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48568

Supelco

Fluorene

analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C13H10
Número CAS:
86-73-7
Peso molecular:
166.22
Beilstein:
1363491
Número CE:
201-695-5
Número MDL:
MFCD00001111
Código UNSPSC:
12000000
ID de substância PubChem:
24872116

grau

analytical standard

Certificado de análise (CofA)

current certificate can be downloaded

embalagem

ampule of 5000 mg

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pb

298 °C (lit.)

pf

111-114 °C (lit.)

aplicação(ões)

environmental

formato

neat

temperatura de armazenamento

2-30°C

cadeia de caracteres 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

chave InChI

NIHNNTQXNPWCJQ-UHFFFAOYSA-N

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Aplicação

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.

Pictogramas

Environment
GHS09

Palavra indicadora

Warning

Frases de perigo

H410

Declarações de precaução

P273 - P391 - P501

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

303.8 °F - closed cup

Ponto de fulgor (°C)

151.0 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificados de análise (COA)

Lot/Batch Number
LRAC8730
LRAC7242
LRAC4033
LRAB7452
LC26573V

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

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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)
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
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
Rui Lu et al.
Environmental science and pollution research international, 20(4), 2220-2225 (2012-07-18)
Polycyclic aromatic hydrocarbons (PAHs) are persistent, bioaccumulative, and toxic chemicals and are listed as priority pollutants by the US EPA. Although they are sparsely soluble in water, their solubility can be increased by binding to dissolved organic matter in natural
C Grazia Bezzu et al.
Advanced materials (Deerfield Beach, Fla.), 24(44), 5930-5933 (2012-09-11)
A highly gas-permeable polymer with enhanced selectivities is prepared using spirobifluorene as the main structural unit. The greater rigidity of this polymer of intrinsic microporosity (PIM-SBF) facilitates gas permeability data that lie above the 2008 Robeson upper bound, which is
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