Pet Safety / Compounds / Bromethalin

Is Bromethalin safe for dogs and cats?

Extreme risk for pets

Bromethalin (N-methyl-2,4-dinitro-N-(2,4,6-tribromophenyl)-6-(trifluoromethyl)benzenamine) is a non-anticoagulant neurotoxic rodenticide increasingly common in the US since EPA restrictions on second-generation anticoagulant rodenticides for consumer use in 2011. Mechanism: uncouples oxidative phosphorylation in neural mitochondria → impaired myelin maintenance → cerebral and spinal cord edema → ascending paralysis. Critically: there is NO antidote for bromethalin. Minimum lethal dose in dogs: approximately 1–2 mg/kg (acute) to 5–10 mg/kg over multiple exposures. A single commercially available bait block may contain sufficient bromethalin to be lethal to a small or medium dog. Onset of clinical signs: 24–96 hours post-ingestion. Signs of acute/severe exposure: hind limb weakness, ataxia, ascending paralysis, tremors, hyperexcitability, opisthotonus, seizures, hyperthermia, death. Signs of subacute/lower-dose exposure: bilateral hind limb paresis, lethargy, vomiting — may persist for days to weeks. Diagnosis is often presumptive (bait product identification). Treatment is limited to aggressive decontamination (emesis + activated charcoal + cathartic — critical if within 1 hour of ingestion; activated charcoal for 24–48 hours due to enterohepatic recirculation), anti-edema measures (mannitol, corticosteroids — evidence limited), and supportive care. ASPCA APCC now receives more bromethalin calls than anticoagulant rodenticide calls in many regions.

What is bromethalin?

The IUPAC name is N-methyl-2,4-dinitro-N-(2,4,6-tribromophenyl)-6-(trifluoromethyl)aniline.

Also known as: N-methyl-2,4-dinitro-N-(2,4,6-tribromophenyl)-6-(trifluoromethyl)aniline, Bromethaline, Vengeance, Bromethalin Bait.

IUPAC name
N-methyl-2,4-dinitro-N-(2,4,6-tribromophenyl)-6-(trifluoromethyl)aniline
CAS number
63333-35-7
Molecular formula
C14H7Br3F3N3O4
Molecular weight
577.93 g/mol
SMILES
CN(C1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])C(F)(F)F)C2=C(C=C(C=C2Br)Br)Br
PubChem CID
44465

Risk for dogs

Extreme risk

Bromethalin (N-methyl-2,4-dinitro-N-(2,4,6-tribromophenyl)-6-(trifluoromethyl)benzenamine) is a non-anticoagulant neurotoxic rodenticide increasingly common in the US since EPA restrictions on second-generation anticoagulant rodenticides for consumer use in 2011. Mechanism: uncouples oxidative phosphorylation in neural mitochondria → impaired myelin maintenance → cerebral and spinal cord edema → ascending paralysis. Critically: there is NO antidote for bromethalin. Minimum lethal dose in dogs: approximately 1–2 mg/kg (acute) to 5–10 mg/kg over multiple exposures. A single commercially available bait block may contain sufficient bromethalin to be lethal to a small or medium dog. Onset of clinical signs: 24–96 hours post-ingestion. Signs of acute/severe exposure: hind limb weakness, ataxia, ascending paralysis, tremors, hyperexcitability, opisthotonus, seizures, hyperthermia, death. Signs of subacute/lower-dose exposure: bilateral hind limb paresis, lethargy, vomiting — may persist for days to weeks. Diagnosis is often presumptive (bait product identification). Treatment is limited to aggressive decontamination (emesis + activated charcoal + cathartic — critical if within 1 hour of ingestion; activated charcoal for 24–48 hours due to enterohepatic recirculation), anti-edema measures (mannitol, corticosteroids — evidence limited), and supportive care. ASPCA APCC now receives more bromethalin calls than anticoagulant rodenticide calls in many regions.

