| Amprolium hydrochloride |
![]() Last updated: 15/09/2025 |
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(Not known by any other names) |
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Amprolium is a thiamine analogue | |
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Mainly used to treat coccidiosis | |
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Poultry; Dogs; Cats; Elephants; Pigeons |
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Approved - usually authorised as a veterinary medicine for general sale (AVM-GSL) | |
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Approved |
| Chemical structure |
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None | |
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C₁₄H₁₉N₄Cl | |
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CCCC1=NC=C(C(=N1)N)C[N+]2=CC=CC=C2C.Cl.[Cl-] | |
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No data | |
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PJBQYZZKGNOKNJ-UHFFFAOYSA-M | |
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InChI=1S/C14H19N4.2ClH/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);2*1H/q+1;;/p-1 | |
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Yes |
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| Common Name | Relationship | Link |
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| amprolium hydrochloride | - | ![]() |
| 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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137-88-2 | ||||||||||||||
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205-307-5 | ||||||||||||||
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1349737338 | ||||||||||||||
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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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315.24 | ||||||||||||||
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5-[(2-methylpyridin-1-ium-1-yl)methyl]-2-propyl-pyrimidin-4-amine chloride | ||||||||||||||
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1-[(4-Amino-2-propyl-5-pyrimidinyl)methyl]-2-picolinium chloride | ||||||||||||||
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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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Current | |||
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Mid 20th century, introduced | |||
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Usually supplied as a concentrate to add to drinking water | |||
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The production of amprolium hydrochloride involves a multi-step synthetic process starting from precursors like butyronitrile and acrylonitrile. Initially, butyronitrile reacts with methanol and ammonia to form butylamidine hydrochloride, while acrylonitrile undergoes methylation to yield alpha-methoxymethyl-beta-methoxylacrylonitrile. These intermediates are then combined to synthesize 4-amino-5-methoxy-2-propylpyrimidine, which serves as the core structure. In the final step, this pyrimidine derivative is reacted with 2-picoline to form the active compound, amprolium, which is then converted into its hydrochloride salt for enhanced solubility and stability. | |||
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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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>8 | R4 R = Peer reviewed scientific publications Slightly persistent4 = Verified data |
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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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> 4000 | Q3 Q = Miscellaneous data from online sources Rat3 = Unverified data of known source |
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| General |
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High (class III) | - | - | ||||||||
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> 4000 | Q3 Q = Miscellaneous data from online sources Rat3 = Unverified data of known source |
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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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Not listed (Not listed) | |||
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amprolium hydrochloride | ||
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chlorhydrate d' amprolium | ||
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hidrocloruro de amprolio | ||
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| Record last updated: | 15/09/2025 |
| 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 |
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