Skip to Content
Merck
All Photos(4)

Documents

128333

Sigma-Aldrich

Fluorene

98%

Synonym(s):

2,2′-Methylenebiphenyl, Diphenylenemethane

Sign Into View Organizational & Contract Pricing
All Photos(4)

About This Item

Empirical Formula (Hill Notation):
C13H10
CAS Number:
86-73-7
Molecular Weight:
166.22
Beilstein:
1363491
EC Number:
201-695-5
MDL number:
MFCD00001111
UNSPSC Code:
12352100
PubChem Substance ID:
24847846
NACRES:
NA.22

Assay

98%

form

chunks
crystalline powder
crystals
powder
solid

bp

298 °C (lit.)

mp

111-114 °C (lit.)

SMILES string

C1c2ccccc2-c3ccccc13

InChI

1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2

InChI key

NIHNNTQXNPWCJQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Fluorene is a rigid, planar polycyclic aromatic hydrocarbon. White crystals of fluorene have violet fluorescence, from which its name derives. It is used as a precursor to other fluorene compounds. Fluorene is used as a chemical intermediate in the formation of polyradicals for resins as well as the manufacture of resinous products and dyes.

Application

Fluorene was used study the extraction of specific, semiconducting single-wall carbon nanotubes (SWCNTs).

Features and Benefits

As a monomer, fluorene exhibits significant solubility while maintaining a high degree of delocalization.

Pictograms

Environment
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

303.8 °F - closed cup

Flash Point(C)

151.0 °C - closed cup

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

Light-emitting diodes based on fluorene polymers
Bernius M, et al.
Thin Solid Films, 363(1-2), 55-57 (2000)
Zhengcai Guo et al.
Bioelectrochemistry (Amsterdam, Netherlands), 135, 107552-107552 (2020-06-12)
Developing a cost-effective and simple micro-analysis tool has long been an important objective in the toxicological detection of fluorene. In this study, a disposable paper-based micro-analysis device (μ-PAD) was designed using graphite doped with multi-walled carbon nanotubes (MWCNTs) to hand
Synthesis and characterization of new imidazole and fluorene--bisphenol based polyamides: Thermal, photophysical and antibacterial properties
Ghaemy M, et al.
Reactive and Functional Polymers, 73(3), 555-563 (2013)
Masayoshi Tange et al.
Nanoscale, 6(1), 248-254 (2013-11-05)
To understand how fluorene-based polymers selectively extract specific semiconducting single-wall carbon nanotubes (SWCNTs), we compared the optical transitions of SWCNTs wrapped with poly(9,9-dioctylfluorene-alt-pyridine) (PFOPy), i.e., structure-selective polymers, with those wrapped with poly(9,9-di-n-dodecylfluorene) (PFD), i.e., non-selective polymers, in organic solvents by
Willian G Birolli et al.
Marine pollution bulletin, 129(2), 525-533 (2017-10-23)
The biodegradation of polycyclic aromatic hydrocarbons (PAHs) by marine-derived fungi was reported in this work. Marine-derived fungi (Trichoderma harzianum CBMAI 1677, Cladosporium sp. CBMAI 1237, Aspergillus sydowii CBMAI 935, Penicillium citrinum CBMAI 1186 and Mucor racemosus CBMAI 847) biodegraded anthracene
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