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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

Quality Level

100

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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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
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
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.
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
Gehad G Mohamed et al.
The Analyst, 136(7), 1488-1495 (2011-02-03)
A screen-printed electrode (SPE) was fabricated for the determination of 1-(ethoxycarbonyl)pentadecyltrimethylammonium bromide (Septonex) based on the use of Septonex-tetraphenylborate as the electroactive substance, and o-nitrophenyloctylether (o-NPOE) as the plasticizing agent. The electrode passes a near-Nernstian cationic slope of 59.33 ±
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