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380520

Sigma-Aldrich

Ammonium tetraphenylborate

99%

Synonym(s):

Tetraphenylboron ammonium

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About This Item

Linear Formula:
NH4B(C6H5)4
CAS Number:
14637-34-4
Molecular Weight:
337.27
Beilstein:
3799683
MDL number:
MFCD00134523
UNSPSC Code:
12161600
PubChem Substance ID:
24863748
NACRES:
NA.22

Assay

99%

reaction suitability

core: boron
reagent type: catalyst

mp

220 °C (dec.) (lit.)

SMILES string

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

InChI

1S/C24H20B.H3N/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;1H3/q-1;/p+1

InChI key

ZWFYDLYRTYMBIL-UHFFFAOYSA-O

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Related Categories

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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S I M Zayed et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 26(1), 45-49 (2010-01-13)
The construction and electrochemical response characteristics of two new polyvinyl chloride (PVC) membrane sensors for the determination of sibutramine hydrochloride were described. The sensors are based on the ion association complexes of sibutramine with sodium tetraphenylborate (NaTPB) or phosphotungstic acid
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
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.
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
Sergio L de Rooy et al.
Chemical communications (Cambridge, England), 47(31), 8916-8918 (2011-06-16)
Herein we report the synthesis of a fluorescent organic salt through anion exchange and the subsequent fabrication of 1D-nanostructures via a facile templating method.
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