| Silver sulfadiazine |
![]() Last updated: 16/09/2025 |
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(Not known by any other names) |
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A topically applied microbial used in veterinary medicine effective against gram-positive and gram-negative organisms | |
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Used to treat skin infections and burns | |
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Dogs; Cats; Horses |
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Not approved | |
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Not approved |
| Chemical structure |
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None | |
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C₁₀H₉AgN₄O₂S | |
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C1=CN=C(N=C1)[N-]S(=O)(=O)C2=CC=C(C=C2)N.[Ag+] | |
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UEJSSZHHYBHCEL-UHFFFAOYSA-N | |
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InChI=1S/C10H9N4O2S.Ag/c11-8-2-4-9(5-3-8)17(15,16)14-10-12-6-1-7-13-10;/h1-7H,11H2;/q-1;+1 | |
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Yes |
| General status |
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Antimicrobial | ||||||||||||||
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Sulfonamide drug | ||||||||||||||
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The silver moiety releases silver ions that disrupt bacterial cell membranes, while sulfadiazine inhibits bacterial folic acid synthesis. | ||||||||||||||
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[DNA, Binder], [Dihydropteroate synthase, Binder] | ||||||||||||||
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22199-08-2 | ||||||||||||||
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244-834-5 | ||||||||||||||
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441244 | ||||||||||||||
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Dermatologicls: Sulfonamides | ||||||||||||||
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QD06BA01 | ||||||||||||||
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No | ||||||||||||||
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357.14 | ||||||||||||||
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silver;(4-aminophenyl)sulfonyl-pyrimidin-2-ylazanide | ||||||||||||||
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| Commercial |
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Current | |||
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1968, discovered; 1990s, vet use adopted | |||
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Topically applied cream or lotion | |||
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The production of silver sulfadiazine involves a straightforward precipitation reaction between silver nitrate and sodium sulfadiazine. First, sulfadiazine powder is converted into its sodium salt by reacting it with sodium hydroxide, often in the presence of a catalyst like trifluoromethanesulfonic acid. Separately, an aqueous solution of silver nitrate is prepared. These two solutions are then simultaneously fed and stirred in a reaction vessel maintained at a temperature between 45–55 DegC, allowing the silver ions to react with sulfadiazine anions and form silver sulfadiazine precipitate. | |||
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For every kilogram of silver sulfadiazine produced, total GHG emissions could range from 50 to 80 kg CO₂e, with silver refinement being the dominant contributor. |
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285 | Q3 Q = Miscellaneous data from online sources 3 = Unverified data of known source |
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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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> 10000 | Q3 Q = Miscellaneous data from online sources Rat3 = Unverified data of known source |
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| General |
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> 10000 | Q3 Q = Miscellaneous data from online sources Rat3 = Unverified data of known source |
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Once absorbed, silver is primarily eliminated via the faeces and its excretion is slow. Sulfadiazine is more readily absorbed and is eliminated through the urine, with approximately 6.6% excreted within five days. | 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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silver sulfadiazine | ||
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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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