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Merck
CN

245917

Pentafluoropropionic acid

97%

Synonym(s):

Perfluoropropionic acid

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About This Item

Linear Formula:
CF3CF2COOH
CAS Number:
Molecular Weight:
164.03
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-021-6
Beilstein/REAXYS Number:
1773387
MDL number:
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Product Name

Pentafluoropropionic acid, 97%

InChI key

LRMSQVBRUNSOJL-UHFFFAOYSA-N

InChI

1S/C3HF5O2/c4-2(5,1(9)10)3(6,7)8/h(H,9,10)

SMILES string

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

vapor density

~5.6 (vs air)

vapor pressure

~40 mmHg ( 20 °C)

assay

97%

form

liquid

refractive index

n20/D 1.284 (lit.)

bp

96-97 °C (lit.)

density

1.561 g/mL at 25 °C (lit.)

application(s)

PFAS testing

functional group

carboxylic acid
fluoro

Quality Level

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Application

Pentafluoropropionic acid (Perfluoropropionic acid) was used in the analysis of gentamicin with Gemini column by liquid chromatographic (LC) methods.
Pentafluoropropionic acid can be used to prepare 2-pentafluoropropylquinazolin-4(3H)-ones, perfluoroalkyl thioethers and perfluoroalkyl-containing 3-azabicyclo[3.1.0]hexanes.

General description

The kinetics of the reaction of pentafluoropropionic acid with fluorine atoms was studied.

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class

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

wgk

WGK 3

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Enantioselective C-H Functionalization-Addition Sequence Delivers Densely Substituted 3-Azabicyclo [3.1. 0] hexanes
Pedroni, Julia and Cramer, Nicolai
Journal of the American Chemical Society, 139(36), 12398-12401 (2017)
E S Vasiliev et al.
The journal of physical chemistry. A, 118(23), 4013-4018 (2014-05-14)
The kinetics of the reaction between fluorine atoms and pentafluoropropionic acid has been studied experimentally at T = 262-343 K. The overall reaction rate constant decreases with temperature: k1(T) = 6.1 × 10(-13) exp(+1166 K)/T) cm(3) molecule(-1) s(-1). The potential
One-Pot Synthesis of Trifluoromethylated Quinazolin-4 (3 H)-ones with Trifluoroacetic Acid as CF3 Source
Almeida, Sofia and Marti, Roger and Vanoli, Ennio and Abele, Stefan and Tortoioli, Simone
The Journal of Organic Chemistry, 83(9), 5104-5113 (2018)
Synthesis of perfluoroalkyl thioethers from aromatic thiocyanates by iron-catalysed decarboxylative perfluoroalkylation
Exner, Benjamin and Bayarmagnai, Bilguun and Matheis, Christian and Goossen, Lukas J
Journal of Fluorine Chemistry, 198, 89-93 (2017)
Sandra Rinne et al.
Journal of chromatography. A, 1119(1-2), 285-293 (2006-03-21)
A fast and sensitive capillary liquid chromatography (cLC) column-switching method with electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS) detection for the simultaneous determination of dopamine (D), epinephrine (E), norepinephrine (NE) and serotonin (SE) was pursued. A sample volume of 100 microl

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