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. 2020 Dec 1;17(2):331–351. doi: 10.1002/ieam.4352

Table 2.

Nonpolymer PFAS toxicity, physical, and chemical properties

Nonpolymer PFAS
Perfluoroalkyl substances Polyfluoroalkyl substances
Description Perfluoroalkyl acids (PFAA) Fluorotelomer alcohols
Substance PFBA PFHxA PFOA PFBS PFOS Hexafluoropropylene oxide (HFPO) dimer acid, ammonium salt 2,2,3‐trifluoro‐3‐[1,1,2,2,3,3‐hexafluoro‐3‐(trifluoromethoxy) propoxy]propanoic acid 6:2 FTOH 8:2 FTOH
CAS number 375‐22‐4 307‐24‐4 335‐67‐1 375‐73‐5 1763‐23‐1 62037‐80‐3 919005‐14‐4 647‐42‐7 678‐39‐7
Structure graphic file with name IEAM-17-331-g014.jpg graphic file with name IEAM-17-331-g015.jpg graphic file with name IEAM-17-331-g016.jpg graphic file with name IEAM-17-331-g017.jpg graphic file with name IEAM-17-331-g018.jpg graphic file with name IEAM-17-331-g019.jpg graphic file with name IEAM-17-331-g020.jpg graphic file with name IEAM-17-331-g021.jpg graphic file with name IEAM-17-331-g022.jpg
Chain length Short Short Long Short Long Short Short Short Long
Molecular weight 214.0384 314.0534 414.069 Da 300.11 500.13 347.084 378.07 364.1 464.12
Physical state, description Liquid Colorless liquid White to off‐white powder Colorless liquid Liquid Clear, colorless liqud Clear, colorless liquid Clear, colorless to pale yellow liquid Waxy solid
Boiling point 120 to 121 °C 157 °C 192 °C 210 to 212 °C 249 °C 108 °C 183 °C 171 °C NDA
Melting point −17.5 °C NDA 54.3 °C NDA NDA 183 to 184 °C NDA 78 °C NDA
Vapor pressure 5866 Pa at 56 °C 263.9 Pa at 25 °C (est) 4.21 Pa at 25 °C 3.57 Pa at 25 °C (est) 0.2667 Pa at 25 °C 2910 Pa at 20 °C 32 Pa at 20 °C 26.6645 Pa at 25 °C 31 Pa at 25 °C
Stability (hydrolysis, photolysis, oxidation, thermal, biological) Stable Concentrations decreased by 0.8% after 106 d of solar irradiation; no other data Stable NDA NDA Stable Stable NDA NDA
Water solubility (USP 2011) 2.14 × 105 mg·L−1 at 25 °C In water, 15 700 mg·L−1 at ambient temperature 9.50 × 103 mg·L−1 at 25 °C In water, 344 mg·L−1 at 25 °C (est) 3.2 × 10−3 mg·L−1 at 25 °C (est) >1000 g·L−1 at 20 °C 100% Soluble in water “insoluble” 18.8 mg·L−1 140 µg·L−1 at 25 °C
Log K OW Not applicable 3.48 (est) 4.81 (est) 1.82 (est) 4.49 (est) NDA 1.89 4.54 NDA
Particle size µm NDA NDA NDA NDA NDA Dried solid 76% >105 microns; 24% < 105 microns NDA NDA NDA
Acute Dermal LD50 NDA Low (>2000 mg/kg) Low (>2000 mg/kg) Low (>2000 mg/kg) NDA Low (5000 mg/kg) Low (5000 mg/kg) Low (5000 mg/kg) NDA
Skin irritant, Y or N Y, corrosive Y Y N N Y Y, mild Y NDA
Eye irritant, Y or N Y (serious damage) Y Y Y Y Y Y Y NDA
Skin sensitizer, Y or N NDA N N N NDA N Y N NDA
90‐d animal feeding study (no effect dose) 6 mg/kg‐day 50 mg/kg‐day 0.06 mg/kg‐day 200 mg/kg‐day 0.4 mg/kg‐day 0.1 mg/kg‐day 10 and 100 mg/kg‐day for males, females 5 mg/kg‐day 5 mg/kg‐day
Mutagen, Y or N NDA N N N N N N N N
Caused tumors in lab rats, Y or N NDA N Y NDA Y Y NDA NDA NDA
Half‐life in humans 69 to 87 h <28 d 3.3 to 3.8 y 24 to 46 d 5.4 to 5.9 y 2.3 h 23 ± 11 d NDA NDA
References (Ding and Peijnenburg 2013; NICNAS 2015; ChemSpider 2018; Sigma Aldrich 2018a; ATSDR 2018) (Savu 1994; USEPA 2012; Environ 2014; Zhao L et al. 2014; ChemSpider 2016; Luz et al. 2019) (Kennedy et al. 2004; Butenhoff et al. 2004; Yalkowsky et al. 2010; Bhhatarai and Gramatica 2011; USEPA 2012; Haynes 2014) (Kosswig 2000; Lewis 2012; USEPA 2012; Sigma Aldrich 2015) (Ashford 1994; Lewis 2012; USEPA 2012) (Biegel et al. 2001; Caverly Rae et al. 2015; Beekman et al. 2016; Hoke et al. 2016; ECHA 2019b; PubChem. 2019) (Gordon 2011; Wang et al. 2013; ECHA 2020) (Daikin 2007, 2009a, 2009b) (Ladics et al. 2008; Climate and Pollution Agency, Norway 2010)

PFAS = per‐ and polyfluoroalkyl substances; PFAA = perfluoroalkyl acids; PFBA = perfluorobutanoic acid; PFHxA = perfluorohexanoic acid; PFOA = perfluorooctanoic acid; PFBS = perfluorobutane sulfonic acid; HFPO = hexafluoropropylene oxide; FTOH = fluorotelomer alcohol; NDA = no data available.