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25C-NBOH

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
25C-NBOH
Clinical data
Other names2C-C-NBOH; NBOH-2CC
Legal status
Legal status
Identifiers
  • 2-({[2-(4-chloro-2,5-dimethoxyphenyl)ethyl]amino}methyl)phenol
CAS Number
PubChemCID
ChemSpider
UNII
Chemical and physical data
FormulaC17H20ClNO3
Molar mass321.80 g·mol−1
3D model (JSmol)
  • COc1cc(Cl)c(OC)cc1CCNCc2ccccc2O
  • InChI=1S/C17H20ClNO3/c1-21-16-10-14(18)17(22-2)9-12(16)7-8-19-11-13-5-3-4-6-15(13)20/h3-6,9-10,19-20H,7-8,11H2,1-2H3
  • Key:VHWXICYYQMMZCW-UHFFFAOYSA-N

25-C-NBOH (2C-C-NBOH,NBOH-2CC) is a derivative of the phenethylamine derived hallucinogen2C-C which has been sold as adesigner drug. It has similarserotonin receptor affinity to the better-known compound25C-NBOMe.[2][3]

Analogues and derivatives

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Analytical chemistry

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25C-NBOH undergoes degradation under routineGas Chromatography (GC) conditions, as well as other NBOH's substances, into 2C-C.[4][5] An alternative method proposed for reliable identification of25I-NBOH usingGC/MS may be used for 25C-NBOH analysis.[6][7]

Legality

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United Kingdom

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This substance is aClass A drug in the United Kingdom as a result of theN-benzylphenethylamine catch-all clause in theMisuse of Drugs Act 1971.[8]

References

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  1. ^Anvisa (2023-07-24)."RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-07-25).Archived from the original on 2023-08-27. Retrieved2023-08-27.
  2. ^Hansen M, Phonekeo K, Paine JS, Leth-Petersen S, Begtrup M, Bräuner-Osborne H, Kristensen JL (March 2014)."Synthesis and structure-activity relationships of N-benzyl phenethylamines as 5-HT2A/2C agonists".ACS Chemical Neuroscience.5 (3):243–9.doi:10.1021/cn400216u.PMC 3963123.PMID 24397362.
  3. ^Hansen M (2010-12-16).Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain (Ph.D. thesis). University of Copenhagen.doi:10.13140/RG.2.2.33671.14245.
  4. ^Arantes LC, Júnior EF, de Souza LF, Cardoso AC, Alcântara TL, Lião LM, et al. (2017)."2A receptor agonist identified in blotter paper seizures in Brazil".Forensic Toxicology.35 (2):408–414.doi:10.1007/s11419-017-0357-x.PMC 5486617.PMID 28706567.
  5. ^Machado Y, Lordeiro RA, Neto JC, Alves RB, Piccin E (2019)."Identification of new NBOH drugs in seized blotter papers: 25B-NBOH, 25C-NBOH, and 25E-NBOH".Forensic Toxicology.38 (2):203–215.doi:10.1007/s11419-019-00509-7.S2CID 209672508.
  6. ^Neto JC, Andrade AF, Lordeiro RA, Machado Y, Elie M, Júnior EF, Arantes LC (2017)."Preventing misidentification of 25I-NBOH as 2C-I on routine GC–MS analyses"(PDF).Forensic Toxicology.35 (2):415–420.doi:10.1007/s11419-017-0362-0.S2CID 32432586.
  7. ^Machado Y, Lordeiro RA, Neto JC, Alves RB, Piccin E (2019)."Identification of new NBOH drugs in seized blotter papers: 25B-NBOH, 25C-NBOH, and 25E-NBOH".Forensic Toxicology.38 (2):203–215.doi:10.1007/s11419-019-00509-7.S2CID 209672508.
  8. ^"The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014".UK Statutory Instruments 2014 No. 1106. www.legislation.gov.uk.
Tryptamines
No ring subs.
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