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77292

Sigma-Aldrich

Pentafluoropropionic anhydride

purum, ≥97.0% (GC)

Synonym(s):

PFPA, Perfluoropropionic anhydride

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About This Item

Linear Formula:
(CF3CF2CO)2O
CAS Number:
356-42-3
Molecular Weight:
310.05
Beilstein:
1806446
EC Number:
206-604-2
MDL number:
MFCD00000429
UNSPSC Code:
12352100
PubChem Substance ID:
329767586
NACRES:
NA.22

grade

purum

Quality Level

200

Assay

≥97.0% (GC)

form

liquid

bp

69-70 °C/735 mmHg (lit.)

density

1.571 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C6F10O3/c7-3(8,5(11,12)13)1(17)19-2(18)4(9,10)6(14,15)16

InChI key

XETRHNFRKCNWAJ-UHFFFAOYSA-N

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Application

PFPA acylates amines, amino acids and other compounds. PFPA derivatives are highly volatile; used in GC separation
Pentafluoropropionic anhydride can be used to synthesize lithium 4,5-dicyano-2-(pentafluoroethyl)imidazole, a novel imidazole-derived salt with potential application as an electrolyte in lithium-ion batteries. It can also be used to prepare 1.3- bis(pentafluoropropionyl)azulene.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Precautionary Statements

P280 - P305 + P351 + P338 - P310

Hazard Classifications

Skin Corr. 1B

Supplementary Hazards

EUH014

Storage Class Code

8A - Combustible corrosive hazardous materials

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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Sigma-Aldrich

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D.R. Knapp
Handbook of Analytical Derivatization Reactions (1979)
New type of imidazole based salts designed specifically for lithium ion batteries.
Niedzicki L, et al.
Electrochimica Acta, 55(4), 1450-1454 (2010)
Chemical Derivatization in Gas Chromatography.
J. Drozd et al.
J. Chromatogr. Library, 19 (1981)
Simple syntheses of 1, 3-bis (perfluoroacyl) azulenes and 1, 3-azulenedicarboxylic acid.
Mathias L J and Overberger C G
The Journal of Organic Chemistry, 45(9), 1701-1703 (1980)
E Ballesteros et al.
Analytical chemistry, 65(13), 1773-1778 (1993-07-01)
A new analytical method that combines on-line derivatization-extraction and gas-liquid chromatography for the determination of N-methylcarbamates is reported. The hydrolysis products of N-methylcarbamates (phenols) are derivatized and extracted in a continuous fashion using pentafluoropropionic anhydride (derivatizing reagent) in n-hexane as
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