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Tin(II) chloride

SIGALD/208256 - reagent grade, 98%

Synonym: Stannous chloride

CAS Number: 7772-99-8
Empirical Formula (Hill Notation): Cl2Sn
Molecular Weight: 189.62
EC Number: 231-868-0
MDL Number: MFCD00011241
Linear Formula: SnCl2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-208256-100G 100 g
$88.00
1/EA
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45-208256-500G 500 g
$252.00
1/EA
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45-208256-2KG 2 kg
$610.00
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 208256-500G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 208256-2KG

 

assay 98%
bp 652 °C (lit.)
form crystalline
  powder or flakes
grade reagent grade
InChI 1S/2ClH.Sn/h2*1H;/q;;+2/p-2
InChI key AXZWODMDQAVCJE-UHFFFAOYSA-L
mp 246 °C (lit.)
pH 2.18 (20 °C)
Quality Level 200 
SMILES string Cl[SnH2]Cl
vapor pressure 33 hPa (~429 °C)
Application: Tin(II) chloride (SnCl2) has been used as a starting material to evaluate the thermal behavior of SnCl2 on heating at the rate of 5°Cmin-1 in air. The product undergoes phase transformation on heating at rate of 5°C min-1 in air, it involves an incomplete evaporation followed by oxidation forming SnO2 nanoparticles. SnCl2 has also been used for the fabrication of Sn-containing carbon nano-structures.
Application: Tin(II) chloride may be used:
• To catalyze the addition of diazo sulfones, diazo phosphine oxides and diazo phosphonates to aldehydes to form β-keto sulfones, β-keto phosphine oxides and β-keto phosphonates, respectively.
• Along with trityl chloride, to catalyze the aldol reaction of silyl enol ethers with acetals or aldehydes and the Michael reaction of silyl enol ethers with α,β-unsaturated ketones.
• As a promoter in the allylic amination of allylic alcohols with amines in the presence of palladium catalyst.
General description: SnCl2 dihydrate reacts with acetic anhydride to yield anhydrous SnCl2. SnCl2 exhibits reducing properties in acidic media. SnCl2 shows superior catalytic action in its molten state. It is a promising raw material for the chemical vapour deposition (CVD) of semiconducting layers. SnCl2 participates in the reduction of aromatic nitro compounds, nitriles, cyanosilyl ethers and organic azides.
Packaging: 100, 500 g in poly bottle
Packaging: 2 kg in poly bottle
Purity 98%
bp 652 °C (lit.)
mp 246 °C (lit.)
UNSPSC 12352300

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