Pentadecafluorooctanoic acid

Pentadecafluorooctanoic acid Basic information
Product Name:Pentadecafluorooctanoic acid
Synonyms:N-PERFLUOROOCTANOIC ACID;PENTADECAFLUOROOCTANOIC ACID;PERFLUOROHEPTANE CARBOXYLIC ACID;RARECHEM AL BO 0424;IPC-PFFA-8;IPC-PFFA-8 HG;Fluorad FC-26;Hexanoyl fluoride, 3,3,4,4,5,5,6,6,6-nonafluoro-2-oxo-
CAS:335-67-1
MF:C8HF15O2
MW:414.07
EINECS:206-397-9
Product Categories:Fluorochemical Surfactants;Analytical Chemistry;Functional Materials;Ion-Pair Reagents for HPLC;LC/MS Ion-Pair Reagents for Basic Samples;Surfactants;Fluorous Chemistry;Fluorous Compounds;Synthetic Organic Chemistry;organofluorine compounds;bc0001
Mol File:335-67-1.mol
Pentadecafluorooctanoic acid Structure
Pentadecafluorooctanoic acid Chemical Properties
Melting point 55-56 °C (lit.)
Boiling point 189 °C/736 mmHg (lit.)
density 1,7 g/cm3
Fp 189-192°C
storage temp. 2-8°C
solubility 3.4g/l
pka0.50±0.10(Predicted)
form Crystalline Powder
Specific Gravity1.7
color White
PH2.6 (1g/l, H2O, 20℃)
Water Solubility 3.4 g/L
BRN 1809678
Stability:Stable. Incompatible with bases, oxidizing agents, reducing agents.
InChIKeySNGREZUHAYWORS-UHFFFAOYSA-N
CAS DataBase Reference335-67-1(CAS DataBase Reference)
IARC2B (Vol. 110) 2017
NIST Chemistry ReferenceOctanoic acid, pentadecafluoro-(335-67-1)
EPA Substance Registry SystemPerfluorooctanoic acid (335-67-1)
Safety Information
Hazard Codes C,Xi,T,F
Risk Statements 22-34-52/53-39/23/24/25-23/24/25-11
Safety Statements 26-36/37/39-45-36/37-16-7
RIDADR UN 3261 8/PG 3
WGK Germany 2
RTECS RH0781000
Hazard Note Corrosive
TSCA T
HazardClass 8
PackingGroup III
HS Code 29159080
Hazardous Substances Data335-67-1(Hazardous Substances Data)
Toxicitydnd-esc 50 mmol MUREAV 89,95,81
MSDS Information
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Pentadecafluorooctanoic acid English
SigmaAldrich English
ACROS English
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Pentadecafluorooctanoic acid Usage And Synthesis
DescriptionConcerns about the potential environmental and toxicological impacts of long-chain perfluoroalkyl sulfonates and carboxylic acids have led to: (1) the phaseout of production of perfluorooctane sulfonate (PFOS) and related compounds and perfluorooctanoic acid (PFOA) by their major global manufacturer in 2000–02; (2) the conclusion of a stewardship agreement between the United States Environmental Protection Agency (US EPA) and eight leading global companies to reduce emissions and product content of PFOA and related chemicals by 95% by 2010 and to work toward their elimination by 2015; (3) a similar agreement between the Canadian environmental and health authorities and five companies to restrict perfluorinated carboxylic acids in products; (4) a European Union Marketing and Use Directive restricting the use of ‘PFOSs’ in the European Union; and (5) the inclusion of PFOS in the Stockholm Convention on Persistent Organic Pollutants as an Annex B substance, i.e., restricted in its use; and other regulatory and voluntary initiatives intended to reduce environmental emissions of this family of compounds.
Chemical PropertiesPerfluorooctanoic acid is a white to off-white powder or colorless flakes. It is very soluble in water.It has a pH of 2.6. Perfluorooctanoic acid has the ability to react with bases, oxidizing agents, and reducing agents. Upon decomposition, PFOA can form carbon oxides and hydrogen fluoride. Additional information related to physical and chemical properties of PFOA are not currently available.
Perfluorooctanoic acid structure
UsesPerfluorooctanoic acid (PFOA) is fluorinated surfactant used, primarily as its ammonium salt (APFO), as an aid in the chemical synthesis of fluoropolymers and fluoroelastomers. As such, it may be found in nonstick cookware and utensils, stain-repellant fabric treatments, and water-proofing treatments for garments. Although an effort is underway by the U.S. EPA to reduce use of and replace perfluoroalkyls with other substances, PFOA is still used in United States industry.
Perfluorooctanoic acid (PFOA, C8, pentadecafluorooctanoic acid, perfluoro caprylic acid) is an eightcarbon compound in the perfluoroalkyl family of chemicals. Perfluorooctane sulfonate is used in a variety of applications, including nonstick cookware, waterproof clothing, leather products, cleaning products, and pesticides. Its main use was as a stain repellent on carpet, furniture, and other consumer products. In 2006, the U.S. Protection Agency along with eight major companies that utilized PFOA embarked on a program to reduce emissions and use of the chemical by 2015 (USEPA, 2012).
UsesPFOA is a completely fluorinated organic acid that is produced synthetically as its salts. The typical structure has a nonbranched chain of eight carbon atoms. The industrial production of perfluoroalkyl carboxylates started in the late 1940s. Two principal production processes are used to manufacture PFOA, viz. electrochemical fluorination and telomerization. PFOA can also appear as a result of degradation of some precursors, e.g., fluorotelomer alcohols. The ammonium salt of PFOA is primarily used as an emulsifier or ‘processing aid’ in industrial applications, for example, in the production of fluoropolymers such as polytetrafluoroethylene, but also produced for fluorosurfactant use. Typical uses include fluoropolymers in electronics, textiles, and nonstick cookware, and fluorosurfactants in aqueous filmforming foams used for fire fighting.
UsesPentadecafluorooctanoic acid solution may be used as an ion-pairing reagent in the development of a chromatographic method for the separation and determination of underivatized proteinic amino acids using liquid chromatography with evaporative light scattering detection (LC-ELSD) and atmospheric pressure ionization-mass spectrometry (LC-API-MS), respectively.
DefinitionChEBI: A fluoroalkanoic acid that is perfluorinated octanoic acid.
General DescriptionPerfluorooctanoic acid is a perfluoroalkyl acid commonly used in the preparation of fluoroacrylic esters, fluoropolymers and fluoroelastmers. It is found to be environmentally persistent and bioaccumulative with a long half-life.
Safety ProfilePoison by intraperitoneal route. Mutation data reported. Whenheated to decomposition it emits toxic vapors of Fí.
Environmental FatePerfluorooctanoic acid found in the environment may result from waste stream releases from manufacture of cosmetics, lubricants, paints, polishes, adhesives, fabric treatments, and fire-fighting compounds. It can partition to the vapor phase in the atmosphere, where it is degraded atmospherically with a half-life of 31 days. It is very resistant to hydrolysis, and immobile in soil. It will not likely evaporate from soil (depending on soil pH) or surface waters. It is not expected to be absorbed to sediments and suspended particles. Perfluorooctanoic acid is not expected to bioaccumulate in aquatic organisms (BCF =3.1–9.4) (NLM, 2013).
Purification MethodsCrystallise the acid from CCl4 and toluene, and distil it. It forms micelles in H2O and the solubility is 1% in H2O. The acid chloride has b 129-130o/744mm. The amide has m 138o. [Bernett & Zisman J Phys Chem 63 1911 1959, Bro & Sperati J Polym Sci 38 289 1959, Beilstein 2 IV 994.]
Toxicity evaluationStudies with animals fed PFOA for a long period showed effects on the stomach, liver, and thyroid hormones. Animal studies also indicate that PFOA may cause cancer at relatively high levels. PFOA has also been shown to be a developmental toxicant, and to have effects on the immune system.
PFOA affects primarily the liver and can cause developmental and reproductive toxic effects at relatively low dose levels in experimental animals. It increases the tumor incidence in rats, mainly in the liver. The carcinogenic effects in rats appear to be due to indirect/nongenotoxic modes of action. Epidemiological studies in PFOA-exposed workers do not indicate an increased cancer risk. There is relatively consistent evidence of modest positive associations between serum levels of PFOA and cholesterol, uric acid, and liver enzyme levels. The critical effects observed in rodents and monkeys are on the liver and include hypertrophy, changes in liver enzyme activity, and proliferation of peroxisomes.
In rodents the anionic form of PFOA induces hepatocellular adenomas, Leydig cell adenomas, and pancreatic hyperplasia. The genotoxic activity of PFOA is a matter of current debate and controversy, with classifications as ‘devoid of significant genotoxicity’ as well as ‘weakly nonspecific genotoxic.’ PFOA does not appear directly genotoxic; animal data indicate that it can cause several types of tumors and neonatal death and may have toxic effects on the immune, liver, and endocrine systems.

