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«Δ^6 /cis or /trans Tetrahydrocannabinol»
CSA Names: Δ6 cis or trans Tetrahydrocannabinol
CSA Location: Schedule I Section (d) Subsection (31)
CSA History: Scheduled in Public Law 91-513, the original CSA of 1970
Names: (6aR)-6,6,9-Trimethyl-3-pentyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-ol (IUPAC)
Molecular formula: C21H30O2
Nominal mass: 314
Average mass: 314.4617
Monoisotopic mass: 314.224580
CAS registry number: 5957-75-5
ChemSpider: 4479481
PubChem: 5321845
Wikipedia:
Erowid:
Drugs-Forum:
Bluelight:
Standard InChI: InChI=1S/C21H30O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9,12-13,16-17,22H,5-8,10-11H2,1-4H3/t16?,17-/m1/s1
Standard InChI key: HCAWPGARWVBULJ-ZYMOGRSISA-N
SMILES: CCCCCc1cc(O)c2c(c1)OC([C@H]1C2CC(=CC1)C)(C)C
Tags: USCSA,cannabinoid
 
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delta8THC.pdf EI MS Agilent MSD
Delta-6 cis or trans Tetrahydrocannabinol (NIST).pdf EI MS Used with the permission of NIST Mass Spectrometry Data Center Collection (C) 2008 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved.
Delta-8-THC.pdf EI MS UV Used with permission of CND Analytical. From "Analytical Profiles of the Hallucinogens"
DELTA-8-THC IRD.bmp GC IRD Used with Permission of Oklahoma State Bureau of Investigation, Forensic Science Center, Controlled Substances Laboratory.
Vendor ID URL
Cayman Chemical 14042 https://www.caymanchem.com/app/template/Product.vm/catalog/14042
Cerilliant T-032 http://www.cerilliant.com/shoponline/Item_Details.aspx?itemno=10c5d53b-1d46-44ef-b61a-dc848fb3b308
Grace Davison (Alltech) 01386 https://grace.com/pharma-and-biotech/en-us/Pages/Drug-Standards.aspx
Lipomed THC-134 http://www.lipomed.com/index.php?eid=128§ion=mediadir&cmd=detail
Sigma Aldrich T2511 http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=T2511|SIGMA&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC
THC Pharm THC-1091 https://biochem.thc-pharm.de/product_info.php?cPath=5&products_id=42
Toronto Research Chemicals T293240 http://www.trc-canada.com/detail.php?CatNum=T293240
Title Publication Date Vol. Iss. Page(s) Remarks
A new pyrazole-carboxamide type synthetic cannabinoid AB-CHFUPYCA [N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(cyclohexylmethyl)-3-(4-fluorophenyl)-1H-pyrazole-5-carboxamide] identified in illegal product Forensic Toxicology 2015-07-01 Vol 33 (367-373) Nahoko Uchiyama et al
Consideration of the major cannabinoid agonists 2009-07-00 Advisory Council on the Misuse of Drugs
Understanding the Spice phenomenon 2009-00-00 European Monitoring Centre for Drugs and Drug Addiction
Further consideration of the synthetic cannabinoids 2012-10-18 Advisory Council on the Misuse of Drugs
GC–MS and FTIR evaluation of the six benzoyl-substituted-1-pentylindoles: Isomeric synthetic cannabinoids Talanta 2014-11-01 Vol 129 (171-182) Forrest T. Smitha et al
Detection and identification of the new potential synthetic cannabinoids 1-pentyl-3-(2-iodobenzoyl)indole and 1-pentyl-3-(1-adamantoyl)indole in seized bulk powders in Hungary Forensic Science International 2012-01-01 Vol 214 (27-32) Péter Jankovics et al
Synthetic cannabinoids and cathinones: prevalence and markets Forensic Science Review 2013-03-01 Vol 25 (7-26) Bretteville-Jensen et al
Identification and analytical properties of new synthetic cannabimimetics bearing 2,2,3,3-tetramethylcyclopropanecarbonyl moiety Forensic Science International 2013-03-10 Vol 226 (62-73) Vadim Shevyrin et al
Spice, bath salts, and the U.S. military: the emergence of synthetic cannabinoid receptor agonists and cathinones in the U.S. Armed Forces. 2012-09-01 Loeffler G, Hurst D, Penn A, Yung K
Synthetic cannabinoid and marijuana exposures reported to poison centers Hum Exp Toxicol 2012-10-31 (1006-1011) MB Forrester et al
Separation and structural characterization of the synthetic cannabinoids JWH-412 and 1-[(5-fluoropentyl)-1H-indol-3yl]-(4-methylnaphthalen-1-yl)methanone using GC–MS, NMR analysis and a flash chromato Forensic Science International 2012-07-12 Vol 220 (e17-e22) Bjoern Moosmann et al
Cannabinoid chemistry: an overview Cannabinoids as Therapeutics 2005-01-01 (23-46) Lumír O. Hanuš and Raphael Mechoulam
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