2,3-MDMA (hydrochloride) (CAS 168968-01-2) | Cayman Chemical
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2,3-MDMA (hydrochloride)

Item № 13970
CAS № 168968-01-2
Purity ≥98%
product image
                (CAS 168968-01-2)

Formulation:  A crystalline solid

SIZE PRICE QUANTITY SUBTOTAL
CART TOTAL
     5 mg $29.00 0.00
     10 mg $55.00 0.00
     50 mg $232.00 0.00

Pricing updated 2018-11-16. Prices are subject to change without notice.

Description
Synonyms
  • 2,3-Methylenedioxymethylamphetamine

2,3-MDMA is an aromatic positional isomer of 3,4-MDMA (ecstasy, Item No. 13971), a euphoric entactogen that is illegal in most countries and is regulated (Schedule I) in the United States.1,2 While 2,3-MDMA exhibits a similar potency to 3,4-MDMA for inhibition of the noradrenalin transporter (IC50s = 6.2 and 6.6 μM, respectively), it is less potent than 3,4-MDMA for inhibition of the serotonin transporter (IC50s = 82 μM and 34.8 μM, respectively).3 This compound is intended for forensic and research purposes only.

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Technical Information
Formal Name
N,α-dimethyl-1,3-benzodioxole-4-ethanamine, monohydrochloride
CAS Number
168968-01-2
Synonyms
  • 2,3-Methylenedioxymethylamphetamine
Molecular Formula
C11H15NO2 • HCl
Formula Weight
229.7
Purity
≥98%
Formulation
A crystalline solid
λmax
234, 283 nm
SMILES
CC(NC)CC1=C(OCO2)C2=CC=C1.Cl
InChI Code
InChI=1S/C11H15NO2.ClH/c1-8(12-2)6-9-4-3-5-10-11(9)14-7-13-10;/h3-5,8,12H,6-7H2,1-2H3;1H
InChI Key
QSEQMDJEMZTQSW-UHFFFAOYSA-N

Warning - this product is not for human or veterinary use.

Shipping & Storage
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
Stability
≥ 2 years
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Additional Information

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References & Product Citations
Product Description References

1. Casale, J.F., Hays, P.A., and Klein, R.F.X. Synthesis and characterization of the 2,3-methylenedioxyamphetamines J.Forensic Sci. 40(3), 391-400 (1995).

2. Chakraborty, K., Neogi, R., and Basu, D. Club drugs: Review of the “rave” with a note of concern for the Indian scenario Indian J. Med. Res. 133, 594-604 (2011).

3. Montgomery, T., Buon, C., Eibauer, S., et al. Comparative potencies of 3,4-methylenedioxymethamphetamine (MDMA) analogues as inhibitors of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines British Journal of Pharmacology 152, 1121-1130 (2007).

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