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466689

Sigma-Aldrich

Potassium tetraphenylborate

97%

Synonym(s):

Potassium tetrakis(phenyl)borate, Potassium tetraphenylboride

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About This Item

Linear Formula:
(C6H5)4BK
CAS Number:
3244-41-5
Molecular Weight:
358.32
MDL number:
MFCD03093877
UNSPSC Code:
12161600
PubChem Substance ID:
24870357
NACRES:
NA.22

Assay

97%

form

solid

reaction suitability

core: boron
reagent type: catalyst

mp

>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

InChI key

MAMCUZQNCMYPCY-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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.
Ian J Casely et al.
Inorganic chemistry, 50(4), 1513-1520 (2011-01-05)
A series of bis(aryl) bismuth compounds containing (N,C,N)-pincer ligands, [2,6-(Me(2)NCH(2))(2)C(6)H(3)](-) (Ar'), have been synthesized and structurally characterized to compare the coordination chemistry of Bi(3+) with similarly sized lanthanide ions, Ln(3+). Treatment of Ar'(2)BiCl, 1, with ClMg(CH(2)CH═CH(2)) affords the allyl complex
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