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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

Quality Level

100

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

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Certificates of Analysis (COA)

Lot/Batch Number
0000262196
0000262196
0000246007
0000274691
MKCP3673

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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
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
Gang Wu et al.
The journal of physical chemistry. A, 112(41), 10359-10364 (2008-09-26)
We report a multinuclear solid-state ( (23)Na, (39)K, (87)Rb, (133)Cs) NMR study of tetraphenylborate salts, M[BPh 4] (M = Na, K, Rb, Cs). These compounds are isostructural in the solid state with the alkali metal ion surrounded by four phenyl
Rosa Peñalver et al.
Talanta, 87, 268-275 (2011-11-22)
Two procedures for the simultaneous determination of organolead (tetraethyllead, triethyllead and trimethyllead) and organomanganese compounds (cyclopentadienyl manganese tricarbonyl (CMT) and methylcyclopentadienyl manganese tricarbonyl (MMT)) are studied. Both procedures involve sample preconcentration by solid-phase microextraction and capillary gas chromatography coupled to
M Chisari et al.
British journal of pharmacology, 164(2b), 667-680 (2011-04-05)
A 'lock-and-key' binding site typically accounts for the effect of receptor antagonists. However, sulphated neurosteroids are potent non-competitive antagonists of GABA(A) receptors without a clear structure-activity relationship. To gain new insights, we tested two structurally unrelated hydrophobic anions with superficially
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