128333
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:
Molecular Weight:
166.22
Beilstein:
1363491
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
chunks
crystalline powder
crystals
powder
solid
crystalline powder
crystals
powder
solid
Assay:
98%
Pricing and availability is not currently available.
Recommended Products
Quality Level
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
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.[1]
Application
Fluorene was used study the extraction of specific, semiconducting single-wall carbon nanotubes (SWCNTs)[2].
Features and Benefits
As a monomer, fluorene exhibits significant solubility while maintaining a high degree of delocalization.[3]
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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)
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
Light-emitting diodes based on fluorene polymers
Bernius M, et al.
Thin Solid Films, 363(1-2), 55-57 (2000)
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
S A Schmid et al.
Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 370(1972), 3787-3801 (2012-07-04)
We have investigated the energy transfer dynamics in a supramolecular linear polymer chain comprising oligofluorene (OF) energy donor units linked by quadruple hydrogen-bonding groups, and oligophenylene (OPV) chain ends that act as energy acceptors. Using femtosecond spectroscopy, we followed the
Active Filters
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
