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3C-E

This article is a stubmissing:
Subjective Effects
Pharmacology
Tolerance
History & Culture
3C-E molecule structure3C-E molecule structure
3,5-Dimethoxy-4-ethoxyamphetamine
3C-Escaline
Chemical Class
3C-x

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold15-25 mg
Light25-35 mg
Moderate35-50 mg
Strong50-70 mg
Heavy80+ mg

Duration

Onset1-2 hours
Peak4-8 hours
Offset3-6 hours
After Effects3-6 hours
Total10-16 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 → orange1
Mecke(ME)
white → brown2 → red2
Mandelin(MD)
yellow2 → brown2 → brown3 → black3
Ehrlich(EH)
No reaction
No reaction
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Pharmacology

Pharmacology not written up yet

Interactions

Dangerous

Highest risk

These combinations are considered extremely harmful and should always be avoided. Reactions to these drugs taken in combination are highly unpredictable and have a potential to cause death.

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Tolerance

Tolerance not written up yet

Harm Potential

Psychosis Risk

Low

Psychosis risk may be increased when combined with lithium or cannabis. Anxiety, paranoia, and panic attacks can occur, particularly at higher doses or when set and setting guidelines are not followed.

Seizure Risk

Low

Seizures appear uncommon, but they may arise in susceptible people, particularly when dehydration, inadequate food intake, overheating, or fatigue place additional strain on the body.

History & Culture

History & Culture not written up yet

Trip Reports

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Legality

By Country

Illegal5
United States flagUnited StatesIllegal (analog/blanket ban)
Germany flagGermanyIllegal (analog/blanket ban)
Japan flagJapanIllegal
Switzerland flagSwitzerlandIllegal (analog/blanket ban)
United Kingdom flagUnited KingdomIllegal

References

Source Pages

  1. Bluelight discussion: 3-halo-4-(1,1-difluoromethoxy)-5-methoxy-phenethylamine homologs (user reports include 3C-E)
  2. Bluelight discussion: 3C-E – 4 Initial Trials
  3. Erowid: 3C-E Vault – dosage, effects and experience reports
  4. Isomer Design (TiHKAL/PiHKAL)
  5. PIHKAL entry #25 – 3C-E
  6. PsychonautWiki
  7. Shulgin & Shulgin, TIHKAL/PIHKAL – overview of substituted amphetamines
  8. TripSit Factsheets
  9. Wikipedia

Citations

  1. PubChem PUG REST: 3C-E (CID 44350137). pubchem.ncbi.nlm.nih.gov (n.d.). https://pubchem.ncbi.nlm.nih.gov/rest/pug/compound/name/3C-E/property/IUPACName,MolecularFormula,MolecularWeight,CanonicalSMILES,IsomericSMILES,InChIKey/JSON1
  2. Neue-psychoaktive-Stoffe-Gesetz (NpSG), Anlage 1. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/anlage_1.html1
  3. Neue-psychoaktive-Stoffe-Gesetz (NpSG), § 2 Begriffsbestimmungen. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/__2.html1
  4. Neue-psychoaktive-Stoffe-Gesetz (NpSG), § 3 Unerlaubter Umgang mit neuen psychoaktiven Stoffen. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/__3.html1
  5. Neue-psychoaktive-Stoffe-Gesetz (NpSG), § 4 Strafvorschriften. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/__4.html1
  6. Neue-psychoaktive-Stoffe-Gesetz (NpSG), current consolidated text. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/BJNR261510016.html1
  7. Deutscher Bundestag Drucksache 18/8579: Entwurf eines Gesetzes zur Bekämpfung der Verbreitung neuer psychoaktiver Stoffe. dserver.bundestag.de (n.d.). https://dserver.bundestag.de/btd/18/085/1808579.pdf1
  8. Betäubungsmittelgesetz (BtMG), Anlage I. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/anlage_i.html1
  9. Betäubungsmittelgesetz (BtMG), Anlage II. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/anlage_ii.html1
  10. Betäubungsmittelgesetz (BtMG), Anlage III. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/anlage_iii.html1

Further Reading

  1. McLean et al. Substitution on Mescaline Analogues Determines 5-HT2A Affinity. J Med Chem 49 (2006): 4269-4280

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.

Recent changes7 human edits · latest

Times are UTCNewest first

24 January 2026

  1. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  2. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  3. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  4. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  5. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  6. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

  7. Josie Kins · Updated the article · also 1,4-Butanediol, 1B-LSD, 1cP-AL-LAD and 573 more

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