257354
1-芘丁酸
97%
别名:
4-(1-芘基)丁酸, PyBA
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关于此项目
经验公式（希尔记法）:
C20H16O2
化学文摘社编号:
分子量:
288.34
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
222-354-7
Beilstein/REAXYS Number:
2140554
MDL number:
产品名称
1-芘丁酸, 97%
InChI key
QXYRRCOJHNZVDJ-UHFFFAOYSA-N
InChI
1S/C20H16O2/c21-18(22)6-2-3-13-7-8-16-10-9-14-4-1-5-15-11-12-17(13)20(16)19(14)15/h1,4-5,7-12H,2-3,6H2,(H,21,22)
SMILES string
OC(=O)CCCc1ccc2ccc3cccc4ccc1c2c34
assay
97%
form
powder
mp
184-186 °C (lit.)
fluorescence
λex 341 nm; λem 376 nm in methanol
λex 342 nm; λem 395 nm (Reaction product)
Quality Level
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Application
PBA可接枝到石墨烯表面，用于制备传感器。它还可制备超级电容电极，作为替代的储能系统。它还可制备光电应用的多层膜。
General description
1-芘丁酸(PBA)是一种共轭聚合物，具有一个大π键和一个羧基基团。它主要用于表面修饰。它具有高荧光效率和稳定性，可用于光电应用。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Wei Song et al.
Biosensors & bioelectronics, 26(7), 3181-3186 (2011-01-25)
A highly efficient enzyme-based screen printed electrode (SPE) was obtained by using covalent attachment between 1-pyrenebutanoic acid, succinimidyl ester (PASE) adsorbing on the graphene oxide (GO) sheets and amines of tyrosinase-protected gold nanoparticles (Tyr-Au). Herein, the bi-functional molecule PASE was
On monolayer formation of pyrenebutyric acid on graphene
Hinnemo M, et al.
Langmuir, 33(15), 3588-3593 (2017)
Ming-Yuan Wei et al.
Biosensors & bioelectronics, 24(9), 2909-2914 (2009-03-27)
A redox-labeled direct competitive electrochemical immunoassay for polycyclic aromatic hydrocarbons (PAHs) was developed. A ruthenium tris(bipyridine)-pyrenebutyric acid conjugate was synthesized as the redox-labeled tracer. Its recognition by an anti-PAH monoclonal antibody was confirmed by surface plasmon resonance. In the immunoassay
Peter Guterstam et al.
Biochimica et biophysica acta, 1788(12), 2509-2517 (2009-10-03)
Cell-penetrating peptides (CPPs) are membrane permeable vectors recognized for their intrinsic ability to gain access to the cell interior. The hydrophobic counter-anion, pyrenebutyrate, enhances cellular uptake of oligoarginine CPPs. To elucidate CPP uptake mechanisms, the effect of pyrenebutyrate on well-recognized
Yongzheng Yang et al.
Organic & biomolecular chemistry, 4(9), 1746-1754 (2006-04-25)
FRET-based fluorogenic substrates for lipases and esterases were prepared in four steps from commercially available building blocks. The substrates are pyrenebutyric acid monoesters of aliphatic 1,2-diols bearing a dinitrophenylamino group as a quencher. The most enzyme-reactive substrate is ester 2a.
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