DESOXY

DESOXY
Names
Preferred IUPAC name
2-(3,5-Dimethoxy-4-methylphenyl)ethan-1-amine
Other names
3,5-Dimethoxy-4-methylphenethylamine
Identifiers
CAS Number
  • 63037-49-0 checkY
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL127679 checkY
ChemSpider
  • 21106289 checkY
PubChem CID
  • 44350128
UNII
  • 424LJJ87HT checkY
CompTox Dashboard (EPA)
  • DTXSID80658381 Edit this at Wikidata
InChI
  • InChI=1S/C11H17NO2/c1-8-10(13-2)6-9(4-5-12)7-11(8)14-3/h6-7H,4-5,12H2,1-3H3 checkY
    Key: LLHRMWHYJGLIEV-UHFFFAOYSA-N checkY
  • InChI=1/C11H17NO2/c1-8-10(13-2)6-9(4-5-12)7-11(8)14-3/h6-7H,4-5,12H2,1-3H3
    Key: LLHRMWHYJGLIEV-UHFFFAOYAV
  • Cc1c(cc(cc1OC)CCN)OC
Properties
Chemical formula
C11H17NO2
Molar mass 195.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references
Chemical compound

4-Desoxymescaline, or 4-methyl-3,5-dimethoxyphenethylamine, is a mescaline analogue related to other psychedelic phenethylamines. It is commonly referred to as DESOXY. DESOXY was discovered by Alexander Shulgin and published in his book PiHKAL.

Effects

The effects of DESOXY vary significantly from mescaline, despite their chemical similarity.[citation needed]

Dosage

A typical dosage is within the range of 40–120 mg and lasts 6–8 hours.[1]

Legality

In 1970 the Controlled Substances Act placed mescaline into Schedule I in the United States. It is similarly controlled in other nations. Depending on whether or not it is intended for human consumption, 4-desoxymescaline could be considered an analogue of mescaline, under the Federal Analogue Act and similar bills in other countries, making it illegal to manufacture, buy, possess, or distribute without a DEA or related license.

DESOXY is also an isomer of 2C-D which makes it a schedule 1 drug in the United States.

References

  1. ^ Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.

External links

  • Alexander Shulgin, Jacob, P. Structure-Activity Relationships of the Classic Hallucinogens and Their Analogs. NIDA Research Monograph 146 (Hallucinogens: An Update), 1994.
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