Skip to main content
L

Not yet reviewed: this article is pending editorial review by Lyrea.

Citation noticeOur citation system is being overhauled

References and citation markers may currently be incomplete, mismatched, or incorrect. This system is being rebuilt and reviewed before the full site launch.

25-DMA

This article is a stubmissing:
Subjective Effects
Pharmacology
Interactions
25-DMA molecule structure25-DMA molecule structure
Chemical Class

25-DMA is a psychoactive substituted amphetamine and the simplest member of the DOx family. It reportedly lacks notable psychedelic effects1 and is primarily used as a precursor in the synthesis of other psychedelic amphetamines, including DOB, DOI, and DON.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold10 mg
Light10-40 mg
Moderate40-80 mg
Strong80-200 mg
Heavy200+ mg

Duration

Total6-8 hours

Subjective Effects

Subjective Effects not written up yet

Reagent Testing

Expected colorimetric results for common reagent tests. Colors show reaction change over 1–2 minutes.

Marquis(MQ)
white → yellow2 → green2
Mecke(ME)
white → yellow2 → green3
Mandelin(MD)
yellow2 → green2
Liebermann(LB)
white → yellow2 → green3
Powered by PROtestkit.eu

Pharmacology

Pharmacology not written up yet

Interactions

Interactions not written up yet

An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.

Check TripSit

Tolerance

Tolerance timelines are rules of thumb, not exact schedules, and vary widely between individuals and use patterns.

Full Tolerance
Tolerance to the effects of 25-DMA develops over several days following ingestion.
Baseline Reset
Tolerance returns to baseline within approximately 7–10 days if no further doses are taken.
Half Tolerance
Tolerance falls to approximately 50% within 3–5 days if no further doses are taken.
Cross Tolerance

Possible but unlikely cross-tolerance with all psychedelics, Possible cross-tolerance with stimulants

Harm Potential

Addiction & Dependence

Psychological

Low

Like many psychedelic substances, 2,5-DMA is not generally regarded as habit-forming, and interest in repeated use may decline with experience. Its stimulant qualities, however, may create some risk of psychological dependence similar to other stimulants.

History & Culture

2,5-DMA was first synthesized in 1939 by Richard Baltzly and Johannes S. Buck in Tuckahoe, New York. Alexander Shulgin later explored its effects in humans and published his findings in PiHKAL (Phenethylamines I Have Known and Loved).2…

Legality

By Country

Illegal4
United States flagUnited StatesIllegal
Germany flagGermanyIllegal
Switzerland flagSwitzerlandIllegal
United Kingdom flagUnited KingdomIllegal (analog/blanket ban)

References

Citations

  1. PiHKAL — #54 2,5-DMA. PiHKAL, Alexander and Ann Shulgin; authorized reproduction hosted by Erowid (1991). https://www.erowid.org/library/books_online/pihkal/pihkal054.shtml1
  2. PiHKAL: A Chemical Love Story — Book II, #54: 2,5-DMA. Transform Press (hosted by The Vespiary) (1991). https://www.thevespiary.org/library/Files_Uploaded_by_Users/llamabox/PiHKAL.pdf1234
  3. Betäubungsmittelgesetz (BtMG), Anlage I (zu § 1 Abs. 1) – nicht verkehrsfähige Betäubungsmittel. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/anlage_i.html1
  4. Betäubungsmittelgesetz (BtMG), § 1 Betäubungsmittel. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/__1.html1
  5. Betäubungsmittelgesetz (BtMG), § 3 Erlaubnis zum Verkehr mit Betäubungsmitteln. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/__3.html1
  6. Betäubungsmittelgesetz (BtMG), § 29 Straftaten. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/__29.html1
  7. Neue-psychoaktive-Stoffe-Gesetz (NpSG), § 1 Anwendungsbereich. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/__1.html1
  8. Betäubungsmittelverzeichnisverordnung (BetmVV-EDI), Anhang 5, Verzeichnis d (Stand am 13. März 2026). fedlex.data.admin.ch (n.d.). https://fedlex.data.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/2011/363/20260313/de/html/fedlex-data-admin-ch-eli-cc-2011-363-20260313-de-html-3.html1
  9. Betäubungsmittelkontrollverordnung (BetmKV), Art. 3 Abs. 2 Bst. d-e (Stand am 23. Januar 2023). fedlex.admin.ch (n.d.). https://www.fedlex.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/2011/362/20230123/de/html/fedlex-data-admin-ch-eli-cc-2011-362-20230123-de-html-3.html1
  10. Betäubungsmittelgesetz (BetmG), Art. 19 Abs. 1 (Stand am 1. September 2023). fedlex.data.admin.ch (n.d.). https://fedlex.data.admin.ch/filestore/fedlex.data.admin.ch/eli/cc/1952/241_241_245/20230901/de/html/fedlex-data-admin-ch-eli-cc-1952-241_241_245-20230901-de-html-8.html1

Further Reading

  1. Glennon et al. 1982 - Behavioral and serotonin receptor properties of 4-substituted derivatives of the hallucinogen 1-(2,5-dimethoxyphenyl)-2-aminopropane

Article Status

  • Josie Kins avatar
    Step 1 · Automated synthesis

    An autonomous workflow built by Josie Kins compiled this article's foundation from information published across the web.

  • Step 2 · First-pass reviewPending

    Not yet reviewed: this article is pending editorial review by Lyrea.

  • Step 3 · Citation reviewPending

    No one has reviewed this article's citations yet. That second pass checks each claim against the source it cites.

Suggest an edit

Spotted a mistake, an outdated claim, or something missing from the 25-DMA article? Send the editors a private note. Feedback lands in a moderation queue and is never shown on the site.

Wish to give generalised feedback? You can do so here.