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48568

Supelco

Fluorene

analytical standard

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About This Item

Formule empirique (notation de Hill):
C13H10
Numéro CAS:
86-73-7
Poids moléculaire :
166.22
Numéro Beilstein :
1363491
Numéro CE :
201-695-5
Numéro MDL:
MFCD00001111
Code UNSPSC :
12000000
ID de substance PubChem :
24872116

Qualité

analytical standard

CofA (certificat d'analyse)

current certificate can be downloaded

Conditionnement

ampule of 5000 mg

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Point d'ébullition

298 °C (lit.)

Pf

111-114 °C (lit.)

Application(s)

environmental

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

C1c2ccccc2-c3ccccc13

InChI

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

Clé InChI

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.

Pictogrammes

Environment
GHS09

Mention d'avertissement

Warning

Mentions de danger

H410

Conseils de prudence

P273 - P391 - P501

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

303.8 °F - closed cup

Point d'éclair (°C)

151.0 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificats d'analyse (COA)

Lot/Batch Number
LRAD5994
LRAC8730
LRAC7242
LRAC4033
LRAB7452

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

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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)
Qianling Cui et al.
ACS applied materials & interfaces, 5(1), 213-219 (2012-12-15)
In the present work, a facile one-pot method is designed to fabricate a core-shell fluorescent nanoparticle (NP) for cellular imaging based on a new cationic conjugated polymer, poly[9,9'-bis(6,6'-(N,N,N-trimethylaminium)fluorene-2,7-ylenevinylene-co-alt-2,5-dicyano-1,4-phenylene] (PFVCN). Gold nanoflowers (AuNFs) are prepared by a seedless method, in which
Fu-Lin Sun et al.
Ecotoxicology (London, England), 21(6), 1651-1660 (2012-06-16)
Polycyclic aromatic hydrocarbons (PAHs) are of great environmental and human health concerns due to their widespread occurrence, persistence and carcinogenic properties. There is now compelling evidence that the mangrove sediment microbial structure is susceptible to PAHs contamination. The study aimed
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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