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345172

Sigma-Aldrich

Tin(IV) acetate

Sinónimos:

Stannic Acetate, Tetraacetoxytin, Tin(4+) Diethanoate, Tin(4+) tetraacetate

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About This Item

Fórmula lineal:
Sn(CH3CO2)4
Número de CAS:
2800-96-6
Peso molecular:
354.89
MDL number:
MFCD00014976
UNSPSC Code:
12352103
PubChem Substance ID:
24861300
NACRES:
NA.23

form

solid

composition

Sn, 31.4-35.5% gravimetric

reaction suitability

core: tin

mp

232-233 °C (lit.)

SMILES string

CC(=O)O[Sn](OC(C)=O)(OC(C)=O)OC(C)=O

InChI

1S/4C2H4O2.Sn/c4*1-2(3)4;/h4*1H3,(H,3,4);/q;;;;+4/p-4

InChI key

YJGJRYWNNHUESM-UHFFFAOYSA-J

Categorías relacionadas

General description

Tin(IV) acetate is a white crystalline solid widely used as a catalyst in organic transformations and a sol-gel precursor to synthesize nanomaterials.

Application

Tin(IV) acetate can be used:
  • As a reducing agent to synthesize silver nanoparticles for conductive inks for printed electronics.
  • As a precursor to prepare tin oxide nanopowder for gas sensors.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Miika Mattinen et al.
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Semiconducting 2D materials, such as SnS2 , hold immense potential for many applications ranging from electronics to catalysis. However, deposition of few-layer SnS2 films has remained a great challenge. Herein, continuous wafer-scale 2D SnS2 films with accurately controlled thickness (2
Non-aqueous synthesis of silver nanoparticles using tin acetate as a reducing agent for the conductive ink formulation in printed electronics
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Journal of Materials Chemistry, 21, 10871-10877 (2011)
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Sn(II) binds to kaempferol (HKaem, 3,4',5,7-tetrahydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one) at the 3,4-site forming [Sn(II)(Kaem)2] complex in ethanol. DPPH• scavenging efficiency of HKaem is dramatically decreased by SnCl2 coordination due to formation of acid inhibiting deprotonation of HKaem as ligands and thus reduces the
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