Skip to Content
Merck
All Photos(1)

Documents

245712

Sigma-Aldrich

Triphenyltin chloride

95%

Synonym(s):

Chlorotriphenylstannane, Fentin chloride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C6H5)3SnCl
CAS Number:
Molecular Weight:
385.47
Beilstein:
524762
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:

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

Looking for similar products? Visit Product Comparison Guide

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - 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)

>302.0 °F

Flash Point(C)

> 150 °C


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
Dawid Kucharski et al.
Molecules (Basel, Switzerland), 25(3) (2020-02-06)
A Quick, Easy, Cheap, Effective, Rugged, and Safe (QuEChERS) extraction method combined with Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) for determination of organotin compounds (OTC) has been newly developed. The novel analytical method was validated and the quality of the results

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service