Phencyclamine

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Phencyclamine
PCPr structure.png
Systematic (IUPAC) name
1-phenyl-N-propylcyclohexanamine
Clinical data
Legal status
Identifiers
CAS Number 18949-81-0
ATC code none
ChemSpider 521518 YesY
Chemical data
Formula C15H23N
Molecular mass 217.349 g/mol
  • N(CCC)C2(c1ccccc1)CCCCC2
  • InChI=1S/C15H23N/c1-2-13-16-15(11-7-4-8-12-15)14-9-5-3-6-10-14/h3,5-6,9-10,16H,2,4,7-8,11-13H2,1H3 YesY
  • Key:KHXNTQRMMGXPQW-UHFFFAOYSA-N YesY
  (verify)

Phencyclamine or PCPr is a dissociative anesthetic drug with hallucinogenic and stimulant effects. It is around the same potency as phencyclidine, although slightly less potent than its ethyl homologue eticyclidine,[1] and has reportedly been sold as a designer drug in Germany and other European countries since the late 1990s.[2][3]

Several other related derivatives have also been encountered, with the n-propyl group of PCPr replaced by 2-methoxyethyl, 2-ethoxyethyl or 3-methoxypropyl groups to form PCMEA, PCEEA and PCMPA respectively.[4][5][6]

PCMEA, PCEEA and PCMPA

See also

References

  1. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  2. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  3. ↑ Christoph Sauer. Phencyclidine Derivatives – A new Class of Designer Drugs. Studies on the Metabolism and Toxicological Analysis. Universität des Saarlandes, 2008
  4. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  5. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  6. ↑ Lua error in package.lua at line 80: module 'strict' not found.


<templatestyles src="Asbox/styles.css"></templatestyles>

Stub icon

This Hallucinogen-related article is a stub. You can help Wikipedia by expanding it.
Retrieved from "https://infogalactic.com/w/index.php?title=Phencyclamine&oldid=5173782"