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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biological Mass Spectrometry 1986-04, Vol.13 (4), p.181-186
Hauptverfasser: Cairns, Thomas, Siegmund, Emil G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 186
container_issue 4
container_start_page 181
container_title Biological Mass Spectrometry
container_volume 13
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
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_bms_1200130406</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>BMS1200130406</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3626-7cd842c1314471dcff74895910a1f5ae47e8b810872c3356ef384dfc73e5cdf83</originalsourceid><addsrcrecordid>eNqFkM9PwjAUxxujQUSv3kx28Dps125tj0IUJSiJ-OvWdF0bihsj7YjiX2_JCMaTp_eS9_m-9_IB4BzBPoIwucor30cJhAhDArMD0EWQZzFnjB1u-zSJOYbZMTjxfgEhZiHUAZ2EY84h7ILpcK4rq2QZ2Xppv2UTSlRJ7yO_0qpxdaUbt4lqExVWzcvalGu5tEUkl0VkGx_QRe2iAMm8Lm2jT8GRkaXXZ7vaAy-3N8_Du3gyHd0PryexwlmSxVQVjCQKYUQIRYUyhhLGU46gRCaVmlDN8vAro4nCOM20wYwURlGsU1UYhnug3-5VrvbeaSNWzlbSbQSCYitGBDHiV0wIXLSB1TqvdLHHdybC_HI3lz7oME4ulfV7jEGCESUB4y32aUu9-eeoGDzM_rwQt1nrG_21z0r3ITKKaSreHkdi8PT6PkDjmRjjH_NLi48</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Chemical ionization mass spectrometry of dichlofluanid and its major metabolite</title><source>MEDLINE</source><source>Wiley Online Library Journals</source><source>Alma/SFX Local Collection</source><creator>Cairns, Thomas ; Siegmund, Emil G.</creator><creatorcontrib>Cairns, Thomas ; Siegmund, Emil G.</creatorcontrib><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><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 &amp; 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 &amp; 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&amp;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 &amp; 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 &amp; Sons, Ltd</pub><pmid>2939900</pmid><doi>10.1002/bms.1200130406</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1052-9306
ispartof Biological Mass Spectrometry, 1986-04, Vol.13 (4), p.181-186
issn 1052-9306
0887-6134
1096-9888
2376-3868
language eng
recordid cdi_crossref_primary_10_1002_bms_1200130406
source MEDLINE; Wiley Online Library Journals; Alma/SFX Local Collection
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T19%3A43%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Chemical%20ionization%20mass%20spectrometry%20of%20dichlofluanid%20and%20its%20major%20metabolite&rft.jtitle=Biological%20Mass%20Spectrometry&rft.au=Cairns,%20Thomas&rft.date=1986-04&rft.volume=13&rft.issue=4&rft.spage=181&rft.epage=186&rft.pages=181-186&rft.issn=1052-9306&rft.eissn=1096-9888&rft.coden=BEMSEN&rft_id=info:doi/10.1002/bms.1200130406&rft_dat=%3Cwiley_cross%3EBMS1200130406%3C/wiley_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/2939900&rfr_iscdi=true