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48570

Supelco

Pyrene

analytical standard

Sinonimo/i:

Benzo[def]phenanthrene

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About This Item

Formula empirica (notazione di Hill):
C16H10
Numero CAS:
129-00-0
Peso molecolare:
202.25
Beilstein:
1307225
Numero CE:
204-927-3
Numero MDL:
MFCD00004136
Codice UNSPSC:
12000000
ID PubChem:
24872119

Grado

analytical standard

Livello qualitativo

100

CdA

current certificate can be downloaded

Confezionamento

ampule of 5000 mg

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Punto di fusione

145-148 °C (lit.)

applicazioni

environmental

Formato

neat

Temperatura di conservazione

2-30°C

Stringa SMILE

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
BBEAQIROQSPTKN-UHFFFAOYSA-N

Informazioni sul gene

human ... CYP1A2(1544)

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Categorie correlate

Descrizione generale

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.

Applicazioni

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.

Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273 - P391 - P501

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

435.2 °F

Punto d’infiammabilità (°C)

224 °C

Dispositivi di protezione individuale

Eyeshields, Gloves

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
LC18172V
LC11829V
LC05267V
LB88435V
LB82213V

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Benzo[a]pyrene analytical standard, for environmental analysis

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48564

Benzo[a]pyrene

Yanna Liang
Pyrene Degradation by Mycobacterium Sp Kms: Biochemical Pathway, Enzymatic Mechanisms, and Humic Acid Effect, 1-4 (2010)
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
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.
Intramolecular pyrene excimer fluorescence: a probe of proximity and protein conformational change.
S S Lehrer
Methods in enzymology, 278, 286-295 (1997-01-01)
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
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