Trifluoroescaline
A synthetic psychedelic compound
Trifluoroescaline (also known as TFE) is a synthetic psychedelic compound belonging to the phenethylamine class. It is structurally related to mescaline, a naturally occurring psychedelic found in the peyote cactus, but with three fluorine atoms replacing hydrogen atoms on the aromatic ring.
Chemical Structure and Properties[edit | edit source]
Trifluoroescaline is a derivative of escaline, which itself is a derivative of mescaline. The chemical structure of trifluoroescaline is characterized by the presence of three fluorine atoms at the 2, 4, and 5 positions of the aromatic ring, and a methoxy group at the 3 position. This trifluorination significantly alters the compound's pharmacological properties compared to its non-fluorinated analogs.
Chemical Formula: C10H10F3NO
Molecular Weight: 217.19 g/mol
Pharmacology[edit | edit source]
The pharmacological effects of trifluoroescaline are not well-documented, as it is a relatively obscure compound with limited research. However, it is believed to act as a serotonin receptor agonist, similar to other psychedelic phenethylamines. The trifluorination may enhance its binding affinity to certain serotonin receptor subtypes, potentially altering its potency and duration of action.
Effects[edit | edit source]
Due to the lack of comprehensive studies, the effects of trifluoroescaline are largely anecdotal. Users have reported experiencing:
- Visual and auditory hallucinations
- Altered perception of time and space
- Euphoria and emotional changes
- Increased introspection and philosophical thinking
The onset of effects typically occurs within 30 to 60 minutes after oral ingestion, with a duration of action lasting 6 to 10 hours.
Safety and Toxicity[edit | edit source]
The safety profile of trifluoroescaline is not well-established. As with many research chemicals, there is a potential for unknown risks and adverse effects. Users should exercise caution and adhere to harm reduction practices when experimenting with such substances.
Legal Status[edit | edit source]
Trifluoroescaline is not specifically scheduled under international drug control treaties. However, its legal status may vary by country, and it could be considered an analog of controlled substances under certain jurisdictions.
History and Research[edit | edit source]
Trifluoroescaline was first synthesized in the late 20th century as part of research into fluorinated phenethylamines. Its synthesis and characterization were documented in chemical literature, but it has not been widely studied in humans or animals.
Also see[edit | edit source]
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD