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1,3-Butanediol Facts

Depressant; Alkanediol; GABA-A receptor positive allosteric modulator

Description

1,3-Butanediol (butane-1,3-diol) is a synthetic depressant of the aliphatic diol class. The liver converts it into β-hydroxybutyrate, a natural ketone body, which drives its depressant effects.[1]

Subjective effects include lowered inhibitions, reduced anxiety, euphoria, dizziness, and sedation. The experience closely resembles ethanol — relaxation and social ease — but without alcohol's stimulatory early phase and compressed into roughly half its duration.[2][3]

Animal studies show chronic use produces physical dependence and alcohol-like withdrawal;[2] acute toxicity is roughly 2.5 times lower than ethanol in animal models.[4] The compound lowers blood sugar — a meaningful added risk for people with diabetes or on glucose-lowering medications.[5]

Dose and durationby route · individual sensitivity varies

Oral(g/kg)
Threshold< 0.1 g/kgLight0.2 – 0.3 g/kgCommon0.35 – 0.5 g/kgStrong0.5 – 0.7 g/kgHeavy0.7+ g/kg

Starts in 20 – 40 minLasts 2 – 4 hoursAfter-effects 1 – 3 hours

Body and dependence

Acute toxicity
Low
Chronic toxicity
Moderate
Physical dependence
Moderate
Psychological dependence
Low
Withdrawal
Moderate · medical supervision
Compulsive redosing
Low

Tolerance

Builds
Moderate
Fully resets after
Not recorded
Carries over to
ethanol

Effectslikely at a common dose

Perception
none likely · 8 possible, including Spatial disorientation, Vestibular distortion, Double vision
Body
Motor control impairment; Sedation; +19 possible, including Dizziness, Nystagmus (eye wobbles), Dehydration sensation
Thinking
Cognitive impairment; +17 possible, including Decision impairment, Information processing suppression, Analysis suppression
Feeling
none likely · 5 possible, including Emotional lability
Self
none likely · 6 possible, including Craving
Time
none likely · 2 possible, including Temporal disorientation

Who shouldn't take it

Absolute
Hypoglycemia susceptibility
Relative
Alcohol use disorder; Diabetes mellitus; Pregnancy; Concurrent CNS depressant use

Combinations60 recorded

Lethal (3)
GHB, Baclofen; Ketamine, DXM, PCP; Opioids
Dangerous (35)
Alpha-2 adrenergic receptor antagonist; Antihistamines; Antipsychotics; Atypical antipsychotics; Benzodiazepines; Cannabis, THC; Clonidine, Guanfacine; GHB, GBL; Naltrexone; NSAIDs; Stimulants; Synthetic cannabinoids; THC; Amphetamines; Anticholinergics; Buprenorphine, Kratom; Caffeine; Cannabis; Dopamine agonists; DXM; Gabapentin, Pregabalin; Ibogaine; Lithium; Local anesthetics; and 11 more, see full page
Caution (17)
See full page: psychedex.org/substances/1-3-butanediol
Not graded (5)
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]
    ^Frye GD, McCown TJ, Breese GR (1983) Characterization of susceptibility to audiogenic seizures in ethanol-dependent rats after microinjection of GABA agonists — The Journal of Pharmacology and Experimental Therapeutics PMID:6317842
  2. [2]
    ^abFrye GD, Chapin RE, Vogel RA, Mailman RB, Kilts CD, Mueller RA, Breese GR (1981) Effects of acute and chronic 1,3-butanediol treatment on central nervous system function: a comparison with ethanol — The Journal of Pharmacology and Experimental Therapeutics PMID:7193248
  3. [3]
    ^(2024) 1,3-Butanediol - PsychonautWiki Link
  4. [4]
    ^McCarthy CG, Waigi EW, Singh G, Castaneda TR, Mell B, Chakraborty S, Wenceslau CF, Joe B (2021) Physiologic, Metabolic, and Toxicologic Profile of 1,3-Butanediol — The Journal of Pharmacology and Experimental Therapeutics doi:10.1124/jpet.121.000796
  5. [5]
    ^Tobin RB, Mehlman MA, Kies C, Fox HM, Soeldner JS (1975) Nutritional and metabolic studies in humans with 1,3-butanediol — Federation Proceedings PMID:1183620
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