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510270

Sigma-Aldrich

Indium(III) acetate

99.99% trace metals basis

Synonym(s):

Indium triacetate

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About This Item

Linear Formula:
In(C2H3O2)3
CAS Number:
Molecular Weight:
291.95
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

99.99% trace metals basis

form

solid

reaction suitability

core: indium
reagent type: catalyst

mp

270 °C (dec.) (lit.)

SMILES string

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

InChI

1S/3C2H4O2.In/c3*1-2(3)4;/h3*1H3,(H,3,4);/q;;;+3/p-3

InChI key

VBXWCGWXDOBUQZ-UHFFFAOYSA-K

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General description

Indium(III) acetate is a white crystalline water-soluble solid that decomposes to indium oxide upon heating. It is used as a catalyst in intermolecular and intramolecular acyl substitution reactions. It is also widely used as CVD precursor to prepare indium oxide thin oxide.

Application

Indium(III) acetate can be used:
  • As a precursor to fabricate In2S3 thin films via chemical spray pyrolysis. These films are used as electron transport layers in highly efficient perovskite solar cells.
  • To prepare indium arsenide quantum dots which are infrared emitting nanomaterials used in optoelectronic and biomedical applications.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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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Kinetics analysis for non-isothermal decomposition ?-irradiated indium acetate.
Al-Resayes SI, et al
Arabian Journal of Chemistry, 3(3), 191-194 (2010)
Characteristics of CuInS2/ZnS quantum dots and its application on LED
Kim H,et al
Journal of Crystal Growth, 326, 90-93 (2011)
Katsukiyo Miura et al.
Organic letters, 10(1), 133-136 (2007-12-13)
In the presence of phenylsilane and a catalytic amount of indium(III) acetate, organic iodides added to electron-deficient alkenes in ethanol at room temperature. Both simple and functionalized organic iodides were applicable to this reaction. A plausible reaction mechanism involves the

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