381721
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/REAXYS Number:
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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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)
K F Faull et al.
Journal of neuroscience research, 27(4), 533-540 (1990-12-01)
In experimental protocols with humans and non-human primates, cerebrospinal fluid (CSF) concentrations of 3-methoxy-4-hydroxyphenylethylene glycol (MHPG), the predominant end-product of norepinephrine metabolism in the mammalian central nervous system (CNS), have been widely used as an index of the rate of
C Legrand et al.
Journal of chromatography. B, Biomedical applications, 663(2), 187-192 (1995-01-20)
Plasma testosterone was measured by gas chromatography-negative-ion chemical ionisation mass spectrometry (GC-MS). The testosterone was extracted from plasma using home-made Extrelut columns and diethyl ether elution. It was quantified as the pentafluoropropionate (PFP) derivative by selected-ion monitoring at m/z 560
T Krishnamurthy et al.
Journal of chromatography, 355(1), 253-264 (1986-03-14)
The pentafluoropropionyl, (PFP) and trifluoroacetyl (TFA) esters of several naturally occurring and synthetically modified simple trichothecenes were synthesized in nanogram amounts and characterized. Optimum conditions for the gas chromatographic (GC) separation of these derivatives and their analysis by negative ion
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