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Amobarbital

Amobarbital molecule structureAmobarbital molecule structure
5-Ethyl-5-isopentylbarbituric acid
Amytal, Sodium Amytal, Amylobarbitone, Blue heavens, Blue velvet

Amobarbital is a barbiturate derivative with sedative-hypnotic properties, first synthesized in Germany in 1923.citation needed Classified as a short to intermediate acting barbiturate,1 it has been used clinically for sedation, short-term insomnia management, and acute seizure control.citation needed Once widely misused, its popularity declined as benzodiazepines offered safer alternatives in overdose. Amobarbital carries a high risk of dependence with continued use, and dose-related central nervous system depression remains a primary safety concern.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~50 mg
Light50-75 mg
Moderate75-150 mg
Strong150-200 mg
Heavy200+ mg

Absorption is faster when taken on an empty stomach.

Duration

Onset10-30 minutes
After Effects2-12 hours
Total5-9 hours

Subjective Effects

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

The amobarbital experience is dominated by heavy sedation and anxiety relief, producing an intoxication that closely resembles alcohol in its disinhibition, sloppiness, and impaired judgment. As the dose increases, cognitive impairment and physical incoordination become pronounced, and memory of the period after ingestion may become patchy or absent. There is little in the way of sensory alteration; the character of the experience is one of suppression rather than enhancement.

Physical

Powerful sedation, muscle relaxation, and a loss of motor coordination define the body experience, manifesting as staggering, clumsiness, and slurred speech. At overdose levels, breathing slows, heart rate drops, and body temperature falls.

Sedation

Uncomfortable

Cognitive

The headspace is clouded and disinhibited, with slowed thinking, reduced anxiety, and impaired judgment. Users may divulge information they would normally withhold, and anterograde amnesia is common at moderate to high doses.

Emotional

Suppressions

Pharmacology

Pharmacodynamics

Amobarbital acts primarily as a positive allosteric modulator of the GABAA receptor, binding at the barbiturate site on alpha or beta subunits, which is distinct from both the GABA and benzodiazepine binding sites.citation needed This potentiates GABAergic inhibition by increasing chloride channel conductance and prolonging inhibitory postsynaptic currents.2 It also antagonizes AMPA and kainate-type glutamate receptors, reducing excitatory neurotransmission, and acts as an antagonist at neuronal nicotinic acetylcholine receptors (alpha-4 and alpha-7 subtypes).

Pharmacokinetics

Amobarbital is metabolized via hydroxylation to form 3'-hydroxyamobarbital3 and via N-glucosidation to form 1-(beta-D-glucopyranosyl)-amobarbital.4

Interactions

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.

1,2-BenzodiazepineAbaloparatideAbemaciclibAcalabrutinibAcebutolol
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Tolerance

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

Cross Tolerance

Barbiturates, Other GABAergic depressants

Harm Potential

Addiction & Dependence

Psychological

High

High abuse potential with significant risk of psychological dependence.citation needed Amobarbital was widely misused recreationally, known on the street as 'Blue Heavens,' 'blue angels,' and 'blue devils,' and is classified as habit-forming.5

Physical

Extremely High

Physical dependence develops with extended use.citation needed Withdrawal mimics delirium tremens and may be life-threatening, requiring medical supervision for discontinuation.

History & Culture

Discovery and Commercial Development

Amobarbital was first synthesized in Germany in 1923, emerging as a short to intermediate acting barbiturate derivative.citation needed The compound gained commercial prominence through Eli Lilly and Company, which manufactured it in the United States under the brand name Amytal. The medication

Legality

By Country

Illegal1
Netherlands flagNetherlandsIllegal
Controlled / restricted3
Canada flagCanadaRestricted
Ukraine flagUkraineRestricted
United Kingdom flagUnited KingdomRestricted
Prescription2
United States flagUnited StatesPrescription only
Germany flagGermanyPrescription only

References

Source Pages

  1. Bluelight: Amobarbital 25 mg tablets, recommended dose?
  2. DrugBank
  3. DrugBank: Amobarbital (DB00321)
  4. Erowid: Amobarbital Vault
  5. PsychonautWiki: Barbiturates
  6. PsychonautWiki: Dangerous Combinations
  7. TripSit: Amobarbital
  8. Wikipedia

Citations

  1. Francisco López-Muñoz, Ronaldo Ucha-Udabe, & Cecilio Alamo. (2005). The history of barbiturates a century after their clinical introduction. Neuropsychiatric Disease and Treatment, 1(4). https://pmc.ncbi.nlm.nih.gov/articles/PMC2424120/1
  2. H‐S Kim, X Wan, D A Mathers, & E Puil. (October 2004). Selective GABA-receptor actions of amobarbital on thalamic neurons. British Journal of Pharmacology, 143(4), 485–94. https://doi.org/10.1038/sj.bjp.07059741
  3. W Kalow, B K Tang, D Kadar, & T Inaba. (1978). Distinctive patterns of amobarbital metabolites. Clinical Pharmacology & Therapeutics, 24(5), 576-82. https://pubmed.ncbi.nlm.nih.gov/699482/1
  4. Tang BK, Kalow W, & Grey AA. (July 1978). Amobarbital metabolism in man: N-glucoside formation. Research Communications in Chemical Pathology and Pharmacology, 21(1), 45–53. https://pubmed.ncbi.nlm.nih.gov/684279/1
  5. AMYTAL SODIUM (amobarbital sodium) for injection, USP — DailyMed Label (setid: a2523317-e071-4e04-9d9f-9053286e0ce2). (n.d.). https://dailymed.nlm.nih.gov/dailymed/fda/fdaDrugXsl.cfm?setid=a2523317-e071-4e04-9d9f-9053286e0ce2&type=display1
  6. Death in Hollywood: Walker, Robert – Strangers on a Train. Emanuel Levy (n.d.). https://emanuellevy.com/profile/death-in-hollywood-walker-robert-age-38-strangers-on-a-train/1
  7. Controlled Drugs and Substances Act, Schedule IV; section 5. laws-lois.justice.gc.ca (n.d.). https://laws-lois.justice.gc.ca/eng/acts/C-38.8/section-sched95660.html1
  8. Controlled Drugs and Substances Act, Schedule IV; section 5. laws-lois.justice.gc.ca (n.d.). https://laws-lois.justice.gc.ca/eng/acts/C-38.8/section-5.html1
  9. Anlage III BtMG. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/anlage_iii.html1
  10. § 13 BtMG. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/btmg_1981/__13.html1

Further Reading

  1. Clarke's Analysis of Drugs and Poisons, 4th Ed.
  2. DailyMed: Amytal Sodium (amobarbital) label
  3. Drugs.com – Amytal Sodium Package Insert
  4. PubChem: Amobarbital (CID 2164)

Article Status

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Recent changes8 human edits · latest

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21 August 2026

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

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

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

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