204722

Tin(II) chloride

≥99.99% trace metals basis

• Sinónimos: Stannous chloride
• Fórmula lineal: SnCl₂
• Número de CAS: 7772-99-8
• Peso molecular: 189.62
• Número CE: 231-868-0
• Número MDL: MFCD00011241
• Código UNSPSC: 12352302
• eCl@ss: 38140204
• ID de la sustancia en PubChem: 57647842
• NACRES: NA.21

Propiedades

• grado: for analytical purposes
• Nivel de calidad: 100
• presión de vapor: 33 hPa (~429 °C)
• Ensayo: ≥99.99% trace metals basis
• Formulario: crystalline powder; flakes
• idoneidad de la reacción: reagent type: catalyst; core: tin
• pH: 2.18 (20 °C)
• bp: 652 °C (lit.)
• mp: 246 °C (lit.)
• cadena SMILES: Cl[SnH2]Cl
• InChI: 1S/2ClH.Sn/h2*1H;/q;;+2/p-2
• Clave InChI: AXZWODMDQAVCJE-UHFFFAOYSA-L

Descripción

Descripción general

Tin(II) chloride (Stannous chloride, SnCl₂) is widely employed as reducing reagent. It plays significant role in diverse fields of science. Since it exhibits superior catalytic action in molten state, it is employed for the hydroliquefaction of coals. It is a promising raw material for the chemical vapour deposition (CVD) of semiconducting layers. It can be prepared by reacting its dihydrate form with acetic anhydride. It exhibits reducing properties in acidic media. It participates in the reduction of the following compounds:

• aromatic nitro compounds
• nitriles
• cyanosilyl ethers
• organic azides

On mixing sodium cyanoborohydride with SnCl₂ in a 2:1 ratio, a reducing reagent mixture is obtained. This reagent is useful for the reduction of tertiary, allyl and benzyl halides.

Aplicación

Tin(II) chloride has been used for the reduction of hydroperxoxides to the corresponding alcohols in a study.

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.

Información de seguridad

• Pictogramas: GHS08,GHS05,GHS07
• Palabra de señalización: Danger
• Frases de peligro: H290,H302 + H332,H314,H317,H335,H373,H412
• Consejos de prudencia: P260 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Clasificaciones de peligro: 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
• Órganos de actuación: Cardio-vascular system, Respiratory system
• Código de clase de almacenamiento: 8B - Non-combustible corrosive hazardous materials
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable
• Equipo de protección personal: Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges