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This timeline of events related to per- and polyfluoroalkyl substances (PFASs) includes events related to the discovery, development, manufacture, marketing, uses, concerns, litigation, regulation, and legislation, involving the human-made PFASs. The timeline focuses on some perfluorinated compounds, particularly perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS)[1] and on the companies that manufactured and marketed them, mainly DuPont and 3M.[2] An example of PFAS is the fluorinated polymer polytetrafluoroethylene (PTFE), which has been produced and marketed by DuPont under its trademark Teflon. GenX chemicals and perfluorobutanesulfonic acid (PFBS) are organofluorine chemicals used as a replacement for PFOA and PFOS.[3]

PFAS compounds and their derivatives are widely used in many products from water resistant textiles to fire-fighting foam.[4][1] PFAS are commonly found in every American household in products as diverse as non-stick cookware, stain resistant furniture and carpets, wrinkle free and water repellant clothing, cosmetics, lubricants, paint, pizza boxes, popcorn bags and many other everyday products.[5]

Timeline

19th century

20th century

21st century

2000s

2010s

2020s

Relevant compounds

Selected compounds
Compound Chemical formula Structural model 3D image Other names Notes
Tetrafluoroethylene (TFE) C2F4 Tetrafluoroethene, Perfluoroethylene, Perfluoroethene Precursor to PTFE (Teflon)
Perfluorooctanoic acid (PFOA) C8HF15O2 perfluorooctanoic acid, PFOA, C8, perfluorooctanoate, perfluorocaprylic acid, FC-143, F-n-octanoic acid, PFO
Perfluorononanoic acid (PFNA) C9HF17O2 As ion: perfluorononanoate Here the health effects of PFNA, one of the ten most common PFAS, has been more widely studied.[81] Some of the "highest levels" of PFNA "ever found anywhere" are present in the Superfund Coakley landfill site in North Hampton, New Hampshire, and Greenland, New Hampshire.[97]
Perfluorooctanesulfonic acid (PFOS) C8HF17O3S As ion: perfluorooctanesulfonate
Polytetrafluoroethylene (PTFE) (C2F4)n Syncolon, Fluon, Poly(tetrafluroethene), Poly(difluoromethylene), Poly(tetrafluoroethylene), Teflon
Perfluorohexanesulfonic acid (PFHxS) C6HF13O3S Perfluorohexane-1-sulphonic acid
Perfluorohexanoic acid (PFHxA) C6HF11O Perfluoro-1-pentanecarboxylic acid
GenX C6H4F11NO3 GenX, FRD-902, Ammonium 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoate Replacement for PFOA developed by DuPont. GenX is created by combining two HFPO molecules to form HFPO-DA fluoride which is then converted to HFPO-DA. GenX is the ammonium salt of HFPO-DA. When GenX contacts water it releases HFPO-DA.

This ammonium salt is the chemical compound trademarked by Chemours as GenX, though many other compounds related to the GenX process are informally referred to as GenX.[122]

Hexafluoropropylene oxide (HFPO) C3F6O 2,2,3-Trifluoro-3-(trifluoromethyl)oxirane Precursor to GenX
Hexafluoropropylene oxide dimer acid fluoride (HFPO-DA fluoride) C6F12O2 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propionyl fluoride Precursor to GenX
Hexafluoropropylene oxide dimer acid (HFPO-DA) C6HF11O3 FRD-903, 2,3,3,3-tetrafluoro-2-(heptafluoropropoxy)propanoic acid Chemical used in the GenX process. GenX hydrolyzes in the presence of water to form HFPO-DA.[122]
Perfluorobutanesulfonic acid (PFBS) C4HF9O3S

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