MDA

Molecular structure via molpic based on CDK

Conformer []

Conformer structure via JSmol

Physical properties []
Molecular mass	179.22 g/mol ^[1]
Appearance	Almost colorless oil ^[1]
Boiling point	157 °C ^[1]
Decomposition	When heated to decomposition it emits toxic fumes of /Nitrogen oxides/. ^[1]
Predicted LogP	1.6 ^[1]

Structural Identifiers []
Molecular formula	C₁₀H₁₃NO₂ ^[1]
IUPAC name	1-(1,3-benzodioxol-5-yl)propan-2-amine ^[1]
SMILES	CC(CC1=CC2=C(C=C1)OCO2)N ^[1]
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 ^[1]
InChIKey	NGBBVGZWCFBOGO-UHFFFAOYSA-N ^[1]

3,4-Methylenedioxyamphetamine

3,4-Methylenedioxyamphetamine (also known as Tenamfetamine, Methylenedioxyamphetamine, Tenamfetaminum, Love, methylene dioxyamphetamine, 1,3-Benzodioxole-5-ethanamine, α-methyl-, Tenanfetamina, EA-1299, α-Methyl-1,3-benzodioxole-5-ethanamine or α-Methyl-3,4-(methylenedioxy)phenethylamine) is a entactogen and stimulant substance of the methylenedioxyphenethylamine class.

Chemistry

Stereochemistry []

3,4-Methylenedioxyamphetamine is a racemic mixture of the enantiomers

Stereoisomers
(R)-3,4-Methylenedioxyamphetamine (S)-3,4-Methylenedioxyamphetamine

Subjective effects []

Physical effects
Abnormal heartbeat Appetite suppression Dehydration Dry mouth Increased blood pressure Increased heart rate Increased libido Restless legs Shakiness Stamina enhancement Stimulation Teeth grinding Vasoconstriction

Cognitive effects
Analysis enhancement Cognitive euphoria Compulsive redosing Disinhibition Ego inflation Empathy, effection, and sociability enhancement Focus enhancement Increased music appreciation Mania Motivation enhancement Suggestibility suppression Thought acceleration Wakefulness

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 1614, 3,4-Methylenedioxyamphetamine. Accessed July 28, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/1614

Anodyne