Lasalocid sodium |
![]() Last updated: 15/09/2025 |
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(Also known as: lasalocid A) |
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A divalent polyether ionophore antibiotic and antiparasitic veterinary drug used to control gram-positive bacteria | |
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Used as a feed supplement for fattening game birds and cattle; Also used for the prevention of coccidiosis caused by Eimeria spp. in game birds. | |
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Turkeys; Chickens; Game birds; Sheep; Cattle |
Approval status |
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Not approved | |
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Not approved |
Chemical structure |
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Lasalocid sodium exhibits stereoisomerism, specifically diastereomerism, due to its complex polyether structure with multiple chiral centres. The molecule contains several cyclic ether rings and hydroxyl groups arranged in a rigid three-dimensional framework, which allows for different spatial configurations of atoms without altering the molecular formula. One notable isomer, sometimes referred to as iso-lasalocid A, differs from the standard lasalocid A in the size and absolute configuration of its terminal cyclic ether, leading to distinct physical properties. These isomers arise naturally during biosynthesis by Streptomyces lasaliensis, and their formation is influenced by the cyclisation mechanisms of the polyether backbone. | |
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C₃₄H₅₃O₈Na | |
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CCC(C1C(CC(O1)(CC)C2CCC(C(O2)C)(CC)O)C)C(=O)C(C)C(C(C)CCC3=C(C(=C(C=C3)C)O)C(=O)[O-])O.[Na+] | |
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CC[C@H]([C@@H]1[C@H](C[C@@](O1)(CC)[C@H]2CC[C@@]([C@@H](O2)C)(CC)O)C)C(=O)[C@@H](C)[C@H]([C@H](C)CCC3=C(C(=C(C=C3)C)O)C(=O)[O-])O.[Na+] | |
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RDHDUYAKDYQPEW-HWLWSTNVSA-M | |
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InChI=1S/C34H54O8.Na/c1-9-25(31-21(6)18-34(11-3,42-31)26-16-17-33(40,10-2)23(8)41-26)30(37)22(7)28(35)19(4)12-14-24-15-13-20(5)29(36)27(24)32(38)39;/h13,15,19,21-23,25-26,28,31,35-36,40H,9-12,14,16-18H2,1-8H3,(H,38,39);/q;+1/p-1 | |
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Yes |
General status |
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Antibiotic, Medicinal drug, Feed additive, Coccidiostat, Antiparasitic | |
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Ionophore | |
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97% | |
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Synthetic | |
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Dissociates the calcium fluxes in muscle fibres. Lasalocid sodium disturbs ionic homeostasis, leading to osmotic lysis of coccidia. | |
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[Ionic homeostasis, Antagonist] | |
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25999-20-6 | |
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247-400-3 | |
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Antiparasitic products, insecticides & repellents: Antiprotozoals | |
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QP51AH02 | |
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No | |
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Allowed substance (Table 1: Poultry) | |
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612.77 | |
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- | |
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(2R-(2α(2S*(3R*,4S*,5S*,7R*),3S*,5S*),5α,6β))-6-(7-(5-Ethyl-5-(5-ethyltetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)tetrahydro-3-methyl-2-furanyl)-4-hydroxy-3,5-dimethyl-6-oxononyl)-2-hydroxy-3-methylbenzoic acid monosodium salt | |
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Benzoic acid, 6-(3R,4S,5S,7R)-7-(2S,3S,5S)-5-ethyl-5-(2R,5R,6S)-5-ethyltetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yltetrahydro-3-methyl-2-furanyl-4-hydroxy-3,5-dimethyl-6-oxononyl-2-hydroxy-3-methyl-, monosodium salt | |
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White to brown coloured powder |
Commercial |
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1951, first reported | |||
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Usually formulated as a medicated feed or feed additive | |||
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Lasalocid sodium is produced through microbial fermentation using the actinomycete Streptomyces lasaliensis, which naturally synthesizes this polyether ionophore antibiotic. The process begins by cultivating the microorganism in a carefully optimised nutrient medium under controlled conditions of temperature, pH, and aeration. During fermentation, lasalocid is secreted into the broth as a secondary metabolite. After sufficient incubation, the culture is harvested and subjected to extraction and purification steps, typically involving solvent extraction, filtration, and chromatographic techniques, to isolate lasalocid in its sodium salt form. | |||
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As microbial-based products tend to use fermentation-based production processes rather than chemical synthesis, they typically have a lower fossil fuel input in formulation and active ingredient creation, and also have reduced downstream emissions due to biodegradability and minimal soil disruption, their life-cycle GHG emissions are expected to be low. Whilst hard and precise data is not available, broad estimates suggest that typically emissions are likely to be below 5 kg CO₂e/kg. |
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50 | F2 F = U.S. EPA ECOTOX database / U.S. EPA pesticide fate database / Miscellaneous WHO documents / FAO data, IPCS INCHEM data (US EPA Databases Related to Pesticide Risk Assessment ) 2 = Unverified data of unknown source |
Moderate | ||||||||
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10000 | Q3 Q = Miscellaneous data from online sources Methanol3 = Unverified data of known source |
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180 | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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1.00 X 102255 | Calculated | - | |||||||
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225 | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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1.119 | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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Substance may enter the environment via the faeces of treated animals or by leaching from spilt medicated feed. |
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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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Soil adsorption and mobility |
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- | R4 R = Peer reviewed scientific publications 4 = Verified data |
Moderately mobile | |||||||
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323 | ||||||||||
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Koc value is for the acid | ||||||||||
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Fate indices |
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Known metabolites |
None
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Terrestrial ecotoxicology |
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122 | 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 |
Moderate | ||||||||
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> 59 | 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 ) Gallus domesticus5 = Verified data used for regulatory purposes |
High | ||||||||
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Aquatic ecotoxicology |
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3.0 | E3 E = Manufacturers safety data sheets Oncorhynchus mykiss3 = Unverified data of known source |
Moderate | ||||||||
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3.6 | E3 E = Manufacturers safety data sheets Daphnia magna3 = Unverified data of known source |
Moderate | ||||||||
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2.4 | E3 E = Manufacturers safety data sheets Desmodesmus subspicatus3 = Unverified data of known source |
Moderate | ||||||||
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General |
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High (class III) | - | - | ||||||||
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122 | 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 |
Moderate | ||||||||
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1400 | 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 ) Rabbit5 = Verified data used for regulatory purposes |
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Intraperitoneal LD₅₀ = 64 mg kg⁻¹ | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Mouse3 = Unverified data of known source |
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Widespread distribution throughout the body once administered. Blood elimination DT50 is ~3hrs in rats. Almost totally excreted by the biliary duct. | 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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Toxic to humans, horses and other species - has low margin of safety Poison by ingestion and intraperitoneal routes |
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When heated to decomposition it emits acrid smoke and irritating fumes IMDG Transport Hazard Class 6.1(b) |
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Not listed (Not listed) | |||
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UN2811 | |||
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Packaging Group III (minor danger) | |||
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lasalocid sodium | ||
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lasalocide sodique | ||
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lasalocido sodico | ||
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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 |