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Merck

M6403

(±)-3,4-Methylenedioxymethamphetamine hydrochloride

Synonym(s):

(±)-MDMA hydrochloride, DL-3,4-Methylenedioxymethamphetamine, DL-MDMA hydrochloride, Ecstasy, XTC hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C11H15NO2 · HCl
CAS Number:
64057-70-1
Molecular Weight:
229.70
NACRES:
NA.77
PubChem Substance ID:
24897006
UNSPSC Code:
12352116
MDL number:
MFCD00079444
Quality level:
200

Key Documents

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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

SMILES string

Cl[H].CNC(C)Cc1ccc2OCOc2c1

InChI key

LUWHVONVCYWRMZ-UHFFFAOYSA-N

drug control

USDEA Schedule I; Home Office Schedule 1; stupéfiant (France); kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada; psicótropo (Spain); Decreto Lei 15/93: Tabela IIA (Portugal)
kontrollierte Droge in Deutschland

Quality Level

200

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

solubility

H2O: soluble

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

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Related Categories

Biochem/physiol Actions

Hallucinogen; releases serotonin and dopamine from axon terminals; selective serotonergic neurotoxin.

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.

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301,H336

Hazard Classifications

Acute Tox. 3 Oral - STOT SE 3

target_organs

Central nervous system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
0000138195
098M4017V
0000095744
029M4056V
13080212

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Zahra Nazari et al.
Iranian journal of basic medical sciences, 25(9), 1091-1096 (2022-10-18)
Ecstasy is a popular recreational psychostimulant with side effects on the central nervous system. This study examined the corpus striatum tissue of adult rats that received ecstasy during the embryonic period for histological and molecular studies. Rats were divided into
G A Ricaurte et al.
Neuropsychobiology, 42(1), 5-10 (2000-06-27)
The popular recreational drug, (+/-)3, 4-methylenedioxymethamphetamine (MDMA; 'Ecstasy') is a potent and selective brain serotonin (5-HT) neurotoxin in animals. MDMA-induced 5-HT neurotoxicity can be demonstrated using a variety of neurochemical, neuroanatomical and, more recently, functional measures of 5-HT neurons. Although
A Lavelle et al.
British journal of pharmacology, 128(5), 975-980 (1999-11-11)
1. We have investigated the effects of methylenedioxymethamphetamine (MDMA, 'ecstasy') on peripheral noradrenergic neurotransmission in the rat. 2. In rat atrial slices pre-incubated with [3H]-noradrenaline and in the presence of desipramine (1 micronM) to prevent effects of MDMA on basal
M M Iravani et al.
Synapse (New York, N.Y.), 36(4), 275-285 (2000-05-20)
We examined the effects of pressure ejected 3, 4-methylenedioxymethamphetamine (MDMA) from a micropipette on direct chemically stimulated release, and on electrically stimulated serotonin (5-HT) or dopamine (DA) release in the caudate putamen (CPu), nucleus accumbens (NAc), substantia nigra pars reticulata
M I Colado et al.
British journal of pharmacology, 126(4), 911-924 (1999-04-08)
1. We investigated whether dopamine plays a role in the neurodegeneration of 5-hydroxytryptamine (5-HT) nerve endings occurring in Dark Agouti rat brain after 3,4-methylenedioxymethamphetamine (MDMA or 'ecstasy') administration. 2. Haloperidol (2 mg kg(-1) i.p.) injected 5 min prior and 55
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