The differentiation of N-butyl pentylone isomers using GC-EI-MS and NMR

Forensic laboratories are faced with an ever-expanding seized drug landscape including the increasing prevalence of novel psychoactive substances (NPS), such as synthetic cathinones, that have varying potencies and scheduling. This study demonstrates a combined gas chromatography-electron ionization...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Forensic science international 2023-10, Vol.351, p.111815-111815, Article 111815
Hauptverfasser: Liliedahl, Ruby E., Hutzel, Elise, Haley, Madison, Predecki, Daniel P., Davidson, J. Tyler
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 111815
container_issue
container_start_page 111815
container_title Forensic science international
container_volume 351
creator Liliedahl, Ruby E.
Hutzel, Elise
Haley, Madison
Predecki, Daniel P.
Davidson, J. Tyler
description Forensic laboratories are faced with an ever-expanding seized drug landscape including the increasing prevalence of novel psychoactive substances (NPS), such as synthetic cathinones, that have varying potencies and scheduling. This study demonstrates a combined gas chromatography-electron ionization-mass spectrometry (GC-EI-MS) and nuclear magnetic resonance (NMR) spectroscopy approach for the differentiation of N-butyl pentylone isomers based on distinct retention times, characteristic EI mass spectra, and NMR characterization. Retention time reproducibility was assessed from 60 replicate measurements for each isomer over the course of a month. In addition, the effect of the mass spectrometer tune and the stability of an identified characteristic ion ratio using spectral data from ±1 scan on either side of the peak apex were also statistically assessed using Welch’s ANOVA testing. The presence of diastereomers for N-sec-butyl pentylone was identified using the developed GC-EI-MS method, which was confirmed using one-dimensional and two-dimensional NMR spectroscopy. The retention time reproducibility of the chromatographic method was ±0.076% or less over the course of a month. An identified characteristic ion ratio between the abundance of the fragment ion at m/z 128 and the fragment ion at m/z 72 enabled the differentiation of the four N-butyl pentylone isomers, even when accounting for the effect of the mass spectrometer tune and mass spectral scans used to calculate the characteristic ion ratio. The 95% confidence interval mean abundance ratio of the fragment ions at m/z 128 and m/z 72 was 17.14 ± 0.14 for N-butyl pentylone, 6.44 ± 0.05 for N-isobutyl pentylone, 3.38 ± 0.02 for N-sec-butyl pentylone, and 0.75 ± 0.01 for N-tert-butyl pentylone. These results highlight the capabilities of a combined GC-EI-MS and NMR approach for the differentiation and characterization of synthetic cathinone isomers. [Display omitted] •Combined GC-EI-MS and NMR approach for differentiating synthetic cathinone isomers•Differentiation by retention time and a characteristic ion ratio for GC-EI-MS•Achieved isomer differentiation even with tune and mass spectral scan variability•Characterized N-butyl pentylone isomers using NMR spectroscopy•Chromatographically separated N-sec-butyl pentylone diastereomers using GC
doi_str_mv 10.1016/j.forsciint.2023.111815
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3153155084</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0379073823002657</els_id><sourcerecordid>2866774512</sourcerecordid><originalsourceid>FETCH-LOGICAL-c409t-f9670b3bf0c32735b9269e0800382d083fd2c4807b888f231b41943b287495cf3</originalsourceid><addsrcrecordid>eNqFkU9LAzEQxYMoWP98BgNevGydJJtN9ihFq6AVtJ7DbjbRlG1Sk12h396UigcvwsDA8HsP5j2ELghMCZDqejW1ISbtnB-mFCibEkIk4QdoQqSgRUUlO0QTYKIuQDB5jE5SWgEA57SaoPnyw-DOWWui8YNrBhc8DhYvinYctj3e5Ou2D95gl8LaxITH5Pw7ns-K24fi6RU3vsOLp5czdGSbPpnzn32K3u5ul7P74vF5_jC7eSx0CfVQ2LoS0LLWgmZUMN7WtKoNSAAmaQeS2Y7qUoJopZSWMtKWpC5ZS6Uoa64tO0VXe99NDJ-jSYNau6RN3zfehDEpRngeDrL8F6Wy4iInJUlGL_-gqzBGnx_ZUZUQJSc0U2JP6RhSisaqTXTrJm4VAbXrQq3Ubxdq14Xad5GVN3ulydF8ORNVhozXpnPR6EF1wf3r8Q2EdpLM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2866774512</pqid></control><display><type>article</type><title>The