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48568

Fluorene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H10
CAS Number:
86-73-7
Molecular Weight:
166.22
EC Number:
201-695-5
UNSPSC Code:
12352200
PubChem Substance ID:
24872116
Beilstein/REAXYS Number:
1363491
MDL number:
MFCD00001111
NACRES:
NA.24
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grade

analytical standard

Quality Level

100

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

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.

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pictograms

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

flash_point_f

303.8 °F - closed cup

flash_point_c

151.0 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
LRAE0306
LRAE0774
LRAD5994
LRAC8730
LRAC7242

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Articles

Polynuclear Aromatic Hydrocarbons Analysis by HPLC for Olive Oil

Highly accurate HPLC-FLD method for evaluating 15 PAHs in olive oil using Ascentis® Express PAH HPLC column and SPE cleanup, following GB 5009.265-2021.

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)
Pierre Lovera et al.
Journal of nanoscience and nanotechnology, 13(7), 5194-5202 (2013-08-02)
Organic nanowires based on a fluorene homopolymer and a copolymer, i.e., poly(9,9-dioctylfluorene), F8, and poly(9,9-dioctylfluorene-co-benzothiadiazole), F8BT, respectively, were synthesised by solution assisted wetting of porous anodic alumina templates. Nanowires ranged between 3 microm and 50 microm in length, and were
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
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Global Trade Item Number

SKUGTIN
4856804061838086525