Structural Characterisation of Degradation Products Formed upon Di-n-Butyl Phthalate Radiolysis by High-Performance Liquid Chromatography Electrospray Tandem Mass Spectrometry
Structural characterisation of 15 degradation products, formed upon di-n-butyl phthalate (DBP) radiolysis, has been achieved using a high-performance liquid chromatography–tandem mass spectrometry (HPLC-MS/MS) coupling. The dissociation behaviour of protonated DBP was first established to be further...
Gespeichert in:
Veröffentlicht in: | European journal of mass spectrometry (Chichester, England) England), 2010-01, Vol.16 (5), p.595-603 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 603 |
---|---|
container_issue | 5 |
container_start_page | 595 |
container_title | European journal of mass spectrometry (Chichester, England) |
container_volume | 16 |
creator | Tintaru, Aura Labed, Véronique Charles, Laurence |
description | Structural characterisation of 15 degradation products, formed upon di-n-butyl phthalate (DBP) radiolysis, has been achieved using a high-performance liquid chromatography–tandem mass spectrometry (HPLC-MS/MS) coupling. The dissociation behaviour of protonated DBP was first established to be further used to characterise structural deviation in the degradation products. Based on accurate mass measurements, compounds shown by HPLC-MS analysis were all found to be DBP oxidation products, amongst which various sets of isomers could be distinguished. Collision-induced dissociation experiments performed on each electrosprayed molecule first allowed unambiguous definition of the location of the additional oxygen atoms; that is, in the alkyl branch or on the aromatic ring. Although location of the oxygen atom in the alkyl branches could not always be precisely determined, relative abundances of some product ions allowed oxygenated functions to be identified |
doi_str_mv | 10.1255/ejms.1096 |
format | Article |
fullrecord | <record><control><sourceid>proquest_hal_p</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_01460297v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1255_ejms.1096</sage_id><sourcerecordid>754012704</sourcerecordid><originalsourceid>FETCH-LOGICAL-c349t-7930bf566d296939f7cee72b5abf7503b31372b4113de2f429e06a11487b62803</originalsourceid><addsrcrecordid>eNptkc1u1DAUhS0Eoj-w4AWQVyAWKXZ-7HjZTlsGaRAjWtbWTXIz8SiJU9tBylPxivUwpWxY2ff687m65xDyjrMLnhbFZ9wP_oIzJV6QUy4LnogyK1_Gey5UwoSQJ-TM-z1jRSmUek1OUlbynJXFKfl9F9xch9lBT1cdOKgDOuMhGDtS29Jr3DlojuXW2Saynt5aN2BD5yk2r00yJldzWHq67UIHPQSkP6Axtl-88bRa6NrsumSLro3fYKyRbszDbJo4z9kBgo0Tpm6hNz3WwVk_OVjoPYwNDvQbeE_vpj8PAwa3vCGvWug9vn06z8nP25v71TrZfP_ydXW5SeosVyGRKmNVWwjRpEqoTLWyRpRpVUDVyoJlVcazWOacZw2mbZ4qZAI4z0tZibRk2Tn5dNSNG-nJmQHcoi0Yvb7c6EOPRXNZquQvHtmPR3Zy9mFGH_RgfI19DyPa2WtZ5IynkuX_VOu4p3fYPktzpg9R6kOU-hBlZN8_qc5VdPuZ_JtdBD4cAQ871Hs7uzE68h-lRzDOqWI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>754012704</pqid></control><display><type>article</type><title>Structural Characterisation of Degradation Products Formed upon Di-n-Butyl Phthalate Radiolysis by High-Performance Liquid Chromatography Electrospray Tandem Mass Spectrometry</title><source>Access via SAGE</source><creator>Tintaru, Aura ; Labed, Véronique ; Charles, Laurence</creator><creatorcontrib>Tintaru, Aura ; Labed, Véronique ; Charles, Laurence</creatorcontrib><description>Structural characterisation of 15 degradation products, formed upon di-n-butyl phthalate (DBP) radiolysis, has been achieved using a high-performance liquid chromatography–tandem mass spectrometry (HPLC-MS/MS) coupling. The dissociation behaviour of protonated DBP was first established to be further used to characterise structural deviation in the degradation products. Based on accurate mass measurements, compounds shown by HPLC-MS analysis were all found to be DBP oxidation products, amongst which various sets of isomers could be distinguished. Collision-induced