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Merck
CN

106887

Ferrocenecarboxylic acid

97%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C11H10FeO2
CAS Number:
1271-42-7
Molecular Weight:
230.04
NACRES:
NA.22
PubChem Substance ID:
24846745
UNSPSC Code:
12352300
EC Number:
215-040-6
MDL number:
MFCD00001430

Key Documents

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Product Name

Ferrocenecarboxylic acid, 97%

InChI key

VUJLGCHOGQEAED-UHFFFAOYSA-N

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;

SMILES string

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

assay

97%

reaction suitability

core: iron
reagent type: catalyst

mp

210 °C (dec.) (lit.)

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Application

Used to esterify complex mixtures of phenols and alcohols for analysis by GCMS.

General description

Papanicolaou is a widely used stain in cytopathology. It is a polychrome stain that has the ability to stain several constituents of cell differentially due to the presence of multiple dyes. Papanicolaou stain consists of a basic dye, haematoxylin that stains the nucleus and three acid dyes like light green, eosin and orange G that stain the cytoplasm.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBC7558
04128TH
08404TH
15401KE
06325JW

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Color Atlas of Pulmonary Cytopathology (2012)
Huilan Su et al.
Biosensors & bioelectronics, 26(11), 4601-4604 (2011-05-31)
A multiple amplification immunoassay was proposed to detect alpha-fetoprotein (AFP), which was based on ferrocenemonocarboxylic-HRP conjugated on Pt nanoparticles as labels for rolling circle amplification (RCA). Firstly, the capture antibody (anti-AFP) was immobilized on glass carbon electrode (GCE) deposited nano-sized
Shunichi Fukuzumi et al.
Chemical communications (Cambridge, England), 48(79), 9801-9815 (2012-07-07)
Anion binding has emerged as an attractive strategy to construct supramolecular electron donor-acceptor complexes. In recent years, the level of sophistication in the design of these systems has advanced to the point where it is possible to create ensembles that
Cedric L Hugelshofer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 22(42), 15125-15136 (2016-09-08)
We present a full account of the development of a strategy that culminated in the first total syntheses of the unique oxetane-containing natural product (+)-dictyoxetane and the macrocyclic diterpene (+)-dolabellane V. Our retrosynthetic planning was guided by both classical and nonconventional
Barry D Fleming et al.
Analytical chemistry, 77(11), 3502-3510 (2005-06-01)
The underlying electron-transfer and coupled chemical processes associated with biologically important catalytic reactions can be resolved using a combination of Fourier transform ac voltammetry with an analysis of the separated dc and ac components. This outcome can be achieved because
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