Frusemide |
![]() Last updated: 15/09/2025 |
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(Also known as: furosemide) |
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A sulfonamide compound used as a diuretic in veterinary medicine | |
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Used for the treatment of congestive heart failure, pulmonary edema, kidney disease, high blood pressure and edema in a range of animals | |
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Horses; Cats; Dogs; 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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C₁₂H₁₁ClN₂O₅S | |
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C1=COC(=C1)CNC2=CC(=C(C=C2C(=O)O)S(=O)(=O)N)Cl | |
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No data | |
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ZZUFCTLCJUWOSV-UHFFFAOYSA-N | |
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InChI=1S/C12H11ClN2O5S/c13-9-5-10(15-6-7-2-1-3-20-7)8(12(16)17)4-11(9)21(14,18)19/h1-5,15H,6H2,(H,16,17)(H2,14,18,19) | |
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Yes |
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Common Name | Relationship | Link |
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frusemide | - | ![]() |
General status |
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Diuretic, Antihypertensive | |
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Sulfonamide | |
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Synthetic | |
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Blocks the absorption of salt and fluid in the kidney tubules, causing diuresis. | |
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[Solute carrier family 12 member 1, Blocker] | |
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54-31-9 | |
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200-203-6 | |
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Cardiovascular system: Diuretics | |
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QC03CA01 | |
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No | |
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Allowed substance (Table 1: All food producing species) | |
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330.75 | |
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4-chloro-2-(furan-2-ylmethylamino)- 5-sulfamoylbenzoic acid | |
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2-furfurylamino-4-chloro-5-sulfamoylbenzoic acid | |
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Pale yellow powder |
Commercial |
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Circa 1970, introduced | |||
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Available in a variety of formulations including solutions for injection and tablets for oral administration | |||
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Frusemide is synthesised through a multi-step chemical process starting with Lasamide as the key intermediate. In the first stage, Lasamide is reacted with furfurylamine under controlled heating and nitrogen purging to form a crude sodium salt of frusemide. The reaction mass is then cooled and neutralised with sodium hydroxide, adjusting the pH to stabilise the product. After quality checks, the crude product undergoes crystallisation using isopropyl alcohol, followed by filtration and drying to yield sodium frusemide. In the final step, the sodium salt is acidified with glacial acetic acid and purified, often using activated carbon, to obtain the finished frusemide compound. | |||
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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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73.1 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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295 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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1.07 X 1002 | Calculated | - | |||||||
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2.03 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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4.30 X 10-05 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) 3 = Unverified data of known source |
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In ethanol: 288nm, 276nm, 336nm In NaOH: 226nm, 273nm, 336nm |
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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 soil and groundwater metabolites |
None
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4-chloro-5-sulfamoylanthranilic acid Note: Minor metabolite |
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Terrestrial ecotoxicology |
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> 2600 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Rat3 = Unverified data of known source |
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Aquatic ecotoxicology |
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General |
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High (class III) | - | - | ||||||||
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> 2600 | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Rat3 = Unverified data of known source |
Low | ||||||||
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Subcutaneous LD₅₀ = 4600 mg kg⁻¹ | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Rat3 = Unverified data of known source |
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Intraperitoneal LD₅₀ = 800 mg kg⁻¹ | V3 V = ChemID Online Databases; Chemspider; PubChem. (ChemID ) Rat3 = Unverified data of known source |
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Excreted largely unchanged in the urine | F4 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 ) 4 = Verified data |
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Health issues |
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kidney, liver, bladder, cardiovascular system toxicant |
Handling issues |
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Do not use water jets to fight fires, use dry chemical, foam or water spray | |||
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Not listed (Not listed) | |||
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frusemide | ||
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furosemida | ||
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furosemidu | ||
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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 |