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Key Documents

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201057

Sigma-Aldrich

Butyltin trichloride

95%

Sinónimos:

Butyltrichlorotin

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About This Item

Fórmula lineal:
CH3(CH2)3SnCl3
Número de CAS:
1118-46-3
Peso molecular:
282.18
EC Number:
214-263-6
MDL number:
MFCD00000515
UNSPSC Code:
12352103
PubChem Substance ID:
24851993
NACRES:
NA.22

Quality Level

100

assay

95%

form

liquid

refractive index

n20/D 1.523 (lit.)

bp

93 °C/10 mmHg (lit.)

density

1.693 g/mL at 25 °C (lit.)

SMILES string

CCCC[Sn](Cl)(Cl)Cl

InChI

1S/C4H9.3ClH.Sn/c1-3-4-2;;;;/h1,3-4H2,2H3;3*1H;/q;;;;+3/p-3

InChI key

YMLFYGFCXGNERH-UHFFFAOYSA-K

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
MKCN8890
MKCS9793
MKCB3215V
MKBZ8055V
MKBT5165V

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Sigma-Aldrich

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Sigma-Aldrich

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L M Allan et al.
AIHAJ : a journal for the science of occupational and environmental health and safety, 61(6), 820-824 (2001-02-24)
An initial screening test compared the use of tropolone (2-hydroxy-2,4-6-cycloheptatrienone) in acetic acid with sodium diethyldithiocarbamate (NaDDC) as chelating agents for the extraction of butyltin chlorides from glass fiber filters and XAD-2 resin tube. NaDDC was chosen for subsequent analyses.
M Monperrus et al.
Analytical and bioanalytical chemistry, 381(4), 854-862 (2004-12-17)
A robust method has been developed for simultaneous determination of mercury and butyltin compounds in aqueous samples. This method is capable of providing accurate results for analyte concentrations in the picogram per liter to nanogram per liter range. The simultaneous
Dagmar D Doering et al.
Steroids, 67(10), 859-867 (2002-09-17)
Butyltins are widely used biocides and accumulate in the food chain. Tributyltin is an imposex-inducing endocrine disrupter in animals. Imposex is characterized by the development of additional male sex organs on females. In a previous study, we identified tributyltin as
J Carpinteiro et al.
Fresenius' journal of analytical chemistry, 370(7), 872-877 (2001-09-25)
A fast and simple procedure is presented for the simultaneous leaching of butyl (mono, di and tributyl) and phenyl organotin species from sediment samples. Leached compounds are further ethylated with sodium tetraethylborate in aqueous medium, and analyzed by gas chromatography.
S Ueno et al.
Archives of toxicology, 69(1), 30-34 (1994-01-01)
The in vivo induction of hepatotoxicity, as evaluated by the activity of ornithine carbamyl transferase in serum, was investigated in mice administered orally with the following three butyltin compounds: tributyltin chloride (TBTC), dibutyltin dichloride (DBTC) and monobutyltin trichloride (MBTC). The
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