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Ethylmorphine

Ethylmorphine molecule structureEthylmorphine molecule structure
3-Ethylmorphine
Codethyline, Dionine, Ethyl morphine
Psychoactive Class
Chemical Class

Ethylmorphine is a semi-synthetic opioid of the morphinan classcitation needed, first created by Merck in 1884 as a weaker alternative to morphine. Its potency is generally placed below morphine and somewhat above codeine, a closely related compound. Today, ethylmorphine is most commonly encountered as an antitussive ingredient in cough syrup preparations1 and is also used in ophthalmic preparations2 to treat eye inflammations.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~20 mg
Light20-50 mg
Moderate50-100 mg
Strong100-200 mg
Heavy200+ mg

Duration

Onset15-30 minutes
Peak2-3 hours
After Effects1-6 hours
Total4-5 hours

Subjective Effects

Legacy content. A statistically backed ontology from Mindstate Design Labs is coming soon.

Effects vary widely by individual, dose, and context.

Physical

The cognitive effects of ethylmorphine can be broken down into several components which progressively intensify proportional to dosage. The general head space of codeine is described by many as one of intense euphoria, relaxation, anxiety suppression and pain relief.

Cognitive

The physical effects of ethylmorphine can be broken down into several components which progressively intensify proportional to dosage.

Forked from Subjective Effect Documentation byJosie Kins September 2015.

Reagent Testing

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

Marquis(MQ)
white → orange2 → purple2
Mecke(ME)
white → green3
Mandelin(MD)
yellow2 → green2
Froe(FR)
white → yellow2 → green2 → blue2
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Pharmacology

Pharmacodynamics

Ethylmorphine produces its effects primarily through activation of μ-opioid receptors, an action mediated largely by its active metabolites, particularly morphine.citation needed The substance has been described as less potent than morphine but slightly more potent than codeine.

Pharmacokinetics

Ethylmorphine functions as a prodrug that requires metabolic conversion to generate its active form, most notably morphine.citation needed As with codeine, there is an upper limit on how much of the parent compound can be converted into its active metabolite.

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.

AlcoholBenzodiazepinesCocaineDXMGHB/GBLKetamineMXEPregabalinTramadol

Unsafe

Avoid

There is considerable risk of physical harm when taking these combinations, they should be avoided where possible.

Caution

Use caution

These combinations are not usually physically harmful, but may produce undesirable effects, such as physical discomfort or overstimulation. Extreme use may cause physical health issues. Synergistic effects may be unpredictable. Care should be taken when choosing to use this combination.

AmphetaminesMAOIsMephedroneNitrous oxidePCP
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Tolerance

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

Full Tolerance
Ethylmorphine tolerance can develop for many effects after ongoing repeated use. Different effects show different timelines, and tolerance to constipation tends to emerge more slowly than tolerance to other opioid effects.
Baseline Reset
1-2 weeks
Half Tolerance
3-7 days
Cross Tolerance

All other opioids

Harm Potential

Addiction & Dependence

Psychological

High

Ethylmorphine has a high potential for abuse and can cause psychological dependence with chronic use.citation needed Compulsive redosing is commonly reported, and cravings develop once addiction forms.

Physical

High

Physical dependence develops with chronic use, with withdrawal symptoms occurring upon sudden cessation.4 Chemical dependence may develop particularly at higher doses.citation needed

Toxicity

Central Nervous System

Long-term chronic use may result in cognitive and affective changes including memory loss and apathy.

History & Culture

Ethylmorphine is a semi-synthetic opioid first synthesized by the pharmaceutical company Merck in 1884. It was developed as a weaker alternative to morphine for therapeutic applications.

Legality

International

Single Convention on Narcotic Drugs 1961 (Schedule III)

By Country

Controlled / restricted4
United States flagUnited StatesSchedule II/III/V (varies by preparation)
Germany flagGermanyAnlage II BtMG
Switzerland flagSwitzerlandVerzeichnis A (controlled)
United Kingdom flagUnited KingdomClass B
Prescription4
France flagFrancePrescription only
Norway flagNorwayPrescription Class B
Russia flagRussiaPrescription only
Sweden flagSwedenPrescription drug

References

Source Pages

  1. DrugBank: Ethylmorphine
  2. Erowid: Ethylmorphine Vault
  3. Isomer Design (TiHKAL/PiHKAL)
  4. PsychonautWiki
  5. TripSit Factsheets
  6. TripSit: Ethylmorphine Factsheet
  7. Wikipedia

Citations

  1. Cosylan «Viatris». Felleskatalogen (n.d.). https://www.felleskatalogen.no/medisin/cosylan-viatris-54767612
  2. PubChem Compound Summary for CID 5359271, Ethylmorphine. National Center for Biotechnology Information (n.d.). https://pubchem.ncbi.nlm.nih.gov/compound/53592711
  3. Aasmundstad TA, Mørland J, & Paulsen RE. (1995). Biotransformation and pharmacokinetics of ethylmorphine after a single oral dose. British Journal of Clinical Pharmacology, 39(6), 611-620. https://doi.org/10.1111/j.1365-2125.1995.tb05720.x1
  4. Rosenthal RN, & Goradia VV. (2023). Opioid Withdrawal. StatPearls. https://www.ncbi.nlm.nih.gov/books/NBK526012/1
  5. Opioid induced hypogonadism. BMJ (2008). https://pmc.ncbi.nlm.nih.gov/articles/PMC2974597/1
  6. J. Hinshelwood. (1904). Dionine: A New Ocular Analgesic. https://doi.org/10.1136/bmj.1.2261.1009-a1
  7. VEGETOSERUM ADULTES, sirop — French Public Medicines Database. base-donnees-publique.medicaments.gouv.fr (n.d.). https://base-donnees-publique.medicaments.gouv.fr/medicament/68338784/extrait1
  8. Anlage II BtMG – verkehrsfähige, aber nicht verschreibungsfähige Betäubungsmittel. Bundesministerium der Justiz (n.d.). https://www.gesetze-im-internet.de/btmg_1981/anlage_ii.html12
  9. Solvipect comp. «Orifarm Healthcare» – Felleskatalogen. Felleskatalogen (n.d.). https://www.felleskatalogen.no/medisin/solvipect-comp-orifarm-healthcare-5640221
  10. Roszdravnadzor consolidated text of Government Resolution No. 681 and its controlled-substances list. roszdravnadzor.gov.ru (n.d.). https://roszdravnadzor.gov.ru/i/upload/images/2026/3/30/1774879151.29078-1-3386659.pdf1

Further Reading

  1. Biotransformation and Pharmacokinetics Study (PMC)

Article Status

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

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

Recent changes8 human edits · latest

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16 August 2026

  1. Lyrea · Changed a word in Dosage & DurationRoutes 1 › Dose ranges › Light

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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