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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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
Effect of phosphonium and arsonium salts on the differential-pulse polarograms of three permitted synthetic food colouring matters.
A G Fogg et al.
The Analyst, 112(9), 1319-1321 (1987-09-01)
K Yoshioka et al.
Experientia, 42(9), 1022-1023 (1986-09-15)
The effect of lipophilic cations such as triphenylmethylphosphonium, tetraphenylphosphonium and tetraphenylarsonium in addition to dibenzyldimethylammonium on thiamine transport in isolated rat hepatocytes was studied. Lipophilic cations at the concentration 10 microM almost completely inhibited thiamine uptake. Kinetic studies showed that