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Merck
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245712

Sigma-Aldrich

Triphenyltin chloride

95%

Sinónimos:

Chlorotriphenylstannane, Fentin chloride

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About This Item

Fórmula lineal:
(C6H5)3SnCl
Número de CAS:
639-58-7
Peso molecular:
385.47
Beilstein/REAXYS Number:
524762
EC Number:
211-358-4
MDL number:
MFCD00000519
UNSPSC Code:
12352103
PubChem Substance ID:
24854753

assay

95%

bp

240 °C/13.5 mmHg (lit.)

mp

108 °C (dec.) (lit.)

SMILES string

Cl[Sn](c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/3C6H5.ClH.Sn/c3*1-2-4-6-5-3-1;;/h3*1-5H;1H;/q;;;;+1/p-1

InChI key

NJVOZLGKTAPUTQ-UHFFFAOYSA-M

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pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - 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_germany

WGK 3

flash_point_f

>302.0 °F

flash_point_c

> 150 °C

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Angeliki Lyssimachou et al.
Aquatic toxicology (Amsterdam, Netherlands), 89(2), 129-135 (2008-07-25)
Long-term exposures to organotin compounds have shown alterations on endogenous steroid levels in gastropods together with the development of imposex. However, information regarding short-term effects of these compounds on the endocrine system of gastropods is lacking. This work aimed at
José J Chicano et al.
Biochimica et biophysica acta, 1558(1), 70-81 (2001-12-26)
Organotin compounds are important contaminants in the environment. They are membrane active molecules with broad biological toxicity. We have studied the interaction of tri-n-butyltin chloride and tri-n-phenyltin chloride with model membranes composed of different phosphatidylethanolamines using differential scanning calorimetry, X-ray
Toshihiro Horiguchi et al.
Analytical and bioanalytical chemistry, 396(2), 597-607 (2009-11-03)
To examine the role of the retinoid X receptor (RXR) in the development of imposex in gastropods, we investigated the time course of expression of the RXR gene in various tissues (ctenidium, ovary or testis, digestive gland, penis-forming area or
Antonio Ortiz et al.
Biochimica et biophysica acta, 1720(1-2), 137-142 (2006-02-14)
Organotin compounds are widely distributed toxicants. They are membrane-active molecules with broad biological toxicity. In this contribution, we study the effect of triorganotin compounds on membrane permeability using phospholipid model membranes and human erythrocytes. Tribultyltin and triphenyltin are able to
Jérôme Darrouzès et al.
Journal of chromatography. A, 1072(1), 19-27 (2005-05-11)
A new methodology for the simultaneous and fast solid-phase microextraction (SPME) of butyl- and phenyltin compounds, as ethylated derivates, is proposed in this paper. The effects of pressure and type of agitation during headspace SPME sampling are evaluated and discussed
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