawan
L. Broto Sugeng Kardono
Siti Isnijah
Muhammad Hanafi
Galuh Widiyarti
Andini Sundowo
spellingShingle Ngadiman
Ermawan
L. Broto Sugeng Kardono
Siti Isnijah
Muhammad Hanafi
Galuh Widiyarti
Andini Sundowo
Preparation Of 2-Aminoethylsulfonic Acid
Makara Seri Sains
2-aminoethylsulfonic acid
esterification
sulfonation
1H-NMR
LC-MS
author_facet Ngadiman
Ermawan
L. Broto Sugeng Kardono
Siti Isnijah
Muhammad Hanafi
Galuh Widiyarti
Andini Sundowo
author_sort Ngadiman
title Preparation Of 2-Aminoethylsulfonic Acid
title_short Preparation Of 2-Aminoethylsulfonic Acid
title_full Preparation Of 2-Aminoethylsulfonic Acid
title_fullStr Preparation Of 2-Aminoethylsulfonic Acid
title_full_unstemmed Preparation Of 2-Aminoethylsulfonic Acid
title_sort preparation of 2-aminoethylsulfonic acid
publisher Universitas Indonesia
series Makara Seri Sains
issn 1693-6671
publishDate 2009-04-01
description Preparation process of 2-aminoethylsulfonic acid (taurine) from ethanolamine, sulfuric acid and sodium sulfite has beenstudied. The process involves two steps of reactions, the first was esterification of ethanolamine (H2N-CH2-CH2-OH)with sulfuric acid to produce the intermediate product of 2-aminoethyl ester (H2N-CH2-CH2-OSO3H) which then wasextended to the second step by sulfonation with sodium sulfite to produce 2-aminoethylsulfonic acid (H2N-CH2-CH2-SO3H). These two process conditions were observed by varying mole ratio of reactants, temperature and time period ofreactions. Taurine product was qualitatively analyzed using 1H-NMR and LC-MS. Physical-chemical analysis weredone by observing its melting point and determining its water, chloride and sulfate contents. Its melting point, watercontent, and sulfate content were 290oC, 0.303%, and 3 ppm, respectively, while its chloride content was undetected.After purification, the yield of process was 25.57%.
topic 2-aminoethylsulfonic acid
esterification
sulfonation
1H-NMR
LC-MS
url http://journal.ui.ac.id/science/article/view/383
work_keys_str_mv AT ngadiman preparationof2aminoethylsulfonicacid
AT ermawan preparationof2aminoethylsulfonicacid
AT lbrotosugengkardono preparationof2aminoethylsulfonicacid
AT sitiisnijah preparationof2aminoethylsulfonicacid
AT muhammadhanafi preparationof2aminoethylsulfonicacid
AT galuhwidiyarti preparationof2aminoethylsulfonicacid
AT andinisundowo preparationof2aminoethylsulfonicacid
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