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M-013

Supelco

(±)-MDMA solution

1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

Synonym(s):

(±)-3,4-Methylenedioxymethamphetamine

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About This Item

Empirical Formula (Hill Notation):
C11H15NO2
CAS Number:
Molecular Weight:
193.24
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

form

liquid

feature

Snap-N-Spike®/Snap-N-Shoot®

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

drug control

Narcotic Licence Schedule D (Switzerland); psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)

concentration

1.0 mg/mL in methanol

technique(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

application(s)

forensics and toxicology

format

single component solution

storage temp.

−20°C

SMILES string

CC(CC1=CC=C(OCO2)C2=C1)NC

InChI

1S/C11H15NO2/c1-8(12-2)5-9-3-4-10-11(6-9)14-7-13-10/h3-4,6,8,12H,5,7H2,1-2H3

InChI key

SHXWCVYOXRDMCX-UHFFFAOYSA-N

General description

This certified Snap-N-Spike® Solution is suitable for use as starting material in calibrators or controls for a variety of LC/MS or GC/MS applications from forensic analysis and clinical toxicology to urine drug testing.

(±)-3,4-Methylenedioxymethamphetamine (MDMA) belongs to the class of racemic amphetamine-type stimulant drugs. It has psychoactive properties and is an active ingredient of the synthetic hallucinogenic drug, ecstasy. It is an illicit drug known by a variety of street names, including "Ecstasy," "E," "X," and "XTC". An analog of the phenethylamine class, MDMA is abused for its euphoric and psychedelic effects.

Application

The Certified Reference Material (CRM) in solution can also be used as follows:
  • Electrochemical detection of morphine and MDMA from human serum and urine samples using a sensitive sensor based on platinum nanoparticles deposited on carbon nanohorns (CNHs)
  • Enantiomeric assessment of seized drugs of amphetamine, methamphetamine, and MDMA by two methods of liquid chromatography coupled with tandem mass spectrometry (MS/MS) and diode array detector (DAD)
  • Development and validation of a stereoselective liquid chromatography-tandem mass spectrometric (LC-MS/MS) procedure for the analysis of MDMA and its metabolites in human plasma samples
  • Matrix-assisted laser desorption/ionization triple quadrupole tandem mass spectrometric (MALDI-QqQ-MS/MS) based analysis of MDMA and its metabolite 3,4-methylenedioxyamphetamine in oral fluid samples
  • Differential pulse voltametric (DPV) identification and quantification of MDMA in seized drug samples using boron-doped diamond electrode (BDDE)

Features and Benefits

  • Fully characterized under ISO/IEC 17025 and ISO 17034 accreditation
  • Accompanied with a comprehensive Certificate of Analysis (CoA) with data on stability, homogeneity, accuracy of concentration, uncertainty, and traceability
  • Rigorously tested through real-time stability studies to ensure accuracy and shelf life
  • Gravimetrically prepared using qualified precision balances to ensure minimal uncertainty
  • Flame sealed under argon into ampoules for long-term shelf life
  • Offered in a convenient, DEA-exempt format to improve laboratory efficiency

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

related product

Product No.
Description
Pricing

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Clara Ros-Simó et al.
Journal of neurochemistry, 125(5), 736-746 (2013-03-26)
Ethanol and 3, 4-Methylenedioxymethamphetamine (MDMA) are popular recreational drugs widely abused by adolescents that may induce neurotoxic processes associated with behavioural alterations. Adolescent CD1 mice were subjected to ethanol intake using the drinking in the dark (DID) procedure, acute MDMA
Tove Abrahamsson et al.
Substance use & misuse, 48(4), 353-357 (2013-02-13)
The aim of the present study was to report independent correlates of ecstasy use in the Swedish general population. Data were drawn from a Swedish national household survey conducted in 2008-2009 on a random, stratified sample of 58,000 inhabitants of
E M O'Sullivan
Community dental health, 29(4), 263-267 (2013-03-16)
This study examines the independent and combined impact of 'alcohol only' and 'alcohol plus drug' abuse on the dental health of Irish alcohol/drug abuse treatment centre residents, comparing their dental caries experience. Four Irish treatment centres were visited periodically over
Amy K Goodwin et al.
The Journal of pharmacology and experimental therapeutics, 345(3), 342-353 (2013-03-22)
(±)-3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy") is a popular drug of abuse. We aimed to characterize the behavioral effects of intragastric MDMA in a species closely related to humans and to relate behavioral effects to plasma MDMA and metabolite concentrations. Single doses of
Re: "Spice, bath salts, and the U.S. Military: the emergence of synthetic cannabinoid receptor agonists and cathinones in the U.S. Armed Forces".
Peter L Platteborze et al.
Military medicine, 178(1), v-v (2013-01-30)

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