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«Δ^1 /cis or /trans Tetrahydrocannabinol»
CSA Names: Δ1 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,7,8,10a-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: 1972-08-3
ChemSpider: 4479482
PubChem: 16078
Wikipedia: Tetrahydrocannabinol
Erowid: Cannabis
Drugs-Forum:
Bluelight: Tetrahydrocannabinol
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/h11-13,16-17,22H,5-10H2,1-4H3/t16?,17-/m1/s1
Standard InChI key: CYQFCXCEBYINGO-ZYMOGRSISA-N
SMILES: CCCCCc1cc(O)c2c(c1)OC([C@H]1C2C=C(C)CC1)(C)C
Tags: USCSA,cannabinoid
 
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delta-9-thc ms.pdf EI MS Agilent MSD
Delta1 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-9-THC.pdf EI MS UV Used with permission of CND Analytical. From "Analytical Profiles of the Hallucinogens"
Delta-9-THC IRD.bmp GC IRD Used with Permission of Oklahoma State Bureau of Investigation, Forensic Science Center, Controlled Substances Laboratory.
Vendor ID URL
Cerilliant T-047 http://www.cerilliant.com/shoponline/Item_Details.aspx?itemno=b045e054-8aad-48f0-9047-700438e8374b
Grace Davison (Alltech) 01387 https://grace.com/pharma-and-biotech/en-us/Pages/Drug-Standards.aspx
Lipomed THC-135 http://www.lipomed.com/index.php?eid=57§ion=mediadir&cmd=detail
Sigma Aldrich T2386-25MG http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=T2386|SIGMA&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC
THC Pharm THC-1295S https://biochem.thc-pharm.de/product_info.php?cPath=5&products_id=95
Toronto Research Chemicals T293200 http://www.trc-canada.com/detail.php?CatNum=T293200
U.S. Pharmacopeia 1651621 http://store.usp.org/OA_HTML/ibeCCtpItmDspRte.jsp?a=b&item=31872
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
CLARIFICATION OF LISTING OF "TETRAHYDROCANNABINOLS" IN SCHEDULE I AND EXEMPTION FROM CONTROL OF CERTAIN INDUSTRIAL PRODUCTS AND MATERIALS DERIVED FROM THE CANNABIS PLANT; FINAL RULES Microgram Bulletin 2003-06-00 Vol 36 (6)
FOLLOWUP TO: CLARIFICATION OF LISTING OF "TETRAHYDROCANNABINOLS" IN SCHEDULE I AND EXEMPTION FROM CONTROL OF CERTAIN INDUSTRIAL PRODUCTS AND MATERIALS DERIVED FROM THE CANNABIS PLANT; FINAL RULES Microgram Bulletin 2003-08-00 Vol 36 (8)
Significance of CYP2C9 genetic polymorphism in inhibitory effect of Δ9-tetrahydrocannabinol on CYP2C9 activity For. Toxicology 2013-01-01 Vol 31 Satoshi Yamaori et. al.
Mass spectrometry of cannabinoids. DOI: 10.1002/jps.2600661025 Journal of Pharm. Sci. 1977-10-01 Vol 66 (10) T. B. Vree
Gas chromatography of cannabinoids : Gas chromatographic behaviour of cis- and trans-tetrahydrocannabinol and isotethrahydrocannabinol. DOI:10.1016/S0021-9673(01)85276-6 Journal of Chromatography 1973-05-01 Vol 79 T.B. Vree, D.D. Breimer, C.A.M. van Ginneken, J.M. van Rossum, N.M.M. Nibbering
Voltammetric determination of Δ9-THC in glassy carbon electrode: An important contribution to forensic electroanalysis For. Sci. Int. 2012-09-10 Vol 221 Marco Antonio Balbino et al
Screening for illicit drugs on Euro banknotes by LC–MS/MS For. Sci. Int. 2011-03-20 Vol 206 Kurt Wimmer, Serge Schneider
Chemical profiling of different hashish seizures by gas chromatography–mass spectrometry and statistical methodology: A case report For. Sci. Int. 2013-10-10 Vol 232 Liv Cadola, Julian Broséus, Pierre Esseiva
Identification of narcotic substances in hemp For. Sci. Int. 1990-05-01 Vol 46 Czesław Szulc, Renata Zarzecka, Andrzej Szuchnik
Some chromatographic aspects of hashish analysis For. Sci. Int. 1974-01-01 Vol 4 Z. Mobarak, N. Zaki, D. Bieniek
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