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About This Item
Linear Formula:
CH3(CH2)3SnCl3
CAS Number:
Molecular Weight:
282.18
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
EC Number:
214-263-6
MDL number:
Assay:
95%
Form:
liquid
InChI key
YMLFYGFCXGNERH-UHFFFAOYSA-K
InChI
1S/C4H9.3ClH.Sn/c1-3-4-2;;;;/h1,3-4H2,2H3;3*1H;/q;;;;+3/p-3
SMILES string
CCCC[Sn](Cl)(Cl)Cl
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.)
Quality Level
Related Categories
signalword
Danger
hcodes
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
WGK 1
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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
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.
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
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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