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M5029

Supelco

(±)-3,4-Methylenedioxymethamphetamine hydrochloride solution

analytical standard, for drug analysis

Synonym(s):

DL-3,4-Methylenedioxymethamphetamine hydrochloride solution, DL-MDMA hydrochloride solution, XTC hydrochloride solution

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About This Item

Empirical Formula (Hill Notation):
C11H15NO2 · HCl
CAS Number:
Molecular Weight:
229.70
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard, for drug analysis

Quality Level

drug control

Home Office Schedule 1; stupéfiant (France); kontrollierte Droge in Deutschland; (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

single component solution

storage temp.

2-8°C

SMILES string

Cl.CNC(C)Cc1ccc2OCOc2c1

InChI

1S/C11H15NO2.ClH/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;1H

InChI key

LUWHVONVCYWRMZ-UHFFFAOYSA-N

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General description

3,4-Methylenedioxymethamphetamine is considered as an illicit drug. It stimulates neurons to release serotonin and dopamine.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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N-substituted piperazines abused by humans mimic the molecular mechanism of 3,4-methylenedioxymethamphetamine (MDMA, or 'Ecstasy').
Baumann MH
Neuropsychopharmacology, 30(3), 550-560 (2005)
Melanie Mueller et al.
The Journal of pharmacology and experimental therapeutics, 344(2), 479-488 (2012-12-05)
The neurotoxicity of (±)-3,4-methylenedioxymethamphetamine (MDMA; "Ecstasy") is influenced by temperature and varies according to species. The mechanisms underlying these two features of MDMA neurotoxicity are unknown, but differences in MDMA metabolism have recently been implicated in both. The present study
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.
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

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