229814
Potassium fluoride
≥99.97% trace metals basis
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About This Item
Linear Formula:
KF
CAS Number:
Molecular Weight:
58.10
UNSPSC Code:
12352302
NACRES:
NA.23
PubChem Substance ID:
EC Number:
232-151-5
Beilstein/REAXYS Number:
3902818
MDL number:
Assay:
≥99.97% trace metals basis
Form:
powder and chunks
Solubility:
water: soluble
assay
≥99.97% trace metals basis
form
powder and chunks
reaction suitability
core: potassium
impurities
≤300.0 ppm Trace Metal Analysis
mp
858 °C (lit.)
solubility
water: soluble
SMILES string
[F-].[K+]
InChI
1S/FH.K/h1H;/q;+1/p-1
InChI key
NROKBHXJSPEDAR-UHFFFAOYSA-M
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.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Mingming Fan et al.
Bioresource technology, 104, 447-450 (2011-12-16)
Transesterification of soybean oil with methanol was carried out in the presence of CaO-MgO and KF-modified CaO-MgO catalysts at atmospheric pressure. While the methyl ester yield for the CaO-MgO catalyst with a ratio of 8:2 (CaO:MgO) was 63.6%, it was
E Gershonov et al.
The Journal of organic chemistry, 74(1), 329-338 (2008-12-05)
A facile solvent-free hydrolysis (chemical destruction) of the warfare agents VX (O-ethyl S-2-(diisopropylamino)ethyl methylphosphonothioate), GB (O-isopropyl methylphosphonofluoridate or sarin), and HD (2,2'-dichloroethyl sulfide or sulfur mustard) upon reaction with various solid-supported fluoride reagents is described. These solid reagents include different
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