Contents

DESOXY

Not to be confused with Desoxyn.

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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 Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL127679 Y
ChemSpider	21106289 Y
PubChem CID	44350128
UNII	424LJJ87HT Y
CompTox Dashboard (EPA)	DTXSID80658381
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 Y Key: LLHRMWHYJGLIEV-UHFFFAOYSA-N Y 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
SMILES 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). Y verify (what is YN ?) Infobox references

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.

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

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

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 analogueofmescaline, 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.

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