| Weight | 195.218 g/mol |
|---|---|
| Formula | C10H13NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
N-Hydroxy mda (74698-47-8)
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- Stimulus effects of N-monoethyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane (MDE) and N-hydroxy-1-(3,4-methylenedioxyphenyl)-2-aminopropane (N-OH MDA) in rats trained to discriminate MDMA from saline (Pharmacology, Biochemistry and Behavior, 1989)
- The pharmacokinetics and liver metabolism of N-hydroxy-3, 4-methylenedioxyamphetamine (NOH MDA) in rats (Life Sciences, 1994)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(CC1=CC2=C(C=C1)OCO2)NO
-
InChIKeyFNDCTJYFKOQGTL-UHFFFAOYSA-N
- Pubchem - N-Hydroxy mda
- Wikipedia - N-hydroxy-3,4-methylenedioxyamphetamine
3,4-Methylenedioxy-N-hydroxyamphetamine (MDOH, MDH, N-hydroxytenamphetamine) is an entactogen, psychedelic, and stimulant of the phenethylamine and amphetamine chemical classes. It is the N-hydroxy homologue of MDA, and the N-desmethyl homologue of MDHMA. MDOH was first synthesized and assayed by Alexander Shulgin.
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N-Hydroxy mda
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