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45798

Supelco

Perylene

analytical standard

Synonym(s):

Dibenz[de,kl]anthracene

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About This Item

Empirical Formula (Hill Notation):
C20H12
CAS Number:
Molecular Weight:
252.31
Beilstein:
1911335
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

grade

analytical standard

Quality Level

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.
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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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)
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)
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)
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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