Is Fenpropathrin safe for dogs and cats?
Low risk for petsDogs tolerate fenpropathrin well at use concentrations; the compound's primary use in ornamental and agricultural settings rather than direct pet products reduces veterinary exposure scenarios compared to permethrin or cypermethrin.
What is fenpropathrin?
The IUPAC name is [cyano-(3-phenoxyphenyl)methyl] 2,2,3,3-tetramethylcyclopropane-1-carboxylate.
Also known as: [cyano-(3-phenoxyphenyl)methyl] 2,2,3,3-tetramethylcyclopropane-1-carboxylate, Meothrin, Rody, Danimen.
- IUPAC name
- [cyano-(3-phenoxyphenyl)methyl] 2,2,3,3-tetramethylcyclopropane-1-carboxylate
- CAS number
- 39515-41-8
- Molecular formula
- C22H23NO3
- Molecular weight
- 349.4 g/mol
- SMILES
- CC1(C(C1(C)C)C(=O)OC(C#N)C2=CC(=CC=C2)OC3=CC=CC=C3)C
- PubChem CID
- 47326
Risk for dogs
Low riskDogs tolerate fenpropathrin well at use concentrations; the compound's primary use in ornamental and agricultural settings rather than direct pet products reduces veterinary exposure scenarios compared to permethrin or cypermethrin.
Risk for cats
Extreme riskFenpropathrin is a type II alpha-cyano pyrethroid — extreme cat toxicity consistent with the class; used in ornamental plant care (Danitol, Tame sprays) and residential spider/mite control; cats in treated ornamental garden areas or homes where sprays have been applied can be exposed through grooming of coat contaminated with residues. The CS syndrome in cats is rapid-onset and severe. Fenpropathrin has both insecticidal and acaricidal properties, making it used more broadly in home and garden settings where cats may roam.
Regulatory consensus
1 regulatory bodyhas classified Fenpropathrin.
| Agency | Year | Classification | Notes |
|---|---|---|---|
| EPA CTX / EPA OPP | — | Not Likely to Be Carcinogenic in Humans |
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 fenpropathrin
- Industrial Facilities — Manufacturing plants, Chemical storage areas, Waste treatment sites
- Occupational Environments — Factories, Warehouses, Transportation vehicles
Safer alternatives
Lower-risk approaches that achieve a similar outcome to Fenpropathrin:
-
Physical/mechanical pest control (IPM)
Trade-offs: More labor-intensive. May not be sufficient for severe infestations.Relative cost: 1.2-2×
Frequently asked questions
Is fenpropathrin safe for pets?
Dogs tolerate fenpropathrin well at use concentrations; the compound's primary use in ornamental and agricultural settings rather than direct pet products reduces veterinary exposure scenarios compared to permethrin or cypermethrin.
What products contain fenpropathrin?
Fenpropathrin appears in: Manufacturing plants (Industrial facilities); Chemical storage areas (Industrial facilities); Factories (Occupational environments); Warehouses (Occupational environments).
See Fenpropathrin in the pets app
Look up products containing fenpropathrin, compare to alternatives, and explore the full data record.
Open in pets View raw API dataSources (2)
- US EPA Pyrethroid Reregistration Eligibility Decision — cypermethrin/deltamethrin/lambda-cyhalothrin/bifenthrin/cyfluthrin/fenvalerate/tau-fluvalinate/fenpropathrin; type I/II classification; aquatic toxicity; cat sensitivity; sodium channel mechanism; human paresthesia; buffer zones (2011) (2011) — regulatory
- ASPCA Animal Poison Control Center: Pyrethroid Toxicosis in Cats and Dogs — type I vs type II CS/T syndromes; extreme cat sensitivity (sodium channel/UGT deficiency); bathing decontamination; methocarbamol tremor control; cyproheptadine; lipid emulsion severe cases (2023) (2023) — veterinary
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 →