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经验公式(希尔记法):
C17H10O
化学文摘社编号:
分子量:
230.26
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
221-196-6
Beilstein/REAXYS Number:
1874889
MDL number:
assay
99%
form
liquid
SMILES string
[H]C(=O)c1ccc2ccc3cccc4ccc1c2c34
InChI key
RCYFOPUXRMOLQM-UHFFFAOYSA-N
InChI
1S/C17H10O/c18-10-14-7-6-13-5-4-11-2-1-3-12-8-9-15(14)17(13)16(11)12/h1-10H
mp
123-126 °C (lit.)
Quality Level
General description
1-芘甲醛(PCA)是一种双官能团分子,具有芘基和一个醛基。芘基通过π-π堆积与碳纳米管(CNT)的侧壁相互作用,实现PCA均匀固定在CNT表面。因此,它被广泛用于CNT的表面功能化。它还可用于制造荧光化学传感器。
Features and Benefits
具有可逆的温度调节性质,并且该性质取决于溶剂环境。
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
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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 204, 425-431 (2018-07-04)
Edge-oxidized graphene oxide (EOGO) nanosheets are good acceptors of electrons. We have employed a suitably designed pyrene-tailed fluorescent probe to establish that the electron acceptability of EOGO can be tuned by undulation of the GO sheet. Comparison between EOGO and
A fluorescence probe study of gemini surfactants in aqueous solution: a comparison between n-2-n and n-6-n series of the alkanediyl-a, w-bis (dimethyl alkylammonium bromides)
Silveira Junior, P. B., V. A. O. Tiera, and M. J. Tiera
Ecletica Quimica , 32(2), 47-54 (2007)
Fluorescence probes for critical micelle concentration determination.
E D Goddard et al.
Langmuir : the ACS journal of surfaces and colloids, 1(3), 352-355 (1985-05-01)
Fluorimetric determination of glibenclamide in plasma using pyrene-1-aldehyde.
P G Takla et al.
The Analyst, 107(1279), 1246-1254 (1982-10-01)
Tamara Zoltan et al.
Scientia pharmaceutica, 78(4), 767-789 (2010-12-24)
The synthesis of the meso-tetra(pyren-1-yl)porphyrin (1) was successfully accomplished by means of the pyrrole condensation with pyrene-1-carb-aldehyde in acidic media. Its metallization was carried out in an almost quantitative yield to obtain the corresponding complexes of Ni(II) (2), Cu(II) (3)
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