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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=3-Fluoroethamphetamine</id>
	<title>3-Fluoroethamphetamine - Revision history</title>
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	<updated>2026-04-26T20:59:15Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wikimd.org/index.php?title=3-Fluoroethamphetamine&amp;diff=5650187&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=3-Fluoroethamphetamine&amp;diff=5650187&amp;oldid=prev"/>
		<updated>2024-04-23T20:54:21Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:3-Fluoroethamphetamine.svg|3-Fluoroethamphetamine|thumb]] &amp;#039;&amp;#039;&amp;#039;3-Fluoroethamphetamine&amp;#039;&amp;#039;&amp;#039; (&amp;#039;&amp;#039;&amp;#039;3-FEA&amp;#039;&amp;#039;&amp;#039;) is a synthetic molecule of the [[amphetamine]] family. Molecules within this class contain a phenethylamine core featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain with an additional methyl substitution at Rα. 3-FEA incorporates a fluorine atom at the third position of the phenyl ring. The pharmacology of 3-FEA is not well-studied, but it is known to act as a releasing agent for [[serotonin]], [[dopamine]], and [[norepinephrine]], with a preference for serotonin. This action is similar to other compounds within the amphetamine class, which typically produce stimulating, euphoric, and empathogenic effects.&lt;br /&gt;
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==Chemistry==&lt;br /&gt;
3-Fluoroethamphetamine belongs to the [[amphetamine]] class of compounds, characterized by a core structure of phenethylamine. The defining feature of 3-FEA, as its name suggests, is the substitution of a fluorine atom at the third position of the phenyl ring. This modification is thought to affect its pharmacokinetics, potentially altering its potency, duration of action, and metabolic stability compared to its non-fluorinated counterparts.&lt;br /&gt;
&lt;br /&gt;
==Pharmacology==&lt;br /&gt;
The mechanism of action of 3-FEA primarily involves the release of monoamines; [[serotonin]], [[dopamine]], and [[norepinephrine]] from their respective storage vesicles in the brain. This release leads to increased concentrations of these neurotransmitters in the synaptic cleft, contributing to the compound&amp;#039;s psychoactive effects. The presence of the fluorine atom at the third position is believed to influence its affinity and selectivity for the monoamine transporters, possibly leading to its reported preference for serotonin release.&lt;br /&gt;
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==Effects==&lt;br /&gt;
Users of 3-FEA have reported a range of effects, from stimulation, focus, and euphoria to empathy, sociability, and enhanced sensory perception. These effects are consistent with other serotonin-releasing agents but may vary in intensity and duration among individuals due to factors such as dose, individual physiology, and the presence of other substances.&lt;br /&gt;
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==Toxicity and Harm Potential==&lt;br /&gt;
The toxicity and long-term health effects of recreational 3-FEA use are not well understood, due in part to the lack of scientific study on the substance. As with other psychoactive substances, potential risks include neurotoxicity, cardiovascular issues, and psychological dependence. Users are advised to exercise caution and harm reduction practices when experimenting with this compound.&lt;br /&gt;
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==Legal Status==&lt;br /&gt;
The legal status of 3-FEA varies by country, with some jurisdictions having specific legislation controlling its possession, production, and distribution, while in others, it may fall under general psychoactive substance bans.&lt;br /&gt;
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[[Category:Psychoactive drugs]]&lt;br /&gt;
[[Category:Amphetamines]]&lt;br /&gt;
[[Category:Stimulants]]&lt;br /&gt;
{{Substance-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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