Description: Inhibitor of 5-HT and dopamine uptake; hallucinogenic
Alternative Names: Methylenedioxymethamphetamine hydrochloride
Chemical Name:N,α,-Dimethyl-3,4-methylenedioxyphenethylamine hydrochloride
Purity: ≥98% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Hallucinogenic compound that inhibits 5-HT and dopamine uptake.
Technical Data
M. Wt
229.7
Formula
C11H15NO2.HCl
Storage
Store at RT
Purity
≥98% (HPLC)
CAS Number
92279-84-0
PubChem ID
71285
InChI Key
LUWHVONVCYWRMZ-UHFFFAOYSA-N
Smiles
CC(NC)CC1=CC(OCO2)=C2C=C1.Cl
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
water
22.97
100
Preparing Stock Solutions
The following data is based on the product molecular weight 229.7. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
4.35 mL
21.77 mL
43.54 mL
5 mM
0.87 mL
4.35 mL
8.71 mL
10 mM
0.44 mL
2.18 mL
4.35 mL
50 mM
0.09 mL
0.44 mL
0.87 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Iravaniet al (2000) Direct effects of 3,4-methylenedioxymethamphetamine (MDMA) on serotonin or dopamine release and uptake in the caudate putamen, nucleus accumbens, substantia nigra pars reticulata, and the dorsal raphe nucleus slices. Synapse 36 275 PMID: 10819905
Fleckensteinet al (2007) New insights into the mechanism of action of amphetamines. Annu.Rev.Pharmacol.Toxicol. 47 681 PMID: 17209801
Boyleet al (2007) MDMA ("ecstasy") suppresses the innate IFN-γ response in vivo: a critical role for the anti-inflammatory cytokine IL-10. Eur.J.Pharmacol. 572 228 PMID: 17689526