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Merck
CN

230227

Tris(4-bromophenyl)ammoniumyl hexachloroantimonate

technical grade

Synonym(s):

Hexachloroantimonate tris(4-bromophenyl)amine, Magic Blue, Tris(4-bromophenyl)aminium hexachloroantimonate, Tris(p-bromophenyl)aminium hexachloroantimonate(1-), Tris(p-bromophenyl)aminium hexachloroantimonate

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About This Item

Linear Formula:
(BrC6H4)3NSbCl6
CAS Number:
24964-91-8
Molecular Weight:
816.48
UNSPSC Code:
12352101
PubChem Substance ID:
24853786
NACRES:
NA.22
Form:
powder

Key Documents

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SMILES string

Cl[Sb-](Cl)(Cl)(Cl)(Cl)Cl.Brc1ccc(cc1)[N+](c2ccc(Br)cc2)c3ccc(Br)cc3

InChI

1S/C18H12Br3N.6ClH.Sb/c19-13-1-7-16(8-2-13)22(17-9-3-14(20)4-10-17)18-11-5-15(21)6-12-18;;;;;;;/h1-12H;6*1H;/q+1;;;;;;;+5/p-6

InChI key

SDHBPVANTRLAKE-UHFFFAOYSA-H

grade

technical grade

form

powder

mp

142 °C (dec.) (lit.)

Quality Level

100

Application

Tris(4-bromophenyl)ammoniumyl hexachloroantimonate can be used as a strong oxidant for the chemical doping of conjugated polymers. It can also be used as a catalyst for the deprotection of tert-butyldimethylsilyl and tetrahydropyranyl ethers.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000489560
0000489560
0000300096
0000300096
MKCV6218

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Chemical doping of conjugated polymers with the strong oxidant magic blue
Hofmann A, et al.
Advanced Electronic Materials, 6, 2000249-2000249 (2020)
A mild and efficient cleavage of tert-butyldimethylsilyl (TBS) and tetrahydropyranyl (THP) ethers using a catalytic amount of TBPA+ SbCl6
Xu Y, et al.
Tetrahedron Letters, 49, 3634-3637 (2008)
Rachel L Meyer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(44), 9905-9914 (2020-03-21)
The rational control of the electrochemical properties of polyoxovanadate-alkoxide clusters is dependent on understanding the influence of various synthetic modifications on the overall redox processes of these systems. In this work, the electronic consequences of ligand substitution at the heteroion
Hong Zhang et al.
Analytica chimica acta, 1107, 107-112 (2020-03-24)
Many important chemical transformations proceed by way of ionic and/or neutral intermediates. Great effort has been expended to understand the mechanism, with only minimum attention given to separate associated ionic and neutral intermediates. Herein, we present a nebulization method followed

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