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About This Item
Linear Formula:
(C6H5)4BK
CAS Number:
Molecular Weight:
358.32
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22
MDL number:
Product Name
Potassium tetraphenylborate, 97%
Quality Level
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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
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
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
