An Analytical Reference Standard
Features
  • This product has been formulated as an exempt preparation which meets criteria established by the US DEA
  • Possession of a DEA Controlled Substance registration is not necessary nor is a DEA 222 form required to purchase this product
  • This product is intended to be used as an analytical reference standard
  • Bulk material is available for academic research at qualified institutions; please contact our sales department for pricing
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N-hydroxy MDA (hydrochloride) (exempt preparation)

Item No. 15688

Exempt Product (US)
Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • MDOH
  • N-hydroxy-3,4-Methylenedioxyamphetamine
Technical Information
Formal Name
N-hydroxy-α-methyl-1,3-benzodioxole-5-ethanamine, monohydrochloride
CAS Number
74341-83-6
Molecular Formula
C10H13NO3 • HCl
Formula Weight
231.7
Purity
≥95%
Formulation
A 1 mg/ml solution in acetonitrile
λmax
236, 287 nm
SMILES
CC(NO)CC1=CC(OCO2)=C2C=C1.Cl
InChi Code
InChI=1S/C10H13NO3.ClH/c1-7(11-12)4-8-2-3-9-10(5-8)14-6-13-9;/h2-3,5,7,11-12H,4,6H2,1H3;1H
InChi Key
DMBCJQVFXIKFJX-UHFFFAOYSA-N
Regulatory Information
DEA Exempt Notification
This product is a DEA exempt preparation of a scheduled compound - does not require DEA Controlled Substance registration or DEA 222 form. For alternate sizes please contact sales.
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
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    1 mg

    $69

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    Product Description

    N-hydroxy MDA is an analog of MDA (Item No. 11554, hydrochloride form) which inhibits reuptake of noradrenaline (IC50 = 87.8 μM) more effectively than serotonin (IC50 = 215 μM).1 Like MDA, N-hydroxy MDA is regulated in the United States. This product is intended for forensic and research applications.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. 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. Br. J. Pharmacol. 152(7), 1121-1130 (2007).