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{{short description|Chemical compound}} |
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{{redirect|3CP|CCCP|Soviet Union}} |
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| image = 3C-P_2d-skeletal.svg |
| image = 3C-P_2d-skeletal.svg |
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| width = 200 |
| width = 200 |
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<!--Clinical data--> |
<!--Clinical data--> |
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| tradename = |
| tradename = |
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| legal_DE = NpSG |
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| legal_UK = Class A |
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<!--Identifiers--> |
<!--Identifiers--> |
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| CAS_number_Ref = {{cascite|changed|??}} |
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| CAS_number = |
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| CAS_number = 501700-11-4 |
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| PubChem = 54929142 |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 21106238 |
| ChemSpiderID = 21106238 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = 4KRX4MHV7L |
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<!--Chemical data--> |
<!--Chemical data--> |
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| C=14 | H=23 | N=1 | O=3 |
| C=14 | H=23 | N=1 | O=3 |
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| molecular_weight = 253.34 g/mol |
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| smiles = CC(N)Cc1cc(OC)c(OCCC)c(c1)OC |
| smiles = CC(N)Cc1cc(OC)c(OCCC)c(c1)OC |
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| InChI = 1/C14H23NO3/c1-5-6-18-14-12(16-3)8-11(7-10(2)15)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3 |
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| InChIKey = KKMCHCCXGKYEKJ-UHFFFAOYAK |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C14H23NO3/c1-5-6-18-14-12(16-3)8-11(7-10(2)15)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3 |
| StdInChI = 1S/C14H23NO3/c1-5-6-18-14-12(16-3)8-11(7-10(2)15)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3 |
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'''3C-P''' is a [[psychedelic]] [[phenethylamine]]. It has structural and pharmacodynamic properties similar to the drugs [[mescaline]], [[proscaline]], and [[amphetamine]]. Little information exists on the human [[pharmacology]] of 3C-P, but a |
'''3C-P''' ('''α-Methyl-4-propoxy-3,5-dimethoxyphenethylamine''') is a [[psychedelic drug|psychedelic]] [[phenethylamine]]. It has structural and pharmacodynamic properties similar to the drugs [[mescaline]], [[proscaline]], and [[amphetamine]]. Little information exists on the human [[pharmacology]] of 3C-P, but a psychedelic dosage appears to be 20–40 mg,{{medcn|date=February 2018}} and is accompanied by [[stimulant]] and [[Psychedelic experience|psychedelic]] effects such as visual enhancement and distortion.{{medcn|date=February 2018}} It can be synthesized from [[syringaldehyde]] by reaction with [[n-Propyl iodide|''n''-propyl iodide]] followed by condensation with nitroethane and reduction.<ref>{{cite journal| vauthors = Trachsel D |title=Synthese von neuen (Phenylalkyl)aminen zur Untersuchung von Struktur-Aktivitätsbeziehungen, Mitteilung 1, Mescalin Derivate|journal=Helvetica Chimica Acta|date=September 2002|volume=85|issue=9|pages=3019–3026|doi=10.1002/1522-2675(200209)85:9<3019::AID-HLCA3019>3.0.CO;2-4}}</ref> |
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Chemically 3C-P is 4-propoxy-3,5-dimethoxyamphetamine, with the formula [[carbon|C]]<sub>14</sub>[[hydrogen|H]]<sub>23</sub>[[nitrogen|N]][[oxygen|O]]<sub>3</sub>. Although its name is similar to the psychedelic phenethylamine [[2C-P]], it is much closer in structure to mescaline, and proscaline. 3C-P is the 3-[[carbon]] [[homologous series|homologue]] of proscaline. |
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==See also== |
==See also== |
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*[[Phenethylamine]] |
*[[Phenethylamine]] |
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*[[3C-AL]] |
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*[[3C-MAL]] |
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==References== |
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{{Reflist}} |
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==External links== |
==External links== |
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*[http://www.erowid.org/chemicals/3cp/3cp.shtml Erowid 3C-P Information] |
*[http://www.erowid.org/chemicals/3cp/3cp.shtml Erowid 3C-P Information] |
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[[Category:Substituted amphetamines]] |
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[[Category:Entheogens]] |
[[Category:Entheogens]] |
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[[Category:Drugs not assigned an ATC code]] |
[[Category:Drugs not assigned an ATC code]] |
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[[Category:O- |
[[Category:O-methylated phenols]] |
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{{hallucinogen-stub}} |
{{hallucinogen-stub}} |
Latest revision as of 02:18, 27 June 2023
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Chemical and physical data | |
Formula | C14H23NO3 |
Molar mass | 253.342 g·mol−1 |
3D model (JSmol) | |
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(what is this?) (verify) |
3C-P (α-Methyl-4-propoxy-3,5-dimethoxyphenethylamine) is a psychedelic phenethylamine. It has structural and pharmacodynamic properties similar to the drugs mescaline, proscaline, and amphetamine. Little information exists on the human pharmacology of 3C-P, but a psychedelic dosage appears to be 20–40 mg,[medical citation needed] and is accompanied by stimulant and psychedelic effects such as visual enhancement and distortion.[medical citation needed] It can be synthesized from syringaldehyde by reaction with n-propyl iodide followed by condensation with nitroethane and reduction.[1]
See also
References
- ^ Trachsel D (September 2002). "Synthese von neuen (Phenylalkyl)aminen zur Untersuchung von Struktur-Aktivitätsbeziehungen, Mitteilung 1, Mescalin Derivate". Helvetica Chimica Acta. 85 (9): 3019–3026. doi:10.1002/1522-2675(200209)85:9<3019::AID-HLCA3019>3.0.CO;2-4.
External links