| Amprolium |
![]() Last updated: 20/10/2025 |
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(Also known as: amprolium ion) |
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Amprolium is a thiamine analogue often used as the hydrochloride | |
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Mainly used to treat coccidiosis | |
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Poultry; Dogs; Cats; Elephants; Pigeons |
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Approved - usually supplied 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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C₁₄H₁₉N₄+ | |
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CCCC1=NC=C(C(=N1)N)C[N+]2=CC=CC=C2C | |
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IPZFPROOBOUEIG-UHFFFAOYSA-N | |
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InChI=1S/C14H19N4/c1-3-6-13-16-9-12(14(15)17-13)10-18-8-5-4-7-11(18)2/h4-5,7-9H,3,6,10H2,1-2H3,(H2,15,16,17)/q+1 | |
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Yes |
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| Common Name | Relationship | Link |
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| amprolium hydrochloride | Variant | ![]() |
| General status |
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Coccidiostat, Antiprotozoal agent, Antiparasitic | ||||||||||||||
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Thiamine analogue | ||||||||||||||
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Synthetic | ||||||||||||||
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A thiamine analogue, blocks the thiamine transporter of Eimeria species | ||||||||||||||
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[Thiamine, Antagonist] | ||||||||||||||
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13082-85-4 | ||||||||||||||
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121-25-5 | ||||||||||||||
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204-458-4 | ||||||||||||||
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2178 | ||||||||||||||
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Antiparasitic products, insecticides & repellents: Antiprotozoals | ||||||||||||||
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QP51AX09 | ||||||||||||||
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No | ||||||||||||||
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Allowed substance (Table 1: Poultry) | ||||||||||||||
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243.33 | ||||||||||||||
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5-[(2-methylpyridin-1-ium-1-yl)methyl]-2-propylpyrimidin-4-amine | ||||||||||||||
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5-[(2-methylpyridin-1-ium-1-yl)methyl]-2-propylpyrimidin-4-amine | ||||||||||||||
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Not approved as a feed additive in EU | ||||||||||||||
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White to off-white coloured powder | ||||||||||||||
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| Commercial |
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Current | |||
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1950s, first synthesised; 1960s, initial vet use; 1970s, start of global expansion | |||
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Usually supplied as a concentrate to add to drinking water | |||
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Amprolium is commercially produced through a multi-step chemical synthesis that begins with intermediates derived from vitamin B1 (thiamine). The process typically involves cyclisation of a pyrimidine derivative, followed by ring-opening hydrolysis to modify the structure. A key transformation is diazotisation, where an amino group is converted into a hydroxyl group, enabling further functionalisation. The final step is a condensation reaction between the modified pyrimidine and a methylpyridinium compound, forming the active amprolium hydrochloride. | |||
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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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| Known metabolites |
None
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| General |
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Rapidly absorbed from the gastrointestinal tract and very rapidly excreted via the urine and faeces | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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| Health issues |
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May cause stomach distress, nausea or vomiting | ||||||||||||||||||||||||||||
| Handling issues |
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No information available | |||
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Health: H361, H372 | |||
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Not listed (Not listed) | |||
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amprolium | ||
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amprolium | ||
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amprolio | ||
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| Record last updated: | 20/10/2025 |
| 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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