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249955

Sigma-Aldrich

Tin(IV) chloride solution

1.0 M in methylene chloride

Synonym(s):

Stannic chloride, Tin tetrachloride

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100 ML
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Estimated to ship onMarch 29, 2025

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4 X 25 ML
$71.50
100 ML
$75.30
800 ML
$219.00

About This Item

Linear Formula:
SnCl4
CAS Number:
7646-78-8
Molecular Weight:
260.52
MDL number:
MFCD00011242
UNSPSC Code:
12352106
PubChem Substance ID:
24855025
NACRES:
NA.22

$71.50

Estimated to ship onMarch 29, 2025

Request a Bulk Order

form

liquid

Quality Level

100

reaction suitability

core: tin
reagent type: catalyst

concentration

1.0 M in methylene chloride

density

1.419 g/mL at 25 °C

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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General description

Tin(IV) chloride shows Lewis acid character[1] and is generally used for the synthesis of SnO2 nanoparticles by sol-gel method.[2]

Application

Tin(IV) chloride solution can be used for chloromethylation reaction of polysulfones to develop polymer electrolyte membranes.[3]

Packaging

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

Legal Information

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

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Danger

Hazard Classifications

Aquatic Chronic 3 - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Central nervous system, Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
0000396970
0000396971
0000396968
0000396969
0000382968

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Solid-State and Solution Structural Study of Acetylacetone-Modified Tin (IV) Chloride Used as a Precursor of SnO2 Nanoparticles Prepared by a Sol- Gel Route.
Briois V, et al.
Chemistry of Materials, 16(20), 3885-3894 (2004)
Phosphoric acid doped polysulfone membranes with aminopyridine pendant groups and imidazole cross-links.
Hink S, et al.
European Polymer Journal, 72(20), 102-113 (2015)
Molecular addition compounds of tin (IV) chloride. I. Interaction with benzonitriles in benzene solution.
Brown TL and Kubota M
Journal of the American Chemical Society, 83(2), 331-334 (1961)
Glycosidation reactions of silyl ethers with conformationally inverted donors derived from glucuronic acid: stereoselective synthesis of glycosides and 2-deoxyglycosides.
Monika Poláková et al.
Angewandte Chemie (International ed. in English), 43(19), 2518-2521 (2004-05-06)
Leo A Paquette et al.
The Journal of organic chemistry, 68(22), 8614-8624 (2003-10-25)
The concept of spirocyclic restriction, when generically applied to nucleoside mimics, allows for the preparation of diastereomeric pairs carrying either a syn- or anti-oriented hydroxyl at C-5'. Reported herein are convenient synthetic routes to enantiomerically pure 1-oxaspiro[4.4]nonanes featuring fully dihydroxylated
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