Tigolaner |
![]() Last updated: 13/09/2025 |
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(Not known by any other names) |
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An bispyrazole antiparasitic verterinary substance used for parasite control | |
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Shown to be efficacious against ticks (Ixodes ricinus, I. holocyclus), fleas (Ctenocephalides felis), and mites (Notoedres cati, Otodectes cynotis) | |
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Cats; Dogs |
Approval status |
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Approved - usually available as a prescription only medicine to be authorised by a veterinarian (POM-V) | |
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Approved |
Chemical structure |
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None | |
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C₂₁H₁₃ClF₈N₆O | |
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CN1C(=C(C(=N1)C(C(F)(F)F)(F)F)C(F)(F)F)N2C=C(C=N2)C3=CC(=C(C=C3)Cl)C(=O)NC4(CC4)C#N | |
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TVAJZOVLQZNNCJ-UHFFFAOYSA-N | |
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InChI=1S/C21H13ClF8N6O/c1-35-17(14(20(25,26)27)15(34-35)19(23,24)21(28,29)30)36-8-11(7-32-36)10-2-3-13(22)12(6-10)16(37)33-18(9-31)4-5-18/h2-3,6-8H,4-5H2,1H3,(H,33,37) | |
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Yes |
General status |
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Antiparasitic, Anthelmintic | |
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Bispyrazole insecticide; Bispyrazole acaricide | |
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Synthetic | |
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Acts as a potent inhibitor of the neurotransmitter gamma-aminobutyric acid (GABA) receptor. Disrupts the insects nervous system function, causing death | |
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[Gamma-aminobutyric acid (GABA) receptor, Inhibitor] | |
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1621436-41-6 | |
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846-825-7 | |
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77847513 | |
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No data found | |
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Antiparasitics: Praziquantel combinations | |
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QP52AA51 | |
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No | |
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552.81 | |
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2-chloro-N-(1-cyanocyclopropyl)-5-[2′-methyl-5′-(pentafluoroethyl)-4′-(trifluoromethyl)-2′H-[1,3′-bipyrazol]-4-yl]benzamide | |
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2-chloro-N-(1-cyanocyclopropyl)-5-[2′-methyl-5′-(perfluoroethyl)-4′-(trifluoromethyl)-2′H-[1,3′-bipyrazol]-4-yl]benzamide | |
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2-chloro-N-(1-cyanocyclopropyl)-5-[1′-methyl-3′-(1,1,2,2,2-pentafluoroethyl)-4′-(trifluoromethyl)[1,5′-bi-1H-pyrazol]-4-yl]benzamide | |
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Commercial |
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Current | |||
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2022, first registered for veterinary use | |||
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Formulated for topical administration such as pour-on and spot-on products usually in combination with praziquanrtel | |||
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The synthesis of tigolaner involves constructing a complex fluorinated heterocyclic scaffold designed for potent ectoparasitic activity. The process begins with the formation of a pyrazine or piperazine-based core, which serves as the central pharmacophore. This core is then functionalised with multiple halogenated aromatic rings, including fluoro and chloro substituents, to enhance lipophilicity and receptor binding. Key steps include selective halogenation, amide coupling, and cyclisation reactions to build the final structure. | |||
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Published GHG data is not available for most pharmaceuticals. However, according to industry, global averages suggest producing 1 kg of a typical active pharmaceutical ingredient can range from 10 to 100 kg CO₂e for small molecule drugs and potentially up to 1000 kg CO₂e for complex biologicals such as vaccines, depending on the drug type, its formulation, complexity of synthesis, solvent recovery, and energy sources used. |
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As this parameter is not normally measured directly, a surrogate measure is used: ‘Photochemical oxidative DT₅₀’. Where data is available, this can be found in the Fate Indices section below. | ||||||||||
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Fate indices |
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Known metabolites |
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Terrestrial ecotoxicology |
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Aquatic ecotoxicology |
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General |
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High (class III) | - | - | ||||||||
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Poorly metabolized and mainly excreted in the faeces | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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Health issues |
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No information available |
Handling issues |
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No information available | |||
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Not listed (Not listed) | |||
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tigolaner | ||
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tigolaner | ||
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Record last updated: | 13/09/2025 |
Contact: | aeru@herts.ac.uk |
Please cite as: | Lewis, K.A., Tzilivakis, J., Warner, D. and Green, A. (2016) An international database for pesticide risk assessments and management. Human and Ecological Risk Assessment: An International Journal, 22(4), 1050-1064. DOI: 10.1080/10807039.2015.1133242 |