2015
DOI: 10.1007/978-3-319-15518-0_17
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Toxicology Data for Alternative “Short-Chain” Fluorinated Substances

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Cited by 20 publications
(17 citation statements)
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“…They contain chains of carbons bonded to fluorines and some contain other functional groups, such as carboxylate or sulfonate moieties. Due to their chemical properties, PFAS are resistant to degradation and persist in the environment and in organisms [1]. Additionally, rodent and human studies have identified a variety of adverse effects associated with PFAS exposure, including liver, endocrine, developmental, and immune toxicity, among others [[2], [3], [4]].…”
Section: Introductionmentioning
confidence: 99%
“…They contain chains of carbons bonded to fluorines and some contain other functional groups, such as carboxylate or sulfonate moieties. Due to their chemical properties, PFAS are resistant to degradation and persist in the environment and in organisms [1]. Additionally, rodent and human studies have identified a variety of adverse effects associated with PFAS exposure, including liver, endocrine, developmental, and immune toxicity, among others [[2], [3], [4]].…”
Section: Introductionmentioning
confidence: 99%
“…79 These alternatives have already been approved by regulators for manufacture, sale and use. 80 As briefly stated above, the second approach to realize environmentally more acceptable anionic fluorosurfactants relies on intersections of fluoroalkylene fragments by ether linkages. Among these ethereal fluororganics, the fluoropolymer processing aids ADONA (ammonium 4,8-dioxa-3H-perfluorononanoate) 81,82 and GenX (ammonium perfluoro(2-methyl-3-oxahexanoate)) 83,84 have already been introduced as replacements of the SVHCs perfluorooctanoic acid and perfluorooctanesulfonic acid, respectively.…”
Section: General Aspects Of Biosafety and Environmental Benignity Of mentioning
confidence: 99%
“…Among these ethereal fluororganics, the fluoropolymer processing aids ADONA (ammonium 4,8-dioxa-3H-perfluorononanoate) 81,82 and GenX (ammonium perfluoro(2-methyl-3-oxahexanoate)) 83,84 have already been introduced as replacements of the SVHCs perfluorooctanoic acid and perfluorooctanesulfonic acid, respectively. 80 A range of structural motifs have emerged from replacement programs of PFASs, but it has been difficult to find substitutes that meet demanding functional and performance requirements. 85 Despite fundamental structural differences, the physicochemical profiles of the novel fluorinated alternatives do not deviate significantly from those of their predecessors.…”
Section: General Aspects Of Biosafety and Environmental Benignity Of mentioning
confidence: 99%
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