Risk for cats

Extreme risk

Cats are highly susceptible to bromethalin toxicosis — the minimum lethal dose is approximately 0.45 mg/kg (lower than dogs), reflecting cats' higher lipophilicity of neural tissue and lower metabolic capacity for bromethalin hydroxylation. Clinical signs in cats often appear as hindlimb paresis, altered mentation, hypersensitivity to stimuli, and seizures at subacute doses. Cats' hunting behavior creates secondary poisoning risk from consuming poisoned rodents containing bromethalin in tissues. Unlike anticoagulant rodenticides, no bioassay-based antidote treatment exists; the prognosis for severely affected cats is poor even with intensive supportive care. Indoor cats with access to rodenticide bait stations and outdoor cats in treated environments (commercial buildings, farms, urban rodent control programs) are both at risk. ASPCA strongly advises keeping bromethalin products inaccessible to cats and checking product labels before purchase, as bromethalin products are visually similar to anticoagulant products and owners may not distinguish them.

Regulatory consensus

1 regulatory bodyhas classified Bromethalin.

AgencyYearClassificationNotes
Unknown

Regulators apply different standards of evidence — animal-data weighting, exposure-pattern assumptions, epidemiological power thresholds — which is why two scientific bodies can review the same data and reach different conclusions. The disagreement is the data.

Where pets encounter bromethalin

  • Industrial FacilitiesManufacturing plants, Chemical storage areas, Waste treatment sites
  • Occupational EnvironmentsFactories, Warehouses, Transportation vehicles

Safer alternatives

Lower-risk approaches that achieve a similar outcome to Bromethalin:

  • Integrated Pest Management (IPM); Biopesticides; Physical controls
    Trade-offs: Combines biological, cultural, and targeted chemical controls; reduces overall chemical use 30-70%; requires trained practitioners and monitoring infrastructure; higher management complexity; proven effective at scale in many crop systems.
    Relative cost: 1.2-2×

Frequently asked questions

Is bromethalin safe for pets?

Bromethalin (N-methyl-2,4-dinitro-N-(2,4,6-tribromophenyl)-6-(trifluoromethyl)benzenamine) is a non-anticoagulant neurotoxic rodenticide increasingly common in the US since EPA restrictions on second-generation anticoagulant rodenticides for consumer use in 2011. Mechanism: uncouples oxidative phosphorylation in neural mitochondria → impaired myelin maintenance → cerebral and spinal cord edema → ascending paralysis. Critically: there is NO antidote for bromethalin. Minimum lethal dose in dogs: approximately 1–2 mg/kg (acute) to 5–10 mg/kg over multiple exposures. A single commercially available bait block may contain sufficient bromethalin to be lethal to a small or medium dog. Onset of clinical signs: 24–96 hours post-ingestion. Signs of acute/severe exposure: hind limb weakness, ataxia, ascending paralysis, tremors, hyperexcitability, opisthotonus, seizures, hyperthermia, death. Signs of subacute/lower-dose exposure: bilateral hind limb paresis, lethargy, vomiting — may persist for days to weeks. Diagnosis is often presumptive (bait product identification). Treatment is limited to aggressive decontamination (emesis + activated charcoal + cathartic — critical if within 1 hour of ingestion; activated charcoal for 24–48 hours due to enterohepatic recirculation), anti-edema measures (mannitol, corticosteroids — evidence limited), and supportive care. ASPCA APCC now receives more bromethalin calls than anticoagulant rodenticide calls in many regions.

What products contain bromethalin?

Bromethalin appears in: Manufacturing plants (Industrial facilities); Chemical storage areas (Industrial facilities); Factories (Occupational environments); Warehouses (Occupational environments).

See Bromethalin in the pets app

Look up products containing bromethalin, compare to alternatives, and explore the full data record.

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Sources (3)

  1. ASPCA Animal Poison Control Center: Bromethalin Rodenticide Toxicosis — Recognition, Management and Prognosis in Companion Animals (2022) — report
  2. US EPA: Bromethalin — Registration Eligibility Decision and Risk Assessment (2013) — regulatory
  3. Dorman DC: Bromethalin Rodenticide Toxicosis. Veterinary and Human Toxicology — Mechanisms and Clinical Presentation (1990) — report

Reference data, not professional advice. Aggregates publicly available regulatory and scientific data; not a substitute for veterinary, medical, legal, or regulatory advice. Why we built ALETHEIA →