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T25305

Sigma-Aldrich

Tetraphenylarsonium(V) chloride hydrate

97%

Synonym(s):

Phenylarsonium chloride, Tetraphenylarsenic chloride

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About This Item

Linear Formula:
(C6H5)4As(Cl) · xH2O
CAS Number:
Molecular Weight:
418.79 (anhydrous basis)
Beilstein:
3580063
EC Number:
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

reaction suitability

core: arsenic
reagent type: catalyst

mp

258-260 °C (lit.)

SMILES string

O.[Cl-].c1ccc(cc1)[As+](c2ccccc2)(c3ccccc3)c4ccccc4

InChI

1S/C24H20As.ClH.H2O/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;1H;1H2/q+1;;/p-1

InChI key

NGDWSDTZKCSLRK-UHFFFAOYSA-M

Application

Cation exchange reagent. Used to prepare arsonium amide, oxime, and carbohydrate derivatives.

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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D Wolff et al.
Biochimica et biophysica acta, 688(1), 138-144 (1982-05-21)
In order to elucidate the mechanism of action of organochlorine insecticides on the ion transport in biological membranes, we have studied the effect of DDT and its analog DDE on the structural parameters of phosphatidylethanolamine (PE) planar bilayers. DDT and
Journal of the American Chemical Society, 114, 5130-5130 (1992)
S Manon et al.
Biochemistry and molecular biology international, 29(2), 375-385 (1993-02-01)
The effect of a group of non-usual inhibitors of ATP synthesis was investigated in yeast mitochondria. Tetraphenylphosphonium, tetraphenylarsonium and ethidium decreased the rate of ATP synthesis but did not decrease the ATP/O ratio. They did not inhibit the ATPase activity
P Gros et al.
Biochemistry, 31(7), 1992-1998 (1992-02-25)
The possibility that simple lipophilic cations such as tetraphenylphosphonium (TPA+), triphenylmethylphosphonium (TPMP+), and diphenyldimethylphosphonium (DDP+) are substrates for the multidrug-resistance transport protein, P-glycoprotein, was tested. Hamster cells transfected with and overexpressing mouse mdr1 or mouse mdr3 exhibit high levels of
E Bibi et al.
Proceedings of the National Academy of Sciences of the United States of America, 90(19), 9209-9213 (1993-10-01)
We describe functional expression of the mouse multidrug-resistance protein (P-glycoprotein; P-gp) in an Escherichia coli mutant defective in the outer membrane protease ompT. Heterologously expressed mdr1 appears as an unglycosylated species with an apparent molecular mass of 140 kDa in

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