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4-Phenyl-4-(1-piperidinyl)cyclohexanol

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4-Phenyl-4-(1-piperidinyl)cyclohexanol
Names
IUPAC name
4-Phenyl-4-(1-piperidinyl)cyclohexanol
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C17H25NO/c19-16-9-11-17(12-10-16,15-7-3-1-4-8-15)18-13-5-2-6-14-18/h1,3-4,7-8,16,19H,2,5-6,9-14H2 checkY
    Key: KPRUAZBLIREHPD-UHFFFAOYSA-N checkY
  • InChI=1/C17H25NO/c19-16-9-11-17(12-10-16,15-7-3-1-4-8-15)18-13-5-2-6-14-18/h1,3-4,7-8,16,19H,2,5-6,9-14H2
    Key: KPRUAZBLIREHPD-UHFFFAOYAM
  • OC1CCC(N2CCCCC2)(C3=CC=CC=C3)CC1
  • OC3CCC(c1ccccc1)(N2CCCCC2)CC3
Properties
C17H25NO
Molar mass 259.391 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

4-Phenyl-4-(1-piperidinyl)-cyclohexanol, also known as PPC, is an organic chemical which is a metabolite of phencyclidine (PCP).[1] It can be detected in the hair of PCP users.[2]

PPC has been shown to cause increases in locomotor activity in lab mice.[3]

See also

  • PCHP, another PCP metabolite

References

  1. ^ Nabeshima, Toshitaka; Yamaguchi, Kazumasa; Fukaya, Hiroaki; Hiramatsu, Masayuki; Furukawa, Hiroshi; Kameyama, Tsutomu (1985). "Simultaneous determination of phencyclidine and its major metabolites in biological samples by high-performance liquid chromatography". Research Communications in Substances of Abuse. 6 (2): 65–78.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^ Nakahara, Yuji; Takahashi, Kazunori; Sakamoto, Tomoaki; Tanaka, Akira; Hill, Virginia A.; Baumgartner, Werner A. (1997). "Hair analysis for drugs of abuse XVII. Simultaneous detection of PCP, PCHP, and PCPdiol in human hair for confirmation of PCP use". Journal of Analytical Toxicology. 21 (5): 356–362. doi:10.1093/jat/21.5.356. PMID 9288587.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ "Behavioral effects of phencyclidine and its major metabolite, (trans)4-phenyl-4-(1-piperidinyl)cyclohexanol, in mice".
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