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Merck

M-013

Supelco

(±)-MDMA solution

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

Sinónimos:

(±)-3,4-Methylenedioxymethamphetamine

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About This Item

Fórmula empírica (notación de Hill):
C11H15NO2
Número de CAS:
Peso molecular:
193.24
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

Quality Level

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

Referencia del producto
Descripción
Precios

signalword

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

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Nicola C Newton et al.
Journal of psychoactive drugs, 44(5), 372-380 (2013-03-06)
The Climate Schools: Ecstasy module is a universal harm-minimisation school-based prevention program for adolescents aged 14 to 16 years. The program was developed to address the need for Ecstasy prevention given the increasing use of Ecstasy use among young Australians.
Stanley C Flavel et al.
PloS one, 7(12), e52025-e52025 (2012-12-29)
Use of illicit stimulants such as methamphetamine, cocaine, and ecstasy is a significant health problem. The United Nations Office on Drugs and Crime estimates that 14-57 million people use stimulants each year. Chronic use of illicit stimulants can cause neurotoxicity
Céline Eiden et al.
Journal of psychoactive drugs, 45(1), 94-97 (2013-05-11)
Typical scenarios of drug-facilitated sexual assaults usually involve victims having ingested a drink after which they had little, partial or no recollection of events for a period of time. We were surprised by the case of a woman who was
Gabrielle Todd et al.
PloS one, 8(2), e56438-e56438 (2013-02-19)
Use of illicit stimulants such as methamphetamine, cocaine, and ecstasy is an increasing health problem. Chronic use can cause neurotoxicity in animals and humans but the long-term consequences are not well understood. The aim of the current study was to
Clifton Chow et al.
Culture, health & sexuality, 15(3), 311-326 (2013-01-15)
Research shows that sexual minorities are at greater risk for illicit substance use and related harm than their heterosexual counterparts. This study examines a group of active drug users to assess whether sexual identity predicts increased risk of substance use

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