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«3,4-Methylenedioxyamphetamine»
CSA Names: 3,4-Methylenedioxyamphetamine
CSA Location: Schedule I Section (d) Subsection (10) DEA code 7400
CSA History: Scheduled in Public Law 91-513, the original CSA of 1970
Names: MDA (other)
1-(1,3-Benzodioxol-5-yl)propan-2-amine (IUPAC)
Molecular formula: C10H13NO2
Nominal mass: 179
Average mass: 179.2157
Monoisotopic mass: 179.094629
CAS registry number: 4764-17-4
ChemSpider: 1555
PubChem: 1614
Wikipedia: 3,4-Methylenedioxyamphetamine
Erowid: MDA
Drugs-Forum: MDA
Bluelight: MDA
Standard InChI: InChI=1S/C10H13NO2/c1-7(11)4-8-2-3-9-10(5-8)13-6-12-9/h2-3,5,7H,4,6,11H2,1H3
Standard InChI key: NGBBVGZWCFBOGO-UHFFFAOYSA-N
SMILES: CC(Cc1ccc2c(c1)OCO2)N
Tags: USCSA,PiHKAL,phenethylamine
 
Property Value Remarks
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MDA base.pdf ATR IR Thermo Nicolet
MDA HCl.pdf ATR IR Thermo Nicolet
MDA ms.pdf EI MS Agilent MSD
3,4-Methylenedioxyamphetamine (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.
MDA.pdf EI MS UV FTIR Used with permission of CND Analytical. From "Analytical Profiles of the Hallucinogens"
3,4-Methylenedioxyamphetamine.bmp GC IRD Used with Permission of Oklahoma State Bureau of Investigation, Forensic Science Center, Controlled Substances Laboratory.
MDA GCMS Cayman.pdf MS Cayman Spectral Library
MDA (free base)-raman.pdf RAMAN GBI DOFS
MDA HCl-raman.pdf RAMAN GBI DOFS
Vendor ID URL
Cerilliant M-012 http://www.cerilliant.com/shoponline/Item_Details.aspx?itemno=15d64bbc-c278-4faa-8df0-13d2da2358dd
Cerilliant NMID842 http://www.cerilliant.com/shoponline/Item_Details.aspx?itemno=abf77f29-18a9-491e-8f30-055707deed5b
Grace Davison (Alltech) 01460 https://grace.com/pharma-and-biotech/en-us/Pages/Drug-Standards.aspx
LGC NMIAD842 http://www.lgcstandards.com/epages/LGC.sf/en_GB/?ObjectPath=/Shops/LGC/Products/NMIAD842
Lipomed MDA-79-HC http://www.lipomed.com/index.php?eid=6§ion=mediadir&cmd=detail
Sigma Aldrich M6267 http://www.sigmaaldrich.com/catalog/ProductDetail.do?lang=en&N4=M6267|SIGMA&N5=SEARCH_CONCAT_PNO|BRAND_KEY&F=SPEC
Toronto Research Chemicals M303965 http://www.trc-canada.com/detail.php?CatNum=M303965
U.S. Pharmacopeia 1429000 http://store.usp.org/OA_HTML/ibeCCtpItmDspRte.jsp?a=b&item=19163
Title Publication Date Vol. Iss. Page(s) Remarks
PiHKAL • info Isomer Design
GC-MS ANALYSIS OF PRODUCTS, INTERMEDIATES, AND BY-PRODUCTS IN THE SYNTHESIS OF MDA FROM ISOSAFROLE Microgram Bulletin 1994-06-00 Vol 27 (6) Clark et al.
ANALYSIS OF METHOXY MDA DERIVATIVES SYNTHESIZED FROM NUTMEG OIL AND 3-METHOXY-4,5-METHYLENEDOXYBENZALDEHYDE Microgram Bulletin 1995-11-00 Vol 28 (11) Clark et al.
