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CERIUM(III) CHLORIDE CAS#7790-86-5

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Chemical Name:CERIUM(III) CHLORIDE

CAS No.7790-86-5

Molecular Formula：CeCl3

Molecular weight:246.48

Sample: Available

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Product Details

Products Description of CERIUM(III) CHLORIDE CAS#7790-86-5

White crystalline particles Cerium trichloride is a colorless, deliquescent block crystal or powder. When exposed to humid air, it quickly absorbs water to form hydrates of uncertain composition. It is easily soluble in water, ethanol and acetone.

CERIUM(III) CHLORIDE Chemical Properties

Melting point	848 °C(lit.)
Boiling point	1727 °C
density	3.97 g/mL at 25 °C(lit.)
Fp	1727°C
storage temp.	Inert atmosphere,Room Temperature
solubility	soluble in H2O, ethanol
form	beads
color	White to Pale Gray
Specific Gravity	3.92
Water Solubility	Soluble in water, ethanol, acids and acetone.
Sensitive	Hygroscopic
Merck	14,1997
Stability:	Stable. Hygroscopic. Incompatible with strong acids, strong oxidizing agents.
InChIKey	VYLVYHXQOHJDJL-UHFFFAOYSA-K
CAS DataBase Reference	7790-86-5(CAS DataBase Reference)
EPA Substance Registry System	Cerium chloride (CeCl3) (7790-86-5)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36
RIDADR	UN 3260 8 / PGIII
WGK Germany	2
RTECS	FK5075000
F	3-10
TSCA	Yes
HS Code	28461090
Toxicity	LD50 in mice, guinea pigs (mg/kg): 352, 110 i.p. (Graca)

Product Application of CERIUM(III) CHLORIDE CAS#7790-86-5

Cerium trichloride can be used as a raw material for the preparation of cerium and other cerium salts, a petroleum catalyst, and a Lewis acid in organic synthesis. Cerium trichloride can be used as a raw material for the preparation of cerium trifluoromethanesulfonate, which is a Lewis acid in organic synthesis and is used in Friedel-Crafts acylation. Cerium trichloride itself is also a Lewis acid and is used in Friedel-Crafts alkylation. Cerium trichloride heptahydrate can be used as a reagent in the Luche reduction reaction when used with sodium borohydride. This reaction is one of the common methods for reducing α,β-unsaturated ketones in organic synthesis.

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