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Sigma-Aldrich

Indium(III) chloride

98%

Synonym(s):

Indium trichloride

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About This Item

Linear Formula:
InCl3
CAS Number:
10025-82-8
Molecular Weight:
221.18
EC Number:
233-043-0
MDL number:
MFCD00011058
UNSPSC Code:
12352302
PubChem Substance ID:
24860216
NACRES:
NA.23

Quality Level

100

Assay

98%

form

powder or flakes (or chunks)

reaction suitability

reagent type: catalyst
core: indium

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 (InCl3) is an indium halide that is a Lewis acid in a variety of organic reactions.

Application

InCl3 can be used for a variety of application such as:
  • fabrication of a photoanode for dye sensitized solar cells
  • a catalyst in Michael addition of silylenol and indoles

Useful catalyst for aqueous organic reactions including C-C bond formation, aldol reactions, and reductions. An efficient, yet mild, Lewis acid for organic synthesis.

Pictograms

Health hazardCorrosion
GHS08,GHS05

Signal Word

Danger

Hazard Statements

H314,H372,H412

Hazard Classifications

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

Target Organs

Lungs

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Babu, S.A.
Synlett, 531-531 (2002)
Fabrication and characterization of ZnO: In thin film as photoanode for DSSC using natural fruit dyes
AIP Conference Proceedings, 1660(1), 070049-070049 (2015)
Satoko Fujimoto et al.
Bioscience, biotechnology, and biochemistry, 66(6), 1389-1392 (2002-08-07)
(R)-(-)-Muscone (3-methylcyclopentadecanone, 1) the key perfumery component isolated from the male musk deer, Moschus moschiferus,* was synthesized from the easily available chiral building block, (R)-3-tert-butoxycarbonyl-2-methylpropanoic acid (2), by employing ring-closing olefin metathesis (RCM). Antipode (+)-1 was also synthesized in a
Indium (III) chloride-catalyzed Michael addition of thiols to chalcones: a remarkable solvent effect
Ranu BC, et al.
ARKIVOC (Gainesville, FL, United States), 3, 44-50 (2005)
Tanmoy Chanda et al.
Chemistry, an Asian journal, 7(4), 778-787 (2012-02-09)
The efficient, regioselective synthesis of functionalized/annulated quinolines was achieved by the coupling of 2-aminoaryl ketones with alkynes/active methylenes/α-oxoketene dithioacetals promoted by InCl(3) in refluxing acetonitrile as well as under solvent-free conditions in excellent yields. This transformation presumably proceeded through the
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