DOx - PsychonautWiki
The generic structure for a DOx compound

Substituted dimethoxyamphetamines (also known as DOx) refers to a class of psychedelic amphetamines originally synthesized and documented by Alexander Shulgin in his investigation of psychoactive phenethylamines in the 1970s. Shulgin later published his findings along with other mescaline-derived compounds in his semi-autobiographical book/organic synthesis reference PiHKAL ("Phenethylamines I Have Known and Loved")[1].

The DOx compounds are highly potent, dose-sensitive, and long-lasting substances which are considered considerably more intense and challenging to use than their counterpart 2C-x analogs as well as the serotonergic lysergamides. The effects of DOx are comprised of strong visuals and an intense body load that is typically accompanied by marked physical and mental stimulation that can persist well past the main duration of its effects (prolonged residual stimulation).

Notably, they are one of the few classes of psychedelic chemicals (the other being the 25x-NBOMe series and the serotonergic lysergamides) potent enough by weight to be laid onto and distributed on blotter paper, where it is has a history of being sold as a substitute for genuine LSD, being significantly easier to produce. On the street, they are notorious for their distinctly bitter taste as well as their unusually long come-up period (which can take up to 3-4 hours before its main effects even begin to present themselves), which has sometimes led inexperienced LSD users to prematurely conclude that their tabs must be weak or from a "bunk batch" and then take more to try to compensate; this has led to a number of accidental overdoses and unpleasant and overwhelming experiences when the substance's effects finally do take hold.[2]



This chemistry section is incomplete.

You can help by adding to it.

All derivatives of 2,5-dimethoxyamphetamine have a amphetamine backbone with two methoxy groups in positions 2 and 5 of the aromatic ring and they further contain different lipophilic substituents in position 4.

List of DOx compounds

Classic DOx compounds

Compound R4 Structure
DOiPR CH(CH3)2  
DOC Cl  
DOB Br  
TMA-2 OCH3  
Aleph SCH3  
Aleph-2 SCH2CH3  
Aleph-4 SCH(CH3)2  
Aleph-6 SC6H5  
Aleph-7 SCH2CH2CH3  

Other compounds, derivated from 2,5-dimethoxyamphetamine

Compound R3 R4 R5 R6 Structure
DOI-2-hemifly CH2- I H H  
DOB-5-hemifly H Br - CH2-  
Bromo-DragonFLY CH= Br H CH=  
F-2 H CH2- (CH3)- H  
F-22 H CH2- (CH3)2- H  

Toxicity and harm potential


This toxicity and harm potential section is a stub.

As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it.
Note: Always conduct independent research and use harm reduction practices if using this substance.

The DOx compounds, as with many other serotonergic psychedelics, should not be taken in combination with SSRIs (selective serotonin reuptake inhibitors) or tricyclic antidepressants in general to avoid serotonin syndrome, a potentially life-threatening condition in which an excess of serotonin builds up past the body's ability to catabolize it (i.e. "break it down"), which can lead to many physical and cognitive health problems. Also, an oft-observed phenomenon of the DOx chemicals is that they have an extremely long onset time relative to other psychedelics (which could prompt users to redose early and repeatedly, potentially causing a drug overdose[2]).

Legal issues

  • Austria: The DOx family is illegal to possess, produce and sell under the SMG (Suchtmittelgesetz Österreich) or the NPSG (Neue-Psychoaktive-Substanzen-Gesetz Österreich).[citation needed]
  • United States: In the US, some of the DOx chemicals are listed as Schedule I substances and all others under the Federal Analogue Act.
  • Australia: Australia has a blanket ban over all substituted phenethylamines including the entire DOx family.[3]
  • Switzerland: DOM, DOB and DOET are illegal to possess, produce and sell.[4]

See also

External links