Study on the degradation and pyrolysis of 2-fluoromethcathinone.

2-fluoromethcathinone Degradation Pyrolysis Reaction pathway Structural identification

Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
20 Sep 2023
Historique:
received: 26 03 2023
revised: 30 05 2023
accepted: 10 06 2023
medline: 28 8 2023
pubmed: 16 6 2023
entrez: 15 6 2023
Statut: ppublish

Résumé

Gas chromatography-mass spectrometry (GC-MS) is the first choice for law enforcement agencies in various countries to analyze new psychoactive substances (NPS) because of its advantages and complete databases. For synthetic cathinone-type NPS (SCat), alkalization and extraction processes before GC-MS analysis are essential. However, the base form of SCat is unstable, causing it to quickly degrade in solution and cause pyrolysis at the GC-MS injection inlet. In this study, we investigated the degradation of ethyl acetate and pyrolysis at the GC-MS injection inlet of 2-fluoromethcathinone (2-FMC), the most unstable SCat. Using gas chromatography-quadruple/time-of-flight mass spectrometry (GC-Q/TOF-MS) combined with the predicted data from theoretical calculations and the analysis of mass spectrometry (MS) fragmentation, the structures of 15 2-FMC degradation and pyrolysis products were identified. Among them, 11 products were produced during degradation, and six products were obtained from pyrolysis (two of which were the same as the degradation products). At the same time, the degradation and pyrolysis pathways of 2-FMC were provided. The balance between keto-enol and enamine-imine tautomerism triggered the primary degradation pathway of 2-FMC. The subsequent degradation started from the tautomer with a hydroxyimine structure, including imine hydrolysis, oxidation, imine-enamine tautomerism, intramolecular ammonolysis of halobenzene, and hydration to generate a series of degradation products. The secondary degradation reaction was the ammonolysis of ethyl acetate to yield N-[1-(2'-fluorophenyl)-1-oxopropan-2-yl]-N-methylacetamide and the byproduct, N-[1-(2'-fluorophenyl)-1-oxopropan-2-yl]-N-methylformamide. In the pyrolysis of 2-FMC, the major reactions were dehydrogenation, intramolecular ammonolysis of halobenzene, and defluoromethane. The achievements of this manuscript not only study 2-FMC degradation and pyrolysis but also lay the foundation for the study of SCat stability and their accurate analysis by GC-MS.

Identifiants

pubmed: 37320973
pii: S0731-7085(23)00294-7
doi: 10.1016/j.jpba.2023.115525
pii:
doi:

Substances chimiques

ethyl acetate 76845O8NMZ
Hydrocarbons, Halogenated 0
Imines 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115525

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests. Xuan Luo reports financial support was provided by Science and Technology Department of Guangxi Zhuang Autonomous Region.

Auteurs

Xuan Luo (X)

School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P. R. China; Guangxi Colleges and Universities Key Laboratory of Applied Chemistry Technology and Resource Development, Guangxi University, Nanning, Guangxi 530004, P. R. China. Electronic address: luoxuan@gxu.edu.cn.

Chunli Feng (C)

School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P. R. China.

Kejian Huang (K)

Institute of Forensic Science, Public Security Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi 500012, P. R. China. Electronic address: huangkejian911@163.com.

Dalong Luo (D)

Wuzhou Institute of Food and Drug Control, Wuzhou, Guangxi 543099, P. R. China.

Xiaofeng Liu (X)

Institute of Forensic Science, Public Security Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi 500012, P. R. China.

Ning Yang (N)

Institute of Forensic Science, Public Security Department of Guangxi Zhuang Autonomous Region, Nanning, Guangxi 500012, P. R. China.

Qiulian Luo (Q)

School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P. R. China.

Hua Wang (H)

Wuzhou Institute of Food and Drug Control, Wuzhou, Guangxi 543099, P. R. China.

Articles similaires

Humans Breast Neoplasms Female Mass Spectrometry Adipose Tissue
Klebsiella pneumoniae Volatile Organic Compounds Metabolomics Ion Mobility Spectrometry Bacterial Proteins
Humans Proteomics Paraffin Embedding Tissue Fixation Organelles
Animals Alzheimer Disease Mice Proteomics Disease Models, Animal

Classifications MeSH