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Key Documents

48568

Supelco

Fluorene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C13H10
CAS Number:
Molecular Weight:
166.22
Beilstein:
1363491
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

Quality Level

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

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

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Certificates of Analysis (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)
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

Protocols

US EPA Method 8270 (PAH only): GC Analysis of PAHs on SLB®-5ms

US EPA Method 610 describes the analysis of polynuclear aromatic hydrocarbons (commonly referred to as PAHs or PNAs) by both HPLC and GC.

HPLC Analysis of PAHs on SUPELCOSIL™ LC-PAH

GC Analysis of Polynuclear Aromatic Hydrocarbons (PAHs) in Salmon on SPB®-608 (20 m x 0.18 mm I.D., 0.18 µm) after QuEChERS Cleanup using Supel™ QuE Z-Sep, Fast GC Analysis

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