Skip to Content
Merck
All Photos(3)

Key Documents

396575

Sigma-Aldrich

Perfluoropentanoic acid

97%

Synonym(s):

Nonafluorovaleric acid, PFPeA, Nonafluoropentanoic acid, Perfluoropentanoic acid

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CF3(CF2)3COOH
CAS Number:
Molecular Weight:
264.05
Beilstein:
1800087
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.294 (lit.)

bp

140 °C (lit.)

density

1.713 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C5HF9O2/c6-2(7,1(15)16)3(8,9)4(10,11)5(12,13)14/h(H,15,16)

InChI key

CXZGQIAOTKWCDB-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Perfluoropentanoic acid, also known as nonafluoropentanoic acid, is a monocarboxylic acid that can be utilized as a surfactant, surface protector, stain repellent, fire-fighting foam, emulsifier, and also in the production of fluoropolymers.

Application

Perfluoropentanoic acid is used as:
  • An emulsifying agent for polymer dispersion, extinction foams, stain repellents, additives for paints, and coatings.
  • A powerful cation exchanger in ion-pairing chromatography.

Pictograms

Health hazardCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Repr. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Application of surfactant-templated ordered mesoporous material as sorbent in micro-solid phase extraction followed by liquid chromatography--triple quadrupole mass spectrometry for determination of perfluorinated carboxylic acids in aqueous media
M Lashgari, et.al.
Talanta, 141, 200-206 (2015)
A Gmiat et al.
Biogerontology, 18(4), 535-548 (2017-03-21)
Mechanisms underpinning age-related decreases in muscle strength and muscle mass relate to chronic inflammation. Physical activity induces an anti-inflammatory effect, but it is modulated by additional factors. We hypothesized that vitamin D, which has also anti-inflammatory activity will modify adaptation
Satoshi Furota et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1095, 191-197 (2018-08-05)
The separation and quantification of underivatized naturally occurring amino acids (AAs) by high-performance liquid chromatography (HPLC) is advantageous for reducing preparation time, running costs, and analytical errors, and is compatible with the isolation of intact AAs. This study establishes and
Quantitation of levodopa and carbidopa in rat plasma by LC?MS/MS: The key role of ion-pairing reversed-phase chromatography
J Chi, et al.
Applied Catalysis. B, Environmental, 1054, 1-9 (2017)
Frédéric J Tessier et al.
Molecular nutrition & food research, 60(11), 2446-2456 (2016-07-10)
Nɛ -Carboxymethyl-lysine (CML) is a prominent advanced glycation end-product which is not only found in vivo but also in food. It is known that a percentage of the dietary CML (dCML) is absorbed into the circulation and only partly excreted

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service