Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

77292

Sigma-Aldrich

Pentafluoropropionic anhydride

purum, ≥97.0% (GC)

Synonym(s):

PFPA, Perfluoropropionic anhydride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CF3CF2CO)2O
CAS Number:
Molecular Weight:
310.05
Beilstein:
1806446
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

purum

Quality Level

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

Looking for similar products? Visit Product Comparison Guide

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

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Skin Corr. 1B

Supplementary Hazards

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’.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

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

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