From The Lycaeum
Jump to: navigation, search
Not to be confused with methoxamine.
File:Methoxetamine 3d.gif
Systematic (IUPAC) name
Clinical data
Legal status ?
Pharmacokinetic data
Half-life 3-6 hours.
CAS number 1239943-76-0 7pxY
ATC code None
ChemSpider 24721792 7pxY
Chemical data
Formula C15H21NO2 
Mol. mass 247.33 g/mol
 14pxY (what is this?)  (verify)

Methoxetamine (MXE), or 3-MeO-2-Oxo-PCE is a dissociative anesthetic that has been sold as a research chemical.[2][1] Methoxetamine differs from many dissociatives such as ketamine and phencyclidine that were developed as pharmaceuticals in that it was designed for grey market distribution, making it a rare instance of a true designer drug.[2][3] Pharmacologically methoxetamine acts as a NMDA receptor antagonist, unlike the related compound ketamine it has appreciable affinity for the serotonin transporter.[4]

Physical properties

Pure methoxetamine hydrochloride is a white powder.[5][unreliable source?] It has low solubility in isopropanol, 6 mg/mL at -10 °C.[6][unreliable source?] It is soluble in ethanol up to 10 mg/ml at 25°C.[7]


The qualitative effects of methoxetamine were first described online in May of 2010 and the compound became commercially available on a small scale in September 2010,[2][1] by November use and sale of the methoxetamine had increased enough for it to be formally identified by the European Monitoring Centre for Drugs and Drug Addiction. By July 2011, the EMCDDA had identified 58 websites selling the compound at a cost of 145–195 euros for 10 grams.[8] MXE remains popular despite bans in many countries


Methoxetamine is reported to have a similar effect to ketamine,[9] with increased potency and duration.[10] Methoxetamine is often believed to possess opioid properties due to its structural similarity to 3-OH-PCP,[2] but this assumption is not supported by data, which shows insignificant affinity for the µ-opioid receptor.[4] Recreational use of Methoxetamine has been associated with hospitalizations in the US and UK.[11][12][13] Acute reversible cerebellar toxicity has been documented in three cases of hospital admission due to methoxetamine overdose, lasting for between one and four days after exposure.[12]

Methoxetamine was designed in part to prevent the urotoxicity associated with ketamine abuse, it was thought the compound's increased potency and reduced dose would limit the accumulation of urotoxic metabolites in the bladder.[2][3] Like ketamine, methoxetamine has been found to produce bladder inflammation and fibrosis after high dose, chronic administration in mice.[14] Reports of urotoxicty in humans have yet to appear in the medical literature.[2]

It is thought that methoxetamine may be an effective, fast-acting antidepressant like other NMDA antagonists. Its activity at other receptors may contribute to this.[10]

Legal status

Methoxetamine powder
Theresa May commented in her reply to the ACMD that "the next step in this process is for the ACMD to undertake a full assessment of methoxetamine for consideration for its permanent control under the 1971 Act." She goes on to say that she hopes the ACMD will do this as a part of the review of ketamine, "including its analogues" and that this review will be completed "within the 12 months from the making of the current order".[20]
On October 18th 2012 the ACMD released a report about MXE, saying that the "harms of methoxetamine are commensurate with Class B of the Misuse of Drugs Act (1971)", despite the fact that the act does not classify drugs based on harm. The report went on to suggest that all analogues of MXE should also become class B drugs and suggested a catch-all clause covering both existing and unresearched arylcyclohexamines.
MXE ceased to be covered by the temporary prohibition on 26 February 2013, when it became classified as a Class B drug. [21]

Media coverage

Mixmag reported in January 2012, that people in the dance music and clubbing community have given methoxetamine the slang name 'roflcoptr'.[26] Vice commented that it was likely that the phrase will only be used by "the same politicians, parents and journalists" who called mephedrone 'meow meow'.[27] After being called mexxy in UK Home Office press releases, the media adopted the name.[28][13]

A literature review was published in March 2012 which looked at scientific literature and information on the web. It concluded that "the online availability of information on novel psychoactive drugs, such as methoxetamine, may constitute a pressing public health challenge. Better international collaboration levels and novel forms of intervention are necessary to tackle this fast-growing phenomenon."[29]


A forensic standard of Methoxetamine is available, and the compound has been posted on the Forendex website of potential drugs of abuse.[30]


