PEA-NBOMe

PEA-NBOMe
Clinical data
Other namesNBOMe; NBOMe-PEA; N-(2-Methoxybenzyl)phenethylamine
ATC code
  • None
Identifiers
  • N-[(2-methoxyphenyl)methyl]-2-phenylethanamine
CAS Number
PubChem CID
ChemSpider
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H19NO
Molar mass241.334 g·mol−1
3D model (JSmol)
  • COC1=CC=CC=C1CNCCC2=CC=CC=C2
  • InChI=1S/C16H19NO/c1-18-16-10-6-5-9-15(16)13-17-12-11-14-7-3-2-4-8-14/h2-10,17H,11-13H2,1H3
  • Key:UTYSBUBGYZSUPZ-UHFFFAOYSA-N

PEA-NBOMe, also known as N-(2-methoxybenzyl)phenethylamine, is a drug of the phenethylamine and N-benzylphenethylamine (NB; NBOMe) families related to phenethylamine (PEA).[1][2] It is the N-(2-methoxybenzyl) derivative of phenethylamine.[1][2] The drug is a parent compound of the NBOMe family of psychedelic drugs, such as 25I-NBOMe.[1][2][3] No data on the pharmacology or toxicity of PEA-NBOMe are available.[1][2] In any case, based on structure–activity relationships, PEA-NBOMe might produce stimulant and/or hallucinogenic effects.[1][2] The drug was encountered as a novel designer drug online in 2024.[1][2] It is not a controlled substance in Canada as of 2025.[4]

See also

References

  1. ^ a b c d e f "PEA-NBOMe". Aipsin (in Russian). Retrieved 8 January 2026.
  2. ^ a b c d e f Pavlovets Y, Haletskaya I, Yurchenko R, Yurchenko L, Piatsetskaya A (January 2025). Psychoactive products market observation. Trend analysis. Monitoring the Psychoactive Product Market. (in Russian). Aipsin Web Electronic Publication. doi:10.13140/RG.2.2.11663.91045.
  3. ^ Brandt SD, Elliott SP, Kavanagh PV, Dempster NM, Meyer MR, Maurer HH, et al. (April 2015). "Analytical characterization of bioactive N-benzyl-substituted phenethylamines and 5-methoxytryptamines" (PDF). Rapid Communications in Mass Spectrometry. 29 (7): 573–584. Bibcode:2015RCMS...29..573B. doi:10.1002/rcm.7134. PMID 26212274. Substances based on the N-(2-methoxybenzyl)phenethylamine template ('NBOMe' derivatives) play an important role in medicinal research but some of these derivatives have also appeared as 'research chemicals' for recreational use which has attracted attention worldwide.
  4. ^ "Controlled Drugs and Substances Act". Department of Justice Canada. Retrieved 19 January 2026.