Cerium(IV) sulfate hydrate, 98%
Cerium(IV) sulfate hydrate, 98%
Cerium(IV) sulfate hydrate, 98%
Cerium(IV) sulfate hydrate, 98%
Thermo Scientific Chemicals

Cerium(IV) sulfate hydrate, 98%

CAS: 95838-16-7 | CeO8S2 | 332.23 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
50 g
250 g
1000 g
Catalog number A10142.30
also known as A10142-30
Price (EUR)
280,00
Each
Quantity:
250 g
Request bulk or custom format
Price (EUR)
280,00
Each
Chemical Identifiers
CAS95838-16-7
IUPAC Nameλ⁴-cerium(4+) disulfate
Molecular FormulaCeO8S2
InChI KeyVZDYWEUILIUIDF-UHFFFAOYSA-J
SMILES[Ce+4].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Yellow or Orange
Formcrystalline powder
Assay (unspecified)>= 97.5% (REO basis)
Cerium(IV) sulfate hydrate is used as a general application for chemical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Cerium(IV) sulfate hydrate is used as a general application for chemical intermediate.

Solubility
Soluble in water.

Notes
Store in cool, dry conditions in well sealed containers. keep container tightly closed
RUO – Research Use Only

General References:

  1. M. P. Singh; H. S. Singh; M. K. Verma. Kinetics and mechanism of the ruthenium(III) chloride catalyzed oxidation of butanone-2 and pentanone-3 by cerium(IV) sulfate in aqueous sulfuric acid medium. J. Phys. Chem. 1980, 84,(3), 256-259.
  2. Oxidizing agent which has been used for the generation of o-benzoquinone from catechol: Liebigs Ann. Chem., 712, 214 (1968).
  3. Promotes the formation of radicals from dialkyl malonates, which undergo substitution reactions with furans and thiophenes: Heterocycles, 27, 2627 (1988).
  4. In the presence of oxygen, oximes can be converted to the parent carbonyl compounds in good yield: Appl. Organomet. Chem., 13, 867 (1999).
  5. In combination with iodine in EtOH, 2-alkylcycloalkanones are ring-opened to ethyl keto esters: J. Chem. Res. (Synop.), 122 (1999).