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About This Item
Linear Formula:
KF
CAS Number:
Molecular Weight:
58.10
Beilstein/REAXYS Number:
3902818
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
assay:
98%
grade:
reagent grade
Recommended Products
grade
reagent grade
assay
98%
mp
858 °C (lit.)
SMILES string
[F-].[K+]
InChI
1S/FH.K/h1H;/q;+1/p-1
InChI key
NROKBHXJSPEDAR-UHFFFAOYSA-M
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Application
A versatile fluoride ion source used in a study of ion-specific swelling and de-swelling of ampholytic polymer gels, in the room temperature oxidation of noble metals in HF, and in the measurement of electronic polarizabilities of ions in polymers of alkali halides.
Other Notes
A -D suffix exists for administrative purposes only.
All -D packages are 100% the same product, same quality, same specification as the package sizes previously sold without a -D.
All -D packages are 100% the same product, same quality, same specification as the package sizes previously sold without a -D.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1
Storage Class
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Characterization of the actual catalytic agent in potassium fluoride on activated alumina systems.
Weinstock LM, et al.
Tetrahedron Letters, 27(33), 3845-3848 (1986)
Natural phosphate doped with potassium fluoride and modified with sodium nitrate: Efficient catalysts for the Knoevenagel condensation.
Sebti S, et al.
Tetrahedron Letters, 43(10), 1813-1815 (2002)
Selective desilylation of tert-butyldimethylsilyl ethers of phenols using potassium fluoride-alumina and ultrasound.
Schmittling EA and Sawyer JS.
Tetrahedron Letters, 32(49), 7207-7210 (1991)
Potassium fluoride on celite. A versatile reagent for C-, N-, O-, and S-alkylations.
Ando T and Yamawaki J.
Chemistry Letters (Jpn), 1, 45-46 (1979)
Lirong Wen et al.
Journal of combinatorial chemistry, 11(5), 799-805 (2009-07-28)
A series of new functionalized thiochromeno[2,3-b]pyridine derivatives have been synthesized via a sequence of Knoevenagel condensation, Michael addition, cyclization, and intramolecular nucleophilic substitution, which is first catalyzed by KF/neutral Al(2)O(3) cooperated with PEG 6000 under microwave irradiation. Experimental results indicated
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