differentiation of N-butyl pentylone isomers using GC-EI-MS and NMR</title><source>Elsevier ScienceDirect Journals</source><creator>Liliedahl, Ruby E. ; Hutzel, Elise ; Haley, Madison ; Predecki, Daniel P. ; Davidson, J. Tyler</creator><creatorcontrib>Liliedahl, Ruby E. ; Hutzel, Elise ; Haley, Madison ; Predecki, Daniel P. ; Davidson, J. Tyler</creatorcontrib><description>Forensic laboratories are faced with an ever-expanding seized drug landscape including the increasing prevalence of novel psychoactive substances (NPS), such as synthetic cathinones, that have varying potencies and scheduling. This study demonstrates a combined gas chromatography-electron ionization-mass spectrometry (GC-EI-MS) and nuclear magnetic resonance (NMR) spectroscopy approach for the differentiation of N-butyl pentylone isomers based on distinct retention times, characteristic EI mass spectra, and NMR characterization. Retention time reproducibility was assessed from 60 replicate measurements for each isomer over the course of a month. In addition, the effect of the mass spectrometer tune and the stability of an identified characteristic ion ratio using spectral data from ±1 scan on either side of the peak apex were also statistically assessed using Welch’s ANOVA testing. The presence of diastereomers for N-sec-butyl pentylone was identified using the developed GC-EI-MS method, which was confirmed using one-dimensional and two-dimensional NMR spectroscopy. The retention time reproducibility of the chromatographic method was ±0.076% or less over the course of a month. An identified characteristic ion ratio between the abundance of the fragment ion at m/z 128 and the fragment ion at m/z 72 enabled the differentiation of the four N-butyl pentylone isomers, even when accounting for the effect of the mass spectrometer tune and mass spectral scans used to calculate the characteristic ion ratio. The 95% confidence interval mean abundance ratio of the fragment ions at m/z 128 and m/z 72 was 17.14 ± 0.14 for N-butyl pentylone, 6.44 ± 0.05 for N-isobutyl pentylone, 3.38 ± 0.02 for N-sec-butyl pentylone, and 0.75 ± 0.01 for N-tert-butyl pentylone. These results highlight the capabilities of a combined GC-EI-MS and NMR approach for the differentiation and characterization of synthetic cathinone isomers. [Display omitted] •Combined GC-EI-MS and NMR approach for differentiating synthetic cathinone isomers•Differentiation by retention time and a characteristic ion ratio for GC-EI-MS•Achieved isomer differentiation even with tune and mass spectral scan variability•Characterized N-butyl pentylone isomers using NMR spectroscopy•Chromatographically separated N-sec-butyl pentylone diastereomers using GC</description><identifier>ISSN: 0379-0738</identifier><identifier>EISSN: 1872-6283</identifier><identifier>DOI: 10.1016/j.forsciint.2023.111815</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Benzodiazepines ; Chromatography ; confidence interval ; Controlled substances ; Diastereoisomers ; Diastereomers ; Differentiation ; drugs ; Forensic science ; Forensic sciences ; Gas chromatography ; GC-EI-MS ; Hallucinogens ; Ionization ; Ions ; Isomers ; Laboratories ; landscapes ; Magnetic resonance spectroscopy ; Mass spectra ; Mass spectrometers ; Mass spectrometry ; Mass spectroscopy ; Narcotics ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; nuclear magnetic resonance spectroscopy ; Psychotropic drugs ; Reproducibility ; Retention ; Retention time ; Scientific imaging ; Seized drugs ; spectral analysis ; spectrometers ; Spectroscopy ; Stimulants ; Synthetic cathinone isomers ; Variance analysis</subject><ispartof>Forensic science international, 2023-10, Vol.351, p.111815-111815, Article 111815</ispartof><rights>2023 Elsevier B.V.