dissociation experiments performed on each electrosprayed molecule first allowed unambiguous definition of the location of the additional oxygen atoms; that is, in the alkyl branch or on the aromatic ring. Although location of the oxygen atom in the alkyl branches could not always be precisely determined, relative abundances of some product ions allowed oxygenated functions to be identified</description><identifier>ISSN: 1469-0667</identifier><identifier>EISSN: 1751-6838</identifier><identifier>DOI: 10.1255/ejms.1096</identifier><identifier>PMID: 20814085</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Chemical Sciences</subject><ispartof>European journal of mass spectrometry (Chichester, England), 2010-01, Vol.16 (5), p.595-603</ispartof><rights>2010 Sage Publications</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c349t-7930bf566d296939f7cee72b5abf7503b31372b4113de2f429e06a11487b62803</citedby><cites>FETCH-LOGICAL-c349t-7930bf566d296939f7cee72b5abf7503b31372b4113de2f429e06a11487b62803</cites><orcidid>0000-0002-6479-7288 ; 0000-0003-3807-8375</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1255/ejms.1096$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1255/ejms.1096$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,780,784,885,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20814085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-01460297$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Tintaru, Aura</creatorcontrib><creatorcontrib>Labed, Véronique</creatorcontrib><creatorcontrib>Charles, Laurence</creatorcontrib><title>Structural Characterisation of Degradation Products Formed upon Di-n-Butyl Phthalate Radiolysis by High-Performance Liquid Chromatography Electrospray Tandem Mass Spectrometry</title><title>European journal of mass spectrometry (Chichester, England)</title><addtitle>Eur J Mass Spectrom (Chichester)</addtitle><description>Structural characterisation of 15 degradation products, formed upon di-n-butyl phthalate (DBP) radiolysis, has been achieved using a high-performance liquid chromatography–tandem mass spectrometry (HPLC-MS/MS) coupling. The dissociation behaviour of protonated DBP was first established to be further used to characterise structural deviation in the degradation products. Based on accurate mass measurements, compounds shown by HPLC-MS analysis were all found to be DBP oxidation products, amongst which various sets of isomers could be distinguished. Collision-induced dissociation experiments performed on each electrosprayed molecule first allowed unambiguous definition of the location of the additional oxygen atoms; that is, in the alkyl branch or on the aromatic ring. Although location of the oxygen atom in the alkyl branches could not always be precisely determined, relative abundances of some product ions allowed oxygenated functions to be identified</description><subject>Chemical Sciences</subject><issn>1469-0667</issn><issn>1751-6838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNptkc1u1DAUhS0Eoj-w4AWQVyAWKXZ-7HjZTlsGaRAjWtbWTXIz8SiJU9tBylPxivUwpWxY2ff687m65xDyjrMLnhbFZ9wP_oIzJV6QUy4LnogyK1_Gey5UwoSQJ-TM-z1jRSmUek1OUlbynJXFKfl9F9xch9lBT1cdOKgDOuMhGDtS29Jr3DlojuXW2Saynt5aN2BD5yk2r00yJldzWHq67UIHPQSkP6Axtl-88bRa6NrsumSLro3fYKyRbszDbJo4z9kBgo0Tpm6hNz3WwVk_OVjoPYwNDvQbeE_vpj8PAwa3vCGvWug9vn06z8nP25v71TrZfP_ydXW5SeosVyGRKmNVWwjRpEqoTLWyRpRpVUDVyoJlVcazWOacZw2mbZ4qZAI4z0tZibRk2Tn5dNSNG-nJmQHcoi0Yvb7c6EOPRXNZquQvHtmPR3Zy9mFGH_RgfI19DyPa2WtZ5IynkuX_VOu4p3fYPktzpg9R6kOU-hBlZN8_qc5VdPuZ_JtdBD4cAQ871Hs7uzE68h-lRzDOqWI</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Tintaru, Aura</creator><creator>Labed, Véronique</creator><creator>Charles, Laurence</creator><general>SAGE Publications</general><general>IM Publications</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-6479-7288</orcidid><orcidid>https://orcid.org/0000-0003-3807-8375</orcidid></search><sort><creationdate>20100101</creationdate><title>Structural