Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material

Research output: Contribution to journalLetterResearchpeer-review

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Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material. / Pasin, Daniel; Nedahl, Michael; Mollerup, Christian Brinch; Tortzen, Christian; Reitzel, Lotte Ask; Dalsgaard, Petur Weihe.

In: Drug Testing and Analysis, Vol. 14, No. 9, 15.09.2022, p. 1645–1651.

Research output: Contribution to journalLetterResearchpeer-review

Harvard

Pasin, D, Nedahl, M, Mollerup, CB, Tortzen, C, Reitzel, LA & Dalsgaard, PW 2022, 'Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material', Drug Testing and Analysis, vol. 14, no. 9, pp. 1645–1651. https://doi.org/10.1002/dta.3333

APA

Pasin, D., Nedahl, M., Mollerup, C. B., Tortzen, C., Reitzel, L. A., & Dalsgaard, P. W. (2022). Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material. Drug Testing and Analysis, 14(9), 1645–1651. https://doi.org/10.1002/dta.3333

Vancouver

Pasin D, Nedahl M, Mollerup CB, Tortzen C, Reitzel LA, Dalsgaard PW. Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material. Drug Testing and Analysis. 2022 Sep 15;14(9):1645–1651. https://doi.org/10.1002/dta.3333

Author

Pasin, Daniel ; Nedahl, Michael ; Mollerup, Christian Brinch ; Tortzen, Christian ; Reitzel, Lotte Ask ; Dalsgaard, Petur Weihe. / Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material. In: Drug Testing and Analysis. 2022 ; Vol. 14, No. 9. pp. 1645–1651.

Bibtex

@article{58a703c292104a8697f2efba7cbe44d2,
title = "Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material",
abstract = "Synthetic cannabinoids (SCs) remain the largest class of new psychoactive substances (NPS), and while the number of NPS that are reported to the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) for the first time each year declines, the number of newly reported SCs still exceeds other NPS classes. This decline can be seen as a result of legislative changes by different jurisdictions which have sometimes transitioned to a more generalized approach when controlling substances by defining common structural scaffolds rather than explicit structures. While the consequences of such legislative changes have been expected over the years, the introduction of so-called “class-wide” bans puts further pressure on clandestine laboratories to synthesize compounds which are out of the scope of the legislation, and thus, these compounds are initially harder to detect and/or identify in the absence of analytical data. Recently, a SC with an indole-3-acetamide core-linker scaffold, AD-18 (i.e., ADB-FUBIATA or ADB-FUBIACA), was reported for the first time in China in 2021. Here, an additional cannabinoid with the indole-3-acetamide scaffold, N-cyclohexyl-2-(1-pentyl-1H-indol-3-yl)acetamide (CH-PIACA), is reported which was identified for the first time in a seized material in Denmark. Structural characterization was performed using gas chromatography–mass spectrometry (GC–MS), liquid chromatography-high-resolution mass spectrometry (LC-HRMS), and nuclear magnetic resonance (NMR) spectroscopy.",
author = "Daniel Pasin and Michael Nedahl and Mollerup, {Christian Brinch} and Christian Tortzen and Reitzel, {Lotte Ask} and Dalsgaard, {Petur Weihe}",
year = "2022",
month = sep,
day = "15",
doi = "10.1002/dta.3333",
language = "English",
volume = "14",
pages = "1645–1651",
journal = "Drug Testing and Analysis",
issn = "1942-7603",
publisher = "JohnWiley & Sons Ltd",
number = "9",

}

RIS

TY - JOUR

T1 - Identification of the synthetic cannabinoid‐type new psychoactive substance, CH‐PIACA, in seized material

AU - Pasin, Daniel

AU - Nedahl, Michael

AU - Mollerup, Christian Brinch

AU - Tortzen, Christian

AU - Reitzel, Lotte Ask

AU - Dalsgaard, Petur Weihe

PY - 2022/9/15

Y1 - 2022/9/15

N2 - Synthetic cannabinoids (SCs) remain the largest class of new psychoactive substances (NPS), and while the number of NPS that are reported to the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) for the first time each year declines, the number of newly reported SCs still exceeds other NPS classes. This decline can be seen as a result of legislative changes by different jurisdictions which have sometimes transitioned to a more generalized approach when controlling substances by defining common structural scaffolds rather than explicit structures. While the consequences of such legislative changes have been expected over the years, the introduction of so-called “class-wide” bans puts further pressure on clandestine laboratories to synthesize compounds which are out of the scope of the legislation, and thus, these compounds are initially harder to detect and/or identify in the absence of analytical data. Recently, a SC with an indole-3-acetamide core-linker scaffold, AD-18 (i.e., ADB-FUBIATA or ADB-FUBIACA), was reported for the first time in China in 2021. Here, an additional cannabinoid with the indole-3-acetamide scaffold, N-cyclohexyl-2-(1-pentyl-1H-indol-3-yl)acetamide (CH-PIACA), is reported which was identified for the first time in a seized material in Denmark. Structural characterization was performed using gas chromatography–mass spectrometry (GC–MS), liquid chromatography-high-resolution mass spectrometry (LC-HRMS), and nuclear magnetic resonance (NMR) spectroscopy.

AB - Synthetic cannabinoids (SCs) remain the largest class of new psychoactive substances (NPS), and while the number of NPS that are reported to the European Monitoring Centre for Drugs and Drug Addiction (EMCDDA) for the first time each year declines, the number of newly reported SCs still exceeds other NPS classes. This decline can be seen as a result of legislative changes by different jurisdictions which have sometimes transitioned to a more generalized approach when controlling substances by defining common structural scaffolds rather than explicit structures. While the consequences of such legislative changes have been expected over the years, the introduction of so-called “class-wide” bans puts further pressure on clandestine laboratories to synthesize compounds which are out of the scope of the legislation, and thus, these compounds are initially harder to detect and/or identify in the absence of analytical data. Recently, a SC with an indole-3-acetamide core-linker scaffold, AD-18 (i.e., ADB-FUBIATA or ADB-FUBIACA), was reported for the first time in China in 2021. Here, an additional cannabinoid with the indole-3-acetamide scaffold, N-cyclohexyl-2-(1-pentyl-1H-indol-3-yl)acetamide (CH-PIACA), is reported which was identified for the first time in a seized material in Denmark. Structural characterization was performed using gas chromatography–mass spectrometry (GC–MS), liquid chromatography-high-resolution mass spectrometry (LC-HRMS), and nuclear magnetic resonance (NMR) spectroscopy.

U2 - 10.1002/dta.3333

DO - 10.1002/dta.3333

M3 - Letter

C2 - 35687099

VL - 14

SP - 1645

EP - 1651

JO - Drug Testing and Analysis

JF - Drug Testing and Analysis

SN - 1942-7603

IS - 9

ER -

ID: 311895255