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Names: JWH-210 (primary)
(4-Ethylnaphthalen-1-yl)(1-pentyl-1H-indol-3-yl)methanone (IUPAC)
Molecular formula: C26H27NO
Nominal mass: 369
Average mass: 369.4987
Monoisotopic mass: 369.209265
CAS registry number: 824959-81-1
ChemSpider: 24617616
PubChem: 45270396
Wikipedia: JWH-210
Standard InChI: InChI=1S/C26H27NO/c1-3-5-10-17-27-18-24(22-13-8-9-14-25(22)27)26(28)23-16-15-19(4-2)20-11-6-7-12-21(20)23/h6-9,11-16,18H,3-5,10,17H2,1-2H3
SMILES: CCCCCn1cc(c2c1cccc2)C(=O)c1ccc(c2c1cccc2)CC
Tags: cannabinoid
Property Value Remarks
Property Value Remarks
Location Type Remarks
JWH 210 ATR IR.pdf ATR IR Thermo Nicolet
JWH-210 MS.pdf EI MS Agilent 5975 MS
9001043-0431271-GCMS.pdf EI MS 8-ethylnaphthyl isomer
9001041-0431269-GCMS.pdf EI MS 6-ethylnaphthyl isomer
9001039-0433376-GCMS.pdf EI MS 3-ethylnaphthyl isomer
9001040-0431268-GCMS.pdf EI MS 5-ethylnaphthyl isomer
9001038-0431267-GCMS.pdf EI MS 2-ethylnaphthyl isomer
9001042-0431270-GCMS.pdf EI MS 7-ethylnaphthyl isomer
10644-0425787-GCMS.pdf EI MS Agilent 5973 MSD
JWH 210 3-ethylnaphthyl isomer.pdf SP-GC-IR 3-ethylnaphthyl isomer (solid phase)
JWH 210 5-ethylnaphthyl isomer.pdf SP-GC-IR 5-ethylnaphthyl isomer (solid phase)
JWH 210 6-ethylnaphthyl isomer.pdf SP-GC-IR 6-ethylnaphthyl isomer (solid phase)
JWH 210 7-ethylnaphthyl isomer.pdf SP-GC-IR 7-ethylnaphthyl isomer (solid phase)
JWH 210 8-ethylnaphthyl isomer.pdf SP-GC-IR 8-ethylnaphthyl isomer (solid phase)
JWH-210 edit.pdf SP-GC-IR DiscovIR
Vendor ID URL
Cayman Chemical 9001043 (8-ethylnaphthyl isomer)
Cayman Chemical 10644
Cayman Chemical 9001040 (5-ethylnaphthyl isomer)
Cayman Chemical 9001042 (7-ethylnaphthyl isomer)
Cayman Chemical 9001038 (2-ethylnaphthyl isomer)
Cayman Chemical 9001041 (6-ethylnaphthyl isomer)
Cayman Chemical 9001039 (3-ethylnaphthyl isomer)
Cerilliant NMID984
THC Pharm THC-1278
Toronto Research Chemicals P279900
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
Identification and Quantitation of two benozylindoles AM-694 and (4-methoxyphenyl)(1-pentyl-1H-indol-3-yl)methanone.... Forensic Toxicol. 2011-03-29 Vol 29 (2) Nakajima et al.
Cannabinoidmimetika: Massenspektren und IR-ATR-Spektren neuer Verbindungen aus den Jahren 2009/2010 (German) Toxichem Krimtech 2011-00-00 Vol 78(1) Kneisel et al.
Identification and quantitation of two new naphthoylindole drugs-of-abuse, (1-(5-hydroxypentyl)-1H-indol-3-yl)(naphthalen-1-yl)methanone (AM-2202) and (1-(4-pentenyl For. Toxicology 2012-01-14 Vol 30 Jun’ichi Nakajima et. al.
Identification and quantitation of two benzoylindoles AM-694 and (4-methoxyphenyl)(1-pentyl-1H-indol-3-yl)methanone, and three cannabimimetic naphthoylindoles For. Toxicology 2013-03-29 Vol 31 Jun’ichi Nakajima et. al.
Identification of Synthetic Cannabinoids in Herbal Incense Blends in the United States J. For. Sci. 2012-09-01 Vol 57 Barry K. Logan et al
The emergence and analysis of synthetic cannabinoids Drug Testing and Analysis 2011-08-01 Vol 3 (466-478) Simon Hudson and John Ramsey
Database ID URL
SWGDRUG Monographs JWH-210 Monograph
Cayman Spectral Database
SWGDRUG Mass Spectral Library
Society of Forensic Toxicologists Designer Drug Monographs JWH-210 Monograph
European Project Response to Challenges in Forensic Drug Analyses JWH-210 Monograph
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