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Documentos

45798

Supelco

Perylene

analytical standard

Sinónimos:

Dibenz[de,kl]anthracene

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About This Item

Fórmula empírica (notación de Hill):
C20H12
Número de CAS:
198-55-0
Peso molecular:
252.31
Beilstein/REAXYS Number:
1911335
EC Number:
205-900-9
MDL number:
MFCD00004142
UNSPSC Code:
41116107
PubChem Substance ID:
329756959

grade

analytical standard

Quality Level

100

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

276-279 °C (lit.)

application(s)

environmental

format

neat

SMILES string

c1cc2cccc3c4cccc5cccc(c(c1)c23)c45

InChI

1S/C20H12/c1-5-13-6-2-11-17-18-12-4-8-14-7-3-10-16(20(14)18)15(9-1)19(13)17/h1-12H

InChI key

CSHWQDPOILHKBI-UHFFFAOYSA-N

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General description

Perylene belongs to the class of polycyclic aromatic hydrocarbons. It is a hydrophobic fluorescent probe used for imaging lipid bilayer membranes.

application

Perylene may be used as an analytical standard along with a mixture of polycyclic aromatic hydrocarbons (PAHs) to determine the spatial distribution and sources of PAHs in surface sediments of rivers. It may also be used as an analytical reference standard for the quantification of the analyte in water samples using spectrofluorimetric technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
BCCK0718
BCBZ5253
SZBE206XV
SZBE014XV
SZB9030XV

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Fluorescence probe partitioning between Lo/Ld phases in lipid membranes
Baumgart T, et al.
Biochimica et Biophysica Acta - Biomembranes, 1768(9), 2182-2194 (2007)
Simultaneous synchronous flourimetric determination of benzo [a] pyrene and perylene in micellar media
Rodriguez SJJ, et al.
Analytica Chimica Acta, 255(1), 107-111 (1991)
Distribution and sources of polycyclic aromatic hydrocarbons in surface sediments of rivers and an estuary in Shanghai, China
Liu Y, et al.
Environmental Pollution (Barking, Essex : 1987), 154(2), 298-305 (2008)
Alessandro Sanguineti et al.
Chemical communications (Cambridge, England), 49(16), 1618-1620 (2013-01-23)
Highly efficient plastic based single layer Luminescent Solar Concentrators (LSCs) require the design of luminophores having complete spectral separation between absorption and emission spectra (large Stokes shift). We describe the design, synthesis and characterization of a new perylene dye possessing
Mykhaylo Myahkostupov et al.
The Journal of organic chemistry, 78(17), 8634-8644 (2013-08-15)
We have synthesized and thoroughly characterized two representative ladder-type acetylene-bridged perylenediimide dimers bearing long alkyl chain solubilizing groups, bis[1-ethynyl-N,N'-bis(1-hexylheptyl)-perylene-3,4:9,10-tetracarboxylic diimide] ([PDICC]2, 1) and 1,1'-ethynyl-bis[N,N'-bis(1-hexylheptyl)-perylene-3,4:9,10-tetracarboxylic diimide] ([PDI]2CC, 2). In these dimeric PDI molecules, NMR-based structural characterization became nontrivial because severe (1)H
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