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48570

Supelco

Pyrene

analytical standard

Sinônimo(s):

Benzo[def]phenanthrene

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About This Item

Fórmula empírica (Notação de Hill):
C16H10
Número CAS:
Peso molecular:
202.25
Beilstein:
1307225
Número CE:
Número MDL:
Código UNSPSC:
12000000
ID de substância PubChem:

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

pf

145-148 °C (lit.)

aplicação(ões)

environmental

formato

neat

temperatura de armazenamento

2-30°C

cadeia de caracteres SMILES

c1cc2ccc3cccc4ccc(c1)c2c34

InChI

1S/C16H10/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h1-10H

chave InChI

BBEAQIROQSPTKN-UHFFFAOYSA-N

Informações sobre genes

human ... CYP1A2(1544)

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Descrição geral

Pyrene belongs to polycyclic aromatic hydrocarbon group. These are organic compounds which have two or more fused benzene rings in linear, angular and cluster arrangements. Pyrene is a four ring PAH.
Pyrene is a neat reference standard, which may be used for environmental analysis.

Aplicação

Pyrene may be used as an analytical reference standard for the quantification of the analyte in environmental tobacco smoke samples using high-performance liquid chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogramas

Environment

Palavra indicadora

Warning

Frases de perigo

Declarações de precaução

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

435.2 °F

Ponto de fulgor (°C)

224 °C

Equipamento de proteção individual

Eyeshields, Gloves


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Semivolatile and particulate polycyclic aromatic hydrocarbons in environmental tobacco smoke: cleanup, speciation, and emission factors
Gundel AL, et al.
Environmental Science & Technology, 259(6), 1602-1614 (1995)
Tomohiro Kato et al.
Journal of the American Chemical Society, 135(2), 741-750 (2012-12-18)
Although distance dependence of Förster resonance energy transfer (FRET) is well-studied and FRET has been extensively applied as "molecular ruler", only limited examples of orientation-dependent FRET have been reported. To create a robust FRET system that precisely reflects the orientation
Aurelio Mateo-Alonso et al.
Organic letters, 15(1), 84-87 (2012-12-22)
A solvent switchable rotaxane equipped with a pyrene stopper and with two ferrocenyl units on the macrocycle is reported, in which three different states, two nondegenerate and one degenerate, can be obtained in different solvents at room temperature. This is
Michael E Østergaard et al.
Chemical Society reviews, 40(12), 5771-5788 (2011-04-14)
Pyrene-functionalized oligonucleotides (PFOs) are increasingly explored as tools in fundamental research, diagnostics and nanotechnology. Their popularity is linked to the ability of pyrenes to function as polarity-sensitive and quenchable fluorophores, excimer-generating units, aromatic stacking moieties and nucleic acid duplex intercalators.
Pentti Somerharju
Chemistry and physics of lipids, 116(1-2), 57-74 (2002-07-03)
Pyrene is one of the most frequently used lipid-linked fluorophores. Its most characteristic features are a long excited state lifetime and (local) concentration-dependent formation of excimers. Pyrene is also hydrophobic and thus does not significantly distort the conformation of the

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