See also


  1. 1.0 1.1 1.2 EMCDDA Annual Report 2010 (Report). European Monitoring Centre for Drugs and Drug Addiction. 2010. Retrieved 2012-01-23.
  2. 2.0 2.1 2.2 2.3 2.4 2.5 Morris, H.; Wallach, J. (2014). "From PCP to MXE: a comprehensive review of the non-medical use of dissociative drugs". Drug Testing and Analysis. 
  3. 3.0 3.1 Morris, H. (2011-02-11). "Interview with a ketamine chemist: or to be more precise, an arylcyclohexylamine chemist". Vice Magazine. Retrieved 2012-01-23. 
  4. 4.0 4.1 "ACMD Methoxetamine Report (2012)". Advisory Council on the Misuse of Drugs. October 2012. pp. 14–15. Retrieved 6 February 2013. 
  5. "Methoxetamine FRANK". Retrieved 2012-04-14. 
  6. "The Big & Dandy Methoxetamine Thread: 9th dose - Tolerance Schmolerance". 2012-04-12. Retrieved 2012-04-14. 
  8. Online sales of new psychoactive substances/‘legalhighs’: Summary of results from the 2011 multilingual snapshots (Report). European Monitoring Centre for Drugs and Drug Addiction. 2011-11-15. Retrieved 2012-01-23.
  9. Kjellgren, A.; Jonsson, K. (2013). "Methoxetamine (MXE) – A Phenomenological Study of Experiences Induced by a "Legal High" from the Internet". Journal of Psychoactive Drugs 45 (3): 276. doi:10.1080/02791072.2013.803647. 
  10. 10.0 10.1 Coppola, M.; Mondola, R. (2012). "Methoxetamine: From drug of abuse to rapid-acting antidepressant". Medical Hypotheses. doi:10.1016/j.mehy.2012.07.002.  edit
  11. Wood, D. M.; Davies, S.; Puchnarewicz, M.; Johnston, A.; Dargan, P. I. (2011). "Acute toxicity associated with the recreational use of the ketamine derivative methoxetamine". European Journal of Clinical Pharmacology 68 (5): 853–856. PMID 22205276. doi:10.1007/s00228-011-1199-9.  edit
  12. 12.0 12.1 Shields, J. E.; Dargan, P. I.; Wood, D. M.; Puchnarewicz, M.; Davies, S.; Waring, W. S. (2012). "Methoxetamine associated reversible cerebellar toxicity: Three cases with analytical confirmation". Clinical Toxicology 50 (5): 438–440. PMID 22578175. doi:10.3109/15563650.2012.683437.  edit
  13. 13.0 13.1 "Pair hospitalised after taking designer drug mexxy". BBC News. April 7, 2014. 
  14. Dargan, P.; Tang, H. (2014). "Three months of methoxetamine administration is associated with significant bladder and renal toxicity in mice". Clinical Toxicology. 
  15. McPherson, P. (2012-02-13). "Health alert over drug sold as 'safe ketamine'". London: The Independent. Retrieved 2012-02-18. 
  17. Johnson, Wesley (2012-03-06). "Bid to ban 'safe' drug Methoxetamine after deaths". The Independent (London). Retrieved 2012-05-12. 
  18. "Statement of evidence - methoxetamine" (PDF). UK Home Office. 2012-02-23. Retrieved 2012-03-29. 
  19. "Methoxetamine". Home Office UK. Retrieved 2012-05-17. 
  20. "Home Secretary's response to the ACMD's advice on methoxetamine". UK Home Office. 2012-03-28. Retrieved 2012-03-28. 
  21. "Home Office circular 004-2013". UK Home Office. 2013-02-20. Retrieved 2013-02-27. 
  22. "Resolution of the Government of the Russian Federation on October 6, 2011 N 822". Retrieved 2012-02-20.  (Russian)
  23. "Ordinance on the lists of narcotic drugs, psychotropic substances, precursors and auxiliary chemicals". Retrieved 2012-02-20.  (German)
  24. "薬事法指定薬物 東京都福祉保健局". Retrieved 2012-06-25.  (Japanese)
  25. "Narkotika-klassning av sex nya substanser". Retrieved 2013-11-26.  (Swedish)
  26. Beaumont-Thomas, B. (2012-01-18). "Methoxetamine is a new chemical analogue of ketamine. It's legal, it's cheap and it's trippy as hell - but is it safe?" (249). London, UK: Mixmag. p. 60. 
  27. Miller, A. (2011-02-11). "We Interviewed the Inventor of Roflcoptr, the New Drug Britain's Panicking About". Vice Magazine. Retrieved 2011-02-11. 
  28. "Legal high drug 'mexxy' banned under new government powers". The Guardian (London). 28 March 2012. 
  29. Corazza, O. et al. (2012). "Phenomenon of New Drugs on the Internet: The Case of Ketamine Derivative Methoxetamine". Human Psychopharmacology: Clinical and Experimental 27 (2): 145–149. PMID 22389078. doi:10.1002/hup.1242.  edit
  30. Southern Association of Forensic Scientists

External links

Personal tools

Lycaeum IRC Chat
TheAntiDrug Diaspora
Starting Points