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217913

Sigma-Aldrich

Tin(IV) chloride

99.995% trace metals basis

Synonym(s):

Stannic chloride fuming

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About This Item

Linear Formula:
SnCl4
CAS Number:
Molecular Weight:
260.52
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

vapor density

9 (vs air)

Quality Level

vapor pressure

10 mmHg ( 10 °C)
18.6 mmHg ( 20 °C)
20 mmHg ( 22 °C)

Assay

99.995% trace metals basis

form

liquid

reaction suitability

core: tin
reagent type: Lewis acid
reagent type: catalyst

bp

114 °C (lit.)

mp

−33 °C (lit.)

density

2.226 g/mL at 25 °C (lit.)

SMILES string

Cl[Sn](Cl)(Cl)Cl

InChI

1S/4ClH.Sn/h4*1H;/q;;;;+4/p-4

InChI key

HPGGPRDJHPYFRM-UHFFFAOYSA-J

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Application

Doping polyaniline, an intensively studied polymer, with SnCl4 stabilizes its solution in nitromethane and allows solution processing.
Lewis acid catalyst

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Jinyan Dai et al.
ChemSusChem, 12(23), 5092-5098 (2019-10-20)
One of the key challenges for the development of lithium-ion batteries is the preparation of high-performance anode materials. In this paper, a micro/nanostructured Si@SnS2 -rGO composite is reported in which Si nanoparticles with a particle size of 30 nm are electrostatically
Bastian Waduge Naveen Harindu Hemasiri et al.
Scientific reports, 7(1), 17868-17868 (2017-12-21)
Indium tin oxide (ITO) still remains as the main candidate for high-performance optoelectronic devices, but there is a vital requirement in the development of sol-gel based synthesizing techniques with regards to green environment and higher conductivity. Graphene/ITO transparent bi-film was
Chemistry Letters (Jpn), 36, 826-826 (2007)
Kulszewicz-Bajer, I. et al.
Chemistry of Materials, 11, 552-552 (1999)
Gerry A Griffith et al.
Journal of the American Chemical Society, 128(40), 13130-13141 (2006-10-05)
Difluorinated alkenoate ethyl 3,3-difluoro-2-(N,N-diethylcarbamoyloxy)-2-propenoate reacts rapidly and in high yield with furan and a range of substituted furans in the presence of a tin(IV) catalyst. Non-fluorinated congener 2-(N,N-diethylcarbamoyloxy)-2-propenoate fails to react at all under the same conditions. These reactions have

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