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Merck

466689

Sigma-Aldrich

Kaliumtetraphenylborat

97%

Synonym(e):

Potassium tetrakis(phenyl)borate, Potassium tetraphenylboride

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About This Item

Lineare Formel:
(C6H5)4BK
CAS-Nummer:
Molekulargewicht:
358.32
MDL-Nummer:
UNSPSC-Code:
12161600
PubChem Substanz-ID:
NACRES:
NA.22

Assay

97%

Form

solid

Eignung der Reaktion

core: boron
reagent type: catalyst

mp (Schmelzpunkt)

>300 °C (lit.)

SMILES String

[K+].c1ccc(cc1)[B-](c2ccccc2)(c3ccccc3)c4ccccc4

InChI

1S/C24H20B.K/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;/q-1;+1

InChIKey

MAMCUZQNCMYPCY-UHFFFAOYSA-N

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Dejan Stekovic et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(16), 4166-4174 (2018-12-28)
The ability to tune the physical properties of bistable organic functional materials by means of chemistry can facilitate their development for molecular electronic switching components. The butylamine-containing biphenalenyl boron neutral radical, [Bu]2 B, crystalline compound has recently attracted significant attention
Beata Paczosa-Bator et al.
Talanta, 81(3), 1003-1009 (2010-03-20)
This paper focuses on the quantitative determination of the loss of the components from plastic membranes of ion-selective electrodes (ISEs) during contact with aqueous bathing solutions. The leaching processes, which affect the ISE responses, are rarely characterized by independent methods.
D C Kapsimali et al.
Talanta, 80(3), 1311-1317 (2009-12-17)
Two different derivatizing reagents were tested for the development of a fast and sensitive method for the determination of selenites (Se(IV)) in human urine. The reagents were sodium tetraethylborate (NaBEt(4)) and tetraphenylborate (NaBPh(4)), respectively, and the procedure is based on
Mirela Samardžić et al.
Talanta, 83(3), 789-794 (2010-12-15)
A sensitive potentiometric surfactant sensor based on a highly lipophilic 1,3-didecyl-2-methyl-imidazolium cation and a tetraphenylborate (TPB) antagonist ion was used as the end-point detector in ion-pair potentiometric surfactant titrations using sodium TPB as a titrant. Several analytical and technical grade
Hiroyuki Hayashi et al.
The Journal of organic chemistry, 73(22), 8683-8693 (2008-10-16)
1-Ethyl-2-(1-oxy-3-oxo-4,4,5,5-tetramethylimidazolin-2-yl)-3-methylimidazolium bromide, [EMINN](+)[Br](-), carrying nitronylnitroxide (NN) in the cation unit, was prepared as a parent molecule and converted to seven salts, [EMINN](+)[X](-) (X = I, TFSI (bis(trifluoromethanesulfonyl)imide), BPh4 (tetraphenylborate), [EMINN](+)(1-3)[BA(1-3)]((1-3)-); BA1 (benzoic acid), BA2 (terephthalic acid), and BA3 (trimesic acid)

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