| Weight | 165.192 g/mol |
|---|---|
| Formula | C9H11NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
HOMOPIPERONYLAMINE (1484-85-1)
3,4-methylenedioxyphenethylamine · HCl of 3,4-methylenedioxyphenethylamine
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- A Synthesis of N-(3-Methoxybenzyl)-N-methyl-3-methoxy-4,5-methylenedioxyphenethylamine (Journal of the American Chemical Society, 1949)
- Preparation of Homopiperonylamine by Hydrogenation of 3,4-Methylenedioxybenzyl Cyanide over Raney Cobalt Catalyst (Journal of the American Chemical Society, 1950)
- Syntheses of N-Acyl Derivatives of -Methyl-3, 4-methylenedioxyphenethylamine and their Analgesic Activity. (Chemical & Pharmaceutical Bulletin, 1963)
- In vivo formation of dopamine from 3,4-methylenedioxyphenethylamine in the rat. (Archives internationales de pharmacodynamie et de thrapie, 1978)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,4-methylenedioxyphenethylamine
- HCl of 3,4-methylenedioxyphenethylamine
-
SMILESC1OC2=C(O1)C=C(C=C2)CCN
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InChIKeyRRIRDPSOCUCGBV-UHFFFAOYSA-N
- Pubchem - HOMOPIPERONYLAMINE
- Wikipedia - Methylenedioxyphenethylamine
3,4-Methylenedioxyphenethylamine ("3,4-MDPEA" or just "MDPEA"), also known as homopiperonylamine, is a substituted phenethylamine formed by adding a methylenedioxy group to phenethylamine. It is structurally similar to MDA, but without the methyl group at the alpha position. According to Alexander Shulgin in his book PiHKAL, MDPEA appears to be biologically inactive.
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HOMOPIPERONYLAMINE
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