Anodyne

4-MA
4-Methylamphetamine
Molecular structure via molpic based on CDK
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Conformer structure via JSmol
Physical properties
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149.23 g/mol [1]
2.1 [1]
Structural Identifiers
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C10H15[1]
1-(4-methylphenyl)propan-2-amine [1]
CC1=CC=C(C=C1)CC(C)N [1]
InChI=1S/C10H15N/c1-8-3-5-10(6-4-8)7-9(2)11/h3-6,9H,7,11H2,1-2H3 [1]
InChIKeyZDHZDWSHLNBTEB-UHFFFAOYSA-N [1]
Dosing
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Elimination half-life6–12 hours

4-Methylamphetamine

4-Methylamphetamine (also known as Aptrol, p-Methylamphetamine, p-Methylamfetamine, P-TAP, PAL-313, -α,4-Dimethylbenzeneethanamine, Benzeneethanamine, α,4-dimethyl-, (+-)-, 1-p-Tolyl-2-propylamine, 4-12-00-02834 or p-.α.-Dimethylphenethylamine) is a stimulant substance of the amphetamine class.

Chemistry

Salts []

4-Methylamphetamine is typically found in the form of its hemisulfate salt.

 []

(RS)-4-Methylamphetamine is a racemic mixture of the optical stereoisomers

Subjective effects []

Experience reports []

There are currently 1 experience reports involving 4-methylamphetamine on OpenErowid:

Legal status []

  • Canada: 4-Methylamphetamine is a Schedule I substance.
  • United Kingdom: 4-Methylamphetamine is a Class A substance.
  • Germany: 4-Methylamphetamine is a Anlage II substance.
  • United States: 4-Methylamphetamine is a List of Schedule II drugs (US)|Schedule II (isomer of Methamphetamine) substance.

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 199116, 4-Methylamphetamine. Accessed June 25, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/199116

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 4-Methylamphetamine. UNII: 9E273KL7HS. Global Substance Registration System. Accessed June 25, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/9E273KL7HS