登录 查看组织和合同定价。
选择尺寸
关于此项目
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
format
neat
storage temp.
2-8°C
正在寻找类似产品? 访问 产品对比指南
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)
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.
Intramolecular pyrene excimer fluorescence: a probe of proximity and protein conformational change.
S S Lehrer
Methods in enzymology, 278, 286-295 (1997-01-01)
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
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持