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Sigma-Aldrich

Pyrene

puriss. p.a., for fluorescence, ≥99.0% (GC)

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:
12171500
ID PubChem:
57652921
NACRES:
NA.32

Grado

for fluorescence
puriss. p.a.

Saggio

≥99.0% (GC)

Forma fisica

crystals

Punto di fusione

145-148 °C (lit.)
151-154 °C

Solubilità

ethanol: soluble

Cationi in tracce

Ca: ≤50 mg/kg
Cd: ≤50 mg/kg
Co: ≤50 mg/kg
Cr: ≤50 mg/kg
Cu: ≤50 mg/kg
Fe: ≤50 mg/kg
K: ≤50 mg/kg
Mg: ≤50 mg/kg
Mn: ≤50 mg/kg
Na: ≤50 mg/kg
Ni: ≤50 mg/kg
Pb: ≤50 mg/kg
Zn: ≤50 mg/kg

Fluorescenza

λex 338 nm; λem 375 nm in DMSO

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

Risultati analitici

In addition to the emission maximum at 375 nm, there are lower maxima at 395, 385, 380, 415 and 445 nm.

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

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Perylene sublimed grade, ≥99.5%

Sigma-Aldrich

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1-Bromopyrene 96%

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391573

1-Bromopyrene

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Anthracene analytical standard

Supelco

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Anthracene

1,6-Diphenyl-1,3,5-hexatriene 98%

Sigma-Aldrich

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1,6-Diphenyl-1,3,5-hexatriene

Chrysene analytical standard

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35754

Chrysene

Anthracene suitable for scintillation, ≥99.0% (GC)

Sigma-Aldrich

10580

Anthracene

Zhaowei Guo et al.
Nature communications, 11(1), 959-959 (2020-02-23)
Hydronium-ion batteries are regarded as one of the most promising energy technologies as next-generation power sources, benefiting from their cost effectivity and sustainability merits. Herein, we propose a hydronium-ion battery which is based on an organic pyrene-4,5,9,10-tetraone anode and an
Yan Fang et al.
Drug delivery, 23(9), 3582-3593 (2016-09-30)
A kind of polymeric lipid vesicles (PLVs) with pH-responsive turning on-off membrane for programed delivery of insulin in gastrointestinal (GI) tract was developed, which was self-assembled from the grafted amphipathic polymer of N-tocopheryl-N'-succinyl-ɛ-poly-l-lysine (TP/SC-g-PLL). By controlling the grafting ratio of
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.
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