Skip to Content
Merck
All Photos(1)

Documents

46264

Sigma-Aldrich

Ferrocenecarboxylic acid

purum, ≥96%

Synonym(s):

Ferrocenemonocarboxylic acid, Ferrocenylcarboxylic acid, (Carboxycyclopentadienyl)cyclopentadienyliron, Carboxyferrocene, Carboxylferrocene, Cyclopentadienecarboxylic acid, Ferrocenoic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H10FeO2
CAS Number:
Molecular Weight:
230.04
EC Number:
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

grade

purum

Quality Level

Assay

≥96%

reaction suitability

core: iron
reagent type: catalyst

mp

210 °C (dec.) (lit.)

SMILES string

[Fe].[CH]1[CH][CH][CH][CH]1.OC(=O)[C]2[CH][CH][CH][CH]2

InChI

1S/C6H5O2.C5H5.Fe/c7-6(8)5-3-1-2-4-5;1-2-4-5-3-1;/h1-4H,(H,7,8);1-5H;

InChI key

VUJLGCHOGQEAED-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Ferrocene carboxylic acid (FCCa) is an organometallic compound comprised of a ferrocene core with a carboxylic acid functional group. It is used as a mediator in electrocatalytic oxidation. Due to its excellent redox properties, it is widely used in electrochemistry, redox probes, and peptide chain modifications. In addition, a direct cross-coupling reaction was explored using ferrocenecarboxylic acid and alkenes.

Application

Ferrocene carboxylic acid can be used as a:
  • Starting material in the synthesize of ferrocene-guanine conjugates.
  • Redox mediator in electrochemical-chemical-chemical (ECC) redox cycling.

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Electrochemical-chemical-chemical redox cycling triggered by thiocholine and hydroquinone with ferrocenecarboxylic acid as the redox mediator
Liu L, et al.
Electrochimica Acta, 139, 323-330 (2014)
New chiral ferrocenyl amidophosphine ligand for remarkable improvement of enantioselectivities in copper-catalyzed addition of diethylzinc to N-sulfonylimines
Wang MC, et al.
Tetrahedron Letters, 46(32), 5413-5416 (2005)
Palladium (II)-Catalyzed Enantioselective C- H Alkenylation of Ferrocenecarboxylic Acid
Huang Y, et al.
Advanced Synthesis & Catalysis, 362(6), 1385-1390 (2020)
New approaches toward ferrocene--guanine conjugates: synthesis and electrochemical behavior
Iurlo M, et al.
Organometallics, 33(18), 4986-4993 (2014)
Ewa Nazaruk et al.
Bioelectrochemistry (Amsterdam, Netherlands), 71(1), 8-14 (2007-02-10)
The monoolein-based liquid crystalline cubic phase was used as the matrix to incorporate redox enzymes--glucose (GOx), pyranose (PyOx) oxidases and laccase. Thin layer of the cubic phase embedding GOx or PyOx activated glucose oxidation in the presence and absence of

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