Perfluoroalkoxy alkanes (PFA) are fluoropolymers. They are copolymers of tetrafluoroethylene (C₂F₄) and perfluoroethers (C₂F₃OR^f, where R^f is a perfluorinated group such as trifluoromethyl (CF₃)). The properties of these polymers are similar to those of polytetrafluoroethylene (PTFE). Compared to PTFE, PFA has better anti-stick properties and higher chemical resistance, at the expense of lesser scratch resistance.

Unlike with PTFE, the alkoxy substituents allow the polymer to be melt-processed. On a molecular level, PFA polymers have a smaller chain length and higher chain entanglement than other fluoropolymers. They also contain an oxygen atom at the branches. This results in materials that are more translucent and have improved flow and creep resistance, with thermal stability close to or exceeding PTFE. Thus, PFA is preferred when extended service is required in hostile environments involving chemical, thermal, and mechanical stress. PFA offers high melt strength, stability at high processing temperatures, excellent crack and stress resistance and a low coefficient of friction. Similarly enhanced processing properties are found in fluorinated ethylene propylene (FEP), the copolymer of tetrafluoroethylene and hexafluoropropylene. However FEP is ten times less capable of withstanding repeated bending without fracture than PFA.

PFA is commonly used as a material for piping and as fittings for aggressive chemicals, as well as the corrosion-resistant lining of vessels in the chemical-processing industry. Typical applications include the construction of gas scrubbers, reactors, containment vessels and piping. In coal-fired power plants, it is used for lining heat exchangers. By channeling crude gas through a PFA-lined apparatus, the gas stream can be cooled below its condensation temperature without damaging the heat exchanger. Its use contributes to increasing the efficiency of the whole plant.

PFA is also used to make sampling equipment in analytical chemistry and for geochemical or environmental in situ studies in the field, when it is particularly important to avoid chemical contamination from metallic ions at trace levels.

PFA is produced as a copolymer of tetrafluoroethylene and a perfluoroether, usually perfluoro(methyl vinyl ether). Preparation of the perfluoroether precursors is more complex than partially fluorinated vinyl ethers, which can be made from the reaction of tetrafluoroethylene with alkoxides:

However, the instability of α-fluoroalcohols makes preparation of most perfluoroalkoxides impractical. Instead, production of vinyl perfluoroethers can be achieved by pyrolysis of a perfluoro(2-alkoxy carboxylate) salt.

This reaction, called dehalocarbonylation, proceeds by the elimination of CO₂ from the carboxylate, forming a carbanion intermediate that then undergoes elimination of fluoride to form the alkene. The vinyl ether can also be prepared directly from an acyl fluoride by using sodium carbonate:

Common trademarks include Teflon-PFA, Hostaflon-PFA and Chemfluor. Chemours claims to be the only U.S. producer of PFA at its Fayetteville Works plant in northern Bladen County.