</rights><rights>2023. Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-f9670b3bf0c32735b9269e0800382d083fd2c4807b888f231b41943b287495cf3</citedby><cites>FETCH-LOGICAL-c409t-f9670b3bf0c32735b9269e0800382d083fd2c4807b888f231b41943b287495cf3</cites><orcidid>0000-0001-9932-8273</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Liliedahl, Ruby E.</creatorcontrib><creatorcontrib>Hutzel, Elise</creatorcontrib><creatorcontrib>Haley, Madison</creatorcontrib><creatorcontrib>Predecki, Daniel P.</creatorcontrib><creatorcontrib>Davidson, J. Tyler</creatorcontrib><title>The differentiation of N-butyl pentylone isomers using GC-EI-MS and NMR</title><title>Forensic science international</title><description>Forensic laboratories are faced with an ever-expanding seized drug landscape including the increasing prevalence of novel psychoactive substances (NPS), such as synthetic cathinones, that have varying potencies and scheduling. This study demonstrates a combined gas chromatography-electron ionization-mass spectrometry (GC-EI-MS) and nuclear magnetic resonance (NMR) spectroscopy approach for the differentiation of N-butyl pentylone isomers based on distinct retention times, characteristic EI mass spectra, and NMR characterization. Retention time reproducibility was assessed from 60 replicate measurements for each isomer over the course of a month. In addition, the effect of the mass spectrometer tune and the stability of an identified characteristic ion ratio using spectral data from ±1 scan on either side of the peak apex were also statistically assessed using Welch’s ANOVA testing. The presence of diastereomers for N-sec-butyl pentylone was identified using the developed GC-EI-MS method, which was confirmed using one-dimensional and two-dimensional NMR spectroscopy. The retention time reproducibility of the chromatographic method was ±0.076% or less over the course of a month. An identified characteristic ion ratio between the abundance of the fragment ion at m/z 128 and the fragment ion at m/z 72 enabled the differentiation of the four N-butyl pentylone isomers, even when accounting for the effect of the mass spectrometer tune and mass spectral scans used to calculate the characteristic ion ratio. The 95% confidence interval mean abundance ratio of the fragment ions at m/z 128 and m/z 72 was 17.14 ± 0.14 for N-butyl pentylone, 6.44 ± 0.05 for N-isobutyl pentylone, 3.38 ± 0.02 for N-sec-butyl pentylone, and 0.75 ± 0.01 for N-tert-butyl pentylone. These results highlight the capabilities of a combined GC-EI-MS and NMR approach for the differentiation and characterization of synthetic cathinone isomers. [Display omitted] •Combined GC-EI-MS and NMR approach for differentiating synthetic cathinone isomers•Differentiation by retention time and a characteristic ion ratio for GC-EI-MS•Achieved isomer differentiation even with tune and mass spectral scan variability•Characterized N-butyl pentylone isomers using NMR spectroscopy•Chromatographically separated N-sec-butyl pentylone diastereomers using GC</description><subject>Benzodiazepines</subject><subject>Chromatography</subject><subject>confidence interval</subject><subject>Controlled substances</subject><subject>Diastereoisomers</subject><subject>Diastereomers</subject><subject>Differentiation</subject><subject>drugs</subject><subject>Forensic science</subject><subject>Forensic sciences</subject><subject>Gas chromatography</subject><subject>GC-EI-MS</subject><subject>Hallucinogens</subject><subject>Ionization</subject><subject>Ions</subject><subject>Isomers</subject><subject>Laboratories</subject><subject>landscapes</subject><subject>Magnetic resonance spectroscopy</subject><subject>Mass spectra</subject><subject>Mass spectrometers</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Narcotics</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>nuclear magnetic resonance spectroscopy</subject><subject>Psychotropic