48570
芘
analytical standard
别名:
苯并[def]菲
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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
EC Number:
204-927-3
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
1307225
MDL number:
NACRES:
NA.24
产品名称
芘, analytical standard
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
analytical standard
CofA
current certificate can be downloaded
packaging
ampule of 5000 mg
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
mp
145-148 °C (lit.)
application(s)
environmental
format
neat
storage temp.
2-30°C
Quality Level
Gene Information
human ... CYP1A2(1544)
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Application
Pyrene may be used as an analytical reference standard for the quantification of the analyte in environmental tobacco smoke samples using high-performance liquid chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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.
Pyrene is a neat reference standard, which may be used for environmental analysis.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
435.2 °F
flash_point_c
224 °C
ppe
Eyeshields, Gloves
Semivolatile and particulate polycyclic aromatic hydrocarbons in environmental tobacco smoke: cleanup, speciation, and emission factors
Gundel AL, et al.
Environmental Science & Technology, 259(6), 1602-1614 (1995)
Yanna Liang
Pyrene Degradation by Mycobacterium Sp Kms: Biochemical Pathway, Enzymatic Mechanisms, and Humic Acid Effect, 1- 4 (2010)
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
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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