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Merck
CN

381721

Sigma-Aldrich

Sodium pentafluoropropionate

98%

Synonym(s):

Pentafluoropropionic acid sodium salt, Perfluoropropionic acid sodium salt

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About This Item

Linear Formula:
CF3CF2COONa
CAS Number:
Molecular Weight:
186.01
Beilstein:
3636648
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level

Assay

98%

form

solid

mp

226-229 °C (dec.) (lit.)

functional group

fluoro

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

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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

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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)
New fluoro intermediates for herbicidal sulfonylureas.
Hamprecht G, et al.
Pestic. Sci., 55(5), 566-570 (1999)
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
Derek A Jackson et al.
Environmental science & technology, 45(19), 8030-8036 (2011-04-07)
Perfluorinated carboxylic acids are widely distributed in the environment, including remote regions, but their sources are not well understood. Perfluoropropionic acid (PFPrA, CF(3)CF(2)C(O)OH) has been observed in rainwater but the observed amounts can not be explained by currently known degradation

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