Para-Fluorophenylpiperazine: Difference between revisions
CSV import Tags: mobile edit mobile web edit |
CSV import |
||
| Line 1: | Line 1: | ||
{{Short description|Chemical compound}} | |||
{{Chembox | |||
| ImageFile = Para-Fluorophenylpiperazine.png | |||
| ImageSize = 200px | |||
| ImageAlt = Structural formula of para-Fluorophenylpiperazine | |||
| IUPACName = 1-(4-Fluorophenyl)piperazine | |||
| OtherNames = pFPP, 4-FPP | |||
| Section1 = {{Chembox Identifiers | |||
| CASNo = 38212-30-5 | |||
| PubChem = 100501 | |||
| ChemSpiderID = 90712 | |||
| UNII = 0F3X4Q3XUS | |||
| SMILES = c1cc(ccc1N2CCNCC2)F | |||
| InChI = 1S/C10H13FN2/c11-9-1-3-10(4-2-9)13-7-5-12-6-8-13/h1-4,12H,5-8H2 | |||
| InChIKey = YXKTVDFXDRQTKV-UHFFFAOYSA-N | |||
}} | |||
}} | |||
== | ==Overview== | ||
'''Para-Fluorophenylpiperazine''' ('''pFPP''') is a chemical compound belonging to the class of [[piperazine]] derivatives. It is structurally related to other phenylpiperazines, which are known for their psychoactive properties. pFPP has been studied for its potential effects on the [[central nervous system]] and is sometimes used in research settings. | |||
Para-Fluorophenylpiperazine | ==Chemical Structure and Properties== | ||
[[File:Para-Fluorophenylpiperazine.png|thumb|right|200px|Structural formula of para-Fluorophenylpiperazine]] | |||
The chemical structure of para-Fluorophenylpiperazine consists of a piperazine ring substituted with a para-fluorophenyl group. This substitution pattern is responsible for its unique pharmacological properties. The presence of the fluorine atom in the para position of the phenyl ring influences the compound's interaction with various [[neurotransmitter]] receptors. | |||
==Pharmacology== | ==Pharmacology== | ||
Para-Fluorophenylpiperazine acts primarily as a [[serotonin receptor]] agonist, with a particular affinity for the 5-HT1A and 5-HT2A receptors. These interactions are thought to contribute to its psychoactive effects, which can include mood alteration and changes in perception. The compound's activity at these receptors is similar to that of other phenylpiperazines, such as [[mCPP]] and [[TFMPP]]. | |||
==Uses and Applications== | |||
While para-Fluorophenylpiperazine is not approved for medical use, it is sometimes utilized in scientific research to study the effects of serotonin receptor agonists. Its ability to modulate serotonin pathways makes it a useful tool in the investigation of [[psychiatric disorders]] and the development of new therapeutic agents. | |||
== | ==Safety and Legal Status== | ||
The safety profile of para-Fluorophenylpiperazine is not well-established, and its use is generally limited to controlled research environments. In some jurisdictions, it may be classified as a controlled substance due to its potential for abuse and psychoactive effects. Researchers handling pFPP must adhere to appropriate safety protocols to minimize risks. | |||
==Related pages== | |||
* [[Piperazine]] | * [[Piperazine]] | ||
* [[Serotonin receptor]] | * [[Serotonin receptor]] | ||
* [[ | * [[Phenylpiperazine]] | ||
* [[ | * [[Psychoactive drug]] | ||
[[Category:Phenylpiperazines]] | |||
[[Category:Serotonin receptor agonists]] | |||
[[Category:Chemical compounds]] | [[Category:Chemical compounds]] | ||
Revision as of 17:42, 18 February 2025
Chemical compound
| Chemical Compound | |
|---|---|
| Identifiers | |
| CAS Number | |
| PubChem CID | |
| ChemSpider ID | |
| UNII | |
| ChEBI | |
| ChEMBL | |
| Properties | |
| Chemical Formula | |
| Molar Mass | |
| Appearance | |
| Density | |
| Melting Point | |
| Boiling Point | |
| Hazards | |
| GHS Pictograms | [[File:|50px]] |
| GHS Signal Word | |
| GHS Hazard Statements | |
| NFPA 704 | [[File:|50px]] |
| References | |
Overview
Para-Fluorophenylpiperazine (pFPP) is a chemical compound belonging to the class of piperazine derivatives. It is structurally related to other phenylpiperazines, which are known for their psychoactive properties. pFPP has been studied for its potential effects on the central nervous system and is sometimes used in research settings.
Chemical Structure and Properties
The chemical structure of para-Fluorophenylpiperazine consists of a piperazine ring substituted with a para-fluorophenyl group. This substitution pattern is responsible for its unique pharmacological properties. The presence of the fluorine atom in the para position of the phenyl ring influences the compound's interaction with various neurotransmitter receptors.
Pharmacology
Para-Fluorophenylpiperazine acts primarily as a serotonin receptor agonist, with a particular affinity for the 5-HT1A and 5-HT2A receptors. These interactions are thought to contribute to its psychoactive effects, which can include mood alteration and changes in perception. The compound's activity at these receptors is similar to that of other phenylpiperazines, such as mCPP and TFMPP.
Uses and Applications
While para-Fluorophenylpiperazine is not approved for medical use, it is sometimes utilized in scientific research to study the effects of serotonin receptor agonists. Its ability to modulate serotonin pathways makes it a useful tool in the investigation of psychiatric disorders and the development of new therapeutic agents.
Safety and Legal Status
The safety profile of para-Fluorophenylpiperazine is not well-established, and its use is generally limited to controlled research environments. In some jurisdictions, it may be classified as a controlled substance due to its potential for abuse and psychoactive effects. Researchers handling pFPP must adhere to appropriate safety protocols to minimize risks.
