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20989

Sigma-Aldrich

Cesium fluoride

BioUltra, ≥99.0% (F)

Sinónimos:

NSC 84270

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About This Item

Fórmula empírica (notación de Hill):
CsF
Número de CAS:
13400-13-0
Peso molecular:
151.90
EC Number:
236-487-3
MDL number:
MFCD00010960
UNSPSC Code:
12352302
PubChem Substance ID:
57647888
NACRES:
NA.25

product line

BioUltra

Quality Level

100

assay

≥99.0% (F)

impurities

insoluble matter, passes filter test
≤0.005% total nitrogen (N)

loss

≤0.5% loss on drying, 110 °C

pH

6.5-7.5 (25 °C, 3 M in H2O)

mp

682 °C (lit.)

solubility

H2O: 3 M at 20 °C, clear, colorless

density

4.115 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤500 mg/kg
sulfate (SO42-): ≤50 mg/kg

cation traces

Al: ≤10 mg/kg
As: ≤0.5 mg/kg
Ba: ≤10 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤30 mg/kg
K: ≤100 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

3 M in H2O

UV absorption

λ: 260 nm Amax: 0.05
λ: 280 nm Amax: 0.05

SMILES string

[F-].[Cs+]

InChI

1S/Cs.FH/h;1H/q+1;/p-1

InChI key

XJHCXCQVJFPJIK-UHFFFAOYSA-M

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Application

Reactant for:
  • Preparation of building blocks for synthesis of fluoroallylic compounds
  • Synthesis of alcohols via hydrolysis of alkyl silyl ethers at neutral pH in buffered mixed organic-aqueous solutions
  • Nucleophilic fluorination of alkynyliodonium salts to form fluorovinylic compounds
  • Nucleophilic aromatic substitution (SNAr) reactions
Used in the successful synthesis of a single-crystal Dion-Jacobson phase, CsLaTa2O7, that has applications in photocatalysis and superconductivity.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Repr. 2 - STOT RE 2

target_organs

Kidney,Adrenal gland

supp_hazards

EUH032

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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L Bertollini et al.
Neuroreport, 5(5), 553-556 (1994-01-31)
The effect of intracellular fluoride ions on voltage-dependent calcium currents was tested during whole-cell voltage-clamp recordings in thalamic neurones acutely dissociated from young adult rats. It is demonstrated that 5-30 mM intracellular fluoride selectively and reversibly suppresses the high voltage-activated
J Fernandez-Bertrán et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(13), 2607-2615 (2002-01-05)
The interactions of alkali fluorides with D-xylose have been studied by X-ray diffraction (XRD), infrared spectroscopy (IR), nuclear magnetic resonance (NMR, 1H and 13C) and atomic absorption spectrophotometry. KF and CsF form complexes with D-xylose in a 1:1 molar ratio.
J Kypr et al.
International journal of biological macromolecules, 13(1), 9-13 (1991-02-01)
Ten DNA fragments containing self-complementary alternating sequences of adenine and thymine differing in length and the starting nucleotide were studied by c.d. spectroscopy. It was found that d(TATATATA) but not d(ATATATAT), d(TATATA), d(CTATATAG) or (dT-dA)20 isomerized into the unusual X-DNA
N Kristianpoller et al.
Radiation protection dosimetry, 100(1-4), 207-209 (2002-10-18)
Optical and dosimetric properties of nominally pure CsGd2F7 crystals and of CsGd2F7 crystals doped with various concentrations of Pr3+ ions were investigated. Effects of X, beta and UV irradiation on these crystals were studied. Methods of optical absorption, X and
Y Sato et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 114(11), 880-887 (1994-11-01)
Benzylammonium N-alkylides were generated by reaction of N-[1-(trimethylsilyl)alkyl]benzylammonium salts with cesium fluoride in DMF or HMPA, and their rearrangement products were investigated. [2,3]Sigmatropic rearrangement of the ylides initially occurred to give isotoluene derivatives and then they were transformed into Sommelet-Hauser
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