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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:
64057-70-1
Molecular Weight:
229.70
MDL number:
MFCD00079444
UNSPSC Code:
41116107
PubChem Substance ID:
329817998
NACRES:
NA.24

grade

analytical standard, for drug analysis

Quality Level

200

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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Certificates of Analysis (COA)

Lot/Batch Number
SLBS5006
SLBH5818V
070M8700V
070M8700
070M8700

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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)
Mariana Angoa-Pérez et al.
Journal of neurochemistry, 125(1), 102-110 (2012-12-05)
Mephedrone (4-methylmethcathinone) is a β-ketoamphetamine stimulant drug of abuse with close structural and mechanistic similarities to methamphetamine. One of the most powerful actions associated with mephedrone is the ability to stimulate dopamine (DA) release and block its re-uptake through its
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
Sílvia Font-Mayolas et al.
Addictive behaviors, 38(3), 1605-1609 (2012-12-21)
This study examined the types of polydrug use among Spanish adolescents. 1501 high school students (50.6% female) aged 12 to 17years old (mean age=14.03, SD=1.28), from public schools in the city of Girona (Catalonia, Spain), completed the survey. In the
J Burucker et al.
Fortschritte der Neurologie-Psychiatrie, 80(12), 684-693 (2012-12-12)
Substance-related disorders are clinically and socially very important. In Germany over a million people of varying ages are affected. Depending on the substance and stage of treatment, drugs and different treatment methods are used. Through a literature search we examined
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