Chemical ionization mass spectrometry of dichlofluanid and its major metabolite
Gas chromatographic/mass spectrometric techniques using chemical ionization have been employed to characterize the fungicide dichlofluanid and its major metabolite. The results have indicated some unusual fragmentation pathways for perhalogenmethylmercapto compounds. Use of deuterated ammonia as rea...
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Veröffentlicht in: | Biological Mass Spectrometry 1986-04, Vol.13 (4), p.181-186 |
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creator | Cairns, Thomas Siegmund, Emil G. |
description | Gas chromatographic/mass spectrometric techniques using chemical ionization have been employed to characterize the fungicide dichlofluanid and its major metabolite. The results have indicated some unusual fragmentation pathways for perhalogenmethylmercapto compounds. Use of deuterated ammonia as reagent gas has permitted a comparative assessment of protonation and exchangeable hydrogens within the major fragment ion structures. Resultant structural information has been employed to confirm residue findings in strawberries at the low part‐per‐million level. |
doi_str_mv | 10.1002/bms.1200130406 |
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The results have indicated some unusual fragmentation pathways for perhalogenmethylmercapto compounds. Use of deuterated ammonia as reagent gas has permitted a comparative assessment of protonation and exchangeable hydrogens within the major fragment ion structures. Resultant structural information has been employed to confirm residue findings in strawberries at the low part‐per‐million level.</description><identifier>ISSN: 1052-9306</identifier><identifier>ISSN: 0887-6134</identifier><identifier>EISSN: 1096-9888</identifier><identifier>EISSN: 2376-3868</identifier><identifier>DOI: 10.1002/bms.1200130406</identifier><identifier>PMID: 2939900</identifier><identifier>CODEN: BEMSEN</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Aniline Compounds - analysis ; Aniline Compounds - metabolism ; Chemistry ; Chromatography, Gas ; Exact sciences and technology ; Fruit - analysis ; Fungicides, Industrial - analysis ; Mass Spectrometry ; Organic chemistry ; Reactivity and mechanisms</subject><ispartof>Biological Mass Spectrometry, 1986-04, Vol.13 (4), p.181-186</ispartof><rights>Copyright © 1986 John Wiley & Sons, Ltd.</rights><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3626-7cd842c1314471dcff74895910a1f5ae47e8b810872c3356ef384dfc73e5cdf83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbms.1200130406$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbms.1200130406$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8043174$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2939900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cairns, Thomas</creatorcontrib><creatorcontrib>Siegmund, Emil G.</creatorcontrib><title>Chemical ionization mass spectrometry of dichlofluanid and its major metabolite</title><title>Biological Mass Spectrometry</title><addtitle>Biol. Mass Spectrom</addtitle><description>Gas chromatographic/mass spectrometric techniques using chemical ionization have been employed to characterize the fungicide dichlofluanid and its major metabolite. The results have indicated some unusual fragmentation pathways for perhalogenmethylmercapto compounds. Use of deuterated ammonia as reagent gas has permitted a comparative assessment of protonation and exchangeable hydrogens within the major fragment ion structures. Resultant structural information has been employed to confirm residue findings in strawberries at the low part‐per‐million level.</description><subject>Aniline Compounds - analysis</subject><subject>Aniline Compounds - metabolism</subject><subject>Chemistry</subject><subject>Chromatography, Gas</subject><subject>Exact sciences and technology</subject><subject>Fruit - analysis</subject><subject>Fungicides, Industrial - analysis</subject><subject>Mass Spectrometry</subject><subject>Organic chemistry</subject><subject>Reactivity and mechanisms</subject><issn>1052-9306</issn><issn>0887-6134</issn><issn>1096-9888</issn><issn>2376-3868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM9PwjAUxxujQUSv3kx28Dps125tj0IUJSiJ-OvWdF0bihsj7YjiX2_JCMaTp_eS9_m-9_IB4BzBPoIwucor30cJhAhDArMD0EWQZzFnjB1u-zSJOYbZMTjxfgEhZiHUAZ2EY84h7ILpcK4rq2QZ2Xppv2UTSlRJ7yO_0qpxdaUbt4lqExVWzcvalGu5tEUkl0VkGx_QRe2iAMm8Lm2jT8GRkaXXZ7vaAy-3N8_Du3gyHd0PryexwlmSxVQVjCQKYUQIRYUyhhLGU46gRCaVmlDN8vAro4nCOM20wYwURlGsU1UYhnug3-5VrvbeaSNWzlbSbQSCYitGBDHiV0wIXLSB1TqvdLHHdybC_HI3lz7oME4ulfV7jEGCESUB4y32aUu9-eeoGDzM_rwQt1nrG_21z0r3ITKKaSreHkdi8PT6PkDjmRjjH_NLi48</recordid><startdate>198604</startdate><enddate>198604</enddate><creator>Cairns, Thomas</creator><creator>Siegmund, Emil G.</creator><general>John Wiley & Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>198604</creationdate><title>Chemical ionization mass spectrometry of dichlofluanid and its major metabolite</title><author>Cairns, Thomas ; Siegmund, Emil G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3626-7cd842c1314471dcff74895910a1f5ae47e8b810872c3356ef384dfc73e5cdf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Aniline Compounds - analysis</topic><topic>Aniline Compounds - metabolism</topic><topic>Chemistry</topic><topic>Chromatography, Gas</topic><topic>Exact sciences and technology</topic><topic>Fruit - analysis</topic><topic>Fungicides, Industrial - analysis</topic><topic>Mass Spectrometry</topic><topic>Organic chemistry</topic><topic>Reactivity and mechanisms</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cairns, Thomas</creatorcontrib><creatorcontrib>Siegmund, Emil G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Biological Mass Spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cairns, Thomas</au><au>Siegmund, Emil G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemical ionization mass spectrometry of dichlofluanid and its major metabolite</atitle><jtitle>Biological Mass Spectrometry</jtitle><addtitle>Biol. Mass Spectrom</addtitle><date>1986-04</date><risdate>1986</risdate><volume>13</volume><issue>4</issue><spage>181</spage><epage>186</epage><pages>181-186</pages><issn>1052-9306</issn><issn>0887-6134</issn><eissn>1096-9888</eissn><eissn>2376-3868</eissn><coden>BEMSEN</coden><abstract>Gas chromatographic/mass spectrometric techniques using chemical ionization have been employed to characterize the fungicide dichlofluanid and its major metabolite. The results have indicated some unusual fragmentation pathways for perhalogenmethylmercapto compounds. Use of deuterated ammonia as reagent gas has permitted a comparative assessment of protonation and exchangeable hydrogens within the major fragment ion structures. Resultant structural information has been employed to confirm residue findings in strawberries at the low part‐per‐million level.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>2939900</pmid><doi>10.1002/bms.1200130406</doi><tpages>6</tpages></addata></record> |
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subjects | Aniline Compounds - analysis Aniline Compounds - metabolism Chemistry Chromatography, Gas Exact sciences and technology Fruit - analysis Fungicides, Industrial - analysis Mass Spectrometry Organic chemistry Reactivity and mechanisms |
title | Chemical ionization mass spectrometry of dichlofluanid and its major metabolite |
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