M-013
(±)-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
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
41116107
EC Number:
200-659-6
MDL number:
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); Pszichotróp anyag / Psychotropic Substance (Hungary), 78/2022. (XII. 28.) BM rendelet, kontrollierte Droge in Deutschland
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.
(±)-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
Other Notes
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
German
Dieses Produkt fällt unter das Betäubungsmittelgesetz (BtMG). Für eine Bestellung dieses Produktes ist eine Erlaubnis nach § 3 BtMG zwingend erforderlich, es sei denn, es greift eine Ausnahme von der Erlaubnispflicht nach § 4 oder § 26 BtMG.
English
This product is subject to the German Narcotics Act. A permit under Section 3 of the German Narcotics Act is mandatory for ordering this product unless an exemption from the permit requirement under Section 4 or Section 26 of the German Narcotics Act applies.
Dieses Produkt fällt unter das Betäubungsmittelgesetz (BtMG). Für eine Bestellung dieses Produktes ist eine Erlaubnis nach § 3 BtMG zwingend erforderlich, es sei denn, es greift eine Ausnahme von der Erlaubnispflicht nach § 4 oder § 26 BtMG.
English
This product is subject to the German Narcotics Act. A permit under Section 3 of the German Narcotics Act is mandatory for ordering this product unless an exemption from the permit requirement under Section 4 or Section 26 of the German Narcotics Act applies.
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
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
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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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
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
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
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.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M-013-1ML | 04061837819445 |
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