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N-Hydroxy-MDA Hydrochloride

CAS No.
74341-83-6
Chemical Name:
N-Hydroxy-MDA Hydrochloride
Synonyms
N-Hydroxy-MDA Hydrochloride;N-hydroxy MDA (hydrochloride) (exempt preparation)
CBNumber:
CB12700686
Molecular Formula:
C10H14ClNO3
Molecular Weight:
231.67606
MDL Number:
MFCD00171386
MOL File:
74341-83-6.mol
MSDS File:
SDS
Last updated:2026-05-27 23:19:50

N-Hydroxy-MDA Hydrochloride Properties

solubility DMF: 10 mg/ml
DMSO: 10 mg/ml
Ethanol: 15 mg/mlPBS (pH 7.2): 5 mg/ml
FDA UNII R0H604RFC0

SAFETY

Risk and Safety Statements

N-Hydroxy-MDA Hydrochloride price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 13958 N-hydroxy MDA (hydrochloride) ≥95% 74341-83-6 5mg $41 2026-04-30 Buy
Cayman Chemical 15688 N-hydroxy MDA (hydrochloride) (exempt preparation) ≥95% 74341-83-6 1mg $69 2026-04-30 Buy
Cayman Chemical 13958 N-hydroxy MDA (hydrochloride) ≥95% 74341-83-6 10mg $75 2026-04-30 Buy
Cayman Chemical 13958 N-hydroxy MDA (hydrochloride) ≥95% 74341-83-6 50mg $312 2026-04-30 Buy
American Custom Chemicals Corporation CHM0293115 N-HYDROXY-3,4-METHYLENEDIOXYAMPHETAMINE HYDROCHLORIDE 95.00% 74341-83-6 5MG $495.94 2021-12-16 Buy
Product number Packaging Price Buy
13958 5mg $41 Buy
15688 1mg $69 Buy
13958 10mg $75 Buy
13958 50mg $312 Buy
CHM0293115 5MG $495.94 Buy

N-Hydroxy-MDA Hydrochloride Chemical Properties, Uses, Production

Description

3,4-Methylenedioxyamphetamine (MDA) is psychedelic and entactogenic drug that is scheduled as a controlled substance in the United States. N-hydroxy-MDA is an analog of MDA (, hydrochloride form) which inhibits reuptake of noradrenaline (IC50 = 87.8 μM) more effectively than serotonin (IC50 = 215 μM). Like MDA, N-hydroxy-MDA is regulated in the United States. This product is intended for forensic and research applications.

Uses

N-Hydroxy-MDA is an 3,4-methylenedioxymethamphetamine (M303985) analogue and was studied as a inhibitor of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines.

References

[1] T MONTGOMERY. Comparative potencies of 3,4-methylenedioxymethamphetamine (MDMA) analogues as inhibitors of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines[J]. British Journal of Pharmacology, 2009, 152 7: 1121-1130. DOI: 10.1038/sj.bjp.0707473
[2] MATTHEW J BAGGOTT. Investigating the mechanisms of hallucinogen-induced visions using 3,4-methylenedioxyamphetamine (MDA): a randomized controlled trial in humans.[J]. ACS Applied Bio Materials, 2010: e14074. DOI: 10.1371/journal.pone.0014074

N-Hydroxy-MDA Hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

N-Hydroxy-MDA Hydrochloride N-hydroxy MDA (hydrochloride) (exempt preparation) 74341-83-6