Perfluorobutanoic acid
|
|
Names
|
Preferred IUPAC name
|
Other names
Perfluorobutanoic acid Perfluorobutyric acid Heptafluorobutyric acid HFBA PFBA [1]C 4 PFCA
|
Identifiers
|
|
|
|
|
Abbreviations
|
HFBA
|
ChEBI
|
|
ChemSpider
|
|
ECHA InfoCard
|
100.006.170
|
|
|
UNII
|
|
|
|
InChI=1S/C4HF7O2/c5-2(6,1(12)13)3(7,8)4(9,10)11/h(H,12,13) NKey: YPJUNDFVDDCYIH-UHFFFAOYSA-N NInChI=1/C4HF7O2/c5-2(6,1(12)13)3(7,8)4(9,10)11/h(H,12,13) Key: YPJUNDFVDDCYIH-UHFFFAOYAI
|
OC(C(F)(F)C(F)(F)C(F)(F)F)=O
|
Properties
|
|
C4HF7O2
|
Molar mass
|
214.039 g·mol−1
|
Appearance
|
colourless liquid
|
Density
|
1.64 g/ml
|
Boiling point
|
120 °C (248 °F; 393 K)
|
|
high
|
Hazards
|
Occupational safety and health (OHS/OSH):
|
Main hazards
|
strong acid
|
GHS labelling:[2]
|
|
|
|
Danger
|
|
H314
|
|
P260, P280, P303+P361+P353, P304+P340+P310, P305+P351+P338
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Chemical compound
Perfluorobutanoic acid (PFBA) is a perfluoroalkyl carboxylic acid with the formula C3F7CO2H. As the perfluorinated derivative of butyric acid, this colourless liquid is prepared by electrofluorination of the corresponding butyryl fluoride.[3]
- ^ Buck, Robert C; Franklin, James; Berger, Urs; Conder, Jason M; Cousins, Ian T; de Voogt, Pim; Jensen, Allan Astrup; Kannan, Kurunthachalam; Mabury, Scott A; van Leeuwen, Stefan PJ (2011). "Perfluoroalkyl and polyfluoroalkyl substances in the environment: Terminology, classification, and origins". Integrated Environmental Assessment and Management. 7 (4): 513–541. doi:10.1002/ieam.258. PMC 3214619. PMID 21793199.
- ^ Sigma-Aldrich Co., Heptafluorobutyric acid. Retrieved on 2022-03-23.
- ^ Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2000), "Fluorine Compounds, Organic", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, doi:10.1002/14356007.a11_349, ISBN 978-3-527-30673-2