T25305
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)
UNSPSC Code:
12161600
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-070-6
Beilstein/REAXYS Number:
3580063
MDL number:
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
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
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Journal of the American Chemical Society, 114, 5130-5130 (1992)
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
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