45798
Perylene
analytical standard
Synonym(s):
Dibenz[de,kl]anthracene
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All Photos(2)
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:
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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.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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)
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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