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Names | |
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IUPAC name
N-ethyl-1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonamide
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Other names
N-Ethylperfluorooctylsulfonamide
N-Ethylheptadecafluorooctanesulfonamide | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.021.801 |
EC Number |
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KEGG | |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C10H6F17NO2S | |
Molar mass | 527.20 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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Sulfluramid (N-EtFOSA) is a chemical compound from the group of sulfonic acid amides and per- and polyfluoroalkyl substances (PFASs) that is effective as an insecticide.
Annual production increased from about 30 tons in 2003 to 60 tons in 2013.[1]
Environmental issues
It is predominantly biotransformed to perfluorooctanesulfonic acid (PFOS),[2] but partly also to perfluorooctanoic acid (PFOA).[3][4] Sulfluramid benefits from an acceptable purpose in the listing of PFOS to annex B of the Stockholm Convention on Persistent Organic Pollutants.
References
- ^ Löfstedt Gilljam, John; Leonel, Juliana; Cousins, Ian T.; Benskin, Jonathan P. (2016-01-19). "Is Ongoing Sulfluramid Use in South America a Significant Source of Perfluorooctanesulfonate (PFOS)? Production Inventories, Environmental Fate, and Local Occurrence". Environmental Science & Technology. 50 (2): 653–659. Bibcode:2016EnST...50..653L. doi:10.1021/acs.est.5b04544. PMID 26653085.
- ^ "Sulfluramid Registration Review Final Decision; Notice of Availability". unblock.federalregister.gov. 2008. Retrieved 2023-02-20.
- ^ Plumlee, Megan H.; McNeill, Kristopher; Reinhard, Martin (2009-05-15). "Indirect Photolysis of Perfluorochemicals: Hydroxyl Radical-Initiated Oxidation of N-Ethyl Perfluorooctane Sulfonamido Acetate (N-EtFOSAA) and Other Perfluoroalkanesulfonamides". Environmental Science & Technology. 43 (10): 3662–3668. Bibcode:2009EnST...43.3662P. doi:10.1021/es803411w. PMID 19544870.
- ^ Liu, Zhaoyang; Lu, Yonglong; Wang, Pei; Wang, Tieyu; Liu, Shijie; Johnson, Andrew C.; Sweetman, Andrew J.; Baninla, Yvette (February 2017). "Pollution pathways and release estimation of perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) in central and eastern China". Science of the Total Environment. 580: 1247–1256. Bibcode:2017ScTEn.580.1247L. doi:10.1016/j.scitotenv.2016.12.085. PMID 28040212.
- ^ Zhang, Wenping; Pang, Shimei; Lin, Ziqiu; Mishra, Sandhya; Bhatt, Pankaj; Chen, Shaohua (March 2021). "Biotransformation of perfluoroalkyl acid precursors from various environmental systems: advances and perspectives". Environmental Pollution. 272: 115908. doi:10.1016/j.envpol.2020.115908. PMID 33190976. S2CID 226973891.
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