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Merck
CN

139718

Trimethylphenylammonium tribromide

97%, powder

Synonym(s):

Phenyltrimethylammonium bromide dibromide, Phenyltrimethylammonium bromide-perbromide, Phenyltrimethylammonium tribromide

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About This Item

Linear Formula:
(CH3)3N(Br3)C6H5
CAS Number:
4207-56-1
Molecular Weight:
375.93
Beilstein:
3919459
EC Number:
224-127-8
MDL number:
MFCD00011789
UNSPSC Code:
12352101
PubChem Substance ID:
24848427
NACRES:
NA.22

Key Documents

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Product Name

Trimethylphenylammonium tribromide, 97%

Assay

97%

form

powder

mp

110-115 °C (dec.) (lit.)

SMILES string

Br[Br-]Br.C[N+](C)(C)c1ccccc1

InChI

1S/C9H14N.Br3/c1-10(2,3)9-7-5-4-6-8-9;1-3-2/h4-8H,1-3H3;/q+1;-1

InChI key

PRXNKYBFWAWBNZ-UHFFFAOYSA-N

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Application

Brominating reagent for 1,2-addition of bromine to the double bond of α,β-unsaturated compounds.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCW8691
MKCF2785
MKBX9040V
MKBN4195V
MKBL6106V

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Heteroatom Chem., 3, 345-345 (1992)
Tetrahedron, 50, 6433-6433 (1994)
Godfrey Lisk et al.
Molecular pharmacology, 71(5), 1241-1250 (2007-02-09)
Human red blood cells infected with the malaria parasite Plasmodium falciparum have markedly increased permeabilities to diverse organic and inorganic solutes. The plasmodial surface anion channel (PSAC), recently identified with electrophysiological methods, contributes to the uptake of many small solutes.
Petr Gebauer et al.
Electrophoresis, 29(5), 1067-1076 (2008-01-26)
In electrophoresis, the introduction of a sample into the BGE creates two new zone boundaries, the front and rear boundary of the sample zone which is sandwiched between the BGE. During an electrophoresis run, these boundaries move and split into
Alec N Salt et al.
Hearing research, 182(1-2), 24-33 (2003-09-02)
Our understanding of the perilymph kinetics of drugs depends largely on data obtained by the analysis of perilymph samples. Although a number of studies have demonstrated qualitatively that perilymph samples may be contaminated by cerebrospinal fluid (CSF), and some investigations
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