Characterisation of Degradation Products Formed upon Di-n-Butyl Phthalate Radiolysis by High-Performance Liquid Chromatography Electrospray Tandem Mass Spectrometry</title><author>Tintaru, Aura ; Labed, Véronique ; Charles, Laurence</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-7930bf566d296939f7cee72b5abf7503b31372b4113de2f429e06a11487b62803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Chemical Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tintaru, Aura</creatorcontrib><creatorcontrib>Labed, Véronique</creatorcontrib><creatorcontrib>Charles, Laurence</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>European journal of mass spectrometry (Chichester, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tintaru, Aura</au><au>Labed, Véronique</au><au>Charles, Laurence</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structural Characterisation of Degradation Products Formed upon Di-n-Butyl Phthalate Radiolysis by High-Performance Liquid Chromatography Electrospray Tandem Mass Spectrometry</atitle><jtitle>European journal of mass spectrometry (Chichester, England)</jtitle><addtitle>Eur J Mass Spectrom (Chichester)</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>16</volume><issue>5</issue><spage>595</spage><epage>603</epage><pages>595-603</pages><issn>1469-0667</issn><eissn>1751-6838</eissn><abstract>Structural characterisation of 15 degradation products, formed upon di-n-butyl phthalate (DBP) radiolysis, has been achieved using a high-performance liquid chromatography–tandem mass spectrometry (HPLC-MS/MS) coupling. The dissociation behaviour of protonated DBP was first established to be further used to characterise structural deviation in the degradation products. Based on accurate mass measurements, compounds shown by HPLC-MS analysis were all found to be DBP oxidation products, amongst which various sets of isomers could be distinguished. Collision-induced dissociation experiments performed on each electrosprayed molecule first allowed unambiguous definition of the location of the additional oxygen atoms; that is, in the alkyl branch or on the aromatic ring. Although location of the oxygen atom in the alkyl branches could not always be precisely determined, relative abundances of some product ions allowed oxygenated functions to be identified</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>20814085</pmid><doi>10.1255/ejms.1096</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6479-7288</orcidid><orcidid>https://orcid.org/0000-0003-3807-8375</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1469-0667 |
ispartof | European journal of mass spectrometry (Chichester, England), 2010-01, Vol.16 (5), p.595-603 |
issn | 1469-0667 1751-6838 |
language | eng |
recordid | cdi_hal_primary_oai_HAL_hal_01460297v1 |
source | Access via SAGE |
subjects | Chemical Sciences |
title | Structural Characterisation of Degradation Products Formed upon Di-n-Butyl Phthalate Radiolysis by High-Performance Liquid Chromatography Electrospray Tandem Mass Spectrometry |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T11%3A10%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_hal_p&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structural%20Characterisation%20of%20Degradation%20Products%20Formed%20upon%20Di-n-Butyl%20Phthalate%20Radiolysis%20by%20High-Performance%20Liquid%20Chromatography%20Electrospray%20Tandem%20Mass%20Spectrometry&rft.jtitle=European%20journal%20of%20mass%20spectrometry%20(Chichester,%20England)&rft.au=Tintaru,%20Aura&rft.date=2010-01-01&rft.volume=16&rft.issue=5&rft.spage=595&rft.epage=603&rft.pages=595-603&rft.issn=1469-0667&rft.eissn=1751-6838&rft_id=info:doi/10.1255/ejms.1096&rft_dat=%3Cproquest_hal_p%3E754012704%3C/proquest_hal_p%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=754012704&rft_id=info:pmid/20814085&rft_sage_id=10.1255_ejms.1096&rfr_iscdi=true |