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Sigma-Aldrich

Tin(II) chloride dihydrate

≥99.97% trace metals basis

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Synonym(s):
Stannous dichloride dihydrate, Stannous chloride dihydrate
Linear Formula:
SnCl2 · 2H2O
CAS Number:
Molecular Weight:
225.65
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥99.97% trace metals basis

reaction suitability

core: tin
reagent type: catalyst

bp

652 °C (lit.)

mp

37-38 °C (dec.) (lit.)

SMILES string

O.O.Cl[SnH2]Cl

InChI

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

InChI key

FWPIDFUJEMBDLS-UHFFFAOYSA-L

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1 of 4

This Item
24352320803531669
Tin(II) chloride dihydrate ACS reagent, 98%

Sigma-Aldrich

243523

Tin(II) chloride dihydrate

Essential Grade
Tin(II) chloride dihydrate puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., ≥98%

Sigma-Aldrich

31669

Tin(II) chloride dihydrate

Essential Grade
reaction suitability

core: tin, reagent type: catalyst

reaction suitability

-

reaction suitability

-

reaction suitability

-

bp

652 °C (lit.)

bp

652 °C (lit.)

bp

652 °C (lit.)

bp

652 °C (lit.)

mp

37-38 °C (dec.) (lit.)

mp

37-38 °C (dec.) (lit.)

mp

37-38 °C (dec.) (lit.)

mp

37-38 °C (dec.) (lit.)

Quality Level

100

Quality Level

-

Quality Level

200

Quality Level

-

Application

Tin(II) chloride dihydrate can be used as a mild Lewis acid catalyst to synthesize:      
  • 3-Aminoimidazo[1,2-a]pyridines via three-component condensation reaction of aromatic aldehydes, 2-aminopyridines, and isonitriles.     
  • Pyrazolo[5,4-b]quinoline derivatives via cyclocondensation reaction of 5-amino-3-(arylamino)-1H-pyrazole-4-carbonitriles with cyclohexane-1,3-dione or dimedone.    
  • Polylactic acid from aqueous lactic acid in the presence of succinic anhydride.

It can also be used as a cocatalyst to synthesize indole derivatives by treating anilines with trialkanolamines in the presence of ruthenium as a catalyst.

Signal Word

Danger

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 Code

8B - Non-combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Xiang-Hui Tan et al.
Organic letters, 5(11), 1833-1835 (2003-05-24)
[reaction: see text] Under the Lewis acid catalysis offered by TiCl(3), SnCl(2) can efficiently mediate the aqueous Barbier reactions between aldehydes and allyl chloride or bromide.
Jonathan J Gridley et al.
Chemical communications (Cambridge, England), (20), 2550-2551 (2003-11-05)
Condensations between the tin(II) enolate 11 of ethyl N-tosylglycinate and conjugated ynals 12 and ynones 14 are highly diastereoselective, in favour of the anti-isomers 13 and 15; similar reactions of enals and enones 17 show lower but still useful levels
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Tin oxide (SnO2) is widely adopted as an electron transport layer in perovskite solar cells (PeSCs) because it has high electron mobility, excellent charge selective behavior owing to a large band gap of 3.76 eV, and low-temperature processibility. To achieve
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Continuously enhanced photoresponsivity and suppressed dark/noise current combinatorially lead to the recent development of high-detectivity organic photodetectors with broadband sensing competence. Despite the achievements, reliable photosensing enabled by organic photodetectors (OPDs) still faces challenges. Herein, we call for heed over
Sharp, S.L. et al.
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