drugs</subject><subject>Reproducibility</subject><subject>Retention</subject><subject>Retention time</subject><subject>Scientific imaging</subject><subject>Seized drugs</subject><subject>spectral analysis</subject><subject>spectrometers</subject><subject>Spectroscopy</subject><subject>Stimulants</subject><subject>Synthetic cathinone isomers</subject><subject>Variance analysis</subject><issn>0379-0738</issn><issn>1872-6283</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkU9LAzEQxYMoWP98BgNevGydJJtN9ihFq6AVtJ7DbjbRlG1Sk12h396UigcvwsDA8HsP5j2ELghMCZDqejW1ISbtnB-mFCibEkIk4QdoQqSgRUUlO0QTYKIuQDB5jE5SWgEA57SaoPnyw-DOWWui8YNrBhc8DhYvinYctj3e5Ou2D95gl8LaxITH5Pw7ns-K24fi6RU3vsOLp5czdGSbPpnzn32K3u5ul7P74vF5_jC7eSx0CfVQ2LoS0LLWgmZUMN7WtKoNSAAmaQeS2Y7qUoJopZSWMtKWpC5ZS6Uoa64tO0VXe99NDJ-jSYNau6RN3zfehDEpRngeDrL8F6Wy4iInJUlGL_-gqzBGnx_ZUZUQJSc0U2JP6RhSisaqTXTrJm4VAbXrQq3Ubxdq14Xad5GVN3ulydF8ORNVhozXpnPR6EF1wf3r8Q2EdpLM</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Liliedahl, Ruby E.</creator><creator>Hutzel, Elise</creator><creator>Haley, Madison</creator><creator>Predecki, Daniel P.</creator><creator>Davidson, J. Tyler</creator><general>Elsevier B.V</general><general>Elsevier Limited</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0001-9932-8273</orcidid></search><sort><creationdate>20231001</creationdate><title>The differentiation of N-butyl pentylone isomers using GC-EI-MS and NMR</title><author>Liliedahl, Ruby E. ; Hutzel, Elise ; Haley, Madison ; Predecki, Daniel P. ; Davidson, J. Tyler</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-f9670b3bf0c32735b9269e0800382d083fd2c4807b888f231b41943b287495cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Benzodiazepines</topic><topic>Chromatography</topic><topic>confidence interval</topic><topic>Controlled substances</topic><topic>Diastereoisomers</topic><topic>Diastereomers</topic><topic>Differentiation</topic><topic>drugs</topic><topic>Forensic science</topic><topic>Forensic sciences</topic><topic>Gas chromatography</topic><topic>GC-EI-MS</topic><topic>Hallucinogens</topic><topic>Ionization</topic><topic>Ions</topic><topic>Isomers</topic><topic>Laboratories</topic><topic>landscapes</topic><topic>Magnetic resonance spectroscopy</topic><topic>Mass spectra</topic><topic>Mass spectrometers</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Narcotics</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>nuclear magnetic resonance spectroscopy</topic><topic>Psychotropic drugs</topic><topic>Reproducibility</topic><topic>Retention</topic><topic>Retention time</topic><topic>Scientific imaging</topic><topic>Seized drugs</topic><topic>spectral analysis</topic><topic>spectrometers</topic><topic>Spectroscopy</topic><topic>Stimulants</topic><topic>Synthetic cathinone isomers</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liliedahl, Ruby E.</creatorcontrib><creatorcontrib>Hutzel, Elise</creatorcontrib><creatorcontrib>Haley, Madison</creatorcontrib><creatorcontrib>Predecki, Daniel P.</creatorcontrib><creatorcontrib>Davidson, J. Tyler</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Toxicology Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Forensic science international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liliedahl, Ruby E.</au><au>Hutzel, Elise</au><au>Haley, Madison</au><au>Predecki, Daniel P.</au><au>Davidson, J. Tyler</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The differentiation of N-butyl pentylone isomers using GC-EI-MS and NMR</atitle><jtitle>Forensic science international</jtitle><date>2023-10-01</date><risdate>2023</risdate><volume>351</volume><spage>111815</spage><epage>111815</epage><pages>111815-111815</pages><artnum>111815</artnum><issn>0379-0738</issn><eissn>1872-6283</eissn><abstract>Forensic laboratories are faced with an ever-expanding seized drug landscape including the increasing prevalence of novel psychoactive substances (NPS), such as synthetic