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380520

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
UNSPSC Code:
12161600
NACRES:
NA.22
PubChem Substance ID:
24863748
MDL number:
MFCD00134523
Beilstein/REAXYS Number:
3799683
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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

pictograms

Exclamation mark
GHS07

signalword

Warning

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Class I Designated Chemical Substances

prtr

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Certificates of Analysis (COA)

Lot/Batch Number
17028PO
16606KR
11703CZ
04414EY

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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.
D C Kapsimali et al.
Talanta, 80(3), 1311-1317 (2009-12-17)
Two different derivatizing reagents were tested for the development of a fast and sensitive method for the determination of selenites (Se(IV)) in human urine. The reagents were sodium tetraethylborate (NaBEt(4)) and tetraphenylborate (NaBPh(4)), respectively, and the procedure is based on
Hajime Katano et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 28(12), 1153-1157 (2012-12-13)
A biopolymer ε-poly-L-lysine (εPL) exists as a fully protonated form (εPLH(n+)) in solutions at pH < 4. Around pH 3.5, at which the tetraphenylborate (TPB(-)) anion is not decomposed immediately, the εPLH(n+) cation associates with the TPB(-) anion to form
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