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48568

Supelco

Fluorene

analytical standard

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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:
12000000
PubChem Substance ID:
24872116

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 5000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

298 °C (lit.)

mp

111-114 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-30°C

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

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Application

Fluorene has been used as a test material in studying its electronic transitions in gas and crystalline phases, and in stretched polymer sheets, measured with synchrotron radiation.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LRAD5994
LRAC8730
LRAC7242
LRAC4033
LRAB7452

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Electronic transitions of fluorene, dibenzofuran, carbazole, and dibenzothiophene: From the onset of absorption to the ionization threshold.
Nguyen D D, et al.
Journal of Molecular Spectroscopy, 264(1), 19-25 (2010)
Michèle J Régimbald-Krnel et al.
The Journal of organic chemistry, 78(17), 8789-8795 (2013-08-15)
Diphenylcarbene (DPC) generated by high-intensity laser photolysis of diphenyldiazomethane rearranges to fluorene (FL) by two distinct mechanisms as revealed by methyl-group labeling. Thus, excimer laser irradiation of p,p'-dimethyldiphenyldiazomethane generates 3,6-dimethylfluorene (3,6-DMF) and 2,7-dimethylfluorene (2,7-DMF), which were identified by fluorescence measurements
Ute B Cappel et al.
Nano letters, 12(9), 4925-4931 (2012-08-24)
Solid state dye-sensitized solar cells (sDSCs) employing the hole conductor 2,2'7,7'-tetrakis-(N,N-di-p-methoxyphenyl-amine)-9,9'-spirobifluorene (spiro-MeOTAD) require the presence of oxygen during fabrication and storage. In this paper, we determine the concentrations of oxidized spiro-MeOTAD within devices under different operating and storage conditions by
Le Bao et al.
The Analyst, 137(17), 4010-4015 (2012-07-12)
This work aims at the development of a fast scanning method for organic pollutants with low-cost small Raman spectrometers. A gold nanoparticles-embedded alginate gel is prepared and applied as the substrate for surface enhanced Raman spectrometric detection of polycyclic aromatic
Shuying Ma et al.
Chemical communications (Cambridge, England), 48(97), 11847-11849 (2012-11-02)
A novel 3D donor material (SF8TBT) based on spiro-fluorene has been developed. Compared with the corresponding 1D linear molecule, the OPVs of this 3D donor exhibited power conversion efficiencies of 4.82%, much higher than that of 1D small molecules (1.69%).
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