| Weight | 209.245 g/mol |
|---|---|
| Formula | C11H15NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
MMDA (13674-05-0)
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- Animal Pharmacology and Human Psychopharmacology of 3-Methoxy-4,5-Methylenedioxyphenylisopropylamine (MMDA) (Pharmacology, 1973)
- Synthesis of deuterium-labelled standards of ()-DOM and ()-MMDA (Journal of Labelled Compounds and Radiopharmaceuticals, 2007)
- Analysis of 1-(3-Methoxy-4,5-Methylenedioxyphenyl)-2-Propanamine(MMDA)Derivatives Synthesized from Nutmeg Oil and 3-Methoxy-4,5-Methylenedioxybenzaldehyde (Journal of Chromatographic Science, 1996)
- Polyamine-sensitive binding of [3H]ifenprodil, a novel MMDA antagonist, to the rat cerebral cortex (European Journal of Pharmacology, 1990)
- Stochastic coefficient regression estimates of the sources of shifts into MMDA deposits using cross-section data (Journal of Econometrics, 1985)
- [Studies on the identification of psychotropic substances (VII). Preparation and various analytical data of standard references of some hallucinogens, 3,4-methylenedioxyamphetamine (MDA), 3,4- methylenedioxymethamphetamine (MDMA) and 5-methoxy-3,4- methylenedioxyamphetamine (MMDA)]. (Bulletin of National Institute of Hygienic Sciences, 1990)
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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)OC)OCO2)N
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- Pubchem - MMDA
- Wikipedia - 5-methoxy-3,4-methylenedioxyamphetamine
MMDA (3-methoxy-4,5-methylenedioxyamphetamine; 5-methoxy-MDA) is a psychedelic and entactogen drug of the amphetamine class. It is an analogue of lophophine, MDA, and MDMA. MMDA was described by Alexander Shulgin in his book PiHKAL.
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