Isomeric discrimination of synthetic cannabinoids by GC-EI-MS: 1-adamantyl and 2-adamantyl isomers ofN-adamantyl carboxamides

Author:

Asada Akiko1,Doi Takahiro1,Tagami Takaomi1,Takeda Akihiro1,Sawabe Yoshiyuki1

Affiliation:

1. Osaka Prefectural Institute of Public Health; 1-3-69 Nakamichi, Higashinari-ku Osaka 537-0025 Japan

Funder

JSPS KAKENH

Publisher

Wiley

Subject

Spectroscopy,Pharmaceutical Science,Environmental Chemistry,Analytical Chemistry

Reference10 articles.

1. Changes in the prevalence of synthetic cannabinoids and cathinone derivatives in Japan until early 2012;Kikura-Hanajiri;Forensic Toxicol.,2013

2. The analytical investigation of synthetic street drugs containing cathinone analogs;Leffler;Forensic Sci. Int.,2014

3. European Monitoring Centre for Drugs and Drug Addiction (EMCDDA), Europol 2016 http://www.emcdda.europa.eu/system/files/publications/2880/TDAS16001ENN.pdf

4. United Nations Office on Drugs and Crime (UNODC) 2016 www.unodc.org/doc/wdr2016/WORLD_DRUG_REPORT_2016_web.pdf

5. Identification of two new-type synthetic cannabinoids, N-(1-adamantyl)-1-pentyl-1H-indole-3-carboxamide (APICA) and N-(1-adamantyl)-1-pentyl-1H-indazole-3-carboxamide (APINACA), and detection of five synthetic cannabinoids, AM-1220, AM-2233, AM-1241, CB-13 (CRA-13), and AM-1248, as designer drugs in illegal products;Uchiyama;Forensic Toxicol.,2012

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