1,3-Butanediol
Lethal interactions
| Combination | Type | Severity | Mechanisms | Confidence |
|---|---|---|---|---|
| GHB, Baclofen | Drug class | lethal | 2 | high |
| Ketamine, DXM, PCP | Drug class | lethal | 2 | medium |
| Opioids | Drug class | lethal | 2 | high |
Dangerous interactions
35 dangerous interactions recorded for this substance.
See the full interactions tableContraindications
| Condition | Severity | Note |
|---|---|---|
| Psychiatric | ||
| alcohol use disorder | relative | Individuals with alcohol use disorder have established neuroadaptive changes that produce cross-tolerance with 1,3-BD. Competitive ADH inhibition with concurrent ethanol makes effects unpredictable. While ketone supplementation may reduce alcohol craving (Li 2024, 2026), the CNS depressant and dependence-producing properties of 1,3-BD pose substitution risk. |
| Metabolic | ||
| diabetes mellitus | relative | 1,3-Butanediol lowers blood glucose in humans (Tobin 1975). Individuals with diabetes mellitus or those taking blood glucose-lowering medications face additive hypoglycemic risk. Blood glucose monitoring is advised if 1,3-BD is consumed. |
| hypoglycemia susceptibility | absolute | Individuals with fasting hypoglycemia, reactive hypoglycemia, or glycogen storage disorders face significant risk from 1,3-BD's documented glucose-lowering properties. Avoidance is recommended. |
| Pregnancy & Breastfeeding | ||
| pregnancy | relative | No human pregnancy safety data have been published. A single rat study showed no adverse fetal outcomes, but this is insufficient to establish safety. Standard precautionary avoidance applies. |
| Other | ||
| concurrent CNS depressant use | relative | No 1,3-BD-specific interaction studies with other CNS depressants exist. Class-level additive CNS depression risk is inferred. Combination with benzodiazepines, opioids, or other sedatives increases risk of excessive sedation, respiratory depression, and loss of consciousness. |