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375187

Sigma-Aldrich

Trimethyltin chloride solution

1.0 M in hexanes

Sinônimo(s):

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

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About This Item

Fórmula linear:
(CH3)3SnCl
Número CAS:
1066-45-1
Peso molecular:
199.27
Beilstein:
3535111
Número MDL:
MFCD00000520
Código UNSPSC:
12352103
ID de substância PubChem:
24863370
NACRES:
NA.22
Preço e disponibilidade não estão disponíveis no momento.

Formulário

liquid

concentração

1.0 M in hexanes

densidade

0.797 g/mL at 25 °C

cadeia de caracteres SMILES

C[Sn](C)(C)Cl

InChI

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

chave InChI

KWTSZCJMWHGPOS-UHFFFAOYSA-M

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Aplicação

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.[1]

Embalagem

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

Informações legais

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

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Central nervous system, Nervous system

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

-9.4 °F - closed cup

Ponto de fulgor (°C)

-23 °C - closed cup

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Certificados de análise (COA)

Lot/Batch Number
MKCS2486
MKCS2490
MKCP9053
MKCN7621
SHBJ8521

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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)
Guangshu Zhai et al.
Chemosphere, 72(3), 389-399 (2008-04-25)
The photodegradation of methyltins, as environmental pollutants, has scarcely been studied so far because of the shortage of rapid and sensitive speciation methods, even though they have very simple structures. The photodegradation of monomethyltin trichloride (MMT), dimethyltin dichloride (DMT) and
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
Erwin van Vliet et al.
Neurotoxicology, 28(6), 1136-1146 (2007-08-19)
Neurotoxicity aims to understand how xenobiotics interfere with the function of the nervous system and to unravel their mechanisms of action. Neuronal activity is the primary functional output of the nervous system and deviations from its resting level may indicate
Jiali Cai et al.
Chemical research in toxicology, 22(9), 1582-1587 (2009-08-07)
In evaluating the cytotoxic effects and the mechanisms of the apoptotic and necrotic actions of trimethyltin chloride (TMT) on human hepatoma G2 (HepG2) cells, the present study focused on the involvement of antiproliferation, DNA damage, cell death, apoptosis-related proteins, and
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