Instrumental Separation of 3,4-Methylenedioxyamphetamine (MDA) from 1-(3,4-Methylenedioxyphenyl)-2-propanol, a Co-Eluting Compound Microgram Journal 2003-06-00 Vol 1 (1-2) Barbara A. Vohlken and Stephen M. Layton
The Separation and Identification of 3,4-Methylenedioxyamphetamine Derivatives (MDA, MDMA, MDEA, and MBDB) in Tablets (Law enforcement restricted publication) Microgram Bulletin 1999-01-00 Vol 32 (1) Nissim et al.
THE ANALYSIS OF ECSTASY (MDMA ANALOGS AND HOMOLOGS) USING AN FT/IR SPECTROPHOTOMETER WITH MICROSCOPE ATTACHMENT (Law enforcement restricted publication) Microgram Bulletin 1998-12-00 Vol 31 (12) John Fox
ANALYTICAL PROPERTIES OF N-HYDROXY-3,4-METHYLENEDIOXYMETHAMPHETAMINE ("FLEA"), A POTENTIAL NEW STREET DRUG (Law enforcement restricted publication) Microgram Bulletin 1996-01-00 Vol 29 (1) Noggle et al.
ARTIFACTS IN THE ANALYSIS OF AMPHETAMINE AND MDA (Law Enforcement Restricted Publication) Microgram Bulletin 1996-04-00 Vol 29 (4) Anneke J. Poortman-van der Meer
GC-MS AND LIQUID CHROMATOGRAPHIC ANALYSIS OFAMPHETAMINE AND AMPHETAMINE-TYPE PRODUCTS FORMED IN THE REACTION OFARYLPROPENES WITH ACETONITRILE AND SULFURIC ACID (Law Enforcement Restricted Publication) Microgram Bulletin 1995-01-00 Vol 28 (1) F.T. Noggle et al.
Synthesis of 2,3- and 3,4-methylenedioxyphenylalkylamines and their regioisomeric differentiation by mass spectral analysis using GC-MS-MS. DOI: 10.1016/S0379-0738(00)00296-6 For. Sci. Int. 2000-12-11 Vol 114 S Bortha, W Hänsel, P Rösner, Th Junge
Liquid Chromatographic and Mass Spectral Analysis of 1-(3,4-methylenedioxyphenyl)-1-propanamines: Regioisomers of the 3,4-Methylenedioxyamphetamines Journal of Chrom. Sci. 1990-03-01 Vol 28 (3) DeRuiter, Clark, Noggle
Differentiation of Side Chain Isomers of Ring-Substituted Amphetamines Using Gas Chromatography/Infrared/Mass Spectrometry (GC/IR/MS). DOI:10.1520/JFS13259J Journal of Forensic Sciences 1991-03-01 Vol 37 (2) WH Soine 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
The synthesis, mass spectrometric properties and identification of some N,N-di-(β-arylisopropyl)formamides related to the synthesis of ring-modified amphetamines For. Sci. Int. 2011-03-20 Vol 206 Dariusz Błachut et al
Rapid and simple method for direct determination of several amphetamines in seized tablets by GC–FID For. Sci. Int. 2005-09-10 Vol 152 Blagoj Mitrevski, Zoran Zdravkovski
Proton and carbon-13 NMR assignments of 3,4-methylenedioxyamphetamine (MDA) and some analogues of MDA For. Sci. Int. 1997-04-18 Vol 86 Terry A Dal Cason, John A Meyers, David C Lankin
GC-FID optimization and validation for determination of 3,4-methylenedioxymethamphetamine, 3,4-methylenedioxyamphetamine and methamphetamine in ecstasy tablets J. Analytical Chem. 2010-09-01 Vol 65 (9) A. Phonchai, B. Janchawee, S. Prutipanlai, S. Thainchaiwattana
Development of a targeted GC/MS screening method and validation of an HPLC/DAD quantification method for piperazines–amphetamines mixtures in seized material Egyptian J. For. Sci. 2014-09-01 Vol 4 (90-99) Yacine Boumrah et al
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