| Chloromebuform (Ref: CGA 22598) |
![]() Last updated: 09/09/2025 |
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(Not known by any other names) |
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An obsolete organochloride insecticide | |
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Possible applications for the control of cattle scabies, ticks, lice, mange mites, stable flies, horse flies and other nuisance flies | |
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Cattle |
| Approval status |
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Not approved | |
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Not approved |
| Chemical structure |
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None | |
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C₁₃H₁₉ClN | |
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CCCCN(C)C=NC1=C(C=C(C=C1)Cl)C | |
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No data | |
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OUDYXRYNDPEKLK-UHFFFAOYSA-N | |
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InChI=1S/C13H19ClN2/c1-4-5-8-16(3)10-15-13-7-6-12(14)9-11(13)2/h6-7,9-10H,4-5,8H2,1-3H3 | |
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Yes |
| General status |
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Insecticide; Acaricide | ||||||||||||||
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Organochloride; Formamidine | ||||||||||||||
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Synthetic | ||||||||||||||
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Unclear but thought to disrupt nervous system signaling, leading to paralysis and death in pests. | ||||||||||||||
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[Unclear - may target octopamine receptors] | ||||||||||||||
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37407-77-5 | ||||||||||||||
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None allocated | ||||||||||||||
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No | ||||||||||||||
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238.76 | ||||||||||||||
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N-butyl-N-(4-chloro-o-tolyl)-N-methylformamidin | ||||||||||||||
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N-butyl-N-(4-chloro-2-methylphenyl)-N-methylmethanimidamide | ||||||||||||||
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| Commercial |
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Considered obsolete but may be available in some countries | |||
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Circa 1975, introduced | |||
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Typically supplied in the form of a powder or dust for topical application on livestock. | |||
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Chloromebuform is produced through a multi-step chemical synthesis involving the formation of a formamidine moiety attached to a chlorinated aromatic ring. While detailed industrial synthesis protocols are not publicly documented, its structure suggests that production likely begins with a chlorinated benzene derivative, which undergoes nucleophilic substitution or condensation reactions to introduce the formamidine group. | |||
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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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Likely to be soluble | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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Based on chemical group | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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| Degradation |
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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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| Fate indices |
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| Known metabolites |
None
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| Aquatic ecotoxicology |
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| General |
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High (class III) | - | - | ||||||||
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Unclear | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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| Health issues |
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No information available | ||||||||||||||||||||||||||||
| Handling issues |
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No information available | |||
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Not classified: Obsolete (Not classified: Obsolete) | |||
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chloromebuform | ||
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chloromebuforme | ||
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| Record last updated: | 09/09/2025 |
| 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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