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Sigma-Aldrich

Indium(III) chloride

99.999% trace metals basis

Sinónimos:

Indium trichloride

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About This Item

Fórmula lineal:
InCl3
Número de CAS:
10025-82-8
Peso molecular:
221.18
EC Number:
233-043-0
MDL number:
MFCD00011058
UNSPSC Code:
12352302
PubChem Substance ID:
24852172
NACRES:
NA.23

assay

99.999% trace metals basis

form

powder or flakes (or chunks)

reaction suitability

reagent type: catalyst
core: indium

impurities

≤15.0 ppm Trace Metal Analysis

density

3.46 g/mL at 25 °C (lit.)

SMILES string

Cl[In](Cl)Cl

InChI

1S/3ClH.In/h3*1H;/q;;;+3/p-3

InChI key

PSCMQHVBLHHWTO-UHFFFAOYSA-K

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General description

Indium(III) chloride is a Lewis acid catalystused in a variety of organic reactions. It also finds application in the fields of catalysis, solar cells, and optoelectronics.

Application

Indium(III) chloride can be used:
  • As a catalyst for the preparation of 1,3-dithiolanes from aldehydes and ketones.
  • For acylation of phenols, thiols, alcohols, and amines.
  • As a precursor to fabricate Indium tin oxide(ITO) thin films for dye-sensitized solar cells.
  • To prepare solution-processed oxide semiconductor thin-film transistors (OS TFTs) that can be used in display devices.

pictograms

Health hazardCorrosion
GHS08,GHS05

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C - STOT RE 1 Inhalation

target_organs

Lungs

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Mecheril Valsan Nandakumar et al.
Chemical communications (Cambridge, England), (26), 2756-2758 (2007-06-28)
The indium-bipyridine-catalyzed, enantioselective ring-opening of meso-epoxides with aliphatic and aromatic thiols furnished 1,2-mercapto alcohols in good yields and excellent enantioselectivities; the crystal structure of the chiral catalyst reveals a pentagonal-bipyramidal coordination geometry around the indium center.
Synthesis, 1712-1712 (2007)
Tetrahedron Letters, 48, 6743-6743 (2007)
Theresa A Proia et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 26(23), 6335-6349 (2020-09-19)
Danvatirsen is a therapeutic antisense oligonucleotide (ASO) that selectively targets STAT3 and has shown clinical activity in two phase I clinical studies. We interrogated the clinical mechanism of action using danvatirsen-treated patient samples and conducted back-translational studies to further elucidate
Naveen Mulakayala et al.
Bioorganic & medicinal chemistry letters, 22(15), 5063-5066 (2012-07-04)
A convenient and practical methodology for the synthesis of 2-aryl quinazolin-4(3H)-ones by the condensation of o-aminobenzamides with aromatic aldehydes under mild conditions using catalytic InCl(3) with good yields and high selectivities. This method has been extended for the synthesis of
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