A new potent serotonin 5-HT2A receptor agonist, 25I-NBOH, was identified in blotter papers by several state-level forensic laboratories in Brazil. The molecule is labile and fragments into 2C-I during routine GC screening, requiring GC-MS, LC-QTOF-MS, FTIR, and NMR for full characterization. Individual doses range from 300 to 1000 μg. Although it is a potent 5-HT2A receptor agonist, 25I-NBOH is not registered with the UNODC and is controlled only in Sweden and Brazil. This is the first scientific report of 25I-NBOH identification in actual seizures.
Discarded screen-printed electrodes can be recoated with a graphite and chitosan mixture to create a reusable sensor for detecting the recreational drug 2C-B in oral fluid and seized samples. The sensor, called SPE-Gr/CTS, detects 2C-B electrochemically with a linear range from 0.05 to 7.5 μmol L⁻¹ and a detection limit of 0.015 μmol L⁻¹. Responses are stable across different electrodes, with relative standard deviation below 5.0%. The method is selective for 2C-B even when seventeen other illicit drugs or adulterants are present. Real seized and oral fluid samples were analyzed, and results matched those from LC-MS. The device offers a rapid, portable, and environmentally friendly screening tool for forensic analysis, using only 50 μL of sample.
A new screening method combining a color change and an electrochemical signal can identify LSD and related drugs (NBOHs, NBOMes, 2Cs) on blotter papers. The method uses Emerson's reagent to produce a color change and a voltammetric measurement on a graphite electrode to detect the drugs. It provides three distinct responses for NBOHs, allowing unambiguous identification, and can distinguish between different drug types. The technique is stable (less than 2.3% variability), sensitive (detection limit of 0.3 μg per mL), and works across a wide concentration range (10 to 1000 μg per mL). When tested on 33 real seized samples, the results matched those from standard confirmatory methods, offering a simple and fast tool for forensic screening.
25I-NBOH, a novel psychoactive substance found on blotter paper in Brazil, can be misidentified as 2C-I by routine gas chromatography–mass spectrometry (GC–MS) because it degrades into 2C-I inside the injector unless a derivatization procedure is used. A slight adjustment to the standard GC–MS method—shortening the solvent delay window—enables detection of an additional early chromatographic peak from the degradation, allowing distinction between 25I-NBOH and 2C-I without derivatization and preventing misidentification.