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202983

Sigma-Aldrich

Cerium(III) chloride heptahydrate

99.999% trace metals basis

Synonym(s):

Cerous chloride heptahydrate

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About This Item

Linear Formula:
CeCl3 · 7H2O
CAS Number:
18618-55-8
Molecular Weight:
372.58
EC Number:
232-227-8
MDL number:
MFCD00149634
UNSPSC Code:
12352302
PubChem Substance ID:
24852136
NACRES:
NA.23

Quality Level

100

Assay

99.999% trace metals basis

form

crystals and lumps

reaction suitability

reagent type: catalyst
core: cerium

impurities

≤15.0 ppm Trace Metal Analysis

density

~3.94 g/mL at 25 °C (lit.)

SMILES string

[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].Cl[Ce](Cl)Cl

InChI

1S/Ce.3ClH.7H2O/h;3*1H;7*1H2/q+3;;;;;;;;;;/p-3

InChI key

KPZSTOVTJYRDIO-UHFFFAOYSA-K

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Application

Cerium chloride heptahydrate is often used to prepare cerium oxide nanoparticles by various methods. It reacts with sodium-oleate to form a cerium-oleate complex which can be further decomposed in hydrocarbon solvents to prepare cerium oxide nanoparticles. Cerium chloride heptahydrate can also be used in the conversion of esters to allylsilanes.

Pictograms

CorrosionEnvironment
GHS05,GHS09

Signal Word

Danger

Hazard Statements

H314,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1C

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000399178
0000350471
0000350471
0000399178
0000212425

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Preparation and characterization of monodisperse cerium oxide nanoparticles in hydrocarbon solvents
Gu H, et al.
Chemistry of Materials, 19.5, 1103-1110 (2007)
Organic Syntheses, 69, 89-89 (1990)
Panthenol-stabilized cerium dioxide nanoparticles for cosmeceutic formulations against ROS-induced and UV-induced damage.
Zholobak NM, et al.
Journal of Photochemistry and Photobiology. B, Biology, 130, 102-108 (2014)
Cerium fluoride nanoparticles protect cells against oxidative stress.
Shcherbakov AB, et al.
Materials Science and Engineering, C, 50, 151-159 (2015)
Xiaoming Tao et al.
Organic letters, 15(1), 72-75 (2012-12-25)
Dynamic kinetic resolution of various α-amido-β-keto phosphonates via asymmetric hydrogenation proceeded efficiently to give the corresponding β-hydroxy-α-amido phosphonates in high diastereo- and enantioselectivities (up to 99:1 syn/anti, 99.8% ee). The addition of catalytic amounts of CeCl(3)·7H(2)O is necessary to achieve
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