908924

Tin(II) chloride

free-flowing, Redi-Dri^™, reagent grade, 98%

• Synonym(s): Stannous chloride
• Linear Formula: SnCl₂
• CAS Number: 7772-99-8
• Molecular Weight: 189.62
• MDL number: MFCD00011241
• UNSPSC Code: 12352302
• NACRES: NA.21
• assay: 98%
• grade: anhydrous; reagent grade
• form: crystals

Properties

• grade: anhydrous; reagent grade
• product line: Redi-Dri^™
• assay: 98%
• form: crystals
• quality: free-flowing
• bp: 652 °C (lit.)
• mp: 246 °C (lit.)
• SMILES string: Cl[SnH2]Cl
• InChI: 1S/2ClH.Sn/h2*1H;/q;;+2/p-2
• InChI key: AXZWODMDQAVCJE-UHFFFAOYSA-L

Description

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.

Application

Redi-Dri^™ is an innovative packaging product line that helps eliminate clumping material by adding extra packaging process steps without any chemical additives, anti-clumping agents, or hydrophobic compounds. Redi-Dri^™offers a more convenient and safer way to handle the products.

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.
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.

Other Notes

Go to Redi-Dri^™ Product Listing 208256

Legal Information

Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Safety Information

• pictograms: GHS08,GHS05,GHS07
• signalword: Danger
• hcodes: H290,H302 + H332,H314,H317,H335,H373,H412
• pcodes: P260 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2 Oral - STOT SE 3
• target_organs: Cardio-vascular system, Respiratory system
• Storage Class: 8B - Non-combustible corrosive hazardous materials
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable