Isolating and Determining the Structures of Colored Products from the Reactions of Cannabinoids with Fast Blue RR

Although cannabis is used in a wide range of fields, including medicine and pharmacology, its use is prohibited in Japan because it contains Δ<sup>9</sup>-tetrahydrocannabinol (Δ<sup>9</sup>-THC), a compound that exhibits narcotic effects. While cannabis is primarily detected via color-based screening methods at crime scenes, the reaction products and mechanisms associated with these screening methods have not been fully elucidated. To address this issue, the colored products were isolated via the diazo-coupling reactions of the major cannabinoids (cannabidiol, cannabinol, and Δ<sup>9</sup>-THC) in cannabis with the Fast Blue RR diazonium salt, and their structures were determined using NMR spectroscopy. As expected, azo compound <b>2</b> was formed from cannabidiol, whereas cannabinol and Δ<sup>9</sup>-THC produced quinoneimines <b>3</b> and <b>4</b>, respectively. This study is expected to lead to the future development of more sensitive color-based reagents that produce fewer false positives.

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Publication Details

Journal
Molecules
Published
2025-08-22
DOI
https://doi.org/10.3390/molecules30173462
Citations
1
Primary Topic
Dye analysis and toxicity
Type
article
Field-Weighted Citation Impact
0.75

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article

Isolating and Determining the Structures of Colored Products from the Reactions of Cannabinoids with Fast Blue RR

Manabu Tokeshi, Ryosuke Arai, Kyohei Higashi, Kayo Nakamura et al.
1 citations
Molecules
Dye analysis and toxicity
0.75
article

Isolating and Determining the Structures of Colored Products from the Reactions of Cannabinoids with Fast Blue RR

Manabu Tokeshi, Ryosuke Arai, Kyohei Higashi, Kayo Nakamura, Akihiko Ishida, Hiroko Abe, Akiyoshi Saitoh, Hideyo Takahashi, H. Nishiguchi, Riho Hamajima
article en
1 citations

Abstract

Although cannabis is used in a wide range of fields, including medicine and pharmacology, its use is prohibited in Japan because it contains Δ<sup>9</sup>-tetrahydrocannabinol (Δ<sup>9</sup>-THC), a compound that exhibits narcotic effects. While cannabis is primarily detected via color-based screening methods at crime scenes, the reaction products and mechanisms associated with these screening methods have not been fully elucidated. To address this issue, the colored products were isolated via the diazo-coupling reactions of the major cannabinoids (cannabidiol, cannabinol, and Δ<sup>9</sup>-THC) in cannabis with the Fast Blue RR diazonium salt, and their structures were determined using NMR spectroscopy. As expected, azo compound <b>2</b> was formed from cannabidiol, whereas cannabinol and Δ<sup>9</sup>-THC produced quinoneimines <b>3</b> and <b>4</b>, respectively. This study is expected to lead to the future development of more sensitive color-based reagents that produce fewer false positives.

MoleculesVol. 30(17)
Tokyo University of Science (JP), Hokkaido University (JP), Japan Institute of Wastewater Engineering Technology (JP)
Japan Science and Technology Agency
Openalex Percentile: Top 27%
Dye analysis and toxicity
0.75
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Isolating and Determining the Structures of Colored Products from the Reactions of Cannabinoids with Fast Blue RR — Manabu Tokeshi, Ryosuke Arai, et al. · Molecules (2025) | TGRS Research Map | TGRS