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«Alpha-methyltryptamine»
CSA Names: Alpha-methyltryptamine
AMT
CSA Location: Schedule I Section (d) Subsection (16) DEA code 7432
CSA History: 69 FR 58050 added (and renumbered subsequent entries) effective 29 Sep 2004
Names: 1-(1H-Indol-3-yl)propan-2-amine (IUPAC)
Molecular formula: C11H14N2
Nominal mass: 174
Average mass: 174.2423
Monoisotopic mass: 174.115699
CAS registry number: 299-26-3
ChemSpider: 8930
PubChem: 9287
Wikipedia: alpha-Methyltryptamine
Erowid: AMT
Drugs-Forum: AMT
Bluelight: AMT
Standard InChI: InChI=1S/C11H14N2/c1-8(12)6-9-7-13-11-5-3-2-4-10(9)11/h2-5,7-8,13H,6,12H2,1H3
Standard InChI key: QSQQQURBVYWZKJ-UHFFFAOYSA-N
SMILES: CC(Cc1c[nH]c2c1cccc2)N
Tags: USCSA,TiHKAL,tryptamine
 
Property Value Remarks
pKa ~10.8 ionization type: +H calculated value ACD/Labs software
solubility soluble in chloroform and dilute acetic acid Clarke's 3rd Edition
Location Type Remarks
AMT Base.pdf ATR IR Thermo Nicolet
AMT HCl.pdf ATR IR Thermo Nicolet
AMT.pdf EI MS Agilent MSD
Alpha-methyltryptamine MS (NIST).pdf EI MS Used with 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.
alpha-Methyltryptamine IRD.bmp GC IRD Used with Permission of Oklahoma State Bureau of Investigation, Forensic Science Center, Controlled Substances Laboratory.
AMT GCMS Cayman.pdf MS Cayman Spectral Library
Alpha methyltryptamine (AMT)-raman.pdf RAMAN GBI DOFS
alpha-methyltryptamine (racemic)-raman.pdf RAMAN GBI DOFS
Vendor ID URL
Alfa Aesar 43642 http://www.alfa.com/en/catalog/43642
Biosynth M-4625 http://www.biosynth.com/en/products/life-science/other-biochemicals/products/M-4625.html
Biosynth M-4620 http://www.biosynth.com/en/products/life-science/other-biochemicals/products/M-4620.html
Biosynth M-4623 http://www.biosynth.com/en/products/life-science/other-biochemicals/products/M-4623.html
Cayman Chemical 11135 https://www.caymanchem.com/app/template/Product.vm/catalog/11135
Cerilliant NMID991 http://www.cerilliant.com/ShopOnline/Item_Details.aspx?itemno=5f6a4f75-5194-4177-afa2-2be7b36240d3
Grace Davison (Alltech) 01647 https://grace.com/pharma-and-biotech/en-us/Pages/Drug-Standards.aspx
LGC NMIAD991 http://www.lgcstandards.com/epages/LGC.sf/en_GB/?ObjectPath=/Shops/LGC/Products/NMIAD991
Title Publication Date Vol. Iss. Page(s) Remarks
TiHKAL • info Isomer Design
TRYPTAMINES Microgram Bulletin 1994-09-00 Vol 27 (9) Chamakuru
AMT And 5-Methoxy-N,N-diisopropyltryptamine Proposed For Emergency Control By DEA Journal of CLIC 2003-01-00 Vol 13 (1) Law Enforcement Restricted
The Identification of 5-Methoxy-alpha-methyltryptamine (5-MeO-AMT) Microgram Journal 2003-12-00 Vol 1 (3-4) Michelle M. Zimmerman
Analysis and Characterization of Designer Tryptamines using Electrospray Ionization Mass Spectrometry (ESI-MS) Microgram Journal 2005-12-00 Vol 3 (3-4) Sandra E. Rodriguez Cruz
- SCHEDULING UPDATE- Microgram Bulletin 2003-05-00 Vol 36 (5) ALPHA-METHYLTRYPTAMINE (AMT) AND 5-METHOXY-N, N-DIISOPROPYL-TRYPTAMINE (5-MeO-DIPT, "FOXY") ARE EMERGENCY SCHEDULED
Trippin’ on Tryptamines The Emergence of Foxy and AMT as Drugs of Abuse (Law enforcement restricted publication) Microgram Bulletin 2002-12-00 Vol 35 (12) No analytical data
Identification of (2-aminopropyl)indole positional isomers in forensic samples. DOI: 10.1002/dta.1508 Drug Testing and Analysis 2014-07-01 Vol 6 (7-8) Kenneth R. Scott et al
AMT (3-(2-aminopropyl)indole) and 5-IT (5-(2-aminopropyl)indole): an analytical challenge and implications for forensic analysis. DOI: 10.1002/dta.1420 Drug Testing and Analysis 2013-03-01 Vol 5 (3) Elliot, Brandt, Freeman, and Archer
Analysis of the chemical drugs among structural isomer. DOI: 10.1248/yakushi.126.815 Yakugaku Zasshi 2006-01-01 Vol 126 (9) Doi K, Miyazawa M, Fujii H, Kojima T.
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