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经验公式（希尔记法）:
C16H10
化学文摘社编号:
分子量:
202.25
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-927-3
Beilstein/REAXYS Number:
1307225
MDL number:
InChI key
BBEAQIROQSPTKN-UHFFFAOYSA-N
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
SMILES string
c1cc2ccc3cccc4ccc(c1)c2c34
grade
certified reference material
agency
BCR®
manufacturer/tradename
JRC
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
145-148 °C (lit.)
format
neat
storage temp.
2-8°C
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General description
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.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)
Analysis Note
For more information please see:
BCR177R
BCR177R
Legal Information
BCR is a registered trademark of European Commission
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
435.2 °F
flash_point_c
224 °C
ppe
Eyeshields, Gloves
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - PBT - vPvB
Yanna Liang
Pyrene Degradation by Mycobacterium Sp Kms: Biochemical Pathway, Enzymatic Mechanisms, and Humic Acid Effect, 1- 4 (2010)
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
Intramolecular pyrene excimer fluorescence: a probe of proximity and protein conformational change.
S S Lehrer
Methods in enzymology, 278, 286-295 (1997-01-01)
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
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