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396575

Sigma-Aldrich

Perfluoropentanoic acid

97%

Synonym(s):

Nonafluorovaleric acid, PFPeA, Nonafluoropentanoic acid, Perfluoropentanoic acid

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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

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

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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’.

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Aerosol synthesis and reactivity of thin oxide shell aluminum nanoparticles via fluorocarboxylic acid functional coating.
Kaplowitz D, et al.
Particle & Particle Systems Characterization, 30(10), 881-887 (2013)
19F, 13C single-and two-bond 2D NMR correlations in perfluoroheptanoic acid.
Ribeiro A
Journal of Fluorine Chemistry, 83(1), 61-66 (1997)
Microwave spectrum of perfluoropentanoic acid.
Pejlovas A, et al.
Chemical Physics Letters, 610, 82-85 (2014)
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
Thomas Albrecht et al.
Scientific reports, 7, 44492-44492 (2017-03-11)
We previously demonstrated that polymorphisms in the carnosinase-1 gene (CNDP1) determine the risk of nephropathy in type 2 diabetic patients. Carnosine, the substrate of the enzyme encoded by this gene, is considered renoprotective and could possibly be used to treat

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