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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:
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

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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

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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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
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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