Legality of Cannabis by U.S. Jurisdiction

DESOXY
Names
Preferred IUPAC name
2-(3,5-Dimethoxy-4-methylphenyl)ethan-1-amine
Other names
3,5-Dimethoxy-4-methylphenethylamine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • 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
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 ?)

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[edit]

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

Dosage[edit]

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

Legality[edit]

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[edit]

  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[edit]