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375187

Sigma-Aldrich

Trimethyltin chloride solution

1.0 M in hexanes

Synonyme(s) :

Chlorotrimethylstannane, Chlorotrimethyltin, Trimethylchlorostannane, Trimethylchlorotin, Trimethylstannyl chloride, Trimethyltin chloride

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About This Item

Formule linéaire :
(CH3)3SnCl
Numéro CAS:
Poids moléculaire :
199.27
Numéro Beilstein :
3535111
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Forme

liquid

Concentration

1.0 M in hexanes

Densité

0.797 g/mL at 25 °C

Chaîne SMILES 

C[Sn](C)(C)Cl

InChI

1S/3CH3.ClH.Sn/h3*1H3;1H;/q;;;;+1/p-1

Clé InChI

KWTSZCJMWHGPOS-UHFFFAOYSA-M

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Application

Trimethyltin chloride solution (1.0 M in hexanes) can be used as a reagent in the synthesis of conjugated polymers based on isoindigo as acceptor and syn- or anti-benzo[1,2-b:5,4-b′]difuran (BDF) as a donor by Stille cross-coupling reaction. It can further be used for the investigation of optical, electrochemical and photovoltaic properties.

Conditionnement

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

Informations légales

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 Inhalation - STOT SE 3

Organes cibles

Central nervous system, Nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

-9.4 °F - closed cup

Point d'éclair (°C)

-23 °C - closed cup


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Synthesis and photovoltaic properties of new conjugated polymers based on syn-and anti-benzodifuran
Hu C, et al.
Polym. Chem., 3(10), 2949-2955 (2012)
Kiyokazu Ogita et al.
Journal of neuroscience research, 82(5), 609-621 (2005-11-08)
The hippocampal dentate gyrus in adult animals is known to contain neural progenitors that proliferate and differentiate into neurons in response to brain injury. Little has been observed, however, on regeneration of the granule cell layer of the dentate gyrus
Katharina Krüger et al.
British journal of pharmacology, 144(2), 283-292 (2005-01-19)
1. Organotin compounds such as trimethyltin chloride (TMT) are among the most toxic of the organometallics. As their main target for toxicity is the central nervous system, the aim of the present study was to investigate the effects of TMT
Xiaojiang Tang et al.
Toxicology, 271(1-2), 45-50 (2010-03-10)
Trimethyltin chloride (TMT), a byproduct of plastic stabilizers, has caused 67 poisoning accidents in the world; more than 98% (1814/1849) of the affected patients since 1998 have been in China. As a long-established toxic chemical, TMT severely affects the limbic
Mengmeng Wang et al.
Toxicology in vitro : an international journal published in association with BIBRA, 22(5), 1136-1142 (2008-04-16)
In this study we intended to evaluate the cytotoxic and genotoxic effects of trimethyltin chloride (TMT), one of the most widely used organometallic compounds, on liver cells with the rat liver epithelial cell line IAR20. The results showed that TMT

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