Skip to main content

1,4-Butanediol Facts

Depressant; Alkanediol; GHB receptor agonist

Description

1,4-Butanediol (butane-1,4-diol) is a synthetic depressant of the aliphatic diol class. It is a prodrug of GHB, meaning it is chemically inert until the body converts it. This conversion produces GHB, which activates GABA receptors in the brain[1][2] and produces the sedation and euphoria characteristic of CNS depressants.

Subjective effects include euphoria, warmth, disinhibition, enhanced sociability, and sedation. The experience resembles a cleaner, more euphoric version of alcohol intoxication — warm and loosening at first, then shifting abruptly into heavy sedation as the dose rises.

1,4-BD produces rapid physical dependence, and the margin between a euphoric and a fatal dose is one of the narrowest among recreational depressants.[3] A genetic variation in the converting enzyme can make the same dose up to four times more potent in some people than others,[4] making individual responses unpredictable.

Dose and durationby route · individual sensitivity varies

Oral(mL)
Threshold< 0.5 mLLight0.5 – 1 mLCommon1 – 2.5 mLStrong2.5 – 4 mLHeavy4+ mL

Starts in 20 – 60 minLasts 3 – 5 hoursAfter-effects 2 – 4 hours

Body and dependence

Acute toxicity
High
Chronic toxicity
Moderate
Physical dependence
High
Psychological dependence
High
Withdrawal
Life-threatening · fatal · medical supervision
Compulsive redosing
High

Tolerance

Builds
Moderate
Fully resets after
10.5 days
Carries over to
baclofen

Effectslikely at a common dose

Perception
none likely · 7 possible, including Spatial disorientation, Vestibular distortion, Double vision
Body
Body high; Motor control impairment; Muscle relaxation; Physical fatigue; Sedation; +23 possible, including Dizziness, Insomnia, Nausea
Thinking
Cognitive impairment; +17 possible, including Analysis suppression, Compulsive redosing urge, Confusion
Feeling
Anxiety suppression; Euphoria; +8 possible, including Emotional lability, Anhedonia, Depression
Self
Disinhibition; +11 possible, including Craving, Communication suppression, Depersonalization
Time
none likely · 2 possible, including Temporal disorientation

Who shouldn't take it

Absolute
Respiratory conditions; Concurrent ethanol use; Concurrent opioid use; Concurrent benzodiazepine use; Other sedative-hypnotics; Operating vehicles or machinery
Relative
Epilepsy or seizure history; ADH1B variant carriers; Pregnancy; NSAID use (diclofenac)

Combinations60 recorded

Lethal (3)
GHB, GBL; Ketamine, DXM, PCP; Opioids
Dangerous (36)
Alpha-2 adrenergic receptor antagonist; Antihistamines; Antipsychotics; Benzodiazepines; Benzodiazepines, Barbiturates; Cannabis, THC; Clonidine, Guanfacine; MDMA, Amphetamines; Synthetic cannabinoids; Amphetamines; Anticholinergics; Atypical antipsychotics; Buprenorphine, Kratom; Buspirone; Caffeine; Cannabis; Dopamine agonists; DXM; Gabapentin, Pregabalin; Ibogaine; Lithium; Local anesthetics; MAOIs; MDMA, MDA; and 12 more, see full page
Caution (14)
See full page: psychedex.org/substances/1-4-butanediol
Not graded (7)
Not listed never means safe.

Seek help immediately if

  • Extreme drowsiness — can't stay awake or be roused
  • Confusion, slurred speech, severe loss of coordination
  • Slow, shallow, or irregular breathing
  • Unconsciousness / unresponsive; limp, floppy body
  • Blue lips or fingertips
  • Vomiting while sedated (choking / aspiration risk)
  • Cold, clammy skin; weak pulse

What to do

  1. Try to wake them — shout, firm sternal rub
  2. If unresponsive or breathing is impaired, call emergency services
  3. Place them in the recovery position — critical, they can choke on vomit
  4. Monitor breathing continuously; be ready to give rescue breaths / CPR
  5. Never leave them alone to "sleep it off"
  6. Do not give other drugs, stimulants, or more depressants

Most depressant overdoses resolve with airway protection, breathing support, and monitoring. The danger is respiratory depression and choking on vomit — sharply worse when combined with opioids or alcohol. GHB/GBL overdoses often involve sudden deep unconsciousness and may self-resolve, but airway protection is essential.

988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE

Version r1 · Not medical advice

References

  1. [1]
    ^Mathivet P, Bernasconi R, De Barry J, et al. (1997) Binding characteristics of gamma-hydroxybutyric acid as a weak but selective GABAB receptor agonist — European Journal of Pharmacology PMID:9083788
  2. [2]
    ^Lingenhoehl K, Brom R, Heid J, et al. (1999) Gamma-hydroxybutyrate is a weak agonist at recombinant GABA(B) receptors — Neuropharmacology PMID:10587082
  3. [3]
    ^Busardò FP, Jones AW (2015) GHB pharmacology and toxicology: acute intoxication, concentrations in blood and urine in forensic cases and treatment of the withdrawal syndrome — Current Neuropharmacology doi:10.2174/1570159x13666141210215423
  4. [4]
    ^Thai D, Dyer JE, Jacob P, Haller CA (2007) Clinical pharmacology of 1,4-butanediol and gamma-hydroxybutyrate after oral 1,4-butanediol administration to healthy volunteers — Clinical Pharmacology and Therapeutics PMID:17192771
Print version
Report an issue