| Oxyclozanide |
![]() Last updated: 19/10/2025 |
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(Not known by any other names) |
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A salicylanide anthelmintic veterinary drug often used as an oral drench or a feed additive in combination with levamisole or oxfendazole | |
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Mainly used in the treatment and control of the parasitic infection, Fascioliasis, in ruminants | |
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Cattle; Sheep; Goats; Buffaloes |
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Approved - usually available as a prescription only medicine to be authorised by suitably qualified person (POM-VPS) | |
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Approved |
| Chemical structure |
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None | |
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C₁₃H₆Cl₅NO₃ | |
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C1=C(C=C(C(=C1Cl)O)NC(=O)C2=C(C(=CC(=C2Cl)Cl)Cl)O)Cl | |
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No data | |
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JYWIYHUXVMAGLG-UHFFFAOYSA-N | |
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InChI=1S/C13H6Cl5NO3/c14-4-1-6(16)11(20)8(2-4)19-13(22)9-10(18)5(15)3-7(17)12(9)21/h1-3,20-21H,(H,19,22) | |
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Yes |
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| Common Name | Relationship | Link |
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| oxyclozanide | - | ![]() |
| oxyclozanide | - | ![]() |
| General status |
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Antiparasitic, Anthelmintic, Medicinal drug | ||||||||||||||
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Salicylanilide; Aromatic halogen | ||||||||||||||
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Synthetic | ||||||||||||||
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Acts by uncoupling of oxidative phosphorylation in flukes | ||||||||||||||
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[Oxidative phosphorylation, Uncoupler] | ||||||||||||||
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2277-92-1 | ||||||||||||||
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218-904-0 | ||||||||||||||
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Antiparasitic products, insecticides & repellents: Anthelmintics | ||||||||||||||
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QP52AE51 | ||||||||||||||
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Allowed substance (Table 1: Ruminants) | ||||||||||||||
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401.46 | ||||||||||||||
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2,3,5-trichloro-N-(3,5-dichloro-2-hydroxyphenyl)-6-hydroxybenzamide | ||||||||||||||
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Marine pollutant | ||||||||||||||
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Current | |||
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Late 1950s, first synthesis, 1960s, characterisation;1970s, introduced into vet medicine | |||
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Available in a variety of formulations including oral suspensions and drenches | |||
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Oxyclozanide is synthesised through a multi-step chemical process involving the condensation of halogenated aromatic compounds. The production begins with the conversion of 3,5,6-trichlorosalicylic acid into 3,5,6-trichloro-2-hydroxybenzoyl chloride using thionyl chloride in the presence of a solvent like monochlorobenzene and a catalytic amount of dimethylformamide (DMF). This acid chloride is then reacted with 2-amino-4,6-dichlorophenol to form the core salicylanilide structure of oxyclozanide. | |||
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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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1.10 X 1006 | Calculated | - | |||||||
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6.04 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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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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| Known metabolites |
None
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| Terrestrial ecotoxicology |
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3519 | A5 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) Rat5 = Verified data used for regulatory purposes |
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| General |
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High (class III) | - | - | ||||||||
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3519 | A5 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) Rat5 = Verified data used for regulatory purposes |
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Around 85% of the administered dose is eliminated within 24hrs in the faeces | A5 A = EU regulatory and evaluation data as published by EC, EFSA (RAR, DAR & Conclusion dossiers), EMA (e.g. EU Annex III PIC DGD) (EU - Pesticides database; EFSA Scientific Publications ) 5 = Verified data used for regulatory purposes |
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| Health issues |
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Possible liver toxicant | ||||||||||||||||||||||||||||
| Handling issues |
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IMDG Transport Hazard Class 9 | |||
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Not listed (Not listed) | |||
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UN3077 | |||
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Packaging Group III (minor danger) | |||
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oxyclozanide | ||
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oxiclozanida | ||
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| Record last updated: | 19/10/2025 |
| 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 |
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