| Cetrimide |
![]() Last updated: 22/10/2025 |
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(Also known as: trimethylcetylammonium bromide; tetradonium bromide) |
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Substance used as a topical antiseptic | |
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Used to treat footrot on hooved livestock | |
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Sheep and many other animals |
| Approval status |
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Approved - usually as 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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C₁₇H₃₈BrN | |
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CCCCCCCCCCCCCC[N+](C)(C)C.[Br-] | |
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- | |
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CXRFDZFCGOPDTD-UHFFFAOYSA-M | |
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InChI=1S/C17H38N.BrH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18(2,3)4;/h5-17H2,1-4H3;1H/q+1;/p-1 | |
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Yes |
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| Common Name | Relationship | Link |
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| cetrimide | - | ![]() |
| General status |
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Antiseptic, Disinfectant, Microbiocide | ||||||||||||||
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Detergent; Surfactant; Microbiocide; Disinfectant; Additive | ||||||||||||||
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Quarternary ammonium compound | ||||||||||||||
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Synthetic | ||||||||||||||
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Broad-spectrum. Acts by preventing microbial growth by interfering with cell wall formation | ||||||||||||||
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[No specific molecular target] | ||||||||||||||
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8044-71-1 | ||||||||||||||
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10182-92-0 | ||||||||||||||
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200-311-3 | ||||||||||||||
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8052 | ||||||||||||||
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14250 | ||||||||||||||
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Dermatologicals: Other dermatological preparations | ||||||||||||||
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QD11AC01 | ||||||||||||||
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No | ||||||||||||||
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Allowed substance (Table 1: All food producing species) | ||||||||||||||
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336.4 | ||||||||||||||
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- | ||||||||||||||
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N,N,N-trimethyl(tetradecyl)azanium bromide | ||||||||||||||
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N-lauryl-N,N,N-trimethylammonium bromide | ||||||||||||||
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Clear to pale yellow viscous liquid | ||||||||||||||
| Commercial |
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Current | |||
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1950s, introduced | |||
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Available in a range of formulations including liquids, aerosols, drenches and as a semi-viscous liquid for cutaneous use with animals | |||
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Cetrimide is produced through a relatively straightforward chemical synthesis. The process begins with the reaction of myristyl chloride with trimethylamine in the presence of a base such as sodium hydroxide, forming myristyl trimethyl ammonium chloride. This intermediate is then converted into cetrimide by reacting it with sodium bromide. | |||
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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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560000 | Q2 Q = Miscellaneous data from online sources 2 = Unverified data of unknown source |
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| Degradation |
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5 | S1 S = Expert judgement 1 = Estimated data with little or no verification |
Non-persistent | |||||||
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Best available 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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| Soil adsorption and mobility |
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- | S1 S = Expert judgement 1 = Estimated data with little or no verification |
Non-mobile | |||||||
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271315 | ||||||||||
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Estimated | ||||||||||
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| Fate indices |
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-1.00 | Calculated | Low leachability | ||||||||||||||||||||||||||
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Low risk | E2 E = Manufacturers safety data sheets 2 = Unverified data of unknown source |
Low risk | |||||||||||||||||||||||||
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Not available | - | |||||||||||||||||||||||||||
| Known metabolites |
None
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| Terrestrial ecotoxicology |
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410 | Q2 Q = Miscellaneous data from online sources Rat2 = Unverified data of unknown source |
Moderate | ||||||||
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| Aquatic ecotoxicology |
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0.46 | Q3 Q = Miscellaneous data from online sources Pimephales promelas3 = Unverified data of known source |
Moderate | ||||||||
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1.81 | Q3 Q = Miscellaneous data from online sources Danio rerio3 = Unverified data of known source |
Moderate | ||||||||
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0.022 | Q3 Q = Miscellaneous data from online sources Daphnia magna3 = Unverified data of known source |
High | ||||||||
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0.0054 | Q2 Q = Miscellaneous data from online sources Raphidocelis subcapitata2 = Unverified data of unknown source |
High | ||||||||
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| General |
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High (class III) | - | - | ||||||||
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410 | Q2 Q = Miscellaneous data from online sources Rat2 = Unverified data of unknown source |
Moderate | ||||||||
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Cetrimide is very poorly absorbed after topical applications | A4 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 ) 4 = Verified data |
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| Health issues |
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May be harmful if swallowed, inhaled or in contact with the skin | ||||||||||||||||||||||||||||
| Handling issues |
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Corrosive | |||
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Health: H302, H312, H314, H318, H332 | |||
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Not listed (Not listed) | |||
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cetrimide | ||
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cétrimide | ||
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Cetrimid | ||
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cetrimide | ||
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cetrimide | ||
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cetrimide | ||
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ketrymid | ||
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| Record last updated: | 22/10/2025 |
| 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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