25D-NBOMe

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25D-NBOMe
25D-NBOMe2DACS.svg
Systematic (IUPAC) name
2-(2,5-dimethoxy-4-methylphenyl)-N-(2-methoxybenzyl)ethanamine
Clinical data
Legal status
  • Illegal in China and Sweden
Identifiers
CAS Number 1354632-02-2
ChemSpider 48059920 YesY
UNII 7RET11HE13 YesY
Chemical data
Formula C19H25NO3
Molecular mass 315.41 g·mol−1
  • COC1=C(C=C(C(=C1)C)OC)CCNCC2=C(C=CC=C2)OC
  • InChI=1S/C19H25NO3/c1-14-11-19(23-4)15(12-18(14)22-3)9-10-20-13-16-7-5-6-8-17(16)21-2/h5-8,11-12,20H,9-10,13H2,1-4H3 YesY
  • Key:UTVHBNXCFSATDB-UHFFFAOYSA-N YesY

25D-NBOMe (or NBOMe-2C-D) is a derivative of the phenethylamine derived hallucinogen 2C-D. It acts in a similar manner to related compounds such as 25I-NBOMe, which is a potent agonist at the 5HT2A receptor.[1][2] 25D-NBOMe has been sold as a street drug since 2010 and produces similar effects in humans to related compounds such as 25I-NBOMe and 25C-NBOMe.[3] It was banned as a Temporary Class Drug in the UK on 10 June 2013 after concerns about its recreational use.[4]

Legal status and scheduling

United States

Unregulated at a federal and state level, though arguably may contravene the Federal Analog Act under certain circumstances given its structural and functional similarity to controlled substance 2C-D.[5]

Sweden

Sveriges riksdag added 25D-NBOMe to schedule I ("substances, plant materials and fungi which normally do not have medical use") as narcotics in Sweden as of Aug 1, 2013, published by Medical Products Agency in their regulation LVFS 2013:15 listed as 25D-NBOMe 2-(2,5-dimetoxi-4-metylfenyl)-N-(2-metoxibensyl)etanamin.[6]

China

As of October 2015 25D-NBOMe is a controlled substance in China.[7]

See also

References

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  2. Hansen, M. Design and Synthesis of Selective Serotonin Receptor Agonists for Positron Emission Tomography Imaging of the Brain. PhD Thesis, University of Copenhagen, 2011.
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  6. http://www.lakemedelsverket.se/upload/lvfs/LVFS_2013-15.pdf
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