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Merck
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30-2490

Sigma-Aldrich

Tin(II) chloride dihydrate

SAJ first grade, ≥90.0%

Sinonimo/i:

Stannous chloride dihydrate

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About This Item

Formula condensata:
SnCl2 · 2H2O
Numero CAS:
10025-69-1
Peso molecolare:
225.65
Numero MDL:
MFCD00149863
Codice UNSPSC:
12352302
ID PubChem:
329753356

Grado

SAJ first grade

Saggio

≥90.0%

Forma fisica

solid

Impiego in reazioni chimiche

reagent type: catalyst
core: tin

Disponibilità

available only in Japan

P. eboll.

652 °C (lit.)

Punto di fusione

37-38 °C (dec.) (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

O.O.Cl[SnH2]Cl

InChI

1S/2ClH.2H2O.Sn/h2*1H;2*1H2;/q;;;;+2/p-2
FWPIDFUJEMBDLS-UHFFFAOYSA-L

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Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Cardio-vascular system, Respiratory system

Codice della classe di stoccaggio

8B - Non-combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

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David J Hallett et al.
Organic & biomolecular chemistry, 10(30), 6130-6158 (2012-04-20)
Reactions of the allyltin trichloride 45 generated from (4S)-4-benzyloxypent-2-enyl(tributyl)stannane 1 with imines prepared from glyoxylates proceed with useful levels of 1,5-stereocontrol in favour of (4E)-2,6-anti-2-(alkylamino)-6-benzyloxyhept-4-enoates 49. This stereoselectivity, controlled by the chirality of the stannane, dominates over any intrinsic stereochemical
Lindsay A Hobson et al.
Organic & biomolecular chemistry, 10(37), 7510-7526 (2012-08-14)
Transmetallation of the 5-benzyloxy-4-methylpent-2-en-1-yl(tributyl)- and -(triphenyl)stannanes 1 and 8 using tin(iv) chloride generates an allyltin trichloride that reacts with aldehydes to give (Z)-1,5-anti-6-benzyloxy-5-methylhex-3-en-1-ols 2. The allyltin trichloride believed to be the key intermediate in these reactions has been trapped by
Caitian Gao et al.
Nanoscale, 4(11), 3475-3481 (2012-05-11)
A high-efficiency photoelectrode for dye-sensitized solar cells (DSSCs) should combine the advantageous features of fast electron transport, slow interfacial electron recombination and large specific surface area. However, these three requirements usually cannot be achieved simultaneously in the present state-of-the-art research.
Liyan Zheng et al.
Dalton transactions (Cambridge, England : 2003), 41(5), 1630-1634 (2011-12-08)
It was found that stannous chloride (SnCl(2)), as a popular inorganic reducing reagent, could obviously enhance the electrochemiluminescence (ECL) of tris(2,2'-bipyridyl) ruthenium(II) (Ru(bpy)(3)(2+)) in aqueous solution. Some factors affecting the ECL reactions between Ru(bpy)(3)(2+) and Sn(2+), including pH, concentrations of
Matthew Currie et al.
Inorganic chemistry, 52(4), 1710-1721 (2012-06-09)
The anionic speciation of chlorostannate(II) ionic liquids, prepared by mixing 1-alkyl-3-methylimidazolium chloride and tin(II) chloride in various molar ratios, χ(SnCl2), was investigated in both solid and liquid states. The room temperature ionic liquids were investigated by (119)Sn NMR spectroscopy, X-ray
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