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T25305

Sigma-Aldrich

Tetraphenylarsonium(V) chloride hydrate

97%

Sinonimo/i:

Phenylarsonium chloride, Tetraphenylarsenic chloride

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About This Item

Formula condensata:
(C6H5)4As(Cl) · xH2O
Numero CAS:
507-28-8
Peso molecolare:
418.79 (anhydrous basis)
Beilstein:
3580063
Numero CE:
208-070-6
Numero MDL:
MFCD00149995
Codice UNSPSC:
12161600
ID PubChem:
24900042
NACRES:
NA.22

Saggio

97%

Impiego in reazioni chimiche

core: arsenic
reagent type: catalyst

Punto di fusione

258-260 °C (lit.)

Stringa SMILE

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
NGDWSDTZKCSLRK-UHFFFAOYSA-M

Applicazioni

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

Pittogrammi

Skull and crossbonesEnvironment
GHS06,GHS09

Avvertenze

Danger

Indicazioni di pericolo

H301 + H331,H410

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
STBK0219
STBH9825
STBG7880
STBF3158V
STBC2940V

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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
A M George et al.
Archives of biochemistry and biophysics, 333(1), 66-74 (1996-09-01)
In this preliminary study, we report the cloning of the human MDR1 cDNA into a prokaryotic expression vector and the consequent functional expression of heterologous P-glycoprotein in Escherichia coli. We demonstrate increased resistance to the P-glycoprotein substrates TPA+, TPP+, and
J A Podcasy et al.
Journal of chromatography, 315, 111-118 (1984-12-19)
The effect of the hetaerons tetraphenylarsonium chloride (Ph4AsCl) and tetraphenylarsonium perchlorate (Ph4AsClO4) on the retention of neutral and cationic metalloporphyrins on a reversed-phase column with an acetonitrile-tetrahydrofuran (85:15, v/v) mobile phase was investigated. The adsorption properties of the two hetaerons
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