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171468

Sigma-Aldrich

Perfluorooctanoic acid

95%

Synonym(s):

Pentadecafluorooctanoic acid, PFOA, Perfluorocaprylic acid, Perfluorooctanoic acid

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About This Item

Linear Formula:
CF3(CF2)6COOH
CAS Number:
Molecular Weight:
414.07
Beilstein/REAXYS Number:
1809678
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

95%

bp

189 °C/736 mmHg (lit.)

mp

55-56 °C (lit.)

SMILES string

OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C8HF15O2/c9-2(10,1(24)25)3(11,12)4(13,14)5(15,16)6(17,18)7(19,20)8(21,22)23/h(H,24,25)

InChI key

SNGREZUHAYWORS-UHFFFAOYSA-N

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Application

PFOA, its salts and related substances are listed in Part A of Annex I of the Persistent Organic Pollutants (POPs) Regulation (EU) 2019/1021. It can only be used for Laboratory-scale research or as a reference standard

Derogations until 4 July 2025 are uses in
  • photolithography or etch processes in semiconductor manufacturing
  • photographic coatings applied to films
  • invasive and implantable medical devices
The use is further allowed in firefighting foams for Class B fires until 4 July 2025

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Lact. - Repr. 1B - Skin Corr. 1C - STOT RE 1

target_organs

Liver

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Yusun Zhou et al.
Scientific reports, 6, 38633-38633 (2016-12-15)
Using a novel magnetic nanocomposite as adsorbent, a convenient and effective magnetic solid-phase extraction (MSPE) procedure was established for selective separation and concentration of nine perfluorinated compounds (PFCs) in surface water sample. Then an ultra high-performance liquid chromatography-tandem mass spectrometry
Lilan Zhang et al.
Environmental pollution (Barking, Essex : 1987), 229, 159-167 (2017-06-09)
With the phaseout of perfluorooctane sulfonate (PFOS) production in most countries and its well known recalcitrance, there is a need to quantify the potential release of PFOS from precursors previously or currently being emitted into the environment. Aerobic biodegradation of
Binding of perfluorooctanoic acid to rat and human plasma proteins.
Han X, et al.
Chemical Research in Toxicology, 16(6), 775-781 (2003)
Effects of perfluorooctanoic acid exposure during pregnancy in the mouse.
Lau C, et al.
Toxicological Sciences, 90(2), 510-518 (2006)
Naomi Kudo et al.
The Journal of toxicological sciences, 28(2), 49-57 (2003-06-25)
Perfluorooctanoic acid (PFOA) is an octanoic acid derivative to which all aliphatic hydrocarbons are substituted by fluorine. PFOA and its salts are commercially used in various industrial processes. The chemical is persistent in the environment and does not undergo biotransformation.

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