cathinones, that have varying potencies and scheduling. This study demonstrates a combined gas chromatography-electron ionization-mass spectrometry (GC-EI-MS) and nuclear magnetic resonance (NMR) spectroscopy approach for the differentiation of N-butyl pentylone isomers based on distinct retention times, characteristic EI mass spectra, and NMR characterization. Retention time reproducibility was assessed from 60 replicate measurements for each isomer over the course of a month. In addition, the effect of the mass spectrometer tune and the stability of an identified characteristic ion ratio using spectral data from ±1 scan on either side of the peak apex were also statistically assessed using Welch’s ANOVA testing. The presence of diastereomers for N-sec-butyl pentylone was identified using the developed GC-EI-MS method, which was confirmed using one-dimensional and two-dimensional NMR spectroscopy. The retention time reproducibility of the chromatographic method was ±0.076% or less over the course of a month. An identified characteristic ion ratio between the abundance of the fragment ion at m/z 128 and the fragment ion at m/z 72 enabled the differentiation of the four N-butyl pentylone isomers, even when accounting for the effect of the mass spectrometer tune and mass spectral scans used to calculate the characteristic ion ratio. The 95% confidence interval mean abundance ratio of the fragment ions at m/z 128 and m/z 72 was 17.14 ± 0.14 for N-butyl pentylone, 6.44 ± 0.05 for N-isobutyl pentylone, 3.38 ± 0.02 for N-sec-butyl pentylone, and 0.75 ± 0.01 for N-tert-butyl pentylone. These results highlight the capabilities of a combined GC-EI-MS and NMR approach for the differentiation and characterization of synthetic cathinone isomers. [Display omitted] •Combined GC-EI-MS and NMR approach for differentiating synthetic cathinone isomers•Differentiation by retention time and a characteristic ion ratio for GC-EI-MS•Achieved isomer differentiation even with tune and mass spectral scan variability•Characterized N-butyl pentylone isomers using NMR spectroscopy•Chromatographically separated N-sec-butyl pentylone diastereomers using GC</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.forsciint.2023.111815</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-9932-8273</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0379-0738
ispartof Forensic science international, 2023-10, Vol.351, p.111815-111815, Article 111815
issn 0379-0738
1872-6283
language eng
recordid cdi_proquest_miscellaneous_3153155084
source Elsevier ScienceDirect Journals
subjects Benzodiazepines
Chromatography
confidence interval
Controlled substances
Diastereoisomers
Diastereomers
Differentiation
drugs
Forensic science
Forensic sciences
Gas chromatography
GC-EI-MS
Hallucinogens
Ionization
Ions
Isomers
Laboratories
landscapes
Magnetic resonance spectroscopy
Mass spectra
Mass spectrometers
Mass spectrometry
Mass spectroscopy
Narcotics
NMR
NMR spectroscopy
Nuclear magnetic resonance
nuclear magnetic resonance spectroscopy
Psychotropic drugs
Reproducibility
Retention
Retention time
Scientific imaging
Seized drugs
spectral analysis
spectrometers
Spectroscopy
Stimulants
Synthetic cathinone isomers
Variance analysis
title The differentiation of N-butyl pentylone isomers using GC-EI-MS and NMR
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-11T11%3A30%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20differentiation%20of%20N-butyl%20pentylone%20isomers%20using%20GC-EI-MS%20and%20NMR&rft.jtitle=Forensic%20science%20international&rft.au=Liliedahl,%20Ruby%20E.&rft.date=2023-10-01&rft.volume=351&rft.spage=111815&rft.epage=111815&rft.pages=111815-111815&rft.artnum=111815&rft.issn=0379-0738&rft.eissn=1872-6283&rft_id=info:doi/10.1016/j.forsciint.2023.111815&rft_dat=%3Cproquest_cross%3E2866774512%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2866774512&rft_id=info:pmid/&rft_els_id=S0379073823002657&rfr_iscdi=true