Cannabicyclohexanol

Structural formula
General
Surname	Cannabicyclohexanol
other names	CP 47,497-C8; (C8) -CP 47,497; 2 - [(1 S , 3 R ) -3-Hydroxycyclohexyl] -5- (2-methylnonan-2-yl) phenol;
Molecular formula	C 22 H 36 O 2
External identifiers / databases
EC number	804-093-6
ECHA InfoCard	100.230.839
PubChem	12788230
ChemSpider	26668381
Wikidata	Q1033359
Drug information
Drug class	Cannabinoid mimetic
Mechanism of action	Cannabinoid receptor CB 1 - agonist
properties
Molar mass	332.52 g · mol -1
safety instructions
GHS labeling of hazardous substances Caution
H and P phrases	H: 319
	P: ?
	As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

Cannabicyclohexanol is a cannabinoid receptor agonist and an analog of the cannabinoid CP-47,497 , which was developed by the Pfizer company in the 1980s . Due to the close analogy (only the side chain was extended by a methyl group ) cannabicyclohexanol is also referred to in the literature as CP 47,497-C8 or (C8) -CP 47,497 .

On January 19, 2009, employees at the University of Freiburg announced that cannabicyclohexanol is the main active ingredient of the drug Spice .

Legal position

Germany

As a pharmacologically active substance , cannabicyclohexanol was classified as a marketable but not prescription narcotic in Germany with its entry in Annex II of the Narcotics Act (BtMG) with effect from January 22, 2009 . Limited to one year, any form of unauthorized manufacture, trade and possession is prohibited.

Austria

Cannabicyclohexanol is not subject to the Austrian narcotics law. However, the sale of "smoking mixtures" with synthetic cannabinoids has been banned since December 18, 2008 in accordance with Section 1, Paragraph 1, Item 5 of the Medicines Act . Furthermore, since February 1, 2012, the substance has been subject to the “Federal Act on Protection against Health Risks in Connection with New Psychoactive Substances” (New Psychoactive Substances Act, NPSG), provided it is intended for human consumption.

Switzerland

With the entry into force of the revised Narcotics Ordinance by Swissmedic on December 1, 2010, cannabicyclohexanol will be subject to the Narcotics Act and will therefore be illegal from that point on. Importation, possession, distribution etc. are punished according to the Narcotics Act.

Individual evidence

↑ Template: CL Inventory / not harmonized There is not yet a harmonized classification for this substance . A label of [No public or meaningful name is available] in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on April 9, 2018, is reproduced from a self-classification by the distributor .
^ University of Freiburg: Main active ingredient of "Spice" identified .
↑ 22nd BtMÄndV of January 19, 2009 ( BGBl. I p. 49 ).
↑ Text of the Swissmedic Narcotics Ordinance, which came into force on December 1, 2010, as a PDF .
↑ Text of the Swiss Narcotics Act as PDF. Relevant criminal provisions: Art. 19 and following. .

[1] Template: CL Inventory / not harmonized There is not yet a harmonized classification for this substance . A label of [No public or meaningful name is available] in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), accessed on April 9, 2018, is reproduced from a self-classification by the distributor .

[2] University of Freiburg: Main active ingredient of "Spice" identified .

[BGBL_vom_090119-3] 22nd BtMÄndV of January 19, 2009 ( BGBl. I p. 49 ).

[4] Text of the Swissmedic Narcotics Ordinance, which came into force on December 1, 2010, as a PDF .

[5] Text of the Swiss Narcotics Act as PDF. Relevant criminal provisions: Art. 19 and following. .