Skip to Content
Merck
CN
All Photos(2)

Documents

309281

Sigma-Aldrich

Iron(III) perchlorate hydrate

crystalline

Sign Into View Organizational & Contract Pricing
All Photos(2)
Synonym(s):
Perchloric acid iron(III) salt hydrate
Linear Formula:
Fe(ClO4)3 · xH2O
CAS Number:
15201-61-3
Molecular Weight:
354.20 (anhydrous basis)
EC Number:
236-908-0
MDL number:
MFCD00149705
UNSPSC Code:
12352000
PubChem Substance ID:
24858725
NACRES:
NA.22

form

crystalline

Quality Level

100

reaction suitability

reagent type: oxidant

impurities

<0.10% chloride

color

yellow

SMILES string

[Fe+3].[H]O[H].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O

InChI

1S/3ClHO4.Fe.H2O/c3*2-1(3,4)5;;/h3*(H,2,3,4,5);;1H2/q;;;+3;/p-3

InChI key

PFPIMAZLJXJVAN-UHFFFAOYSA-K

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Catalyst for synthesis of:
  • Fullerene-fused lactones
  • α-Carbonyl furans via one-pot cyclization
  • Fullerodioxolanes via heterocyclization
  • Dialylated indoles via double alkylation
  • Aryl esters via oxidative esterification

Used as chemical actinometer based on photolysis of ferrioxalate in presence of polyoxometalate in aqueous solution

Oxidant for conducting polymer nanoparticles synthesized in ionic liquid by chemical polymerization
Iron(III) perchlorate hydrate is a useful starting material for the synthesis of a tris-salicylate Fe(III) complex having bidentate chelating units and in photolysis of ferrioxalate in presence of polyoxometalate in aqueous solution.

It can be used as a catalyst for synthesis of:
  • Fullerene-fused lactones
  • α-Carbonyl furans via one-pot cyclization
  • Fullerodioxolanes via heterocyclization
  • Fulleroxazolidines
  • Dialylated indoles via double alkylation
  • Aryl esters via oxidative esterification

Useful starting material for the synthesis of a tris-salicylate Fe(III) complex having bidentate chelating units which allow two coordination modes.

Pictograms

Flame over circleExclamation mark
GHS03,GHS07

Signal Word

Danger

Hazard Statements

H272,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Diverse redox chemistry of photo/ferrioxalate system.
Wang Z, et al.
Royal Society of Chemistry Advances, 4(84), 44654-44658 (2014)
Ferric Perchlorate Promoted Reaction of [60] Fullerene with N-Sulfonyl Aldimines: Synthesis and Functionalization of Fulleroxazolidines.
Liu TX, et al.
The Journal of Organic Chemistry, 80(24), 11986-11992 (2015)
Iron salt-catalyzed cascade type one-pot double alkylation of indole with vinyl ketones.
Kobayashi JK, et al.
Tetrahedron, 66(22), 3917-3922 (2010)
A facile access to [60] fullerene-fused 1, 3-dioxolanes: Reaction of [60] fullerene with aldehydes/ketones promoted by ferric perchlorate.
Li FB, et al
Organic Letters, 12(14), 3258-3261 (2010)
Structural characterization of a tris-salicylate coordination for iron (III) with the tripodal ligand O-TRENSOX.
Serratrice G, et al.
Inorganic Chemistry, 38(5), 840-841 (1999)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service