PERFLUORO-N-OCTANOIC ACID-1-13C 4-VINYLBENZYL PERFLUOROOCTANOATE Tetramethylammoniumperfluoroctanoat Pentadecafluorooctanoic acid butyl ester,Pentadecafluorooctanoic acid butyl ester Ethyl 2-(Chlorosulfonyl)acetate potassium perfluorooctanoate Tris(pentadecafluorooctanoic acid)chromium(III) salt,Tris(pentadecafluorooctanoic acid)chromium(III) salt Ascoric Acid Pentadecafluorooctanoic acid (PFOA),Pentadecafluorooctanoic acid (PFOA) Pentadecafluorooctanoic acid anhydride,Pentadecafluorooctanoic acid anhydride N-BUTYL PERFLUOROOCTANOATE ALLYL PERFLUOROOCTANOATE VINYL PERFLUOROOCTANOATE 2-(5-METHYL-3-NITRO-PYRAZOL-1-YL)-PROPIONIC ACID ETHYL ESTER Bis(pentadecafluorooctanoic acid)1,6-hexanediyl ester,Bis(pentadecafluorooctanoic acid)1,6-hexanediyl ester OCTADECYLAMINOPERFLUOROOCTANOATE Bis(pentadecafluorooctanoic acid)1,5-pentanediyl,Bis(pentadecafluorooctanoic acid)1,5-pentanediyl PENTADECAFLUOROOCTANOIC ACID MONOHYDRATE,PENTADECAFLUOROOCTANOIC ACID MONOHYDRATE Perfluorooctanoic Acid

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