Skip to Content
Merck
All Photos(2)

Documents

381721

Sigma-Aldrich

Sodium pentafluoropropionate

98%

Synonym(s):

Pentafluoropropionic acid sodium salt, Perfluoropropionic acid sodium salt

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
CF3CF2COONa
CAS Number:
378-77-8
Molecular Weight:
186.01
Beilstein:
3636648
EC Number:
206-830-1
MDL number:
MFCD00066167
UNSPSC Code:
12352100
PubChem Substance ID:
24863834
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

mp

226-229 °C (dec.) (lit.)

SMILES string

[Na+].[O-]C(=O)C(F)(F)C(F)(F)F

InChI

1S/C3HF5O2.Na/c4-2(5,1(9)10)3(6,7)8;/h(H,9,10);/q;+1/p-1

InChI key

SCWLIHXXYXFUFV-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

General description

Sodium pentafluoropropionate is an aryl fluorinated building block.

Application

Sodium pentafluoropropionate may be used in the preparation of:
  • tributyltin pentafluoropropionate (Bu3SnO2CC2F5)
  • trimethyltin pentafluoropropionate
  • new o-fluoroalkyl-benzenesulfonamide precursors

Storage Class Code

11 - Combustible Solids

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

New fluoro intermediates for herbicidal sulfonylureas.
Hamprecht G, et al.
Pestic. Sci., 55(5), 566-570 (1999)
Atmospheric pressure deposition of fluorine-doped SnO2 thin films from organotin fluorocarboxylate precursors.
Mahon MF, et al.
Applied Organometallic Chemistry, 19(5), 658-671 (2005)
[Recent development of C-terminal sequence analysis of proteins].
A Tsugita
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme, 43(7), 857-865 (1998-06-23)
C T Mant et al.
Journal of chromatography. A, 1125(2), 211-219 (2006-07-04)
The present study set out to investigate whether observed relative hydrophilicity/hydrophobicity values of positively charged side-chains (with Lys and Arg as representative side-chains) or hydrophobic side-chains (with Ile as the representative side-chain) were context-dependent, i.e., did such measured values vary
Wenche Langseth et al.
Rapid communications in mass spectrometry : RCM, 24(17), 2641-2649 (2010-08-27)
This paper reports the mass spectra, obtained after electron ionisation (EI) at 70 eV, of 34 trichothecenes and five culmorin compounds after acylation with pentafluoropropionic anhydride. The derivatised fungal metabolites were separated by gas chromatography, and the mass spectra were
View All Related Papers

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