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Sigma-Aldrich

Kaliumhexafluorphosphat

99.5% trace metals basis

Synonym(e):

Potassium fluophosphate, Potassium hexafluorophosphate, Potassium hexafluorophosphate (KPF)

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About This Item

Lineare Formel:
KPF6
CAS-Nummer:
17084-13-8
Molekulargewicht:
184.06
EG-Nummer:
241-143-0
MDL-Nummer:
MFCD00011412
UNSPSC-Code:
12352302
PubChem Substanz-ID:
24873857
NACRES:
NA.23

Assay

99.5% trace metals basis

Form

solid

Verunreinigungen

≤5500.0 ppm Trace Metal Analysis

mp (Schmelzpunkt)

575 °C (lit.)

Dichte

2.75 g/mL at 25 °C (lit.)

SMILES String

[K+].F[P-](F)(F)(F)(F)F

InChI

1S/F6P.K/c1-7(2,3,4,5)6;/q-1;+1

InChIKey

YZDGRYDIGCWVND-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung

  • Multifunctional potassium hexafluorophosphate passivate interface defects for high efficiency perovskite solar cells: Potassium hexafluorophosphate (KPF6) is used to enhance the interface between SnO2 quantum dots and perovskite (Z Wang et al., 2021).
  • Potassium hexafluorophosphate additive enables stable lithium–sulfur batteries: An optimized amount of KPF6 added to the electrolyte improves the cycling stability of lithium-sulfur batteries (J Li et al., 2020).
  • Dual electrolyte additives of potassium hexafluorophosphate and tris (trimethylsilyl) phosphite for anode-free lithium metal batteries: KPF6 and tris(trimethylsilyl) phosphite enhance the electrochemical performance of anode-free lithium metal batteries (TM Hagos et al., 2019).

Piktogramme

Corrosion
GHS05

Signalwort

Danger

H-Sätze

H314

Gefahreneinstufungen

Eye Dam. 1 - Skin Corr. 1B

Lagerklassenschlüssel

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Analysenzertifikate (COA)

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Anil K Gorle et al.
Dalton transactions (Cambridge, England : 2003), 43(44), 16713-16725 (2014-10-02)
A series of inert tri- and tetra-nuclear polypyridylruthenium(II) complexes that are linked by the bis[4(4'-methyl-2,2'-bipyridyl)]-1,n-alkane ligand ("bb(n)" for n = 10, 12 and 16) have been synthesised and their potential as antimicrobial agents examined. Due to the modular nature of
Anil K Gorle et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 21(29), 10472-10481 (2015-06-05)
Ruthenium(II) complexes containing the tetradentate ligand bis[4(4'-methyl-2,2'-bipyridyl)]-1,n-alkane ("bbn "; n=10 and 12) have been synthesised and their geometric isomers separated. All [Ru(phen)(bbn )](2+) (phen=1,10-phenanthroline) complexes exhibited excellent activity against Gram-positive bacteria, but only the cis-α-[Ru(phen)(bb12 )](2+) species showed good activity
Kosuke Doki et al.
Drug metabolism and pharmacokinetics, 30(4), 257-262 (2015-07-22)
The aims of this study were to clarify whether the ratio of S- to R-flecainide (S/R ratio) in the serum flecainide concentration was associated with the stereoselectivity of flecainide metabolism, and to investigate the effects of the cytochrome P450 (CYP)
Jeffrey A Therrien et al.
Inorganic chemistry, 53(24), 12962-12972 (2014-10-23)
A series of pyridine- and lutidine-linked bis-N-heterocyclic carbene (NHC) palladium pincer complexes were electrochemically characterized and screened for CO2 reduction capability with 2,2,2-trifluoroethanol, acetic acid, or 2,2,2-trifluoroacetic acid (TFA) as proton sources. The lutidine-linked pincer complexes electrocatalytically reduce CO2 to
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