A Colour Reaction for Thiosulphinates
INVESTIGATIONS of the chemistry of the thiolsulphinates, both synthetic and of natural provenance, would be aided if a rapid colorimetric test for these compounds were available. Aliphatic thiolsulphinates can be characterized, in part at least, by reaction with thiamine 1 or with cysteine 2 to yiel...
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Veröffentlicht in: | Nature (London) 1959-06, Vol.183 (4676), p.1673-1673 |
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container_title | Nature (London) |
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creator | CARSON, JOHN F WONG, FRANCIS F |
description | INVESTIGATIONS of the chemistry of the thiolsulphinates, both synthetic and of natural provenance, would be aided if a rapid colorimetric test for these compounds were available. Aliphatic thiolsulphinates can be characterized, in part at least, by reaction with thiamine
1
or with cysteine
2
to yield crystalline derivatives; but these methods do not generally distinguish thiolsulphinates from thiolsulphonates, since the latter compounds will also react with these reagents. The addition of sodium nitroprusside
3
solution followed by base will yield orange to red colours in the presence of aliphatic thiolsulphinates or thiolsulphonates. This procedure has found application in paper chromatography
3
in investigations of the formation of thiolsulphinates in plants of the genus
Allium
. In our experience, the colour, however, is very fugitive and is apparently not produced by some aromatic thiolsulphinates. |
doi_str_mv | 10.1038/1831673b0 |
format | Article |
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1
or with cysteine
2
to yield crystalline derivatives; but these methods do not generally distinguish thiolsulphinates from thiolsulphonates, since the latter compounds will also react with these reagents. The addition of sodium nitroprusside
3
solution followed by base will yield orange to red colours in the presence of aliphatic thiolsulphinates or thiolsulphonates. This procedure has found application in paper chromatography
3
in investigations of the formation of thiolsulphinates in plants of the genus
Allium
. In our experience, the colour, however, is very fugitive and is apparently not produced by some aromatic thiolsulphinates.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/1831673b0</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Humanities and Social Sciences ; letter ; multidisciplinary ; Science ; Science (multidisciplinary)</subject><ispartof>Nature (London), 1959-06, Vol.183 (4676), p.1673-1673</ispartof><rights>Springer Nature Limited 1959</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c321t-ab86ab4f840f9c0b24258e12e26ce52120a951929c9ef34483614d3674de81cf3</citedby><cites>FETCH-LOGICAL-c321t-ab86ab4f840f9c0b24258e12e26ce52120a951929c9ef34483614d3674de81cf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2727,27924,27925</link.rule.ids></links><search><creatorcontrib>CARSON, JOHN F</creatorcontrib><creatorcontrib>WONG, FRANCIS F</creatorcontrib><title>A Colour Reaction for Thiosulphinates</title><title>Nature (London)</title><addtitle>Nature</addtitle><description>INVESTIGATIONS of the chemistry of the thiolsulphinates, both synthetic and of natural provenance, would be aided if a rapid colorimetric test for these compounds were available. Aliphatic thiolsulphinates can be characterized, in part at least, by reaction with thiamine
1
or with cysteine
2
to yield crystalline derivatives; but these methods do not generally distinguish thiolsulphinates from thiolsulphonates, since the latter compounds will also react with these reagents. The addition of sodium nitroprusside
3
solution followed by base will yield orange to red colours in the presence of aliphatic thiolsulphinates or thiolsulphonates. This procedure has found application in paper chromatography
3
in investigations of the formation of thiolsulphinates in plants of the genus
Allium
. In our experience, the colour, however, is very fugitive and is apparently not produced by some aromatic thiolsulphinates.</description><subject>Humanities and Social Sciences</subject><subject>letter</subject><subject>multidisciplinary</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1959</creationdate><recordtype>article</recordtype><recordid>eNptz81KxDAUhuEgCtbRhVdgNy4UquckaZouh-IfDAgyrkOaSZwOtRmSduHdG6mMG1dn83D4XkIuEe4QmLxHyVBUrIUjkiGvRMGFrI5JBkBlAZKJU3IW4w4ASqx4Rq6XeeN7P4X8zWozdn7InQ_5etv5OPX7bTfo0cZzcuJ0H-3F712Q98eHdfNcrF6fXprlqjCM4ljoVgrdcic5uNpASzktpUVqqTC2pEhB1yXWtDa1dYzzNAf5homKb6xE49iC3Mx_TfAxBuvUPnSfOnwpBPXTpw59yd7ONiYzfNigdiljSPP-xVczTjlTsH9vD-IbpTpYKw</recordid><startdate>19590613</startdate><enddate>19590613</enddate><creator>CARSON, JOHN F</creator><creator>WONG, FRANCIS F</creator><general>Nature Publishing Group UK</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19590613</creationdate><title>A Colour Reaction for Thiosulphinates</title><author>CARSON, JOHN F ; WONG, FRANCIS F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c321t-ab86ab4f840f9c0b24258e12e26ce52120a951929c9ef34483614d3674de81cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1959</creationdate><topic>Humanities and Social Sciences</topic><topic>letter</topic><topic>multidisciplinary</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CARSON, JOHN F</creatorcontrib><creatorcontrib>WONG, FRANCIS F</creatorcontrib><collection>CrossRef</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CARSON, JOHN F</au><au>WONG, FRANCIS F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Colour Reaction for Thiosulphinates</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><date>1959-06-13</date><risdate>1959</risdate><volume>183</volume><issue>4676</issue><spage>1673</spage><epage>1673</epage><pages>1673-1673</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><abstract>INVESTIGATIONS of the chemistry of the thiolsulphinates, both synthetic and of natural provenance, would be aided if a rapid colorimetric test for these compounds were available. Aliphatic thiolsulphinates can be characterized, in part at least, by reaction with thiamine
1
or with cysteine
2
to yield crystalline derivatives; but these methods do not generally distinguish thiolsulphinates from thiolsulphonates, since the latter compounds will also react with these reagents. The addition of sodium nitroprusside
3
solution followed by base will yield orange to red colours in the presence of aliphatic thiolsulphinates or thiolsulphonates. This procedure has found application in paper chromatography
3
in investigations of the formation of thiolsulphinates in plants of the genus
Allium
. In our experience, the colour, however, is very fugitive and is apparently not produced by some aromatic thiolsulphinates.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><doi>10.1038/1831673b0</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Humanities and Social Sciences letter multidisciplinary Science Science (multidisciplinary) |
title | A Colour Reaction for Thiosulphinates |
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