MDA | |
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Salts [] | |
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3,4-Methylenedioxyamphetamine hydrochloride | |
Molecular structure via molpic | |
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Molecular formula | C10H13NO2 |
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Molecular mass | 179.22 g/mol |
Appearance | Almost colorless oil |
Predicted LogP | 1.6 |
Boiling point | 157 °C |
Decomposition | When heated to decomposition it emits toxic fumes of /Nitrogen oxides/. |
Chirality | racemic |
Identifiers [] | |
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IUPAC name | 1-(1,3-benzodioxol-5-yl)propan-2-amine |
SMILES | CC(CC1=CC2=C(C=C1)OCO2)N |
InChI | InChI=1S/C10H13NO2/c1-7(11)4-8-2-3-9-10(5-8)13-6-12-9/h2-3,5,7H,4,6,11H2,1H3 |
InChIKey | NGBBVGZWCFBOGO-UHFFFAOYSA-N |
3,4-Methylenedioxyamphetamine
3,4-Methylenedioxyamphetamine (also known as Tenamfetamine, Methylenedioxyamphetamine, 3,4-Methylenedioxy-amphetamine, Tenamfetamine, MDA (pharmaceutical), Tenamfetamina, Tenamfetaminum, methylene dioxyamphetamine, 1,3-Benzodioxole-5-ethanamine, alpha-methyl- or Tenanfetamina) is a hallucinogens substance of the amphetamine class.
Chemistry
3,4-Methylenedioxyamphetamine is typically found in the form of its hydrochloride salt.
Stereochemistry
3,4-Methylenedioxyamphetamine is a racemic mixture of the optical stereoisomers:Stereoisomers [] | |
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(+)-3,4-Methylenedioxyamphetamine | (-)-3,4-Methylenedioxyamphetamine |
See also
- Hallucinogens
- Antidepressant
- Depressant
- Amphetamine
- Substituted amphetamines
- Substituted methylenedioxyphenethylamines
- Bluedark
External links
- 3,4-Methylenedioxyamphetamine (Wikipedia)
- 3,4-Methylenedioxyamphetamine (Wikidata)
- 3,4-Methylenedioxyamphetamine (DrugBank)
- 3,4-Methylenedioxyamphetamine (PubChem)
- 3,4-Methylenedioxyamphetamine (ChemSpider)
- 3,4-Methylenedioxyamphetamine (ChEMBL)
- 3,4-Methylenedioxyamphetamine (ChEBI)
- 3,4-Methylenedioxyamphetamine (Common Chemistry)
- 3,4-Methylenedioxyamphetamine (HMDB)
- 3,4-Methylenedioxyamphetamine (KEGG)
- 3,4-Methylenedioxyamphetamine (UNII)
- 3,4-Methylenedioxyamphetamine (EPA DSSTox)