N-hydroxy MDA (hydrochloride) (CAS 74341-83-6) | Cayman Chemical
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N-hydroxy MDA (hydrochloride)

Item № 13958
CAS № 74341-83-6
Purity ≥95%

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 2018-05-26. Prices are subject to change without notice.

Description
Synonyms
  • MDOH
  • N-hydroxy-3,4-Methylenedioxyamphetamine

3,4-Methylenedioxyamphetamine (MDA) is psychedelic and entactogenic drug that is scheduled as a controlled substance in the United States.1 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).2 Like MDA, N-hydroxy-MDA is regulated in the United States. This product is intended for forensic and research applications.

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Technical Information
Formal Name
N-hydroxy-α-methyl-1,3-benzodioxole-5-ethanamine, monohydrochloride
CAS Number
74341-83-6
Synonyms
  • MDOH
  • N-hydroxy-3,4-Methylenedioxyamphetamine
Molecular Formula
C10H13NO3 • HCl
Formula Weight
231.7
Purity
≥95%
Formulation
A crystalline solid
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
Schedule
I

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. Baggott, M.J., Siegrist, J.D., Galloway, G.P., et al. Investigating the mechanisms of hallucinogen-induced visions using 3,4-methylenedioxyamphetamine (MDA): A randomized controlled trial in humans. PLoS One 5(12), 1-13 (2010).

2. 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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