| Promacyl (Ref: CRC 7320) |
![]() Last updated: 16/09/2025 |
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(Not known by any other names) |
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An obsolete carbamate insecticide | |
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Once used to control tick infestations | |
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Cattle; Horses |
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Not approved | |
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Not approved |
| Chemical structure |
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None | |
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C₁₆H₂₃NO₃ | |
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CCCC(=O)N(C)C(=O)OC1=CC(=CC(=C1)C(C)C)C | |
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DXEMHWAAAJAXBG-UHFFFAOYSA-N | |
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InChI=1S/C16H23NO3/c1-6-7-15(18)17(5)16(19)20-14-9-12(4)8-13(10-14)11(2)3/h8-11H,6-7H2,1-5H3 | |
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Yes |
| General status |
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Ixodicide | ||||||||||||||
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Carbamate insecticide; Carbamate acaricide; Phenyl methylcarbamate insecticide; Phenyl methylcarbamate acaricide | ||||||||||||||
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Synthetic | ||||||||||||||
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Acetylcholinesterase (AchE) inhibitor. | ||||||||||||||
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[Cholinesterase, Inhibitor] | ||||||||||||||
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34264-24-9 | ||||||||||||||
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No data found | ||||||||||||||
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None allocated | ||||||||||||||
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36733 | ||||||||||||||
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No data found | ||||||||||||||
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None allocated | ||||||||||||||
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No | ||||||||||||||
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277.36 | ||||||||||||||
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3-methyl-5-(propan-2-yl)phenyl butanoyl(methyl)carbamate | ||||||||||||||
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5-methyl-m-cumenyl butyryl(methyl)carbamate | ||||||||||||||
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3-methyl-5-(1-methylethyl)phenyl methyl(1-oxobutyl)carbamate | ||||||||||||||
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Brown liquid | ||||||||||||||
| Commercial |
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Considered obsolete but may be available in some countries | |||
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1970s-1980s, developed; 1980s, first approvals; 1990s, start of usage decline | |||
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Usually supplied as an emulsifiable concentrate for sprays or plunge dips | |||
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Promacyl is synthesised through a multi-step chemical process that begins with the preparation of its key intermediates, typically involving a carbamate backbone and aromatic components. These raw materials are combined in an organic solvent and subjected to distillation and dehydration, often using techniques like spray heating or membrane evaporator heating to ensure continuous processing. During this phase, wet-process smashing, blending, and packaging are integrated to streamline production. A notable innovation in the process involves the simultaneous complexation of maneb and zinc within the solvent system, which occurs alongside dehydration to facilitate crystal transformation. | |||
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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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158 | L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
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0.996 | L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
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400000 | L3 L = Pesticide manuals and hard copy reference books / other sources 3 = Unverified data of known source |
Highly volatile. If applied directly to plants or soil, drift is a concern & mitigation is advisable | ||||||||
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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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| Soil adsorption and mobility |
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| Fate indices |
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| Known metabolites |
None
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| Terrestrial ecotoxicology |
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> 1220 | L3 L = Pesticide manuals and hard copy reference books / other sources Rat3 = Unverified data of known source |
Moderate | ||||||||
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> 4000 | L3 L = Pesticide manuals and hard copy reference books / other sources Gallus domesticus3 = Unverified data of known source |
Low | ||||||||
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| Aquatic ecotoxicology |
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| General |
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Low (class I) | - | - | ||||||||
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> 1220 | L3 L = Pesticide manuals and hard copy reference books / other sources Rat3 = Unverified data of known source |
Moderate | ||||||||
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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 further information available | ||||||||||||||||||||||||||||
| Handling issues |
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IMDG Transport Hazard Class 6,1 | |||
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II (Moderately hazardous) | |||
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UN3005 | |||
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promacyl | ||
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promacyle | ||
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| Record last updated: | 16/09/2025 |
| 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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